FAQ/Help |
Calendar |
Search |
Today's Posts |
![]() |
#5 | |||
|
||||
Wisest Elder Ever
|
Quote:
We have to be our own advocate. Research and double check what your Neuro tells you. They aren't the ones having to take these meds and suffer the side effects. I'm at the point where I'm tired of being made to feel ungrateful (by my Neuro) for the fact we have access to all these meds. Last visit he told me I should be thankful there are so many choices. I am.....if I can find one that works for me. ![]() ![]()
__________________
These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here. |
|||
![]() |
![]() |
|
|
![]() |
||||
Thread | Forum | |||
Tecfidera | Multiple Sclerosis | |||
Starting with tecfidera | Multiple Sclerosis | |||
Day 25 of Tecfidera | Multiple Sclerosis | |||
Tecfidera | New Member Introductions | |||
Tecfidera & PML ??? | New Member Introductions |