Friedreich’s ataxia (FA) affects my abilities, mood, energy levels, major musculoskeletal functions, and choices. It determines my days in ways far beyond what a 23-year-old newly diagnosed me could imagine. It is a lot to process. But, like most things, I get kind of “used to” it. New adaptations can…
My Darling Disability
— Kendall Harvey
Kendall Harvey is a wife and mother of two in Austin, Texas. She has been navigating life with Friedreich’s ataxia (FA) since her diagnosis in 2013 at the age of 25. She worked in marketing before “retiring” to be a stay-at-home-mom. She is an optimistic warrior fighting for a better future free of FA. Until that day comes, she aspires to inspire others with her column by detailing personal life lessons about grit and grace. Kendall shares a message of hope despite disability.
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I am sure that we have all been around that person who seems to always have it all together — beautiful with hair and makeup done, effortlessly trendy clothes, happy kids sent to school with lunch boxes filled with perfectly well-balanced meals, volunteers for everything, gets praised for being awesome,…
Last in a series. Read part one. In the 10 days since my nose-fracturing accident and the three days since my reconstruction surgery, I’ve had a lot of time to reflect. As I mentioned last week, this isn’t the first time I’ve required surgery after falling due to the…
First in a series. When I broke, fractured, and dislocated my ankle in 2018, I earnestly prayed that it would be my first and only surgery resulting from a fall due to poor balance and coordination — symptoms of my Friedreich’s ataxia (FA). I hoped those two reconstructive plates…
In December 2025, my husband, Kyle, and I traveled to the Children’s Hospital of Philadelphia to see neurologist David Lynch. It was the first time I had traveled for Friedreich’s ataxia (FA) care since transitioning to predominantly using a wheelchair. Therefore, much of the discussion centered on this transition.
Friedreich’s ataxia (FA) is all-consuming. When I allow my experience with it to consume my thoughts, life with FA can seem like an insurmountable problem with no hope of rescue or normalcy. Living with FA and its symptom progression is entirely beyond my control. So what can…
This morning, I did something I rarely do: I asked my children for help with writer’s block. Every Monday morning, I sit down at my computer to write about whatever is in my heart or on my mind as it relates to living with Friedreich’s ataxia (FA).
My husband, Kyle, who will turn 38 next month, has been involved in sports since the age of 5. He played baseball in college and learned numerous life lessons that have shaped him into the kind of husband, father, co-worker, coach, and volunteer he is today. To provide some background,…
Friedreich’s ataxia (FA) shook up my life in every way imaginable. I started to notice a loss of balance and coordination in early 2013, which resulted in a five-month diagnostic journey and then a diagnosis of FA that August. It’s fair to say that in those early days,…
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