Multiple sclerosis bay area

Common Questions and Answers about Multiple sclerosis bay area

multiple-sclerosis

Ya I just got back my MRI the third one in 1 year and the results are the same, the MRI shows an area 9mm in length on the left side of my brain, it represents an area of demylenation, I have now been too 3 neurologists and none of them know what it is, I was hoping I could list some of my symptoms and someone here could help me out, here goes Right side of my body only numbness face, Vertigo, insomnia, anxiousness, stress, trembling, spasms in my face, ear and leg, my stomach also will jerk fro

I'm a Limbo Lander, so I don't have a diagnosis of Multiple Sclerosis. Humidity doesn't effect most neurologic conditions, but heat does. Any time it's in the high 80's or above, I hide in the air conditioning. I love it when fall and winter come to Colorado. I'm much more comfortable with the cold. As far as sunlight, we have over 300 sunny days a year here, and I don't seem sensitive to the sunlight.

One of them said it is all due to ur anxiety ( Cause i do not have any bladder problems and dizziness, numbness tingling all is due to anxiety) but one said its Multiple Sclerosis+ anxiety. My MRI and EEG were clear. Currently i have high frequency of muscle tingling through out my body only when i am lying on bed plus i see double vision of any statement especially ( white in colour) on TV and laptop. Is it MS? Should I start taking Med for MS or just let it be and hope it will go away?

my sister (24) was diagnosed Multiple Sclerosis in 2010, responded to steroid. now she suffered sudden & complete loss of vision in her left eye. she has been put on SOLUMEDROL. please suggest any available treatment modalities world over ? chances of return of vision ??

org/brochures and you can get many publications from The Basic Facts, The History of Multiple Sclerosis, to publications on Newly Diagnosed, Employment issues, Staying Well, Managing Specific Issues, Managing Major changes, And the list goes on and on.

i had been diagonised with multiple sclerosis in the year 2001. now i am not able to walk. i am also not able to see clearly. my speech is also not clear. i think my type of ms is primary progressive since my condition has worsened gradually. pl suggest some medicines or other alternative therapy.

Recommended