I have been on Copaxone over 9 years. Diagnosed in 2009. My MRIs have been stable for several years even tho my balance is bad, I walk with a cane and my left side is negatively affected. I can’t count how many reactions I’ve had to the Copaxone shots. My reactions to the daily shots have been so bad (can’t breathe, excruciating back spasms, body shaking and chills to the point I shake for hours) that I want to change meds. I am scared of the damage to the liver by the other meds. That’s why I… read more
That is what I take Gileyna and I have not had any problems. My MRI came back with some improvement last year. My lesions had reduced in size. I've been taking it since 2015. I hope you don't mind me answering your question too just thought it might help.
MSF 291 DMTs Published on Apr 23, 2018
I hope this helps.
Disease modifying therapies (DMTs) – the front line in our fight against MS. Some data presented by percentage:
@ Avonex decreases relapses by 30% and has no effect on brain atrophy.
@ Copaxone
Decreases relapse rates by 30%
Decreases brain atrophy by 20%
@ Aubagio Tablet
Decreases relapse rates by 30%
Decreases brain atrophy by 20%
@Gelenya
Decreases relapse rates by 60%
Decreases MRI activity by 60 to 70%
Decreases brain atrophy by 34%
Chance to improve symptoms is moderately high.
@ Tysabri:
Decreases relapse rates by 67%
Decreases MRI activity by 80%
Decreases brain atrophy by 45%
do not use this medication if you are JCV positive.
@ Tecfidera. Tablets
Decreases relapse rates by 50%
Decreases MRI activity by 50%
Decreases brain atrophy by 30% @ Rebif is Interferon beta 1a, which is also sold under the brand name of Avonex. Avonex is a slightly different formulation.
@ Ocrevus
decreases relapse rates by 80%
decreases MRI activity by 95%
decreases brain atrophy by 45%
Chance of improving symptoms is very high in RRMS.
Decreasing relapse rates should be a must when fighting MS because a relapse can be unexpectedly horrific.
I used to take copaxone for a few years and the shots were really painful and were just not pleasant. I would get like a bruise across my whole inner thigh with the copaxone. Then i switched to plegridy for the past 2-3 years and its been great. Site reactions are beter but my only complaint is that my lymph nodes swell after the shot and hurt. But i havent heard anyone else having that reaction. I do recomend plegridy.