MSA

Feb 20, 2016

Multiple Systems Atrophy

Error

I have had neurological problems for a number of years but was not able to get relief or a diagnosis. We decided to see a neurologist/ movement disorder specialist at the University of Michigan. They spent several hours listening to my story, reviewing MRIs and performing tests/ questioning me. I was videotaped and my story shared with other movement specialists. With frequent falls, blood pressure swings, ataxia, sexual problems, bladder difficulties, and trouble following objects with my eyes as initial symptoms ( have added more), I was diagnosed with MSA ( probable) in March of 2015. After a year, the changes continue and include more severe mobility problems and exhaustion.

Know someone who should read this story? Share it

Tell my story

0 comments

MSA

Feb 20, 2016

Know someone who should read this story? Share it

Login or register to leave a comment

Multiple Systems Atrophy diet. Is there a diet which improves the qual...

How do I know if I have Multiple Systems Atrophy?

Which advice would you give to someone who has just been diagnosed wit...

Celebrities with Multiple Systems Atrophy

What are the latest advances in Multiple Systems Atrophy?

What is the history of Multiple Systems Atrophy?

Does Multiple Systems Atrophy have a cure?

Can people with Multiple Systems Atrophy work? What kind of work can t...