|
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
![]() |
TuesdayCOPAXONE TIP #1
Since I started injecting manually, I have had noticeably
reduced injection site reactions. A friend of mine who was just
diagnosed and was ready to give up on the Copaxone because
of the site reactions just did the same (with the permission of
her MS nurse) and is now able to stay on the drug because of
it. To anyone who is having bad reactions, discuss with your
nurse or doctor the possibility of doing the shots manually as you may be surprised at the difference! It's super scary, I know (I cried for an hour before I did it the first time) but it gets better. Just offering another possibility if the above doesn't help! Hope everyone's experiences are improved by the shared solutions advice. Labels: Copaxone (glatiramer acetate) |