Quote:
Originally Posted by hankster1
Hi NeuroTalkers,
I hope all of you are doing well today. This is my second set of posts. I went to a new Neurologist yesterday and rheumatologist the day before - (I tried posting a link to my previous thread, but it wouldn't allow me because I don't have 10 or more posts yet) - but if you click on my name, you can see my earlier post - I posted it in 2 forums.
I was told that I likely won't have a condition that is out there... so no MG or CIDP or anything like that, maybe some variant? I know my Neurologist brought up multifocal motor neuropathy which I had never heard before. They're trying to decide if my condition is inflammatory or autoimmune response so they can figure out whether to treat me with IVIg or Steroids.
My question today is, I have had progressive muscle weakness..
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Hi, Something I found really REALLY surprising when I had tetanus, before I knew I had it, was weakness. One day I could move a chair on my deck, the next it was as if the chair had suddenly become 10 times heavier. I thought my kitty had gained weight when it was hard to lift her.
In fact the problem was my nerves, though what I experienced made it feel as if the problem was my muscles.
If you have symptoms of low vitamin B12 you may want to create a Time Line of your symptoms and start using sublingual methylcoblamin, recording how you feel each day, along with the amount of B12 you use.
For me, when I used B12 in a rather intense way, nerve damage that doctors had told me was permanent... went away. Well, the pain went away. I'm not totally healthy.
But, the sooner you replace B12 if you are low, the more recovery you can experience.
Karen