Carrie & Haidyn Fowler

Carrie & Haidyn Fowler Haidyn Grace’s fight against Sanfilippo Syndrome- Mucopolysaccharidosis lllA

•heal• 🫶🏼

We got big sissy all moved into her dorm room yesterday. While we will miss her incredibly much, we are so so so proud o...
08/15/2026

We got big sissy all moved into her dorm room yesterday. While we will miss her incredibly much, we are so so so proud of her.

We love you SO MUCH, B. See you soon sister girl. 💜🥹

In case you were wondering how tall Haidyn is now •• the first picture is a good reference. I’m about 5’4. Also, she may...
08/07/2026

In case you were wondering how tall Haidyn is now •• the first picture is a good reference. I’m about 5’4.

Also, she may look JUST LIKE her daddy but I see my facial structure behind those beautiful features.. and the second two pictures show it. 😍

First day of FIFTH GRADE for the second time! 💜✌🏼Big sissy got to go with us this morning - 10 days until she moves into...
08/05/2026

First day of FIFTH GRADE for the second time! 💜✌🏼

Big sissy got to go with us this morning - 10 days until she moves into college. 🥹🪄

Today I am angry. Anger fills my chest like fire. Listening to Haidyn’s cries for the last few days almost feels like I’...
07/22/2026

Today I am angry.

Anger fills my chest like fire. Listening to Haidyn’s cries for the last few days almost feels like I’m filled with rage. A heartbroken, soul-burning, rage. Not with her, but with Sanfilippo Syndrome and the suffering it brings.

As I’ve spent the day allowing it to move through me, I am reminded that I’ve always been familiar with fire. Growing up, I spent many nights around a roaring fire with my dad, my uncle and cousins. As an adult and a mother, I now understand that I’ve always had a raging fire inside of me. Maybe that’s why I was mesmerized by its almost violent yet seemingly poetic, dancing flames, flickering until it burnt out.

I am angry at her suffering - a suffering that no child deserves. I am angry because there are brilliant scientists dedicating their lives to diseases like my daughter’s, and yet treatments remain trapped in years of waiting while Sanfilippo continues moving forward without permission. Neurodegeneration does not wait on paperwork to be finished, another meeting to be scheduled, or profit margins to be met. As parents, we don’t get to file an extension with Sanfilippo Syndrome.. the clock keeps ticking and the syndrome keeps progressing.

I am angry because medication like an antibiotic can put out one fire, while igniting another. It can save her from an infection and also throw her gut into chaos. Can we create something that can heal and doesn’t have to destabilize another system in the process?

Western medicine saves lives yet fails to treat the body as a whole living ecosystem. Haidyn’s gut speaks to her brain, her brain speaks to her neuro-storms and seizures, her seizures speak to her sleep, her sleep speaks to her nervous system, her nervous system speaks to every part of her body. Every part of the body speaks to each other. Yet, we are still dividing medicine into pieces and specialties as if the body ever agreed to such boundaries.

The neurologist studies the brain, gastroenterologist studies the gut, geneticist studies the genes, cardiologist studies the heart, infectious disease studies the infection and so on. As helpful as they each can be divided, Haidyn doesn’t live in specialties. She lives in one, amazingly connected body and a body where nothing happens in isolation. Even as Sanfilippo syndrome is still wildly misunderstood, it is obvious that her entire body is all connected.

Much like life, Sanfilippo continues to teach me that it cannot be placed into a multitude of neat, tiny compartments. Everything belongs to everything. Everything is impacted by everything. Remember? An ecosystem and a paradox.

Organs, emotions, genetics, nervous systems, environment, grief, hope… LOVE. It’s all in conversation together.

I have watched this disease ripple through every piece of my child, her life and our family. I no longer believe that anything exists alone because I do not have the luxury to look away.

So yes, I am angry. I am angry to be in a world that looks away and avoids FEELING the very anger that I feel. A world that avoids feeling almost anything by scrolling, distracting, intellectualizing, telling others that everything happens for a reason or rushing them towards acceptance before they’ve even had a chance to scream… because their grief causes discomfort. All directly intertwines with why we are missing so many connections - emotionally, biologically, medically and environmentally.

I do not have the privilege to look away. I spend my days administering medications and researching their interactions/reactions. I am prepping and cleaning feeding tubes and stocking medical supplies. I witness the suffering I cannot fix, after trying everything in my smorgasbord of remedies. I am holding her through seizures, pain and discomfort. I am rubbing her little face through sleepless nights. Even when her cries make me feel as if I could run 100 miles, I do not get to leave when it feels inconvenient or unbearable. My family is forced to feel it and face it.

Honestly, I think that’s a lot of the divide. It’s not just healthy and sick or modern medicine vs nature. It’s between those that have the privilege of looking away and those who love someone so much that they can no longer fathom looking away. That deep, heavy and unconditional love has made me incapable of indifference. Many have stated that parents like me are so strong.. but many of us have simply lost the ability to pretend that suffering isn’t happening just because it may make another less comfortable.

Today, I am angry because love leaves me no other honest feeling. I don’t want this fire to consume me. I also pray it never goes out, because the day it does is the day I have learned to look away.. and I REFUSE.

