Seeing Beyond: The Connection Between Nature and Self

Nature does nothing uselessly.

-Aristotle

I went to Beaver Creek Conservation Area for a walk last week. Only one tick! But many, many mosquitoes. While in their interpretive centre, I read about plant blindness. Plant blindness means missing all the plants on your trail. It is experienced when we are walking in nature. Yet completely missing the beauty and wonder of what is right in front of us. We miss the beauty of all the plants and flowers, even wildlife. Perhaps focusing on the end of the trail instead of the journey.

How is your “plant sight”? Today on the blog we will make connections with plant blindness. As it applies to nature. And taking it further to see how we can see ourselves in the plants that are being missed. Or misunderstood for what they have to offer. Are you one of those plants? I felt like one just last week.

First, as always, I invite you to join me on Facebook, Instagram and X. We are holding walks and making big plans! Don’t miss out. Follow my social media to stay up to date. I also have uplifting thoughts and quotes to share. Find all the links in my link tree.

Confessions of a Partial Plant Blindness Victim!

I have to admit, I have partial plant blindness. I miss things that are right in front of me. Until they are pointed out. I have a friend who has 20/20 plant sight. She sees it all. She says she has been raised that way. She is teaching me how to see what is right in front of me. And to appreciate it. We are loving our plant identification app Seek. It keeps track of the plants we have seen. And can provide more information on them too.

When I see the plants. And I have used my app to identify them. I know them better. I see those plants everywhere once I have taken the time to slow down and develop a connection. I would like to apply this process to seeing, identifying, knowing and connecting with each other. As fellow humans.

Humans in Their Natural Habitat

We all need to feel seen. I speak of my life experience since that is what I know. In chronic illness being seen is wonderful. To feel noticed is to feel embraced. To know that someone can identify what I am experiencing is even more calming. I don’t have to explain everything to them. They already know. Often this comes from having similar experiences. My chronic comrades understand me. They can identify when I am struggling. And when I am in more pain than usual. We come to know one another. This connection is life-giving. And life-altering. I love my chronic comrades.

We see in one another the common strains. That the healthy might not see or comprehend. The shame in trying to fix it and only getting worse. The getting worse while others have a health crisis then get better and carry on with their lives. The constant getting behind in housework and self care. The financial strain and feeling beholden to others. Having felt burned in the past by those who were supposed to help. Feeling blamed for circumstances not within my control. Lack of resources and information for our conditions. Not knowing if there will be a pain I cannot treat or handle. Feeling abandoned while society carries on. Being over reactive due to our strained nerves. The loss. The mental and emotional exhaustion. Feeling missed and misunderstood.

I love those who seek to understand our world. Last week I experienced a moment where I felt unseen by someone trying to help. In that moment, I felt the gulf between us, where I hoped to have sensed connection.

So Here’s The Low-Down…

A four-year degree has not fit in my life. As such, I am limited on what I can offer the world. I highly regard those who go back to school at any time, especially those in my age group. And I highly regard getting an education.

In the past I have spoken of going back to school wistfully. And been bombarded with counter arguments of why I should just go and do it. This happened again last week. There seems to be a movement of well-wishers and dream-pushers. “You can do it!” “Just try!” “Believe in yourself” “It’s never too late”. “Spread your wings and fly!” But some of us were not meant to fly.

The Irony of Explaining Things: A Guide to Not Being Understood

People with chronic conditions will always be capable of accomplishing anything and everything. But where we choose to place our energy HAS to be the right thing. We have to be picky. And our experience is still valid and monumental, despite the lack of paycheck that would suggest otherwise 😉.

I have not found the right words to explain to the masses, my level of brain function. It dangerously closely resembles getting older and being tired. So many of us live there!

It seems a ridiculous thing to defend. But my brain function is worse than your brain function. Years of pain and stress and overload have maxed my brain’s capacity. Now, the best it can do, is not great. And I’ve come to terms with it. When a well-meaning individual tries to persuade me otherwise. That I just need to start using it again and it will be fine. The gulf seems wider between me and the rest of humanity.

They were correct in assuming I am capable of going back to school. I would pass the classes and get all the credits. But what I’d lose in the process has to be taken into consideration.

Your garden isn’t thriving because every time a flower blooms you cut it to prove to someone else that you’re a gardener. Focus, please.

-Unknown

Maneuvering the Costs and Stresses of Chronic Illness

My life is a constant cost: benefit ratio analysis. I have done the math. School is not in the cards. Let me be wistful and let it go. Trust that I know what I can handle. Trust that it is different from what a typical body can handle. Mine does not handle stress well. Putting it through four years of stressful situations would be a terrible idea!

All of us chronic comrades have been through years of our own scholarship program. Like me, maybe you have no degrees. No fancy letters after your name. But we have learned. We have gained. We have built and then rebuilt. We have understanding no school can ever teach. And we have much to offer the world in our various capacities.

Like a wildflower; she spent her days, allowing herself to grow, not many knew of her struggle, but eventually all; knew of her light.

-Nikki Rowe

A Quirky Academy for the Chronically Challenged

We are not on the same plane as the rest of humanity. We have our own training and instructors. And we do not need to force our bodies to a pace and strain they cannot handle. To prove we are the same. We are not. And the good news is, we are not supposed to be.

I know my body. My pain requires time and energy. Time for nature and grounding. Energy to rest and digest. I push myself to my own limits. In my own time frame. Within peace. I need time for therapies. Even a micro dose of therapies. E.g, Forest therapy!

Art therapy!

This is how I survive my high pain days. I could choose to put it all aside for a time and focus on a formal education. It would take days, not weeks, for my body to start shutting down. As it took on more pain and stimuli than usual. It has done this before.

All I need to do is participate in life for more than a day or two in a row. My body will throb. I will feel like I have been hit by, then dragged behind a truck. Not from getting sick but from engaging in too much life. I won’t have to talk about the toll it’s taking. There will be signs 👇🏼 .

The C Factor: Six Key Traits

Instead I would like to center my life and focus on where I have been and what I have gained. In these six characteristics for example:

  • Compassion– I am learning compassion for myself and others. When my life looks different from others’. I take time to feel my sadness and frustration. Then I move forward trusting in my own intuition.
  • Curiosity– I know that when I get angry, there is another option, I can get curious. When a car cuts me off in traffic. I can be curious as to why they did that instead of zipping around him indignantly. Perhaps he was distracted by a child in the back seat.
  • Calm– This word was not in my vocabulary as a working mom in constant pain. I would laugh and think there was no time or space to be calm. I see now that everyone needs time and space for their nervous system to be calm. A time where despite what is happening around you, peace exists. Now I know the word and the feeling.
  • Clarity– I am cultivating a sense of clarity. This comes with practice. And trusting my intuition to guide me to what is right for me, even when that looks vastly different from the lives of others around me.
  • Courage– Now I know. Courage looks different for everyone. Courage to face another day. Courage to keep fighting. Courage to go back to school. Courage to not go back to school. Courage to stand in what I know.
  • And Creative!- I placed little importance on creativity after my elementary years. Such a waste of time, my brain told me. Who needs it? Boy, was I wrong!

Meliorism (noun)- the belief that we can contribute to positive change and improve the world through acts of love, creativity, compassion, and kindness.

livefreelaurad

The Two Hemispheres: Battling Personas?

We all know the brain has two hemispheres.

The left is about productivity. Control. Fear. Our society thrives on living in our left hemisphere. And (somewhat) rightly so! Our society is built on people accomplishing and achieving. We benefit from their ideas and efforts.

On the other side we have the right hemisphere. Its focus is about enjoyment. Meaning. Purpose. Delight and creation. Our society’s less sought-after focal points.

Here’s something I find fascinating about the two hemispheres.

The left hemisphere has a quality where it does not realize that anything but itself exists. That its own world view is the only thing in existence. Do you know that guy? We are all that guy. The left brain is that guy who thinks he knows everything.

The right hemisphere, on the other hand, does not have this quality. It knows the left hemisphere is doing things that are different and it watches with amused tolerance. I also know these people.

Who would you rather spend all your time with between these personas, represented by the two hemispheres? You don’t have to choose between the two hemispheres. You just need to find your correct balance.

Progress with Purpose

At no day, no hour, no time are you required to do more than you can do in peace.

-Melody Beattie

I love this quote. It rests in my bones and resonates with truth. School would require more than I could do in peace. Through this experience I felt misunderstood and I wanted so much to convince the other party that I was right. I needed a step back to see where the hurt was hiding. And how to manage a confrontation like that in the future.

I tell you all this in hope that some of you can relate. Maybe not exactly the same way. But we have all felt missed and misunderstood. Have you been tempted to base your life on what people think you should do?

So many people are living a life that’s not right for them and using substances or stimuli of other kinds to numb their feelings or to pull themselves up to a sense of okayness.

-Martha Beck

Martha Beck is Oprah’s life coach. She says when you are living a life that is not yours. It’s like standing on a nail and taking opium to make yourself not feel the nail. But the cure is not taking the drugs. The cure is taking the nail out of your foot.

See. Identify. Know. Connect. With others. Listen to and trust the assessment that others give to their own life. Focus on your therapies you know you need. And traits like the six key traits. Beware the battle of the brain hemispheres. You are only required to do what you can do in peace. If you are living a life that is not yours, take the nail out. And step in the right direction.

As we Canadians prepare to go to the lake for the long weekend. I leave you with these words of how you can be more like water.

Be Like Water

  • You can go with the flow of others or find your own current to take you where you want to go
  • Make new paths. By the power of steady single drops of water new pathways can be made through any terrain.
  • Let go. Sometimes we just need to let the rain pour. The tears flow. The old to be washed away.
  • Sparkle. Be you and shine. Don’t imitate the sparkle of others, you have your own.
  • Be still. Take time to be still. To see what’s under the surface. To allow for change.
  • Reflect. In those moments of stillness, reflect. On your good life. On the good you have to offer. On the wild and exciting ride ahead.

Every particular in nature, a leaf, a drop, a crystal, a moment of time…partakes of the perfection of the whole.

– Ralph Waldo Emerson

Unlocking Joy: Embrace Play and Creativity

To watch spring unfold is to see the earth smile after its long nap.

-Author Unknown

Do you know how to play? I have learned the importance of play and what it does for my nervous system. In this post I offer suggestions of forms of play. Caution for my chronic comrades regarding play. How to incorporate play into our already busy lives. Why play continues to be important for us as adults. Followed by a tribute to Mother Nature for Mother’s Day. Finally I’ll introduce you to my cousin Kate.

Think back, what did play look like for you as a kid?

Then, make sure you are subscribed to the blog. We are changing things up for an opportunity I have upcoming. How my business runs will be significantly altered and I am so excited to share it all with you. Stay tuned for that!

Kefi: Celebrating the Essence of Life and Joy

Kefi is a Greek philosophy. According to kefiyoga.com, “kefi is an overpowering emotion you have when you completely let go in the moment, release inhibition, and allow yourself to joyfully feel the life pulsing through your body and soul.”

What creates this type of feeling in you? Before learning the type of living described by the Greek philosophy of kefi, I enjoyed things. But I didn’t recognize the life fulfillment and easing of symptoms I would experience in truly celebrating life and joy.

From Playgrounds to Paperwork: When Did Fun Take a Backseat?

Art, music, dancing, there was a time that these were top-priority areas to develop. Now they are skills in which to work and succeed at high levels only. We do them to get good at them not because it is something our soul needs to do. As a career choice they are absurd. So say the masses.

Balancing Act: The Cost: Benefit Ratio of Playing, While In Chronic Pain

For most people, play is an energy giver. When you are low on energy, introducing play into your daily activities can be a great idea. But as a chronic comrade we have to do a little more thinking and planning ahead. This is where I think of play in a cost: benefit ratio. There is a cost every time we rise from bed or take an outing in our world. Play is one area that I encourage you to find a way. I hope you find a way to play where the cost is worth the benefit that comes from it. We should all be so lucky.

👆🏼Sometimes this is the best we can do, is it worth the pain👆🏼 I have some things that are.

This is my form of play. I enjoy wearing this goofy helmet cover and making people laugh. Some of my favorite reactions are from dogs that don’t know what to think. Moms that laugh and try to get their teens to laugh. *said teen looks up from phone, emotionless expression engaged, looks back down.* Little old ladies laugh out loud. People who see and laughter erupts from them. This is play to me.

Also this 👇🏼. We aren’t there quite yet this year, but my lake looks ready to play. I went to check it out on Saturday.

Playtime Hosts: From Board Games to Bad Decisions

We don’t all have the same play styles as adults. Makes sense since as kids we had different play styles too. Here are some adult play styles I have witnessed.

