#copaxone - Shift.ms

Copaxone (glatiramer acetate) is an injectable disease modifying treatment (DMT) for relapsing remitting multiple sclerosis, taken daily. Read about the experiences of other MSers using Copaxone.

Sort 1330 results by

@jumpingJacks

11 Aug 2025 17:36 EditedLast reply 11 Aug 2025 22:27

RRMS SPMS Treatments Ranked by How Well They Stop Relapses That Cause Damage to Your Brain, Spinal Cord & Optic Nerves

Relapses in MS are attacks where your immune system wrongly attacks important nerves inside your central nervous system (CNS) that means your brain, spinal cord, and the nerves connecting your eyes to your brain. These attacks cause damage that can lead to disability. The right treatments help stop...

First posted on the Shift.ms app

@julie1975

5 Aug 2025 12:12

2 years on Kesimpta already

Yesterday was my 2 year anniversary of being on Kesimpta. Can't get over how quick it's gone. But I still get very nervous of doing it. Got Copaxone to thank for that. Horrendous treatment. Still no side effects what's so ever. I love it

First posted on the Shift.ms app

@HasekHoward

4 Aug 2025 03:43Last reply 4 Aug 2025 16:49

Keysympa vs copaxone what are the pr⅚

First posted on the Shift.ms app

@MarnieV

24 Jun 2025 18:17Last reply 25 Jun 2025 05:35

My doctor said if I didn't have any new lesions after my mri I could stop taking the Copaxone injection and take a pill. Does anyone know what pill that would be? Want to do some research before I get it. Oh yeah and there were NO NEW LESIONS!!!! After 15 years of injections I need a break

First posted on the Shift.ms app

@Dellkan

14 Jun 2025 19:08Last reply 17 Jun 2025 14:50

Might need a new MS DMT

Hi all, I was diagnosed with MS in 2020, and started Ocrevus shortly after. However, after 5 successful years on the drugs (no relapses!), I was diagnosed with very early stage breast cancer. Thankfully, we caught it early and post-mastectomy, I don’t need chemo. Still, my MS neurologist is strongl...

First posted on the Shift.ms app

@Leah89

6 Jun 2025 07:45 EditedLast reply 8 Jun 2025 13:23

Hi, I got diagnosed in January and started on medication after a very long wait about a month ago, unfortunately I had a very severe reaction to copaxone....I need to start another treatment however it's limited what I can take due to the fact me and my partner are trying for another baby just wondering what anyone else is or has taken whilst trying to conceive? My ms nurse keeps trying to push the infusion but due to the severe reaction I had after only 4 jabs I don't fancy 6 months worth at a time going into my body. Thanks for reading

First posted on the Shift.ms app

@PoppyJo

19 May 2025 07:38

Hi, has anyone got experience of starting a DMD after years of finishing and essentially opting out? I've been assigned a new consultant and I'm looking into being approved for one? Has anyone been turned down? Back in the day I had Copaxone and Avonex for a few years.

First posted on the Shift.ms app

@Holls

14 May 2025 11:15Last reply 15 May 2025 07:25

🤗

Anyone on copaxone injections and how are you finding them? 😊

First posted on the Shift.ms app

@Carlos

12 May 2025 11:55Last reply 12 May 2025 12:26

Hi I have rrms but latley I seem to be having more episides than usual , I am pretty used with tingling down one leg and regular pain in my sides which I believe is somthing called the ms hug which is reall annoying, but latley I have been experiencing servere pain in my lower jaw and teeth which happen when I touch a certain part of my bottom lip, even licking my lip can set it of, a few days ago it got scary when I was unable to talk due to the pain when simply trying to speak, I am currently on copaxone, this is the first time I have spoke about my ms on a forum apart from speaking to my long suffering partner ( who has to endure my whinging ) I just would like to know if anyone else has this sort of pain and any advice on how to deal with it . Thanks David

First posted on the Shift.ms app

@Chrissykain

11 May 2025 02:39Last reply 11 May 2025 23:48

cladribine

So I was dx 2009. Copaxone nearly killed me. Tecfidera caused me severe acne. I lost the feeling from my neck down September last year and finally had an mri in April. I broke my shoulder in October (slipped on holiday in Bulgaria) had surgery there and had plates and pins , they flew me home too ...

First posted on the Shift.ms app

Shift.ms is better if you're logged in

Topics