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Story about Stiff Person Syndrome .

Me. :)

Feb 17, 2017

By: Stacy


> My name is Stacy Mayle and I'm 47 years old. I was diagnosed with Stiff Person Syndrome (SPS) 4 years ago, after developing symptoms at age 37. It took 10 years to diagnose since it is such a rare disorder. Causing the muscles in my body to become stiff and/or spasm which is extremely painful. I can no longer completely care for myself. Because of this I've have to live with my parents.  I am currently being treated with IV immunoglobulin (IVIG) for 6 hours for  2 days every 3 weeks. I take multiple muscle relaxers and pain killers medications to try to keep the pain and spasms under control. Some days are better than others, but I live in pain 24/7. But, it could be worse!!

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2 comments
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<p>Hi Stacy. I’m Susan Greenberg. I have a similar combo. DM type 1, toxic thyroid nodule, now fully ablated thyroid, and SPS just diagnosed. I’m looking for a Doctor that can see my whole picture, not just their specialty. &#13; Wishing you lots of good days!</p>

Commented 8 years ago susan 510
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<p>Thanks Susan! I wish you the same! Let’s hope our SPS and all other problems progress slowly!! &#13; 🙂</p>

Commented 8 years ago Stacy 110

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