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Genetics
April 2024: After 25 years of research, scientists at the University of Utah have uncovered the genetic cause of Spinocerebellar Ataxia 4 (SCA4), a rare and progressive neurological disorder. This discovery gives affected people hope for future therapies. Spinocerebellar Ataxia 4 (SCA4) is a rare, debilitating condition that disrupts movement. Symptoms often start with difficulty...
Mary Hogan’s journey delves deep into her family’s genealogy, unraveling the mysteries of a pervasive genetic disorder known as SCA27B.  Unlike the casual exploration many people undertake on genealogy websites, Mary’s journey is driven by a profound familial connection to Ataxia SCA27. Which has afflicted numerous members of her family. Nicknamed the “Darby Glide” in...
Testing for genetics has experienced significant growth and innovation since the completion of the Human Genome Project 20 years ago. This technology has become a vital tool in diagnosing a wide range of diseases, from rare genetic conditions to certain cancers. Moreover, genetic testing empowers patients and healthcare providers by guiding treatment decisions and preventive...
Keep your face always toward the sunshine – and shadows will fall behind you. Walt Whitman Look up the definition of Ataxia and most of the time, the definition will be “a neurological condition that affects coordination, balance, and muscle control.”  But the world of ataxia is so much more complex.  Living with ataxia presents...

My purpose

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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