FAQ/Help |
Calendar |
Search |
Today's Posts |
![]() |
|
Myasthenia Gravis For support and discussions on Myasthenia Gravis, Congenital Myasthenic Syndromes and LEMS. |
|
Thread Tools | Display Modes |
![]() |
#31 | |||
|
||||
Member
|
I don't know if THIS might be a factor.................
My MG doc also works at the MDA clinic AND treats ALS patients. I LOVE this doc -- he has been mighty kind to me. BUT, if I "compare" myself to the other non-MG patients he sees, I would have to admit that my problems/symptoms seem "mild". I have sat in his waiting room...........other patients in wheelchairs, with walkers, hooked up to oxygen, not able to hold their heads up.........makes ME count my blessings! I REMIND myself all the time -- MGers are probably the most "normal" patients my doc sees. My headache neuro sees a LOT of stroke and MS patients. In comparison, I probably look/seem pretty healthy to him, too. When someone talks about "normal" -- I AM able to walk, feed myself, dress myself, breathe "regular" air, sleep in a regular bed....actions that MS, MD, ALS often don't allow. Perhaps a doctor's definition of living a "normal life" considers these things. ![]()
__________________
~jana |
|||
![]() |
![]() |
|
|
![]() |
||||
Thread | Forum | |||
RA in remission. Why is SFN not better? | Peripheral Neuropathy | |||
Remission in MG | Myasthenia Gravis | |||
Remission | Myasthenia Gravis | |||
is it possible to be in remission and..... | Multiple Sclerosis | |||
RSD in Remission | Reflex Sympathetic Dystrophy (RSD and CRPS) |