FAQ/Help |
Calendar |
Search |
Today's Posts |
![]() |
#2 | |||
|
||||
Member
|
Best wishes. Decreasing the depth is good advice. Works for many people. But, doesn't work for everybody. Didn't for me.
I don't understand why they'd want you to stop icing. That's the only thing that gets me through the burning after my injections. They've usually included icing in their advice to me for what I should do. ~ Faith
__________________
aka MamaBug Symptoms since 01/2002; Dx with MS: 10/2003; Back in limbo, then re-dx w/ MS: 07/2008 Betaseron 11/2003-08/2008; Copaxone 09/2008-present Began receiving SSDI 11/2008 |
|||
![]() |
![]() |
"Thanks for this!" says: | Debbie D (01-15-2009) |
|
|
![]() |
||||
Thread | Forum | |||
Looks like I will be trying copaxone again | Multiple Sclerosis | |||
Does Copaxone cause b*&chiness? | Multiple Sclerosis | |||
Started Copaxone | Multiple Sclerosis | |||
My Copaxone froze! | Multiple Sclerosis | |||
Copaxone question | Multiple Sclerosis |