View Single Post
Old 12-12-2012, 09:28 PM
KittyLady's Avatar
KittyLady KittyLady is offline
Member
 
Join Date: Apr 2012
Location: Indiana
Posts: 430
10 yr Member
KittyLady KittyLady is offline
Member
KittyLady's Avatar
 
Join Date: Apr 2012
Location: Indiana
Posts: 430
10 yr Member
Default

Im sorry you have to go thru all this. When I was on ivsm, I had it for 5 days, then taper with the prednisone. Had that for about 3 weeks. It never made me energetic, I was always sleepy and tired and for the life of me I couldnt stay awake. I had the best sleep I'd had in years. Once the ivsm was out of my system, I was back to insomia land It took almost 4 months for me to notice any improvement at all. This whole thing is such a wait and see game. Wait and see how it affects you, wait and see if the meds work, ugh !! Hang in there, we're all pulling for you!
__________________
Dx RRMS April 1992
Yearly flares from 92 to 11
MS induced seizures 2002
Flare Oct 2011
Flare Dec 2011
Left disabled after 2 previous flares
Betaseron '02, Copaxone '12, Tecfidera '13
(allergic reaction to all)
No longer taking any MS therapy meds
KittyLady is offline   Reply With QuoteReply With Quote
"Thanks for this!" says:
AynaDee (12-13-2012), dmplaura (12-15-2012), Jappy (12-13-2012), SallyC (12-12-2012)