I had a similar experience when I was diagnosed. I had unexplained symptoms in the months leading up to the official diagnosis which were passed off by GPs as "some kind of virus". Having read about MS online I insisted on being referred to a neurologist who finally confirmed I had relapsing remitting MS. I was upset but at the same time relieved that I finally had an explanation for my symptoms.
I 've been on Copaxone now for almost a year and a half and during that time I have had no symptoms
6 weeks now, I've had what I'll call MS symptoms. Foggy head, Occipital nuralgia, numbness, tingling hands and feet, eye and facial twitching. Neuro said MRI has 2 UBO's could be nothing. report says, demylination. I have thryroid disease. Numbness and tingling has progressed, mostly in right side feels arthritic. 2nd opinion doc wants to send me to another neuro. Did you have lesions on brain and spine? Did you have MRI of spine too? Did you have a lumbar puncture?
when I'm ready to inject I heat the area first then clean it,, when I pull the cap off the injector I give it a little tap on the side with my fingers in case thers any copaxone in the needle then I sit on my couch relax and inject,,, then i press with a clean cotton ball and then i ice the area i find it helps allot,, I get very little burning
i sit for a bit relax for about 15 min. only cause I want to then I get up and get ready to go to work.
Glad you got your diagnosis. Limbo SUCKS! While it's not the 'best' news, when I got my diagnosis, after at least 2 years of symptoms, a sense of relief washed over me. I hugged my neurologist with a grin on my face.
I've been on Copaxone since May 08 (diagnosed March 08). I'm also a migraine sufferer.
Best Copax advice I got, after the shot, take the cotton ball, press firmly 30 sec (don't rub). This will reduce lumps!
Best of luck sweetie, keep up the good fight and the great videos!
Skin reactions: the burning and stinging you heard of... It's different in every individual and from one body part to another. The injection itself is no worst than a mosquito bite. But as copaxone is acid, it is not uncommon for people to feel a burning sensation right after the injection. From experience, I can tell you that it is VERY bearable. In my case, I would say that it happens once or twice each month and it doesn't last more than a couple of seconds.
For some, the dx comes as a tragedy and for others, it's welcomed as a relief. You're doing the right thing by educating yourself.
Effectiveness of all ABCR is similar. You can concentrate on which best fits your lifestyle and medical needs. Given your medical history, it seems that copaxone might be a wise choice.
Aside from occasional skin reactions, there are no common side effects. You may want to ask your doctor about other side effects...
I had a similar experience when I was diagnosed. I had unexplained symptoms in the months leading up to the official diagnosis which were passed off by GPs as "some kind of virus". Having read about MS online I insisted on being referred to a neurologist who finally confirmed I had relapsing remitting MS. I was upset but at the same time relieved that I finally had an explanation for my symptoms.
I 've been on Copaxone now for almost a year and a half and during that time I have had no symptoms
Sozymandias 3 years ago
Good.
Alexknobsob 3 years ago
6 weeks now, I've had what I'll call MS symptoms. Foggy head, Occipital nuralgia, numbness, tingling hands and feet, eye and facial twitching. Neuro said MRI has 2 UBO's could be nothing. report says, demylination. I have thryroid disease. Numbness and tingling has progressed, mostly in right side feels arthritic. 2nd opinion doc wants to send me to another neuro. Did you have lesions on brain and spine? Did you have MRI of spine too? Did you have a lumbar puncture?
hrwitch 3 years ago
Glad you were finally officially diagnosed. Limbo is annoying. Good luck with Copaxone my sister is on that and I'm on Tysabri.
spikegrl1000 3 years ago
when I'm ready to inject I heat the area first then clean it,, when I pull the cap off the injector I give it a little tap on the side with my fingers in case thers any copaxone in the needle then I sit on my couch relax and inject,,, then i press with a clean cotton ball and then i ice the area i find it helps allot,, I get very little burning
i sit for a bit relax for about 15 min. only cause I want to then I get up and get ready to go to work.
yiasas1962 3 years ago
Glad you got your diagnosis. Limbo SUCKS! While it's not the 'best' news, when I got my diagnosis, after at least 2 years of symptoms, a sense of relief washed over me. I hugged my neurologist with a grin on my face.
I've been on Copaxone since May 08 (diagnosed March 08). I'm also a migraine sufferer.
Best Copax advice I got, after the shot, take the cotton ball, press firmly 30 sec (don't rub). This will reduce lumps!
Best of luck sweetie, keep up the good fight and the great videos!
dmplaura 3 years ago
Skin reactions: the burning and stinging you heard of... It's different in every individual and from one body part to another. The injection itself is no worst than a mosquito bite. But as copaxone is acid, it is not uncommon for people to feel a burning sensation right after the injection. From experience, I can tell you that it is VERY bearable. In my case, I would say that it happens once or twice each month and it doesn't last more than a couple of seconds.
sophieadd 3 years ago
Seems like you've done your homework Nicole!
For some, the dx comes as a tragedy and for others, it's welcomed as a relief. You're doing the right thing by educating yourself.
Effectiveness of all ABCR is similar. You can concentrate on which best fits your lifestyle and medical needs. Given your medical history, it seems that copaxone might be a wise choice.
Aside from occasional skin reactions, there are no common side effects. You may want to ask your doctor about other side effects...
sophieadd 3 years ago
Sorry to hear this has happened.
I wish you all the best.
bornaangel 3 years ago
I'm sorry to hear and I hope you the best .
nightladymagic 3 years ago