Are there other MS-ers who don't really have numbness? Oh I get a tingle every so often or a slight feeling of numbness, but it is far from my main symptom.
Just wondering.
Just wondering.
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Marti
The only cure for insomnia is to get more sleep.
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Me neither. I have had numbing, tingling, but not continuous areas that go numb.
I feel I am lucky in many ways.
Be well, my friend,
JanI believe in miracles~!
2004 Benign MS 2008 NOT MS
Finally DX: RR MS 02.24.10 -
Originally posted by mjan View Post
Thanks Jan. It's been a very, very stressful few weeks. We are having an auction Saturday and also trying to auction the whole farm. Bought a much smaller house... easier for me to get around without stairs. I do very well, but have to do my laundry in the basement here. Getting a little harder. Anyway it is breaking my heart to leave here after 36 years. I will HATE living "in town". Acquiring more and more autoimmune things all the time. I don't think there is an inch of my body that has not been affected somehow. Even my teeth sting. Hope you are hanging in. I always enjoy reading your posts.Marti
The only cure for insomnia is to get more sleep.Comment
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Strangely enough, as my balance has deteriorated and my motor skills have kind of disappeared, my sensation has improved.
I can feel my feet really well, hypersensitive if anything, and they were pretty numb. They just don't work properly anymore.Comment
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