My Nonprofit Reviews

My Name is Rosalind Miale, I have had MdDS for the last 7 years, I was 64 at that time. My motion came on from car rides I took in that summer. We drove from NY to Vt for a wedding. After the 3-4 hr ride I got out of the car saying that I was still moving, swaying and bobbing. I didn’t think much of it, figured it would eventually stop, but it didn’t.
I ignored it danced and drank at the wedding- big mistake!
We returned home after an overnight, still moving and I had another wedding a week later 1&1/2 hrs away. Foolishly I danced and drank again, still thinking it would stop.
One week later someone in the last wedding- family, passed. I had to go back for the wake.
That was the last straw, I was holding on to walk and was frightened. This was family, how could I not go to the funeral, so I did.
After these events I was at level 8, and I had great regrets for my actions, too late.
Feeling like a lost sole, I researched symptoms, Mdds foundation came up, they had a list and I had them all. At least I wasn’t crazy and alone.
From their site, I looked up doctors, things I could do and felt comfort, good advice. I’ve gone to several doctors, Mt Sinai, and balance rehab.
All helped, but I still have it today, learned to watch my activity and am at level 0-1.
The MdDS foundation was and is wonderful tool for people like me.