Haidyn has a form of “childhood dementia,” called Sanfilippo Syndrome. Yet, dementia never sat comfortably with me as a ...
07/15/2026

Haidyn has a form of “childhood dementia,” called Sanfilippo Syndrome. Yet, dementia never sat comfortably with me as a description. It is so much deeper, like a lake created from a mountain runoff, deep in the forest.

It is an ecosystem & a paradox… like humans.
Biologically her body cannot break down toxic waste. As years have passed and a treatment yet to be released.. (Hey, U.S. Food and Drug Administration 👋🏻) we have witnessed the destruction from inside out.

Ecologically, I imagine a forest. One tree becomes sick. Nothing exists in isolation. Everything changes. The soil, the fungi, the bugs, the birds, and even the amount of sunlight peeking through the weak and broken branches. The forest will re-organize itself because every tree belongs to the surrounding ecosystem. I have witnessed Sanfilippo re-organize how my child’s body functions. Much of it is incredibly heartbreaking, while we also experience miracles with neuroplasticity. A paradox - the brain is both dying and growing at the same time.

When I think of SF as an ecosystem, I think of ripples. A pebble thrown into water changes the shorelines. Wind moves through the trees and adjusts the forest floor. Rivers change flow when a wolf re-enters Yellowstone. “Cascading effects,” as an ecologist would say. Our life has been such. SF has impacted both of my children, our marriage, family, finances, dreams, medical staff, therapists, her service dog, community, the questions we ask and every choice that we make.

Biologically, you learn what the disease is but that doesn’t begin to tell you what it does to the living ecosystem around it.

As a paradox lover - because life is full of multiple truths held in our hands, I can’t help but to look at SF as a paradoxical reality (and not because of new medications 😆).

It is devastating and reveals beauty.
It takes away and it uncovers what it really means to be human.
It narrows a life and breaks hearts while also expanding the very same hearts.
It annihilates certainty and control and creates space for surrender and presence.
None of this takes away from the harshness of this disease but it does remind us that reality is filled with paradoxes.

Haidyn has taught us so much. Including, both the ecological and paradoxical reality of being human. Being human should have never been defined by productivity, cognition, independence or achievements.

Nobody escapes the ripples of life - so what does it mean to be fully human?
Perhaps, we keep trying to remember how living systems reorganize around profound loss without losing their capacity for beauty, connection and meaning.

Love you. 🩵🪄

07/11/2026
Tonight, on our evening walk I felt led to elaborate on why we rarely share. The last six years, since H’s Sanfilippo di...
07/08/2026

Tonight, on our evening walk I felt led to elaborate on why we rarely share.

The last six years, since H’s Sanfilippo diagnosis, feels like many lifetimes. To look back and see the many versions of Haidyn, myself, my husband and our oldest feels almost like a fever dream. This journey has forever changed us in a multitude of ways and heavily.

Where we are now is a place of presence. Sometimes it feels stagnant, heavy and lonely. Other times, it is filled with peace and easy solitude. I have spent years trying to change the future. About a year and a half ago, during a complete break down, I found myself processing the grief, what was ahead and how to slowly accept it. For years, I had advocated my way out of actually feeling and sitting with most of it.

We are not prioritizing changing the future for our Haidyn - we have accepted what is and what will be, to the best of our ability. Even if at times it continues to feel as if I could throw up, kick, scream and rip the world apart. Honestly, I never thought I could find any acceptance in the life we/she had been given. Sitting in my grief was humbling.

Still, each day arrives with the sunrise and we are choosing to soak in each drop of life we have now. We have little control over the future but we have a choice in this moment, to put phones down and absorb each other’s presence… in the stillness, the chaos and the mundane. We have been so blessed to have our own home again, and to share it together. We enjoy walks with the sun sneaking through the trees and kissing our skin. We find more joy in the cooking, cleaning, yard work and responsibilities because we are doing it here, together. We spend time with family and friends every chance we get as time is fleeting.

We are no longer stuck on how to change her future or how to prepare to lose her. We understand that every ordinary moment, right now, is us living the memories that we will spend the rest of our lives wishing we could return to.

We encourage you to do the same. Love your people - leave the rest. Haidyn shows me everyday how to exist outside the parameters of this modern era.. and to be happy within it. I will always follow her lead. 🩵

Thankful for invites to pool days and fireworks with the best of friends! Even if it looks a little different for us.. (...
07/05/2026

Thankful for invites to pool days and fireworks with the best of friends! Even if it looks a little different for us.. (peep the gtube feed running in the second picture)

Also, adding that our friends had our girl covered with shade and a fan to help prevent overheating. It may seem small to some but that is HUGE to us. 🫶🏼🖤

07/02/2026
Happy Father’s Day to my best friend & husband… and also to the coolest, old man that I am lucky enough to call, “Dad.”H...
06/22/2026

Happy Father’s Day to my best friend & husband… and also to the coolest, old man that I am lucky enough to call, “Dad.”

Happy Father’s Day to all the good men in my life and throughout the world. 🖤

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