Here are the symptoms I've been experiencing . I think that the length of time this has been going on, even though the
weaknessWeakness is progressing, means that
ALS is not a possibility.
I'm experiencing significant
weaknessWeakness in my left
handHand or foot spasms
Hand tremor and it has been slowly progressing for over 6 months now. In addition to the
weaknessWeakness, I am unable to
lift my
fingersAmputated finger
Amyloidosis on the fingers
Clubbed fingers
Cryoglobulinemia - of the fingers
Finger pain
Herpes zoster (shingles) on the hand and fingers
Janeway lesion on the finger
Kawasaki's disease, peeling of the fingertips
Nail abnormalities
Replantation of digits
Ringworm, tinea manuum on the finger individually and am limited on the range of
motionMotion sickness
Motion sickness less drowsy of my thumb. I can fully extend or fully close my fingers by using my other hand or
something inanimate to force them into the position and it does not hurt but I am unable to do it with that hand itself. I have no pain and no loss of
sensation in that hand, no tingling or numbness. I do, however, have fasciculations in my left hand and forearm. Occasionally I have strong muscle spasms in
the left forearm.
In addition over the last couple of months I've noticed that my legs are incredibly stiff when I get up from any chair if I have been sitting for longer than
about 10 minutes. Once I'm moving, the pain/stiffness in my legs goes away.
I have an appointment to see a neurologist in early November. I there something my regular doctor could test for prior to my visit to the neurologist that
might be helpful? Or that might make the visit to the neurologist more productive? What could this be? I think that any nerve impingement would be
accompanied by some pain or change in sensation - am I right about that?
Any thoughts would be appreciated.
thanks:
1) Sorry for the extra line breaks in the original posting.
2) I'm a 50yo female
I really started to worry when it became cronic and the fatigue set in. My MRI was normal and I didn't have anything show up in emg or other nerve tests. I insisted on having a lyme test. (Thanks to Hikerunner on the site) My doctor didn't want to do one, but he finally agreed.
I'm positive. I've never had a tick byte or had other symptoms of lyme but if your neurologist hasn't a clue and tells you that anxiety is your problem get a lyme test. I feel sooooo much better knowing that I have lyme and not ALS or MS.
Just stay positive.