  • Kinesthetic- we all know the guy that gets so excited when things are fun that they start sensory seeking. I am married to that guy @saskmunk . He put his knees through the ceiling of a buddy’s place while swinging down the stairs. He slid down a sand hill scraping his entire back up. He flipped for the crowd and broke a rib. He has calmed down in his old age. Do you enjoy a kinesthetic play style?
  • Competitor- How about a friendly-not-so-friendly board game or sport? This is so far from my play style it makes me uncomfortable. Perhaps because of the one I grew up with that claimed this style. @carrierice134 If this is you, lean into it. Be courteous and all, but find other people who like to test their limits against the skills of someone else. Be competitive!
  • Creator- When you have an art room and love all things art, you fit perfectly in the creator play style. @soulfullifebyamanda Whether it is with paints, rocks, doodles, words, the options are endless. You are constantly seeing ways to enhance the world around you.
  • Joker- As long as it is not at someone else’s expense, I am all for jokes. I heard someone say. The Tickle Me Elmo was a good example of how to make someone laugh and to laugh along. We don’t pick up the Elmo and just laugh at him. That’s not funny. Not until the other guy is laughing. See if this one works for you. Text another joker at 7am and say you are on your way to their place. When you have no plans with them. Just to make their day a little more fun. 😆 My father in law is front of mind when I think of this type of play and fun.
  • Director- You know who you are. You love to lead. You love to come up with the idea and have others follow along. Sometimes it’s your little sister. Who is taller than you, louder than you, and you are just a little bit scared of her. @kristajulseth Don’t hide your strengths! Be bold with those who want to follow. I am one who likes to be guided. To each her own.
  • Storyteller- Gather your tribe. And share your stories. The best stories are filled with laughter. The first thing I noticed about my friend Sharla is that she tells stories with her whole heart and hands. @sharlaboehme I love that about her. Or you can gather your stories and share in a unique way. I filled photo albums with pictures of my boys as they grew. And goofy stories of what they did when they were young. They are a gift treasured by both grandmas that received them.
  • Introverted experience- this will take many shapes, for those who enjoy a quiet space. It looks different from other types of play. Possibilities include collecting and exploring, perfect things to do in Forest Therapy! For this I gotta go with my other, other sister. @lmfinch51 is the queen of enjoying an introverted experience. We can all learn from her!

What type of play most resonates with you? Think about that type of play and how to incorporate it into work times and rest times. As you peruse the rest of this post.

Work, Meet Playtime; Playtime, Meet Work

When you are at work, you owe your time and your skills to your employer. I do not want to suggest that we should slack off or be dishonest about our work time. I propose that there is a way to incorporate play in a way that will check both boxes. If you are a telemarketer, see if you can casually bring up a random word you and a co-worker choose. If you drive deliveries, create a playlist that will rock your world and keep adding to it. In your rest hours, you will have more options.

Why Adults Should Play: A List of Compelling Reasons

Why is play so important? We know kids will learn things way faster if we incorporate play into their day. Can it still benefit us as adults? The answer is a resounding YES! Here is my top ten list of reasons why play continues to be important as adults.

  1. Play encourages creative thinking and boosts problem-solving skills
  2. Play can improve physical health as there is usually movement involved
  3. Play helps us practice using good communication skills, to keep it fun we work together
  4. Play increases resilience helping us see a more positive outlook
  5. Play improves mood when dopamine is released (dopamine is our pleasure and reward hormone)
  6. Play enhances learning by keeping us curious and engaged
  7. Play can be a way to practice working together in our relationships and this can transfer to other arenas where we need those skills
  8. Play is a way to strengthen our longevity, giving us a reason to keep going
  9. Play has been shown in research to increase productivity, those encouraged to take a short break and engage in play came back more focused
  10. Play amplifies our quality of life. When we take time to play in any area of interest, life becomes a little more sweet.

Latin lesson for the week. That I realize I have no business giving but this is what google says. It resonates with me as a chronic comrade, so I will share. In Latin, Audere est Facere means “To do is to dare”. Where can you apply this principle? Dare to play! Dare to laugh! Dare to rise! It’s good for you.

Mother Nature: The Ultimate Caregiver

This week as we prepare for Mother’s Day, I think of my mother and grandmothers. My sisters and friends that are mothers and all those that have a mothering heart. Another mother that I recently recognized for her mothering attributes, is mother nature. How can you allow mother nature to nurture you as a mother would this week and through the year?

Her Sunlight provides vitamin D, energy and regulation of sleep patterns

Her Plants provide nourishment and healing, reducing stress and anxiety

Her Water cleanses, hydrates, and relaxes.

Her Bird’s Songs lower cortisol, and encourage mindfulness.

Her Trees purify the air, boost immunity and calm anxiety.

If you are still overwhelmed or unsure of how to get started, meet Kate @mate8219. I have a cousin named Kate. She is one of the best examples of play to me. She still has a contagious aura of fun when we gather our crew. I appreciate her example of joy. It makes me want to be better. Let’s all be a little more like Kate and see ways to play in our work and rest times.

Lesson I’ve Learned From Kate To Get You Started:

  1. Laugh- laughter really is one of the best forms of medicine, Kate has THE best laugh, find times and places, and people to laugh with, watch something that makes you giggle
  2. Play with kids/grandkids- this one is my favorite, even when he puts a rib out, it was worth the cost, follow them and see what makes them come alive, I remember following Kate as a little one
  3. Stay curious- our kids are great examples of this, they don’t decide they know and close their mind, they stay open and filled with wonder and curiosity
  4. Try something new- a dance, a blog, a recipe, anything that speaks to you, Kate is always the first one to jump on a chance to try something new and exciting
  5. Creative endeavors- we all need a creative outlet, what will yours be? will it be incorporated in your play for the day? maybe singing into a karaoke mic whatever comes to mind (that’s what Kate does 😉).

As my mother always said in this type of weather, now go outside and find something to play!

My favorite weather is bird chirping weather.

-Terri Guillemets

Transforming Obligation Exhaustion into Obligation Anticipation

Outside it is warm and blue and April.

-Sylvia Plath, The Journals of Sylvia Plath

Obligation Exhaustion: Is It Just Me?

Are you exhausted by your obligations? Where did this idea come from that our time is being stolen by our obligations? That obligations are the enemy? I just want to sit in my blanket fort and pretend I don’t hurt while I color with my grandson. I have wondered if ignoring all of my obligations was the answer. As someone who suffers from chronic pain, do I ever get to have any freedom or autonomy? I have learned a better solution. Obligation anticipation. What does obligation anticipation look like? And how does forest therapy apply? These are the questions I’ll be tackling today. Beside all this I have a crocus tea party to share. AND a confession from the bedroom! 😳

But First! We are so close to actual, boots on the ground, forest therapy. I would be thrilled to have you join me for a forest therapy walk. Our first group walk will be held on Saturday, May 3rd at 10am. The cost is $25 for 2-3 hours of healing through a connection with nature. All you need is a good pair of shoes. The trail we will take is dry. This walk will be a moderate level. Meaning you should be able to step up and down stairs. And get down into a seated position for a short time. You can expect a short intro to forest therapy at the beginning of our walk. A portion of our walk will be in silence. Other portions will be seated on the ground with socks and shoes off. I will give invitations of beginner-level meditation. If you have any questions and to book your spot, contact me on my How To Get in Touch page. You can fill out the subscribe form and include a message requesting a spot. Or you can email me directly, pam.munkholm@gmail.com. Our first walk will be held at Cranberry Flats, just outside Saskatoon city limits to the south on Lorne Avenue. Payment can be made at the trail head by cash or e-transfer to pam.munkholm@gmail.com. I will post a pin and a reminder on all of my social media on Friday. Check there if you need any help getting to our meeting location and for final confirmation. We will meet at the head of the trail by the parking lot. I hope to see you out there!

CRANBERRY FLATS CONSERVATION AREA April 25, 2025

Back to obligation exhaustion. Obligations are not the enemy. You can have freedom, not by controlling outside circumstances. (pssst! you can’t control outside circumstances, stop trying, it’s exhausting!) but by doing something within your control. Sound too good to be true? Keep reading.

Autonomy: Your Great Escape Artist?

You have choices and control in your life. So if you are looking for autonomy, you have it. Who scheduled your day? Who decided to go to work, school, driving kids around, or otherwise. You could say, “well, I have to go to work or I will lose my house.” That is you choosing to be autonomous. You are choosing that you want a house and you want to fulfill your financial responsibilities. That is you using your freedom.

Have you ever scheduled your life so tight that you have no room to breathe? That is also you using your freedom. You may say “well, I have kids and they need to get to activities.” That is you using your autonomy to say, my kids are important to me. Their fitness and social development are a priority and I believe sports will help them learn those values. So I am choosing to put time and energy to this.

One way to avoid obligation exhaustion is to recognize that our non-choices are choices too. When we get sucked in to the social norm. This is also our choice. Do not be distracted by non-choices.

When we take this first step to recognize that we have a choice, our day is not less full. But our experience is changed. Obligation exhaustion is not all about what we do and when we do it. But our relationship to what we are doing. This is an inner experience that we have 100% control over. Regardless of the external circumstances.

We think of a life with no deadlines, no obligations, no responsibilities to others as a life of autonomy. But this logic is flawed and will set us up for disappointment, Every time! Bringing us to this breaking point:

We all live and work with others. This means there will always be external constraints. But the good news is that our brain does not discern the difference between external choice and perceived choice. When we believe we are making a choice. Even if that choice is made within constraints. Our brain activates the rewards centers associated with autonomy and motivation.

By contrast, when we perceive we have no choice, it activates the stress response. This in turn impairs cognitive function. And decreases motivation. Think about it, when you are over-scheduled, how do you feel? Awful! This may also stem from a developing sense of victim-hood.

There is an obligation illusion. I expect my chronic comrades are familiar. “I have to…” “I need to…” We feel trapped by our lives. Where is our choice?

Answers in Strategies; Not Just Semantics

It is not word play. Try this.

When you “have to” take care of yourself. When you “need to” follow up with another doctor. You are trapping yourself. Reframe it. When you change the words and the energy to I “get to” take care of myself. So I can support my family when they need me. Or I “am pursuing” a path to better health. The best way to navigate that path is to see the next doctor.

This is the way you can go from entrapped to empowered.

Feeling empowered leads to the brain activating centers associated with motivation, creativity, and resilience. Feeling entrapped leads to feelings of stress, threat, and overwhelm.

A note here to my chronic comrades. Your first job is to ask yourself, should I be doing this thing. Because able bodied people will often ask us, “can you do the thing?” Our response may be: “yes, BUT it will hurt me later/ ruin tomorrow/ trigger a flare/ exhaust me/ make things worse and then I will need to up my dosage/ spend a day in bed/ cancel all other plans”. Able bodied people will hear the ‘yes’: “excellent! so you can do it.” Our first question should be: am I supposed to be here? Once that has been established, carry on to these three steps to go from obligation exhaustion to obligation anticipation.

Our first step towards obligation anticipation is to recognize that we have a choice. Second, reframe how you think and speak about the obligation. Our stories and language matter. Third, recognize the value that you are expressing in your freedom of choice. Is this for my family? For me? Keep using your obligation anticipation muscle and it will get stronger.

Those who have chronic everything can benefit from practicing micro moments of autonomy. Maybe I can’t get outside today. But I can open the curtains and get the sun on my face. Maybe I have to cancel plans with a friend. But I can get my feet in the grass. Find and appreciate the wins.

If you want to learn more about this idea, visit the https://neillwilliams.com/success-genius-podcast. Most of the information I share here is based on her podcast Episode 272: Beyond ‘Have To’: Reclaiming Choice in a World of Commitments

Obligation: An Illness-Inspired Game of Survivor!

When you suffer from chronic pain and illness, what is your obligation? Taking care of yourself has to come first. That means a career and/or school will move to the back burner or come off the stove all together. It’s a hard choice either way. Obligations change in chronic illness.

Is “Back Off” A Socially Acceptable Response?

I struggle to answer the question, so what do you do? Do you have kids at home? Going back to school? Work outside the home? The answer is no. And then what? My latest attempt is something like, “I am taking care of me”. But that sounds like I am listening to a self help course from the 80s.

I think I am getting closer with this response. Yes I do have a job. My job is to take care of myself and try to be my version of healthy. If further explanation is required, That includes getting enough rest. Jumping through hoops to find correct medications and therapies. Getting outside and healing in nature. Or something of the sort. What do you think?

My obligation to myself is to re-wild my heart, my soul, my being. To be at home in nature. To schedule it into my life on a regular basis. As part of this effort I had an impromptu crocus tea party with a dear friend. We checked out Cranberry Flats by Saskatoon. We planned a picnic. The crocuses were a charming surprise.

First the howling blizzard woke us,
Then the rain came down to soak us,
And now before the eye can focus,
CROCUS!
-Lilja Rogers

We both felt drawn to the experience so much. We needed it. And all it was, was sunshine, water, fresh air and our feet in the sand. How can that be so healing? To curb your expectations, I can’t answer that question. But I can claim that it has been and continues to be a healing experience for me.

