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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.

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@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.

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@Holls

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

🤗

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

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@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

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@Chrissykain

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

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 ...

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@Hough1981

4 May 2025 09:19Last reply 4 May 2025 18:52

Copaxone side effects

Morning all. I was using Copaxone for many years, but stopped around three years ago due to experiencing awful side effects. I used to inject myself in privacy when nobody was at home. One occasion I injected into my right thigh, then experienced what can only be described as a feeling that I was h...

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@MarnieV

30 Apr 2025 04:44Last reply 2 May 2025 00:48

I've been taking copaxone for 16 years has anyone else been taking it for this long. Do you still have places to shoot without bleeding or lumps. The shots are getting more painful every time and I hate having to take the injections every 48 hours

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@Shelleyjo1969

23 Apr 2025 03:17Last reply 24 Apr 2025 09:38

Copaxone or tec fidera? Have had some progression sence i switched from copaxone

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@Shaystar37

21 Apr 2025 12:49Last reply 3 May 2025 10:41

So I was on Copaxone for like 3 years it was working great. Then all of a sudden my relapses were happening more often. Just moved to Chicago 7 months ago and have now established care here. My Neurologist is wanting to start me on Kesimpta. Has anyone ever been on it? If so what were some side affects? Also side note I don't have a Pancreas so I am extremely nervous about trying new medications.

Calumet Park, United States

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@CurlyEm

15 Apr 2025 17:16Last reply 16 Apr 2025 06:50

Copaxone

Just spoke to my nurse about my twitching nose. She's booking me for an MRI. On another note!. she was telling me about cases of people taking Copaxone having anaphylactic shocks, even when they've been taking it for a while. Your thoughts.....

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@irmarisdavila

5 Apr 2025 23:47Last reply 23 Apr 2025 20:49

Copaxone

Who is here taking copaxone? How does it do for u?

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