Hey guys. My partner of 9 years was recently diagnosed with MS. We're both 27 years old and of course a little worried and scared and don't know where to go from here.
Alicia's doctor has prescribed her copax injections. The 40mg 3x a week. I'm curious if anyone has any advice about copax. What was your experience?
I forgot to add: she hasn't started the copax yet and seems to be putting it off because she is nervous about having a reaction to it. We are waiting for a home health nurse to come help show us how the injection process works and such.
Also, the insurance company she goes through wont pay for her perscription. The copay is about $4900 every three months. We have copay assistance through Mylein Advocates but that won't cover the entire year. Anybody know where else we can get help with the cost?
Any and all advice is greatly appreciated. Thanks for taking time out to read. :)
Hi I'm sorry to hear about her diagnosis. I believe that they have other programs through the ms association that may help. Also they have auto injunctors that they will give you through the pharmacy you just have to request it. It makes it easier to do your injunctions.
Thank you very much. We will check out the association to see if they can help as well.
I have been on copaxone since November. For me, it does cause pain (varying in intensity) and sometimes redness or a lump that eventually goes away. Aside from that, I have not had any side effects! I'm glad to be avoiding the possible flu like side effects that meds like Avonex can cause. It's annoying to give the shots, but it's not difficult (especially using the autoinjector). Having the nurse there with you the first time will probably help with peace of mind. Best wishes!
Thanks so much. She did get an auto injector and we are just waiting on a nurse to come over and help. :)
Have you noticed any changes with your MS symptoms since starting on copax? Alicia seems to be having a lot of brain fog and tingly sensations in her rib area. We are curious if the copax has helped relieve some symptoms for others.
No, I haven't noticed any change in symptoms. I don't think this med, or even most of the meds, are supposed to help with symptoms unfortunately. :( My current symptoms aren't bad, just mainly off and on tingling or pinprick like sensations in my hands and feet mostly. Sometimes what I wonder if it is brain fog (or could be just lack of sleep, lol), and occasional very mild dizziness.
I'd recommend giving us a call and connecting with our MS Navigator program- that would allow us to ask a few more questions to gather information to see what programs we may know of that could assist. 1 800 344 4867, option 1.
For now, here's additional resources: Finding Lower Priced Drugs
Jess, MS Navigator
Thanks so much. We will be calling sometime soon :)
I been on copaxon for four years. Sheer solutions is the pharmaceutical Company that manufactures copaxon. They have a program where they picked up your co-pay . I have never paid a dime for it. The only side effect is a sore injections site . I put a small ice pack on it . They have a website teaching you how to take the injections along with the nurse coming very very helpful.
I’ve been on Copaxone for 6 years. Started with the daily injections and now take the 40mg 3 times a week. Shared Solutions is the name under which Teva Pharmaceuticals administers Copaxone, offers support, etc. Shared Solutions was very helpful to me during the early days of my diagnosis.
Sounds familiar dr just put me on same thing I chose it cause it seemed like the least side effects of the 3 he suggested the auto injection system seems easy to use. Let's keep in touch we can compare notes. I'm starting Wednesday.
How's it going with your injections?
Sorry didn't see your post. I decided to wait and follow my original dr's idea of waiting to do another MRI before starting treatment the dr that prescribed it was the one I got a second opinion from. I just started to feel uncomfortable with him (no bedside manner) just felt like a number on his to do list. I expressed my concern to my dr and he moved MRI up to may 10th and we are sitting down to discuss treatment the 15th . I want to get started on treatment asap cause it seems like everyone agrees the sooner the better. My dr was only waiting cause I had other issues to deal with but I am no longer comfortable waiting. I'll keep a better eye on website and update on what is happening. Hope all is going well for you.