Spring Fling Lessons

There are always lessons in nature. See what other lessons you can find from spring. This is my list:

  • Plant the seeds you want to see grow (obligation frustration or obligation anticipation)
  • Even after dark times, there is still life (seasons are cyclical and so is our sense of entrapment and empowerment if we aren’t careful, keep coming back to empowerment)
  • Growth does not happen all at once (like the lilies growing in my yard, we all start somewhere and then we keep reaching for understanding, suddenly we see we are taller and more beautiful than before)
img_5037
  • Positive changes can look scary (a thunderstorm can bring fear until you see the blessings that it is bringing)
  • We don’t all bloom at the same time (I see people my age flourishing in different arenas, it seems they are fully formed while I’m barely above the ground, but we never see what’s developing in the roots)
  • Take time to notice the beauty (I am excited for ‘new green’ as I watch for all the buds to break open)
Photo by Aibek Skakov on Pexels.com
  • Challenges are required for growth (plants need the heat and the water, they can also be scorched or drown, we can face challenges, but should watch our stress levels and adjust before the elements are too much)

Trees, Please! Let’s Get Lost in Forest Therapy!

Here’s a suggestion for a forest bathing exercise I have enjoyed recently. THE STUDY OF CREATURES. Find a comfortable spot in nature and become quiet in your generation of sound and in your energy. In a short time you will be privileged to get a glimpse into another world.

An ant. A bird. A ladybug. A butterfly. Any creature will suffice. As you watch your fine specimen ask yourself questions like this:

  1. How does it move?
  2. How would you describe it to someone that cannot see?
  3. Is it interacting with other creatures? Who and how?
  4. What type of behavior is being exhibited?
  5. How would you describe it in words to someone that cannot hear?

Grab your nature journal and write down what you are witnessing. Or discuss with a friend what you are noticing to make the experience more memorable and to expand your understanding. We are seeking a certain type of chill. The chill demonstrated by this photo 👇🏼

Let’s be honest. Nobody can achieve this level of chill. But we can try.

Managing chronic pain can feel like an obligation. But allowing this type of thinking further entraps the mind and body into a prison of unhappiness. Resulting in losing our chill. How can this be reframed?

Where do you see that your chronic anything has been a blessing in your life? I’ll go first.

Seven Ways Chronic Pain Has Been a Blessing In My Life

  1. I am loved with a special love by those who seek to understand my suffering
  2. I have learned to appreciate the little things in life
  3. I have found a better version of me through my experience
  4. I have gained a different perspective on life
  5. I have learned sisu- a special form of resilience
  6. I have learned to problem solve
  7. I have a greater empathy for the suffering of others

Things won’t always be easy to frame this way. But every exercise in doing so will bring you energy.

Embracing the Art of Fumbling Gracefully

As we learn these lessons and grow stronger and better:

Be kind to all the past versions of you. They are the soil in which you now bloom.

-Arielle Estoria

When we have experienced trauma in our life, including chronic pain. putting up walls can feel like we are just trying to keep everyone out. We build boundaries that can make us feel trapped. Alone. But as we go through our own distinct healing, we see that the walls are really beneficial boundaries. And we can show all those willing to work within those boundaries where the door is.

The Little Plant
From The Baby Plant and Its Friends
By Kate L Brown

In the heart of a seed,
Buried deep, so deep,
A dear little plant
Lay fast asleep.

'Wake,' said the sunshine,
'and creep to the light'
'Wake,' said the voice
Of the raindrops bright.

The little plant heard,
And it rose to see
What the wonderful
Outside world might be.

And Finally, A Bedroom Confession 😳

As chronic comrades we need to get out. And then we need to be in. I love the forest. And I love my bed. My confession from my bedroom is that I use my bed for EVERYTHING! It is my office where I write these posts. It is my dining room where I eat most of my meals. It is where I have all my phone calls and zoom meetings. It is where I watch TV and listen to podcasts. The forest and my bed are my comfort zones. Quite literally.

Take care out there and I hope to see those of you in the area this Saturday.

The Realities of Hypermobility: Shared Experiences and Advice

The sun was warm but the wind was chill. You know how it is with an April day.

-Robert Frost

I return in this post to my hypermobile syndrome. If you’ve just joined us, I have an undiagnosed hypermobile condition, akin to Ehlers-Danlos Syndrome (EDS). I am extremely bendy. This week I was introduced, by a dear friend, to another tool that I can use to treat my pain. Tuning forks! I have been struggling with scar tissue. When I attempt to massage it out, the area becomes so inflamed that I can’t touch it without pain. The tuning fork is extremely useful for removing the scar tissue that my fingers couldn’t get. In my excitement I removed most of the scar tissue in my neck. This area has been bothering me since my second to last slip on the ice this winter. It felt so good to release so many tight, pinching spots. This sounds like it would be a good thing. It. Decidedly. Was. Not. The scar tissue was holding me together. I see that now. I should have removed it slowly. Now my neck feels like it is hanging on by a thread while the muscles work overtime.

A person with chronic conditions will have many moving parts and factors to consider in every decision. Often we will think, “wait, why did I do that?” “I knew better!” Do you know anyone that would benefit from the community we have here? Or someone that would appreciate knowing they are not the only one suffering through chronic conditions? And at times making terrible decisions in how to treat their pain? Share this post with them. I invite everyone to follow my social media. We are watching the trails and reattaching my neck muscles to prepare.

Let’s talk hypermobility. Collagen is the glue that holds our bodies together. It gives the body strength and elasticity. When the collagen is genetically altered due to a condition such as EDS, function of many bodily systems is affected. Collagen affects skin, tendons, bones, cartilage, eyes, and internal organs. It is more than just joints. When these systems are all out of order, mayhem ensues.

I am not a doctor. I have no training in this specialty. But I have lived it. I only share the symptoms that I am having or have had in the past. This is not medical journal material. Not based on book studies and lab work. It is based on me. My lived experience. 

My 18 Irksome Evidences of Hypermobility

In no particular order, I share here 18 ways that I am affected by my hypermobility condition. I do this to highlight how all of us chronic comrades are suffering more than you know. In ways we can’t put into words. Unless you are very close to someone who is suffering. You will only ever know a small part of what they are experiencing. This blog has helped me put my pain into words.

1} Neuropathic pain– stemming from problems with the signals from the nerves. Felt as shooting, stinging, burning, tingling, numbing. Particularly difficult to treat. Often caused by pinched nerves due to shifting joints.

2} Inadequate passageway between the base of the neck and the armpit. Causing compression of nerves or blood vessels. Or both. This results in a wide variety of symptoms. Including pain in the shoulder and along the top of the clavicle. This pain can spread to the inside edge of the arm and down to the hand. Often numbness and tingling are present. Activities that most aggravate this area are driving, writing, carrying and lifting.

This explains the nights of excruciating pain after a day of working and driving and yard work years ago. Now I know better and I plan better. I no longer work. I drive only when necessary and only short distances. Yard work has to be done carefully and in short sessions.

Ipseity- (noun) sense of selfhood. The feeling of being the individual subject of one's own experience. A core aspect of consciousness. The inherent sense of being. 

How does this fit with chronic pain? I think it is accepting myself. As I am. Today. And that is a person with pain. It is my experience. It has become part of who I am. Can you claim your ipseity with a renewed perspective regarding any chronic conditions or illnesses you have? You are not a hypochondriac. You are not overreacting and complaining. You are not lazy. If you are doing your best. It is enough. Period.

3} Riding in a car is also exhausting. Think of all the micro adjustments you need to make as you bump along in a car. While your body has to keep adjusting to stay upright, you don’t even notice. A flexy body bumping along trying to stay upright is working against already tired muscles. And painful spots that inflame on being used repeatedly. There is also so much extra sensory input to process.

My husband drives us everywhere. But I’m the one that needs to nap when we get there. Now I have an explanation for why. It may be good to occasionally open your body’s task manager to see what’s going on in the control center.

4} Hearing issues. Caused by mobility of the joints in the inner ear. Creating problems with effective sound conduction through the middle ear. This can lead to mild or moderate conductive hearing loss. This can also cause problems with dizziness as the inner ear is responsible for balance.

I wandered lonely
As a cloud
That floats on high
O'er vales and hills,
When all at once
I saw a crowd,
A host, of golden
Daffodils;
Beside the lake,
Beneath the trees,
Fluttering and dancing
In the breeze.

-William Wordsworth

5} Low back pain. The ligaments that are supposed to support and stabilize the spine and pelvis are often too loose. This means the muscles end up supporting the upper body. Loose lips may sink ships. But loose hips make it hard to stabilize the pelvis. All this can aggravate the sciatic nerve. And can lead to sciatica. A painful condition where pain runs through the buttocks and radiates down the leg.

Getting ready for Monday. Or a hypermobile person just trying to survive the day.☝🏼

6} Anxiety and panic disorder. The hypermobile body tends to overreact to stress and creates an excess of adrenaline. This can be mistaken for mood disorders. But is more likely linked to ongoing pain and fatigue. This could explain why counselling which is suitable in some cases, will not prove effective for all.

Thole– (verb) in American English- to suffer, to endure, to undergo.

You have tholed, you are tholing, and the toll it takes can be front and center in our lives.

7} The impossibly fine line we all walk between moving too much and moving too little. Movement causes pain. Movement can also cause injury. However, without movement our muscles decondition. Causing further strain on the joints where the muscles can’t hold it. Causing more pain and increased risk to injury.

8} Due to the collagen deficiencies linked to the condition, swallowing and speech difficulties may occur. If you have heard me speaking and then suddenly my words are slurring together. You’ll notice I start to enunciate clearly for a few words. Then my brain and mouth seem to get back on track. Unless I have been speaking for a while and then there is no coming back once the slurring starts. Making the muscles of my mouth work to swallow is also an issue at times.

I was just sittin’ here enjoyin’ the company. Plants got a lot to say, if you take the time to listen.

-Eeyore

9} Local anesthetic may not hold or work as well. I have experienced this myself and I have seen it in my son enduring dental work. It makes me squirm to think about it. Now I know the “drill”.

As I spend time in the forest, I am learning to pay closer attention to my body signals. Because it doesn’t lie to me. And I am attempting to pay less attention to my mind because it lies to me all the time.

10} Anything repetitive is out of the question. Overuses the same muscle group and strains already inflamed nerves in the process. My body never adjusts to the increased work load. It just stays weak and bendy. Like an uneducated peanut!

11} Muscle spasms are painful and regular. This is new to me in the last few years. It is down right annoying most days. It makes typing this post take much longer since I hit the wrong key and double hit another. It shows up in various and embarrassing ways. I have spilled the sacramental cup of water more than once at church.

12} We sit and stand in weird body positions. This is to hold the right spots together. We often fidget. Sitting or standing the same way for too long will result in a slipped joint.

13} We are often thought of as clumsy. I still run into walls when I get tired. Something I thought I would have outgrown by now. The truth is, between our unstable joints and dizziness we should be praised for all the time we are successful in staying upright!

ASAP
As Slow As Possible
As Soft As Possible
As Sustainable As Possible
As Sincere As Possible
As Steady As Possible
Allow Space And Pause
-Unknown

14} Oral and dental issues. Teeth are prone to fracture from relatively minor trauma. Gums can bleed after minor trauma such as brushing teeth. Chewing or sleeping wrong have both contributed to subluxations in my temporo-mandibular joint. I attribute my crooked teeth that are always on the move to my hypermobility.

15} Chronic neck strain. Due to weakness in the shoulders, activities that use the shoulders also use neck muscles. The ligaments meant to support the head are too loose. Neck muscles get overworked and strained.

This is me today, except I am wearing clothes and female, otherwise the resemblance is uncanny!

16} Difficult and painful to write. This one hits home for me. I shake when I write. Not because I am nervous. But because my hand muscles are spasming and weak. If I have just washed dishes or had a shower, good night! You will not be able to read my scrawls. The warm water loosens things even more than they were. It is also painful to write for any period of time.

If the sight of blue 
skies can fill you
with joy,
If a blade of grass
springing up in
the fields has the
power to move you,
If the simple
things of nature
have a message that
you understand,
Rejoice~
For your soul is
alive...
-Eleonora Duse

17} Disc problems. Discs may be less rigid than usual in hypermobile people. Soft discs are more prone to rupture or leak. Disc material leaks out and pinches nerves.

18} Brain fog has already been a topic of conversation here. Brain fog in the hypermobile may be due to lack of blood flow to the brain. This is thought to be from blood pooling in the legs thanks to our stretchy blood vessels.

Chronic illness is not so fun. It is easy to think about who I would be without this disability. It is easy to think about all the hopes and dreams I once had that have to go. But what about who I will be now, with it? What hopes and dreams can I create now that this is my reality?

