FAQ/Help |
Calendar |
Search |
Today's Posts |
![]() |
#12 | |||
|
||||
Senior Member
|
Another SPMS person here and I just turned 65 this past Friday. Dx in 1990 with RRMS but think I've had "IT" since 1976 when I developed optic neuritis after my third child was born. Remission until '90. Been taking LDN for over three years after bad reactions to the injectables. The neuro says I seem to be stable, but deal with LOTS of pain. Meds: LDN, Zoloft, Oxybutynin, Omeprazole, Aleve, Atenolol for mitral valve prolapse, Warfarin for atril fibrillation, iron, Diazapam for spasms, generic Tegretol when nerve pain is extra bad and dexamethasone pills for any type of flare since a needle will no longer stay in my veins. Hope that answers your questions. I do use a powerchair or scooter all the time but still live alone with some help.
![]()
__________________
_____________________________________________ .....Judy SPMS -- FIBROMYALGIA -- Ouch! and Ouch! . |
|||
![]() |
![]() |
"Thanks for this!" says: |
|
|
![]() |
||||
Thread | Forum | |||
does RRMS always become SPMS? | Multiple Sclerosis | |||
A question for those with SPMS | Multiple Sclerosis | |||
Roll-Call-PPMS and SPMS | Multiple Sclerosis | |||
Possible new tx for SPMS | Multiple Sclerosis | |||
MBP8298 Enrolling Patients in SPMS Trial | Multiple Sclerosis |