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Emotional
Sometimes the most honest answer is, ‘I’m doing the best I can,’ and that’s more than enough. It’s a simple question: “How are you doing?” But when someone asks you this after you haven’t seen them for a while, especially when you’re living with a condition like Ataxia, it can feel like a loaded one....
Life is made up of a bunch of little moments, each with its special meaning.  But when we step back, we see how those small actions can make a big difference.  Just like throwing a pebble in a pond, our actions can create waves that affect way more than just us. We all want to...
I just read a great article on PR Newswire, and it could be an exciting opportunity.  But please, talk to your own medical professional about your options.  Disclaimer: This article is intended for informational purposes only. It is not a substitute for professional medical advice, diagnosis, or treatment. Always consult with a qualified healthcare professional...
Raising awareness is the first step toward change. Together, we can bring hope, inspire action, and create a world where Ataxia no longer limits lives. What is Ataxia Awareness Day? Ataxia Awareness Day, September 25th, is a global event to raise awareness about Ataxia, a group of neurological disorders affecting coordination, balance, and speech. This...
Acceptance is not a sign of weakness; it’s a declaration of strength. It’s the courage to face reality and the wisdom to find a way forward. We’ve all faced moments where life feels like it’s throwing us a curveball. Whether it’s a health diagnosis, a significant life change, or just a series of tough breaks, it’s...
Catherine Meredith’s life took an unexpected turn when she was diagnosed with Ataxia at the age of forty-nine, during her fifth year as a fourth-grade school teacher.  Initially dismissing her symptoms as minor issues like a sore knee, Catherine’s journey with Ataxia began to unfold when she started experiencing difficulties with speech and walking. Despite...
I have some fantastic news to share with you today. At MichaelMantz.com, we constantly strive to provide the best content and resources to help you stay informed and empowered about overall health and Ataxia awareness. I’m excited to share our recent changes and additions to our website with you. Let’s dive into the details! Introducing...
In 1956, Josephine’s son was born healthy and seemingly normal. By nine months, he walked with assistance, and his language skills developed well, though speaking proved difficult. Frequent falls and coordination issues marked his early years. At 5, doctors discovered severe vision problems, and while glasses helped, his balance and coordination continued to worsen. His...
At twenty-three, Yesenia Ramos from Edmond, Oklahoma, reflects on her life with Friedreich’s Ataxia (FA), a condition she was diagnosed with at the tender age of six. Her Mexican heritage is a significant source of pride, and she lives with her supportive parents and an older brother who also has FA. Yesenia’s path to diagnosis...
Life is about accepting the challenges along the way, choosing to keep moving forward, and savoring the journey Roy T. Bennett In Richard’s insightful blog post, he shares his journey of adapting to life with Ataxia through practical solutions and supportive technology.   When he and his wife moved into their forever home in 2013,...
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michael mantz
Life rarely goes as planned. This blog is about navigating what actually happens – major disruptions, health challenges, and the quieter work of figuring out who you are through all of it. I write from inside that process. I have Spinocerebellar Ataxia (SCA 15), a rare neurological condition that shapes my perspective but doesn’t define this space. Some articles are personal. Some are practical. All of them are honest.

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