Watch for the Signs!

There are signs to watch for in healing. Chronic is chronic. Cure is not in our vocab. But healing is available. Healing means acceptance. Softening. Learning and growing within our new reality. There are also signs to watch for at this time of year. Have you seen any of these signs of Spring?

  • a nest being built
  • a bird carrying a worm
  • a muddy puddle
  • blossoms
  • a lamb or other baby animal
  • spring flowers
  • insects
  • a bumble bee
  • buds on a tree
  • a singing bird

What have you already noticed this year? Write in the comments.

Just like the poems, quotes and uplifting thoughts laced throughout this list. The beauty of life and nature can be sprinkled throughout our days. To lift and cheer our souls. To lend beauty and joy to an often troubled heart. Go out and get some forest therapy today! We will be together in the forest soon!

Everybody needs beauty as well as bread, places to play in and pray in, where nature may heal and cheer and give strength to body and soul alike.

-John Muir

What’s in a Flare?: A Pain Like No Other

Pain never arrives alone. It always brings with it strength and resilience.

-often attributed to Maya Angelou

I am in a flare. My latest fall, leading to my latest physio adjustment has me looking for the knot to untangle my insides. It is not stress. I do not just need to go for a walk. In adjusting some joints back to their intended position we uncovered the really ugly spots. But not until a couple of days after I left the appointment. So now I wait. While the flare moves through my system and interrupts my life.

I expect to be out on the trail as soon as this flare passes. There are some bio-mechanical issues to be sorted out. Then I can show those who are interested in booking a forest therapy walk, what we’ve been discussing here. Follow me on social media. And subscribe to the blog to be the first to know when booking is available. I am so excited to show you what this is all about!

What to Expect on the Blog:

What is a flare? How can you support yourself or another person in calming a flare? and How can forest therapy help? These are the questions we will be exploring together on the blog today.

Pain Flares: When Your Body Goes Off Script!

Flares comes in all shapes and sizes and for so many reasons. @ferociousfighters defines a flare as “A sudden exasperation of a disease. Different from the day to day variation of symptoms that patients with chronic illnesses experience and is characterized as large and rapid increase in a patient’s symptoms.

Flares can be triggered by physical stress, psychological stress. Traveling or other schedule changes. A change in the weather or medication. A common illness, interrupted sleep. Overexertion.

A description of nitroglycerin comes to mind. “Unfortunately, nitroglycerin was unstable. If you dropped it from a small height, it’d blow up. If it got too hot, it’d blow up. If it got too cold, it’d blow up. Even placed in a cool, dark room and left alone, it’d eventually blow up” (Elder Dale G Renlund). I am nitroglycerin. I always end up blowing up into a flare. Despite my greatest efforts. My chronic comrades will relate.

Sometimes there is a reason. Sometimes it is totally uncalled for.

The Not-So-Amusing Tale of My Not-So-Epic Fall

This time, I triggered the pain by a fall, which is causing a flare of so many symptoms. In sharing this experience, I do not seek your sympathy. But your understanding for all those who suffer.

This is how my flare looks this time. It all started with a “minor” slip on March 17th. I was taking my grandson for a walk in his wagon. It was a day that had a skiff of snow on top of the melting ice. I should have known better.

Suddenly I was on the ground. I knew instantly that I would need an adjustment. Joints had definitely shifted. James waited patiently. I’m sure he wondered what game we were playing.

During the first wait to see my physiotherapist, my pain level stayed around a 4. During the evenings and the worst of it I was up to a 7. I saw my wonderful physio and she adjusted a few areas.

Unfortunately, I missed a spot that needed adjusting. It’s difficult to sense it all until all the joints settle into place from the main adjustment. I share all this to say, since I realized something was not right since that adjustment. I have been living at a 7 and getting up to a 9. The discomfort is one thing. What it does to my body is what triggered my flare.

This is my layman’s understanding. My little stabilizer muscles are working overtime to hold me upright. The muscles that are supposed to be doing that job are stabilizing joints that are not set correctly. I have a constant headache while I write. Something is pulling on the back of my neck.

The Empty Plate: A Restaurant Running on Fumes!

Let’s say my body is a restaurant. All of my joints are my employees. The joints that have settled incorrectly, all those employees have called in sick. They are just trying to hold their own little spot together. So now I have multiple areas that aren’t doing their job. The rest of the employees are left to try to hold the restaurant together. As it goes on and on the strain and exhaustion on those few employees that are left builds.

While this is happening in my muscles, my easily overwhelmed nerves are taking some of the fallout. All of the upset clients coming out of the restaurant are complaining to them, if you will. (Me: okay nerves I’m going to need you to take some of the strain. My nerves: (crying, laughing, then igniting the nitro) Me: 😳😑)

The restaurant looks fine. The tables are set as though all is well. Meanwhile this is happening:

Window of Tolerance: The Fine Line Between Zen and Zany!

I expect all of us are familiar with the window of tolerance. There is a space where I am emotionally secure. Triggers come and go but with self acceptance and emotional resilience, I am okay. I can stay comfortable within that window. When I go over that window of tolerance, I am hyper aroused. I feel as though I will explode like a volcano. When I go under my window of tolerance, I am hypo aroused. I feel down and depressed.

When I am in a flare, that window of tolerance is very small. I am easily over aroused by sounds and lights. I like my slow times of the day that help me focus. I am also easily dragged down by my thoughts. I think of all the things I could be doing if I were well. I see others living their dream and I want to live mine. Knowing this window of tolerance is small and taking care of myself, becomes indispensable during a flare.

I Need a Nap So Bad, I’m Already Tired Tomorrow

Last week I described different types of sad. Here are some different types of tired. Can anyone relate? Beat, I just want to sleep all the time. Drained, my thoughts and energy leak out of me like a leaky faucet. Apathetic, it becomes really hard to care about the needs of others. Frazzled, when I can only feel buzzing and everything needs to stop. Broken, too tired to do anything but not so tired that I don’t miss the things I could be doing. Wiped, when there is nothing left of me. Zonked, can I repeat what I just said? No, I have no idea what we were talking about. Burned out, I am crispy and short with others around me.

How to Pamper Yourself When Life Throws a Flare!

During a flare. Take care of you. Whatever feels right. Cold or heat. Being propped up with blankets or going for a walk. Find the right balance for this time. I’d love to be out and enjoying this actual spring-like weather today. But for now, inside is the place to be. But I am loving seeing the blue sky through my window and feeling the sunlight.

It is important that the right people know what you are going through. Your people will be there to support you. Let them know what you need. Do not cover up pain with those people. There are levels of okay and not okay. Stay in tune to your body and in touch with your people. “I am currently eggshell-fine. Doing okay but easily crushed.”

Wear the right clothes. Eat the foods that will nourish and that are easy to prepare. Take time for doing nothing. Where your body can speak to you. Wear the slippers. Say the affirmations. Sleeeep. And then sleep some more.

Your worth does not change with what you can or cannot do. Your worth is and always has been great. Even if your house is covered in dog hair. Even if your meals are subpar at best lately. Your tired body is worthy. Your misfiring brain is worthy. Your yearning heart is worthy. You have worth. No matter what you can and cannot do. Truth be told. That may be more of a pep talk for me than anyone else.

What do you have in your flare basket? Mine has fuzzy blankets. My housecoat. Slippers. Essential oils. Tea. My Spotify flare playlist. An eye mask. Noise canceling headphones. Epsom salts. Snacks. Water. Pain killers. And the all important hair ties. Full disclosure, I have no basket. But this is what would be in it if I were to make one. What am I missing?

As we discuss ways to move through a flare, I find this graphic very helpful. See if it speaks to you:

Branching Out: Forest Therapy for Flare Relief

How can forest therapy help? I don’t know about the rest of you but I want to live this lady’s life. Wrap me up and set me by the water. With my bare feet on the sand and the sun on my face. Feeling the steady lapping of the waves as I watch them roll in. This is healing.

It doesn’t take much to get a lot out of nature. Her gift is freely given with love. During your own flare. Or when supporting someone in a flare. When struggling with any number of life’s conundrums, find a space in nature. Take time to be quiet. Time to be still. There are multiple exercises that I can lead you through when you join me. This enhances the support and healing of nature.

BRIVET (British)- to wander an area or look through items without purpose, often in a sneaky way.

With me or on your own, find your space in nature. Use all five senses to connect. Breathe deeply. Find your center. Relax. Bare skin to the earth. Sense the vibrancy and wonder.

This is Forest Therapy!

Soak your life
with wildflowers
and rivers.

Breathe in honey
and the moon.

Bring in softness
wherever you can.

Softness can carry you
over the sharpest
of grounds.

Like wind and water.

-Victoria Ericson

How to Transform Mindset for Better Living With Chronic Pain

and she gracefully danced on the fine line between a hard mind and a soft heart.

“Pick up the slack!” These words went through my mind as I was trying to make my hands work. They are getting slower and tighter these days. During my latest fall one hand took the brunt of the impact. As I tried to hold the vacuum and quickly do the job, I got frustrated.

What is slacking? It is careless, negligent, sluggish. Am I really slacking? I pictured saying the same thing to my grandson as he tried his best to get his work done. It made me so sad thinking of saying it to him. Especially if he is trying hard. That could be damaging to his self esteem. So why would I even have this as a passing thought to myself?

Where does your brain go next when you are in a similar spot? Does it try to speak kindly to you like you would a small child you love? To support and put tools in place to garner success for the future? I know. I didn’t used to do that either. But after an intensive series of unfortunate events. I felt I had no other choice but to learn how to build and support a healthy mindset. That is what we will discuss in the blog today. Some of those tools I have learned to use, in managing and living with chronic everything. I have far from the worst diagnosis, but this is my story.

Have you checked out my social media lately? I post something to my Facebook/ Instagram and X everyday (except Sundays). This snow we are getting in Saskatoon is not helping us get closer to trail time. But forest therapy time will come. And this is where I will post my schedule for forest therapy walks. In the meantime, follow me on X to see daily, different reasons why I practice forest therapy. And on my Facebook/ Instagram I post reminders of the blog. As well as other quotes and pictures that will support you in seeking a connection with the forest. Especially when it comes to chronic conditions, pain and fatigue.

Hit Pause on Your Brain: Put it in Timeout

Have you heard of the power of the pause? When you respond to stimuli instantly, you react by instinct. Unless you recognize the power of the pause.

We all have triggers. Those things that send us into base instinct mode. But if we train our brains to pause. We can have power over our thoughts, and thereby our emotions, leading to power over our outcomes.

Triggers without the pause lead to unwanted outcomes. Triggers, followed by a pause will hopefully lead to more favorable responses.

What to do with the pause? There are different options. Or you can do a combination. Find what works for you and use the power of the pause. You can count to ten. Or count backwards from 100 going down by 7. You can connect to your senses by naming three things you can see. Three things you can touch Three things you can smell. And three things you can hear in your immediate surroundings. You can label any emotions going through your body. How do they feel? Ground yourself by thinking big perspective.

The power of the pause is mighty. When you find the way that works for you and use it consistently. The path it starts, becomes a crevice. Where your pause is your superpower. To stay in your own, genuine energy.

When you find yourself unable to manage tasks that used to be a breeze. When the daily routine has to change, again. To cope. And to make things more functional. The brain can take this chance to destroy your peace. Will you allow those thoughts to drag you down? Or can you practice with the power of the pause?

☝🏼 Also remember this ☝🏼 we are going to need practice this ☝🏼 it is not a one and done.

Mushroom Wisdom: The Fungi You Never Knew You Needed

Today let’s take some advice from a mushroom 🍄. Here are my top five ✋🏼 life lessons from a mushroom 🍄.

  1. Do your best work when nobody is looking. Keep a low profile. Mushrooms suddenly appear. Or they seem to. They do most of their work under the ground. Then they pop open as though they’d been there all along. Work on your own and know when to pop up and share. Silence the inner commentary of what others will think of you or your work.
  2. Support the ones around you. Mushrooms work in a community. Through their branching network, all the fungi support and provide nutrients to each other. We have become less of a community in recent years. I find supportive community is vital to my healthy brain narratives.
  3. I am not just what you see. By the same token, I know that what I see of others is not the whole story. There is more depth to all of us. Especially those of us who live down to earth. When I give others room to improve. Knowing there is more to them than meets the eye, I give myself more room for improvement. When I have this space, my brain isn’t as restrained for quick fixes.
  4. Flourish even in the dark. Mushrooms thrive in dark corners. I have lived in dark spaces. Literally and figuratively speaking. On occasion, that’s where I needed to be. Other times it’s where I chose to be. But even in those times of darkness, there was a spark of life. And that helped me see the importance of kind self talk.
  5. Communication is key. This comes with the community in #2. We know when to keep the low profile of #1 and when to bring in the community of #2. We give support and nutrients to one another. In this arena we want to stay open to what others have to say. Use the power of the pause. Build skills starting from a ground up perspective. When my self talk is healthy, I use more effective spoken language when communicating with others.
Taken by my friend Amanda 📷@soulfullifebyamanda in
British Columbia, Canada

Joyful Words: For The Purpose of the Conversation

VORFREUDE- (German) joyful , intense anticipation that comes from imagining future pleasures.

