Copaxone: Hi all, Im out of meds, my dr... - My MSAA Community

My MSAA Community

9,440 members21,223 posts

Copaxone

SunnyDays202 profile image
14 Replies

Hi all,

Im out of meds, my dr has switched me off copaxone and i want my old friend.

I really could do with help. If anyone has spare please let me know its urgent.

Thanks

E

Written by
SunnyDays202 profile image
SunnyDays202
To view profiles and participate in discussions please or .
Read more about...
14 Replies
tadpole0623 profile image
tadpole0623

why switched off Copaxone?

Sandyz profile image
Sandyz

I would suggest you ask your Dr took you off the medication.

I no longer take copaxone. My Dr switched me off of it when it no longer worked for me. I then went to aubagio. I am now on Ocrevus. It's been 6 years with no progression or flares.

MrStripey profile image
MrStripey

They've stopped making the Autoject, and my insurance no longer covers Copaxone, so I was switched to Mylan's generic in January. That may be the reason you were switched as well—ask! I don't like the Mylan autojector as well as Copaxone's, but the meds seem to be okay. You might actually prefer their autojector since it comes in a hard-sided case. What I don't like is that you have to assemble it Every. Freaking. Time. and it only has certain depth settings rather than being infinitely adjustable. Annoying, but you do what you gotta do.

Frances_B profile image
Frances_B

Why do you think it is appropriate to join an online forum where you are anonymous and the same day you join you ask other people in the group to provide you with a prescription only medication?

If your doctor has taken you off Copaxone and you are not happy about that then you need to discuss that with your doctor instead of illegally trying solicit other people to provide you with the medication - and if anyone did provide you with the meds they would also be breaking the law.

BettysMom profile image
BettysMom in reply toFrances_B

Well said, Frances. Thank you.

OSU13 profile image
OSU13

Hi SunnyDays202!

I switched from Copaxone to Abagio 8 years ago. I am very happy with the change. I was on Copaxone for 20 years. I've had MS for 31 years. I could wait to stop giving myself a needle. And all the side effects that came with it!

SvenKj profile image
SvenKj

I started Copaxone when diagnosed in 2000. My fatigue was worsening over the years and finally put me in a retirement community last year. Since I started Copaxone my MRIs have shown no additional lesions and this year at 62 my neurologist told me that my MS was "done", or no longer active, and gave me the option to stop. I have been off the med since March and haven't experienced anything different. Just happy to not be poking myself daily.

BettysMom profile image
BettysMom

What you suggest is illegal. Please remove your message from this site.

Xvettech profile image
Xvettech in reply toBettysMom

That’s exactly what I was thinking. Thank you for saying and confirming it

johnMSAA profile image
johnMSAAPartner

We are sorry you are having trouble with your disease modifying treatments. As other members have mentioned above, this forum does not allow actions like this, as you can imagine.

What we can suggest is that you are free to contact MSAA's Helpline to speak with our Client Services Specialists for more information on medication assistance, how best to talk to your doctors about such subjects, and other questions related to MS:

Phone: (800) 532-7667, ext. 154

Email: clientservices@mymsaa.org

Online Chat: mymsaa.org/mschat

- John, Multiple Sclerosis Association of America (MSAA)

stepsforNeeC profile image
stepsforNeeC

Hi SunnyDay, Did you ask your doctor why without a “medication plan” of smooth transitioning? I understand Copaxone is expensive but, everyone has their own story. I’ve been on it for years, but have other health issues and had to consider the other medications may interfere with other prescriptions. In my sixties now, I may gradually come off in a few years if I continue on a good path so scary and I read the research. Always do what’s best for you, but quiet as it’s kept, a patient should never suffer without medication. States are also trying to impose Step Therapy/ Fail First (read about it) I recently posted about it. Stay strong be encouraged ❤️💐

MSbeGone profile image
MSbeGone

hello, did your doctor say why you were switched off copaxone. The progression of your disease could be the reason to be switched off.

SunnyDays202 profile image
SunnyDays202

Hi anyone who can help please pm me thanks. Im in the UK in a nightmare situation

SunnyDays202 profile image
SunnyDays202

Thanks for your comments and taken under advisement, nonetheless if anyone could help pm me id appreciate it. Terrible situation sadly

Not what you're looking for?

You may also like...

For Copaxone Users

I'm sure you already have a handle on site reactions, but thought I'd share what has worked best...
greaterexp profile image

Copaxone users??

Twice now when I got to inject (I inject manually), the plunger does not want to “plunge”. I try to...
Tulip77 profile image

Copaxone

Just out of curiosity, what time of day do you take and/or recommend taking your Copaxone shot? I...
Jesmcd2 profile image
CommunityAmbassador

Copaxone 3 day

Can anyone tell me the difference between Copaxone 7 day vs Copaxone 3 day other than the obvious...

Secondary Progressive taking Copaxone

Has anyone moved from RR into Secondary Progressive and continued taking Copaxone? I have been for...
LindaHen profile image

Moderation team

See all
johnMSAA profile image
johnMSAAPartner

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.