FAQ/Help |
Calendar |
Search |
Today's Posts |
![]() |
#8 | |||
|
||||
Member
|
Quote:
I was fairly certain after some research that I did that I had PPMS, after being finally told that it now looks like my mystery illness looks like a neurological problem. I had also looked at the recommended treatment, none? I could easily accept that, it seemed better than the limited options offered give the risks associated with them. It will be a lot harder and more costly to get insurance after a diagnosis of MS? Some are willing to try anything? I like to see a 50/50 chance of help at least.
__________________
ditched the witch . |
|||
![]() |
![]() |
"Thanks for this!" says: | SallyC (06-01-2014) |
|
|
![]() |
||||
Thread | Forum | |||
Spinal Haemangioma Question ? | General Health Conditions & Rare Disorders | |||
Question about Spinal Tap | Multiple Sclerosis | |||
Spinal Tap ...Question | Multiple Sclerosis | |||
Spinal Stenosis Question.... | Peripheral Neuropathy | |||
question about spinal tap results need help | New Member Introductions |