Can you bring some Vorfreude into your life to quiet and calm the unhealthy brain talk? Focusing on future joys, at times can bring us out of those darker places.

Amygdala Hack: When Overreacting Has Become Your Go-To

Another powerful trick is the amygdala hijack. The amygdala is responsible for such brain functions as emotional processing. Emotional memories (a more vivid memory, often related to fear or trauma). Social cues which contribute to social behavior and anxiety. And finally, motivation and reward. It’s an important little almond shaped portion of the brain.

Think of your brain as a fist. Your thumb inside your fist is the amygdala. Your fingers wrapped around the thumb are your prefrontal cortex.

When you have a big emotion, your brain puts the amygdala in charge. This is not good news. We turn back to that kid that was traumatized until the thinking part of the brain takes control again. Turn things around by taking deep breaths. Doing so will put the prefrontal cortex back in charge. This is the part of the brain in charge of higher order cognitive functions. We want this part in control.

Mind vs. Body: A Commentary on Living Accommodations

Are you a person that lives in your head? Or lives in your body? A person that lives in their head is constantly distracted. Focused on the future and worried about it. Focused on the past and about everything that went wrong. They have racing thoughts. They are so preoccupied with what isn’t happening, they run on autopilot for what is. The same thoughts come in and out like a revolving door. Does this sound like you?

By contrast, living in your body looks like being connected to the world around you. You are open to new experiences and growth. You are grounded. You can exist in the present moment. You live with intention. You use the power of the pause. You are willing to let go of what no longer serves you.

And yet I still find myself here 👆🏼 . Where I am out of my comfort zone while going about regular life. I think it’s okay to recognize the stretch. As long as we keep doing the things.🤷🏼‍♀️ What do you think? Go ahead and add your thoughts to the comments.

We all have a comfort zone. I think it is good to push the boundaries within what our life and brain health can handle. I think this is growth. What do you think? Should we just respect our comfort zones as they are?

Leaf Your Worries Behind: Forest Therapy for Chatty Minds

Forest therapy is my favorite way to support my brain health. If you’ve been reading the blog. You’ll know that connecting to the forest with all your senses is a great way to find healthy brain support. Following are five more ways to up-level your forest experience:

  1. Touch interesting textures. You may have already done this. But have you touched those textures to your knees? Your nose? Your toes?
  2. Bring your dog. You’ve probably already done that. But have you walked while looking at the world through the eyes of your pet?
  3. Bring a child with you. Preferably one you know. Do not just grab a random child. This is frowned upon. All kidding aside, you’ve probably walked with a child. But have you asked them general questions about what you are seeing? How does their perspective change yours?
  4. Take a picture. You’ve probably already done this. But have you put away the phone and burned a mental snapshot? These stick. And you can pull it up anytime for peace or clarity.
  5. Look for special features that catch your eye. If you’ve been following the blog you’ve probably already done this. But have you brought along a magnifying glass and closely inspected those things that caught your eye?

Enjoy these and other invitations on a forest walk with me!

Your nervous system will naturally feel calm around people with pure intentions and authentic energy. Trust it.

-@masteringlawofattraction

Let’s Keep Our Sanity: Free Therapy Sessions Available?

Talking to people is important. Especially YOUR people. My mom just got back from her winter in Yuma, Arizona. SHE is my people. When you talk to your people, describe your feelings. This is something we always hear. But what does it actually look like?

I missed my mom but I would squish her like a bug if I sat on her lap 😉

I can describe my sad. Some days it is big and over my head. Like a big ol’ rain cloud. Overshadowing me. Some days it is small and I can hold it in the palm of my hand. But it is still there. Some days it is a light sprinkling of sad. Like a rain shower that is not drenching me but it is constant little gentle reminders of sadness. Some days it is rising up and I think it will drown me. If it keeps getting higher. Some days it is sharp. I see it coming but there is nothing I can do. Some days I am confusingly sad. Everything seems to be in order but I can’t enjoy it. Some days my sad is heavy. And when I talk to others it can feel like they are carrying it along with me. Some days my sad creeps up on me and I suddenly am in its grip. It is constricting and tight.

Can you describe your emotions? Name it. Where is it in your body? How does it feel? These tools are ways I have found to dissolve all of my sads. The sad can still be there but it’s not so concentrated. When I can talk to my people, the emotion does not turn to negative self talk.

When Chronic Pain Crashes Your Mom Life: Can I Get a Time-Out While the Kids Run Amok?

Lastly, I want to talk to my mom-era friends. It can be tough to be a mom with chronic anything. You are a hero. Just keep doing the things. Here is a list for you of what to do when you are feeling burned up and burned out.

  1. For toddlers, time them while they… anything, run laps, bring you all the spoons in the house, turn their socks inside out and put them back on
  2. Puzzles. Everyone loves a good puzzle for some sit down time.
  3. Give them a building challenge and a box of things to use for that build, then have them return and present their creation
  4. Read books, or better yet, have them read to you, any way they want
  5. Bath time, depending on the age, add a popsicle for bonus points
  6. Facetime with grandparents, etc, have them read to your littles
  7. Go for a walk or a drive, something they will enjoy and crank your music while they take in the view
  8. Look at old pictures together, or add some filters and create new goofy photos
  9. Bubbles or stickers are nice and slow
  10. Play board games on the couch

Laughter: The Best Medicine for a Sharp Mind!

To thine own self be true.

Keep Calm and Ditch the Debbie Downer Vibes!

Brains tend to be the Debbie Downer of the party. Unless managed in such a way as to bring you up. Follow these tips to take your Debbie Downer to a Sunny Susan. Or a Breezy Ben. Radiant Rachel? Optimistic Olivia. I’ll show myself out.

Here are my suggestions to you on how to manage your brain. Use the power of the pause and find a strategy that works best for you in the pause. Learn from a mushroom how to keep a low profile, support community, flourish in the dark and communicate. Find time and space for Vorfreude. Hacking your amygdala and getting back to your prefrontal cortex is a few deep, cleansing breaths away. Choose to live in your body and not just your head. The accommodations are much friendlier. Forest therapy is great. I offer you today five ways to up-level your forest therapy experience. For more ideas and to see how it all works. Join me for a forest therapy walk when the trails are clear. Get that free therapy from your closest people. Talk about your emotions to clear those thoughts that are relentlessly taking up residence in your brain. Even mom life is doable with some ideas of how to take it easy on yourself. You are in a marathon, not a sprint, use your time and energy wisely. Find times to laugh!

I would rather be among the forest animals and the sounds of nature, than among city traffic and the noise of man.

-Anthony Douglas Williams

That’s it for today. Take it easy on the trails in Saskatoon. Watch your self talk and learn to manage your brain! Until next time, chronic comrades. I leave you with these fabulous photos taken by Amanda 📷 @soulfullifebyamanda in beautiful British Columbia.

Embrace Nature: The Power of Forest Therapy in ME-CFS

Fjellro (Norwegian)- means “mountain peace” or “a quiet place in the mountain”.

I could use some mountain peace. My diagnosis of Myalgic Encephalomyelitis- Chronic Fatigue Syndrome (ME-CFS) demands that I find time and places for peace. Outdoors- if at all possible. The winter months make it less than practical in Saskatchewan. But the forests and spaces of nature are melting and inviting us to join their tip toe into spring. I will explore this diagnosis and why nature is so beneficial in today’s post.

Before that, if you haven’t already,

☝🏼 Me today ☝🏼

I slipped on the ice again yesterday. Just a mini whoopsy daisy that would be nothing for the average Joe. But I am me. And it is not nothing.

This has been an atrocious year for ice. This is my third fall. Every time I fall I have to put in a herculean effort to get back to where I was physically. Which also takes a toll mentally and emotionally.

It means more painful days. And harder to sleep nights. It takes weeks (sometimes months), a few physio appointments to figure out what is happening and then I fall again!

Frustration at the setback is not a strong enough word. Exasperation. Fury at myself over such a mistake. Rage at the prospect of what this means for the days, weeks and months ahead.

Faith is a bluebird we see from afar. It’s real and sure as the first evening star. You can’t touch it, or buy it, or wrap it up tight, but it’s there just the same- making things turn out right.

-The Rescuers

My ME-CFS Diagnosis: The Mystery Illness That Would Have Ruined My Social Life If I’d Had One

Such an accurate depiction. Just getting dressed feels out of reach. Taking care of kids is a stretch but worth it. Although that knocks out fitness and and career (you can’t have it all!) Plans, hopes and dreams feel too far away to try to reach.

In my last post on Myalgic Encephalomyelitis (ME) Chronic Fatigue Syndrome (CFS) Living with ME/CFS: A Journey Through Chronic Fatigue I explained that when broken down the term means, inflammation of the brain and spinal cord with muscle pain. After years of wondering and then months of testing, I was told the master plan was to manage the symptoms and treat the pain. Forever.

Rubatosis is a newly coined term by John Koenig. He defines it in his book “The Dictionary of Obscure Sorrows”. It speaks to me because it is derived from the musical term rubato. I played piano for years. I loved songs with rubato. Rubato literally means ‘robbed time’.

When playing a piece of music that calls for rubato, the musician subtly speeds up and slows down. This ‘robs time’ from one spot and gives it to another. This inclines the ear of the listener as it is not what is expected.

Rubatosis is being aware of your own unsettled heartbeat. Sensing a nervous, irregular rhythm. Unlike the steady beat of a metronome, it feels erratic and frantic. This is one of the sensations I feel with ME. Along with that feeling of sorrow as originally intended. I sense a physically unsettled feeling that never shows up on any test. Doctors and their machines cannot find it. But the sensation persists.

From There To Here: Now What?

How does one keep fighting against such odds and thrive, not just survive this life? I believe this is where SISU can come in. I discuss sisu in another post if you want to learn more. Sisu: The Art of Thriving in Adversity.

Sisu is where perseverance and grit end. It is the second wind we find to go on. When you feel you have reached your limits, can you find your sisu? Can you meet yourself in this place of suffering and give yourself the time to grieve? And then push past your perceived limits. Those places that other people don’t have to go. Feel the frustration. And then advance. Arise. Flourish. Shine.

Also know when it is time to stop shining and go to bed. 😉

I recommend doing all you can to make your physical environment peaceful and comfortable.

Guilt-Free Zone: Moving Past Disability Guilt

Do you feel guilty about your disability? I feel like a burden on others. I see my inabilities and put aside my abilities. Let’s discuss the guilt that comes along with disabilities. Bring it out into the light so there is no shame here. You are not the only one.

  • I feel guilty when I struggle with an everyday task like walking the garbage to the trash can outside. I feel incompetent. I feel like a whiner. I feel powerless. So I do it anyway. And I slip on the frozen lake that is our driveway.
  • I feel guilty when I need to ask for help. I would rather just take care of things myself. But I have seen the repercussions in the past. It is an ongoing internal battle of pros and cons for the most menial of tasks.
  • I feel guilty for needing accommodations. My back starts to spasm when I think of sitting on an upright chair for any length of time. If I can’t recline, all the joints that are “out” have to work too hard. Little, tiny muscles are asked to do too much. And then they start to complain loudly. With inflammation and pain. But to bring a recliner camp chair with me wherever I go is demeaning. Even the super old people are fine in upright chairs. What’s the matter with me?
  • I feel guilty for needing more rest than others. It is a need I cannot ignore. I can pretend to be a “normal person” for one day. Maybe two. But then I will pay dearly for time that should have been spent resting &/or sleeping.
  • I feel guilty for quitting my job. I see others fighting through exhaustion and pain. Continuing to work. There are so many days I just want to ignore my body and join the rest of the world. Even typing that sentence makes my body react adversely.
  • And I feel guilty for not showing up. I want to be there. I want to do more. I want to see you. But my condition is not meant for this world. I have to create my own if I want to thrive.

The Vast Spectrum of Struggles: Understanding This Essentially Invisible Condition

What’s stressful about having an ‘invisible illness’ is that others expect you to have the same energy levels and stamina as people who are healthy, because you ‘look healthy’, which usually means you push your body past where you should in order to not appear ‘weak’ or ‘needy’.

-Hannah Lindgren

The symptoms and severity of this condition vary widely person to person. Some are home bound. Others even bed bound. I was there. I know what I, personally, need to do to keep myself from going back. This is what I can share with you.

It is not a cure all. Every journey with this serious neurological illness will be different. One thing sufferers will see in common is an exacerbation of symptoms with physical and mental exertion. Resting is ineffective at alleviating the symptoms. Waking exhausted is the daily norm.

ME-CFS is characterized by a profound dysfunction of the regulatory control network within and between the nervous system.

This interacts with immune and endocrine systems affecting virtually all body systems cellular metabolism and ion transport.

Rosalynde Lemarchand

A Nod to Jeff Foxworthy and a List of My Own: Both of Which Are Not to be Taken Too Seriously

Instead of Jeff Foxworthy’s famous, You Might be a Redneck, let’s play You Might Have ME-CFS. Disclaimer: I am not a doctor or medical professional. This is not intended to diagnose, it is for entertainment and introductory informative purposes only. If you have any questions, talk to your doctor. Also despite the fact that I said let’s play, this will not be fun.

You Might Have ME-CFS-

If you experience severe and debilitating exhaustion on a daily basis. if you have ever been too tired to answer a simple question, to turn your head to look at someone, to get to your bed and so you lay down wherever you are, you might have ME-CFS

If you have sensitivities to noise, lights, sounds, foods, odors and chemicals, if your guts are grinding and your brain is buzzing, your limbs are cramping, your eyes are tingling and your muscles are spasming and your extremities are numb, you might have ME-CFS

If your body overreacts to temperature changes, if the cold makes you convulse and the heat makes you nauseous and you get stuck feeling one or the other, then back and forth with no sense of order or balance, if your skin feels like a million pin pricks with each change in temperature, you might have ME-CFS

If you experience daily unexplained pain in your muscles and joints, if you have muscle weakness and reoccurring headaches, if you wonder what you will do when you are 80 since your body feels like it has aged 10 years in the last year, you might have ME-CFS

If you have brain fog to the point that it is often embarrassing and off-putting in a conversation, if you constantly struggle for the right word, forget the names of your friends, and lose track of what you were going to say every, single, time, you might have ME-CFS

If you struggle through exhaustion all day and then equally struggle to get to sleep and stay asleep all night, if you have night sweats and chills, if you have extra pajamas by your bed, just in case you sweat through the first round, you might have ME-CFS

If you struggle with lymphatic fluid blocks and swollen or tender lymph nodes, if you know the spots to massage and what to leave alone, if you struggle with nasal passages staying clear and swollen glands, you might have ME-CFS

Pretend You Have ME-CFS: The Hilariously Not Funny Guide

The symptoms are one thing, how they dismantle our lives is another. I have a different list in my other post on ME. Here is a new list of how to duplicate the feeling of having ME for anyone that wants to know. Like a partner trying on a pregnancy suit to find empathy for their expectant wife. Here we go. How to replicate the symptoms of ME-CFS:

  1. drink a bottle of wine and all the espressos you can hold (I don’t drink either but you get the point, something to make you sleepy and something to keep you up for 3 days straight)
  2. dump a load of rocks onto your bed and lie down
  3. have someone lay multiple weighted blankets on you
  4. invite someone with the flu virus to cough in your face and wait for that to take effect
  5. call on a friend with a toddler to jump all over you, especially directly on your joints
  6. inject your muscles with lactic acid until it feels your limbs will fall through the mattress with dead weight
  7. ensure you have live bare wires placed around you, the shocks you get will be equivalent to the body shocks we are so fond of
  8. have someone dump all the ice cubes they can find on and around you, touching your bare skin until the sensation of pin pricks starts, then have someone prick you with pins, small pins are fine
  9. turn on all the florescent lights and place them directly over your eyes, no blinking!
  10. Lastly, have your niece that is learning violin over to practice directly by your ear

Chronic illness is tricky. People don’t know what to say. When someone has an illness that they beat, they are applauded for their ability to overcome. As they should be! When someone dies, we remember them for their strength to the end. As we should! But in chronic illness, people ask if you are better yet. What will the doctors do? As though you haven’t tried everything. They look for improvement and see none and wonder when you will start trying.

I’m Not Tired, Just in a Long-Term Relationship With my Bed!

Recherche Women

Some women are made
of steel, stones, tears, 
dust, bones and scars
Others are made of books, music, 
rainfall, stardust, moonlight,
flowers, daydreams
And wild adventures.
The rare ones are made of both. 

-Omoehi Ehixojie

Just because the past is painful, doesn’t mean the future will be.

-Meet the Robinsons

Forest Therapy: The Only Time Talking to Trees Isn’t Considered Crazy

I need to be alone for certain periods of time or I violate my own rhythm.

-Lee Krasner

My way through. Forest therapy. I don’t openly share the invitations that I use in my forest therapy practice. They are what I use when I take individuals or groups on walks. There is an added benefit to utilizing silence, meditation and the many practices I have to offer.

Click to my How To Get in Touch page to reach out if you have any questions. If you’d like to know when my walks get scheduled, follow me on social media. Search sunbeam acres on Instagram, Facebook and X.

Tickling All Five Senses for a Brilliant Nature Connection Adventure

Engaging all five senses is tantamount to the forest therapy walk. Enlist your eyes, ears, nose, fingers, and taste buds to join you. Following is an example of how that looks.

Sight- (this one is easy, you can look at a book of nature to get that, but you are missing four other senses when that is all you have) take time in nature to notice what is around you, the colors, the shapes, the relationship between the forest and fauna.

Sound- the birds are singing their songs, we can hear the breeze, what else do you hear, listen for what is near, and then further and further away, then nearer and nearer

Smell- what trees are near, do they have a scent, is there mud or dirt, decaying wood, pinpoint different scents and then how would you describe the overall scent of this space in nature

Touch- a variety of textures are accessible in any space in nature, the bark of the tree and any body of water nearby are what come to mind first, what else is handy, a ladybug to crawl on your hand, a light brush over a patch of grass, toes digging into the sand or dirt, what else

Taste- this one can be tricky, lots of forest therapists bring a thermos of hot water and add bits of the forest to use in a tea ceremony at the completion of the forest therapy walk, make sure you know what you are putting in if you decide to go this route, only use what you are very familiar with, some of the places I go have Saskatoon berries or honeysuckle (just don’t eat their berries) use what you know and learn more about what is safe in your area, you can always bring a snack from home to engage this sense while on your forest bathing walk

It’s Not Woo Woo: It’s Science, Just with a Side of Quirk!

Connecting with the forest through all these and more sense helps me to balance a nervous system. And that is not an easy feat with my life! I promise you it is worth feeling a little quirky at first. For those that think this is alternative medicine linked to the supernatural. Let me assure you, it is no such thing. The science behind the practice is proving the benefits.

If you’d like to look at a couple of those scientific studies:

👉🏼Here is one that shows how woodland sounds help with relaxation more than meditation apps.

👉🏼Another on how the sounds of nature relax our bodies and help them go from fight-or-flight to rest-and-digest mode.

👉🏼And one more that shows the psychological and physiological benefits of forest bathing in bamboo forests.

These studies are copied from Forest Bathing Central You can head to their page to find a monster list of the research they’ve compiled on the physical, emotional and mental effects of forest bathing. Forest Bathing Central check them out!

Ralph Waldo Emerson knew where it was at. He was a forest therapist long before it was a term. Check this out, he said:

Few people know how to take a walk. The qualifications are endurance, plain clothes, old shoes, an eye for nature, good humor, vast curiosity, good speech, good silence and nothing too much.

I’d go for a walk with him any day. Take care my friends. Watch out for the icy patch!

Understanding Depression in Chronic Illness: Signs and Strategies

I walked a mile with Pleasure
She chatted all the way;
But left me none the wiser
For all she had to say.

I walked a mile with Sorrow
And ne’er a word said she;
But, oh! The things I learned from her,
When Sorrow walked with me.

-Robert Browning Hamilton

Have you found learning in your greatest sorrows? Chronic pain has changed the landscape of my life. Through the sadness and heartache. It has been my own school. A specific training.

Searching for Joy in the Gloomy Neighborhood

As humans, we all experience seasons of grief and depression. There are times in this life that those emotions are the correct and measured response. Chronic everything has led me to more than one season of grief. But I don’t want to live in the neighborhood of depression. It is appropriate and healthy to visit grief and sadness at times. However, I believe that to live in the community of peace and joy will give me the greatest satisfaction.

Today I will explore the relationship between chronic illness and depression. I will share what I have noticed, and what has helped me.

I want to take a moment to send a shoutout to all those that have subscribed to the blog. And a big thank you for all the loving feedback. If you know someone that suffers with chronic illness, chronic pain, &/or chronic fatigue. Take a minute to share either my landing page: sunbeamacres.ca or any specific post. There are so many people that are hurting and have tried it all. They have lost hope. I was there. I don’t want anyone to suffer the way I did for a moment longer than is necessary. Offer them a sunbeam of hope.

Do you know the signs of depression? Would you recognize it in yourself or others?

Disclaimer: I am not a trained counselor or psychologist. This post is meant to be used as suggestions from a friend. A friend who has been there. If you have medical issues, talk to your doctor. If you have mental health concerns, talk to your therapist. If you are looking to break the cycle of unmanaged pain and fatigue, that’s where I can help.

What You Need To Know

Here is a my list of things to watch for in regards to depression. This is not meant to diagnose. Just to raise a red flag for you to talk to your doctor.

  1. Brain fog- this is tricky because brain fog is a side effect of our illness, our medications, our inability to sleep, but if you notice an increase in brain fog, take note (literally, write it down or you will forget)
  2. Messy- there may be a lack of care for appearance and living space, again some people are just messy, this is more mess than usual, and not caring about it
  3. Feeling worse around others- you know the people in your life that lift you up, if you feel dull and dragged down around your tribe, that indicates something is off
  4. Your own thoughts drag you down- have you heard of ANTs (automatic negative thoughts) these are powerful and constant, pay attention to the ANTs, the way you talk to yourself internally
  5. Hobbies are not energizing- we all need creative and physical outlets, those activities that normally bring you joy suddenly seem like a chore
  6. Acting more irritable and trying to drag others down with you when going into a depression spiral
  7. Wanting to be at home, alone, all the time- some of us are home bodies, but having a desire get out and socialize is part of our beings, we get to choose the tribe and the activity, I don’t think we can choose to not need anyone
  8. Constant fatigue- again, tricky with meds and side effects and flares, but for no other reason, you are more fatigued than usual
  9. View of the world is negative- we all have to navigate this world we live in, it can be tricky, but when all we can see is the dark side of everything, something is up
  10. Losing dreams and goals- lack of mental energy to plan ahead, all you can see is a dreary future

Do you see yourself or someone you love in this list? How about in this image? 👇🏼 When we ignore the signs of depression, it will start to manifest in physical symptoms.

The Wacky World of Chronic Illness Factors

Do you have triggers that initiate your depression? It’s good to know your triggers. And yet, in my experience, anything can trigger depression in chronic illness. Cold weather. Holidays. Waking up. Going to bed. Getting together with friends. Not getting together with friends. There are so many layers of emotion.

are u ok? im literally a forest fire and i am the fire and i am the forest and i am the witnesses watching it

@fringeffect

I used to daydream of a time when I would have no more pain. My life would realign with the trajectory I’d planned for it. But waiting and waiting for something that is never coming led me to despair. With each setback I slipped farther and farther.

Maybe you are like me. When all these emotions hit me, I pushed through. Thinking there were no other options. And (no surprise), the next stop for me was burnout.

Burnout is sneaky because you don’t realize you’re borrowing from tomorrow to push through today.

Emily Leahy

Brain Power Showdown: Healthy Minds vs. Chronic Pain

I have seen images of healthy brains and the brain of someone with chronic pain. My limited understanding (also not a neurologist) is that a brain can be damaged over time. In someone with chronic illness. There is constant activity in centers that should normally be at rest. Information starts to be processed differently. This could explain why over time we develop symptoms such as anxiety, depression, sleep disorders, and difficulty making decisions. The toll our brains take on a daily basis when dealing with pain is no joke.

When I am in crisis mode mentally. My brain is not to be trusted. It is overwhelmed and overworked. Our brains are designed to protect us. But left to their own devices, they do a terrible job. We have to manage them. Especially when they are also dealing with chronic illness. But don’t worry. You are still inside there.

Don’t think the garden loses its ecstasy in winter. It’s quiet, but the roots are down there riotous.

-Rumi

Brain Games: Boosting Your Mental Superpowers

I am learning to manage my brain and my emotions when depressive thoughts come up. Part of that work is affirmations. I can find the words to let go of what is not useful or regain balance with what is useful. For example:

Over generalization thought: “I failed at this so I am a failure at everything.” Counteracting affirmation: “A bad day does not equal a bad life”

Minimizing thought: “Sure I’ve done hard things. But other people are better.” Counteracting affirmation: “My chronic illness does not define me. I can still do hard things.”

Apathetic thought: “I will never get better, why do I even try to manage it?” Counteracting affirmation: “I am worthy of healing.” (healing is different than cure)

Catastrophizing thought: “This is awful and it will never get better.” Counteracting affirmation: “There are good days ahead.”

Isolation thought: “I don’t belong with my loved ones anymore.” Counteracting affirmation: “Not all my thoughts are true, depression lies to me.”

Perceived burdensome thought: “I make their lives harder because I am this way.” Counteracting affirmation: “I am not a burden on those around me, I only think I am.”

Comparison thought: “What is wrong with me? Why do I need so much more sleep?” Counteracting affirmation: “Rest is important and my body deserves it.”

Give Your Negative Thoughts a Run for Their Money: Six Questions to Ask

When an affirmation isn’t enough to chase those negative thoughts away. Here are 6 questions to ask yourself:

  1. Is this thought true? Can it be proven in a court of law? e.g. Thought: I am too much for people. True? Not necessarily. Maybe for some people. Or in some situations. It is an opinion. It is not a fact.
  2. Is there evidence to prove it? Thought: I can’t handle the pain. Evidence? It sure feels like it some days. But the evidence would suggest that you have been and will continue to handle the pain.
  3. What is a more helpful thought? Make sure it is a true thought that you offer yourself. e.g. Maybe I am too much for some people now that I have a chronic illness. And maybe that’s okay. Maybe I like being my true self more than catering to the needs of other people.
  4. Is there another way to look at it? Going back to the second example, the thought that I can’t handle the pain. What do I need to survive this flare? Who are my people and what are my supports in place? Start to see the way out.
  5. Am I jumping to negative conclusions? Maybe I was never too much for anyone in the first place. The amount of negative energy we spend on anxiety over something that never has and never will happen, is ginormous.
  6. What would I say to a dear friend in the same situation? I would speak gently and lovingly to a friend in pain. I would not expect more than she was able to give. I would honor her needs. Can we learn to do that for ourselves?

Healing: A Hike, Not a Sprint!

Instead of absorbing all of the thoughts that your brain produces. Try observing as though you were on the outside looking in.

I do not want to give the impression that if you follow this simple list. Poof! Your depression will be gone. The journey out of depression takes time. It takes mending.

Mending is a story on a sleeve. Mending is resiliency. Mending cheers the heart and soothes the mind. Mending is clever, ancient and wise. Mending is hope. And mending is healing.

How are you healing? I find chronic pain is best survived by surrounding myself with people who understand and commend my quiet, everyday courage. The bravery shown by just getting up some mornings. To a body that does not behave. And a life that is more stressful than most.

Something else ancient and wise that soothes a body and soul. FOREST THERAPY!

Connect with Nature Through Forest Therapy!

We often forget that we are nature. Nature is not something separate from us. So when we say that we have lost our connection to nature, we have lost our connection to ourselves.

-Andy Goldsworthy

I feel this in the winter months. I lose a connection to myself. And to the healing that is available through the earth. I miss having time in nature.

The mountains are in my bones. 
The rivers my veins.
The forests are my thoughts,
And the stars are my dreams.
The ocean is my heart,
Its pounding is my pulse.
The sounds of the earth write
The music of my soul.

-Wild Woman Sisterhood

I love nature. I love its music and rhythms and breath. I love its beauty and majesty. It has been my greatest earthly physician.

Live in each season as it passes; breathe the air, drink the drink, taste the fruit, and resign yourself to the influence of the earth.

-Henry David Thoreau

Wrapping It All Up with a Bow!

Chronic everything is heavy. Visit the land of grief and sadness but do not get trapped in the neighborhood of depression. Recognize the signs in yourself or your loved ones. We have a lot of triggers. Including a different life than the one we had planned. I did not plan to spend my 40s living like the grandparents in Charlie and the Chocolate Factory. But some days. 🤷🏼‍♀ h️ere we are. Be aware of burnout. Chronic pain actually changes the way our brains look and work. Do not discount your struggle. Practice managing your brain by countering negative thoughts with positive truths. Challenge sticky negative thoughts with the six questions. Mending and healing happen best around those who understand the struggle. Forest therapy helps!

Watch my social media to stay up to date on my forest therapy schedule. TBD once the trails are clear.

I’ve Got a Question for You: Enriched with a Gaelic Blessing

You get to decide who you will be. I choose to be the girl on the right. I choose to be a success story. For anyone that wants to join me in this. Here’s my advice: Wear your best clothes! Light your best candles. Get excited about your health and wellness goals. Don’t save them for a future version of you. You are worthy of good things. Now! In whatever form that may be. Get going on your best life. It will look a little different than you had planned, but you are trusted to carry this burden. If you look around, you will see people you are teaching as you go through your suffering. It is not without purpose.

To help you find the strength to keep digging, I leave you with this Gaelic blessing:

Deep peace of the running wave to you
Deep peace of the flowing air to you
Deep peace of the quiet earth to you
Deep peace of the shining stars to you
Deep peace of the gentle night to you
Moon and stars
pour their healing light on you...
Deep peace to you.

(doesn't that make you want to go into the forest?!?)

Coping with Chronic Pain: When to Break the Silence

Winter sunlight is a warm old soul, spreading love in the bitter cold.

-Angie Weiland- Crosby

Exulansis

Have you ever heard of the emotion, exulansis? It is the tendency to give up trying to talk about an experience. Because people are unable to relate to it.

Can my chronic comrades relate?

I have lived in that space. Until I started this blog. It is a way to talk about my journey. It was lonely to keep it all in. It felt like I was the only one. But I keep hearing of people who are reading the blog and have had similar experiences. We are not alone.

Have you subscribed to the blog yet? Go to the bottom of the page. Hit subscribe. Just fill in your name and email. And you’ll get a weekly email with a link to the newest post. Please share with anyone who would benefit. From the discussion here. Or from a walk in the forest. And watch my social media. (Instagram, Facebook, and X). For upcoming forest therapy walk dates and times as the weather warms up.

Masking the Pain

I try to hide the pain. In social settings I smile and visit and try to be present. When I see photo evidence I recognize I am not as sneaky as I think I am. Why do we do this? Why do we hide chronic pain?

I have some thoughts. But I’d love to hear yours. Comment why you think we hide the pain in chronic illness? Here’s my non- comprehensive list of why I think we hide the pain:

  1. With invisible illness there is a fear of not being heard or taken seriously
  2. Some people choose to be private about what they are going through
  3. When people know, they treat you different
  4. Previous negative experiences when sharing
  5. It is almost impossible to put it all into words and the emotion is close to the surface
  6. Social pressure to be normal- to make others comfortable
  7. Shame and guilt- in all its forms
  8. Avoiding the feeling of being a burden, needing pity or sympathy
  9. Fear of judgment- have you met people? They’re awful!
  10. Denial of the illness and its effects- ‘I can do this on my own’ type of attitude

☝🏼 Can you see yourself in this list? What would you add? ☝🏼

The Health- Privileged

Those privileged enough to know only health do not understand. How could they?These are the ones that will ask if you are better. They are watching only for improvements and progression to a cure. It does not occur to them that your chronic illness does not come with such commodities.

While this can be frustrating. I find it helpful to have a sound bite ready to go for such cases. Instead of staring blankly while your mind searches frantically for where to start. Not everyone needs the whole story. Just a few sentences. ‘My illness is chronic. I have better days and worse days. And for now that is as good as it gets.’

This method is not foolproof. ☹

We can honor our own progress in a way superior to what someone on the outside can provide. From past experience we know how this goes. It might be hard today, easier tomorrow and hard again the next day. I choose to meet myself where I am. Regardless of improvements and progression in the standard way. And that is my route to healing.

The health- privileged will not understand. But as a group of chronic comrades we can provide that understanding for one another. It is said, Health is a crown and only the sick can see it.

Chronic Comrades

I THINK IT'S BRAVE
by Lana Rafaela

i think it's brave that you get up
in the morning even if your soul is very weary
and your bones ache for a rest

i think it's brave that you keep on
living even if you don't know how to
anymore

i think it's brave that you push
away the waves rolling in everyday
and you decide to fight

i know there are days when you
feel like giving up but i think it's brave
that you never do

I am thankful for the few on the outside that want to understand and help. Here are some helpful tips for those of us that live with and love those with chronic illness. Here are some things that seem small but are actually big to those that are suffering:

  1. checking in on us makes us feel loved- even if we can’t hangout, the connection is significant
  2. being heard- having someone hear us and trust our ability to handle it, not take over and offer unsolicited advice
  3. when I say I need to rest and someone rests with me- I don’t need to be motivated, I need to be supported
  4. comfy clothes- they are the only way for my arms to get through a day
  5. going at my pace- whether walking or making a plan, I appreciate being able to move at my own pace
  6. when someone asks how I am and I answer with the standard ‘Fine’ they ask, but how are you really? I feel seen.
  7. meeting people going through something similar- another reason for this blog

You Should Know

It’s important to know that people with chronic illness will have stomach issues, dizziness, nausea, headaches, joint pain, muscle pain, fatigue, and more everyday. These are all essentially invisible. Especially for those who have learned to cope. My grandma knew how to cope. I hope I can emulate her example. Remember you never know who is in pain just by looking.

Coping vs Shutting Down

Is this is the main reason to hide the pain? Is it a coping mechanism? We cannot moan in pain all day long. Learning to listen to your body and ignore the pain is a skill. What are the right coping mechanisms in chronic illness?

Dr Gabor Mate said, When you shut down emotion, you’re also affecting your immune system, your nervous system. So the repression of emotion, which is a survival strategy then becomes a source of physiological illness later on.

Is this also true in a way for shutting down pain centers? What is the difference between coping and shutting down? To me, coping is a way through the pain. Through the darkness to the other side. Shutting down is staying stuck in the discomfort with no plans to get out. This is where I found despair. When we grin and bear it instead of answering the call for what our bodies need, what does it cost? Does it take a bad situation and make it worse?

Maybe you have had a similar experience to mine this week. A new symptom appeared. Instantly, I have so many questions. Is this a symptom I will have as my new baseline? Is it just a flare? How will this affect everything else? Can I handle this?

I’m sick not ugly, thank you very much!

Hiding Below the Surface

We often fill our day until it is overflowing. I believe that this is true especially for women with chronic illness. Then everyone wonders why this Mom is such a mess. At least that’s what happens at my house. 🤷🏼‍♀️

Like a water balloon that can only handle so much weight before it tears. Ask yourself, what was in that balloon that it could not handle one more drop of water? What is already happening under the surface that is filling your balloon to bursting over an insignificant event? Here are some possibilities:

Emotional dysregulation. We all have emotions. Do you know how to handle the negative ones? If not, they can sit and fester like a wound. Chronic illness comes with its share of negative emotions. Constantly filling our cup up to and over the brim if we don’t learn how to process them. In a healthy way.

Lack of understanding, empathy and compassion. We all crave being understood and cared for. In chronic illness there is an added bonus of feeling misunderstood in the medical world. Finding that understanding somewhere is vital and replenishing.

Mental exhaustion. It is not just physical fatigue we deal with. Trying to figure out what to make for supper when the mental exhaustion has set in is awful. Like trying to thread a chicken through the eye of a needle. Mental exhaustion is not something that can be ignored. It is in your face.

Self deprecating thoughts about how you should be able to do more. No matter what we do as moms and women, we want to do more. Exponentially so in chronic illness. We think we should be able to do what we used to do. We wish we could be ourselves again. We think we should have the ability to push through. Just like the rest of the general population.

I was sick yesterday. Having a minor cold or infection is a big deal in chronic illness. It causes a flare in my other symptoms. My body aches were quite enough before this bug. The fatigue that comes and stays with any upset in the baseline is debilitating. What little time or energy I had is sapped out of me. And recovery is not quick. It is a long and slow process.

Add to the list: anxiety, frustration trying to find the words to communicate, sensory issues, and hormones.

Once overstimulation hits, I know I have already passed the point of no return. Overstimulation is not being able to focus. Everything feels overwhelming. I can’t remember or process anything. Everything is irritating.

From Overstimulation to Emotionally Regulated

Then what? What can you do to move through this situation and come out with minimal effect? How do we cope and not shut down?

Please congratulate me on my new position. It is the fetal position. I will be in it for a while.

-@kristen_arnett

The first step is to remember that you are not selfish if you need to remove yourself from the overstimulating situation. You are allowed to care for yourself. You are allowed to opt out of overwhelming environments. Getting adequate rest is not an indulgence but a necessity. Crying is one way the body regulates itself. Go ahead and cry. It is not weak. Forgive yourself for any reactions. You have limits and that is okay. Learn to listen to them. Honor them.

Unlocking Your Full Potential

You are meant to thrive. Not just survive. My veins are filled with stories of survival. Surviving looks like flight, shutdown, protection, fighting, impulsivity, mistrust, rigidity, critical of others, anxious, anger, defensive, collapsing, freezing, fear, submitting, shame, despair.

While thriving includes regulation, connection, resilience, prosperity, goodness, passion, love, contentment, expansion, well being, ease, play, rest, repair, joy, trust, growth, stillness, presence, and health in all its forms.

Shout out to all those making their life with chronic illness a life of thriving. You don’t let anyone see your darkest moments. Nobody knows the effort. I know how hard it is to transform yourself. Silently battling and winning. Be proud of every little step you are making. Keep going! You’ve got this!

I find it easier to thrive when I am with the right people. They are the ones that help me to feel sunshine when I am around them.

Forest Therapy has been my way of coping. It is healthy and beneficial in so many ways. This is not a hike, this is deliberate invitations that lead to learning and healing. Join me in the forest when the ice has melted. We can get on the trails in and around Saskatoon for some much needed forest therapy. My body does not winter well. I am anxiously awaiting. Spring! Dates and times TBD. Watch my social media to see when and where. If you have any questions reach out to me.

Tell me, when was the last time you ran through a field just to feel the freedom of creating your own wind.

-Author Unknown

Explaining and Embracing Life with Hyper Mobility Issues in My Tissues

And a softness came from the starlight and filled me to the bone.

-W B Yeats

I yearn for this type of softness. Nature provides the way. Even if nature and I are not currently on the best of terms.

Gluggaveour (Icelandic)- (n.) “window- weather”; a weather that looks so nice and picturesque through the window, until you’re actually outside in it; a weather best enjoyed only behind the window. (If that doesn’t describe Saskatoon these days, I don’t know what does)

I. Am. Cold. My body does not like to be cold for several reasons. One of them being my hyper mobility issues. My bones are on a subluxation mission this week. Making my muscles work overtime to hold me together. When I go outside and my muscles tighten up in response to the cold, there isn’t much left to tighten. It feels like I am full of rubber bands that will snap at any time. Today I will be sharing more information on hyper mobility issues. And what to do about it, here on the 124th of February and when spring arrives!

Is there nothing to sing about today? Then borrow a song from tomorrow; sing of what is yet to be. Is this world dreary? Then think of the next.

-Charles H Spurgeon

Forest Therapy Helps

First take a moment to think of one person you could share this blog with. Someone with chronic issues. When we tell our stories, we don’t feel as alone. It is a chance to lift others. If you know someone who will benefit from the camaraderie. Take a moment to hit the share button and send this post or my landing page (sunbeamacres.ca) to them. Make sure you are subscribed. To keep up on all things forest therapy in the spring. Find me on instagram, facebook and X! Tell the others.

Reality vs TV Dramas

My chronic comrades, am I the only one who sees the irony of medical dramas? Maybe there are such hospitals. And maybe there are such doctors. But I have not run across the ones who pause their lives for hours. I’m confident they don’t sit in their office thinking only of me. They don’t throw a ball in a repetitive manner while trying to solve the complex issue of my body. They haven’t run all the tests and stopped at nothing to provide me with answers. Until suddenly, they have the answer (after their hour of regularly scheduled programming obviously). I have not experienced this. Have you?

More like, “After minimal deliberation, we’re pretty sure you are faking it.” First of all, how dare you, sir.

Chronic

Recently I was asked what the doctors are going to do. Because it seems like I am not getting better. I didn’t have the words in the moment. But chronic is chronic. And not every condition has a name. And they definitely don’t all have solutions.

If someone is unable to find solutions to their chronic condition, it is surely not for lack of trying. Hope in chronic illness does not mean hoping for answers. Or miraculous recovery. Or even hope of regaining a certain level of functioning. Those are out of our hands. Even if we are doing all the “right” things. Hope with chronic illness involves trusting your ability to manage whatever your condition throws at you. You will be capable of handling it. And your life can still be full of joy. It is worth living!

Hyper mobility/ Ehlers- Danlos Syndrome

If you missed my last post about my hyper mobility syndrome, I have an undiagnosed connective tissue disorder. Akin to Ehlers- Danlos Syndrome (EDS). I share many of the same symptoms.

This is a fitting description of my symptoms. Resulting in chronic pain.

Having hyper mobility, Ehlers- Danlos ish Syndrome is like if you ordered your structural collagen from Wish. Skin from Shein. Organs from Temu. It looks like it should function. Just not quite up to par.

Describing Chronic Pain

Chronic pain is part and parcel of what I have. If I were to describe that pain. It’s like leg day at the gym was yesterday. Everyday. All the time. Forever. And it’s not just my legs. I have that pain everywhere. Some other people describe what it’s like to live with hyper mobility/ EDS.

It feels like I’m 80. But I’m only 40. – Kimberly A Bates

It feels like having the flu. All the time. -Linnie Lin

I’m slowly disintegrating into particles. – Sarah- Marie Zeraphic- McFarlane

I feel like a marionette and someone else is in charge of the way I move. – Nicole Hess

It’s like riding a bicycle with very loose bolts. – Melissa Drennan

EDS is living the day after a car accident in perpetuity. – Sabrina Winchester

You cannot trust your body to do what it is supposed to. – Emma Stathopoulos

The hair on my skin hurts. – Mary Carlson

I feel like I am falling apart at the seams. – Lisa Sinnott

EDS is feeling insane for years because people tell you there is nothing physically wrong with you, when you know there is. – Sarah Elizabeth Erwin Bloom

The cruelest symptom of our disease is disbelief by medical personnel. – Mary Carlson

It’s like falling down the up escalator indefinitely while bystanders speculate about how you got there, what your injuries might be, and if you really even look hurt. – Jess Elsen

Hormone Changes

One negative aspect of my hyper mobility is the hormone changes that come with being female. Progesterone is known to increase subluxations. Especially leading up to the week of menstruation. Joints loosen and pain tightens muscles. A tragic combination.

During pregnancy there are other hormones present that loosen joints further. Creating a need for the muscles to work overtime. Then add to that the trauma of pregnancy. And giving birth. Looking back I can see why my body gave up on me in my 30s. My 20s were super hard on it. How many of you could say the same?

I miscarrried a baby in 2013. While the loss broke parts of me, the physical strain would have been too much at that time. We had 16 weeks together and I would have gone all the way if it had been up to me. But it wasn’t. I was blessed to have all 3 of my boys in my early 20s. When my body was up to the challenge.

I wanted that one more baby so, so bad. For so, so long. The loss was devastating. Following a short time, I was advised to get a hysterectomy. To solve a large part of the hormone cycle- subluxation cycle- pain cycle. It was all getting to be too hard on me. The idea of letting go of my little caboose to fill out our family, was heartbreaking. I still miss that precious one. But the physical damage was increasing in severity. Spreading to my nerves. So I made the heartbreaking decision to have a hysterectomy. That’s all I’m ready to share on the matter at this time.

We are often told if something doesn’t kill you it will only make you stronger. I agree. But some days I don’t want to be any stronger.

The Chronic Cycle

There are other parts of hyper mobility that can be draining. For me, it is a never ending cycle of going to physiotherapy and having everything put back in place. I leave feeling so much better. One wrong move. Or too much exercise. Or sleeping the wrong way. Or a slip on the ice. Then it’s waiting for physio. Get put back in place. Everything feels good. One wrong move. And we begin again. This cycle is painful in so many ways.

The pain of this is so real to me.

I am very flexible. But in hyper mobility that is a bad thing. It has been said only the cognitive and emotional flexibility we develop is truly a good thing. Through having to navigate a medical system that doesn’t understand and therefore is unable to help us manage our condition.

Brain Fog

Let’s talk about how our thoughts feel as though they are swimming in molasses. Or swirling in a cloud of cotton candy. Like the Lord poured in my brains with a teaspoon and somebody jostled His arm (Apple Dumpling Gang). When the brain is not braining. The struggle is so real.

Or teaching a lesson to a bunch of ladies at church. I often fake it until I remember or change the subject. How many of my friends can tell?😳😊

Brain fog affects more of us than just those with chronic illness. Between stress and medication and toxins. Many of us are suffering some level of brain fog. I forget what I am doing every time I get distracted. I forget what I am saying every time another thought comes along. I forget where I am driving on a regular basis. I cannot access parts of my brain that used to work. I used to be an avid speller. I got people’s names right. I remembered long passwords made up of random letters and numbers. I kept my family on track and on time. Those parts of my brain have fled or have taken refuge somewhere. I d0 not have access to them.

Brain fog is not just forgetfulness, confusion or feeling out of it. I often feel isolated from my reality. And parts of my personality. I feel detached. Like an outside observer. There are days when the effects of my brain fog are debilitating. And extremely frustrating. Until I can let that go. Which is sometimes easy. Wait! What was I talking about?

These symptoms are minimal to those that have not experienced them. I’ve been asked how my symptoms interfere with my daily activities. **Blank stare**. My symptoms ARE my daily activities. My life is planned around them. And I often half function in a hurried state when trying to get something accomplished. I see the amount of stuff to be done. And the number of spoons. The math doesn’t math. I feel similar to what a sloth must feel being chased by a cheetah. There was never a chance.

Hard Pills to Swallow

In addition, there are pills that come with hyper mobility, other than the actual pills. That are hard to take. These are the pills I find hard to swallow that come with any chronic condition:

  1. Giving up a career- I loved teaching piano. It was so hard to say good bye to my students. Packing up my piano supplies has been even harder. After five years I have started to pick away. But the grief surfaces and I set it aside again.
  2. Losing or changing relationships- I have amazing friends. Some that have lasted for years and changing lives. Other people have slipped away. They took more energy than I had or the other person couldn’t handle a different me. Chronic illness has changed me. The process has eroded me to my most essential parts. That means the way some relationships look is different now. Not the way I would have planned.
  3. Accepting the term chronic- It has taken time to come to terms with the fact that this condition is chronic. There is no cure. There is a lot I can do to manage it. But it will always be a part of me. I will always have pain. And then the pill of others not understanding. If they are not familiar with chronic, they might have a hard time accepting the limits of the medical world.
  4. Accepting physical limitations- I like to be strong. I used to do the P90X workouts. I had muscles I previously did not know existed. Now I need to bring my husband with me to pick up a chair. I need to sit often. My brain does not function as it should. I need reminders for everything. And then there are still times where something important falls through the cracks. And I need to acknowledge and accept. Then work within my capacity.
  5. Great desires to do what I used to do- I am so happy I can run. For years I just wanted to run again. And now I can! There are other movements or actions I am working towards. But I need to curb my expectations. Some days I get on the treadmill and I am so fast! Like a gazelle. An old one. With arthritis. Run over by a truck. Seven days ago.

Are there pills you find hard to swallow with chronic illness?

Puddle of Exhaustion

Which brings me to my next point. All of this is mentally and physically exhausting. The hyper mobility and resulting pain is tiring. The cycle of subluxations is tiring. Brain fog is tiring. We are just tired. I always feel like I’m about four days past my bedtime.

So many moments of my day, I wish there was a rope available to hang over. I have no more strength to hold my upper body and those muscles greatly desire to let go. So if you see me looking like the people in the picture, rope or no, now you know why. I’m just hung over. (I haven’t been pickled in decades)

One More

Proprioception. I have none. And from that point it gets worse as I get more tired. Actually, I can tell where I am in a space. But navigating within that space gets less easy as I get more tired. When I have subluxations, I am essentially crooked. So unless I am paying attention I walk crooked. I run into walls. I walk into people. I take a step and end up on the exact thing I was trying to avoid.

There is so much more to EDS and hyper mobility.

This post is getting too long and there is more about my EDS/ hyper mobility. So I will revisit this condition in the future. I hope this information is useful and that you can relate to parts, if not the whole condition. We all have parts that need healing.

Before we go I want to share some ways to handle any chronic issues.

Number one on the list as always is:

FOREST THERAPY!

Join me in the spring to see what forest therapy looks like. It is not just walking around in the forest. It is mindful and focused work. And then you will see the healing begin. I still struggle and suffer at times. But the forest brings me back to life. Back to joy.

If you have any questions feel free to email me on my How To Get in Touch page. I’d love to hear from you. Remember to subscribe and share with anyone you think could use a little forest therapy.

Once There Was a Snowman

Until that time. To help us navigate these terribly cold and icy days. Take some advice from this cute little snowman.

  1. Be a jolly, happy soul
  2. Spend time outdoors (unless it is even too cold for the snowmen)
  3. Stay COOL
  4. It’s okay to be bottom heavy
  5. Stay in the environment and energy that will help you avoid meltdowns
  6. Be well rounded
  7. Make others happy
  8. Remember life is short

You are strong, chronic comrade. You are not alone and you can do this. And if you feel broken…

Oh but the irony is, broken people are not fragile.

-Clinton Sammy Jr