Search
Search
About
Log in
Join
Experiences with
Copaxone
Posts
Communities
228 public posts
Filter results
Finally
I don’t know how i did it but I finally managed to take my first
copaxone
injection. And of course it went really well just minor stinging which was gone within 20 minuets. I wish I had just done it sooner.
I don’t know how i did it but I finally managed to take my first
copaxone
injection. And of course it went really well just minor stinging which was gone within 20 minuets. I wish I had just done it sooner.
Jeremyhess1980
in
My MSAA Community
6 years ago
Response to Gilda5
However, the daily
Copaxone
injection had become a standard, almost automatic, part of my daily morning routine. The
Copaxone
is working well for me. There are now some oral & other med options that might or might not work as well.
However, the daily
Copaxone
injection had become a standard, almost automatic, part of my daily morning routine. The
Copaxone
is working well for me. There are now some oral & other med options that might or might not work as well.
LJMC
in
My MSAA Community
6 years ago
Newbie here, just saying hi!
I'm currently taking 40mg of
Copaxone
3 times a week (but the injection site reactions have been pretty bad, so I don't know how long I'll stick with it.) The worst of the ongoing symptoms I've had so far is just the unrelenting fatigue, and the bladder issues.
I'm currently taking 40mg of
Copaxone
3 times a week (but the injection site reactions have been pretty bad, so I don't know how long I'll stick with it.) The worst of the ongoing symptoms I've had so far is just the unrelenting fatigue, and the bladder issues.
acguinn0215
in
My MSAA Community
6 years ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
Hello
I’ve been on
Copaxone
, Tecfedera and Gilenya; I am currently taking that one. I have relapsing remitting ms. I felt relieved to finally have a diagnosis. It took about 6 years to get a diagnosis. I’m losing some weight and taking care of myself.
I’ve been on
Copaxone
, Tecfedera and Gilenya; I am currently taking that one. I have relapsing remitting ms. I felt relieved to finally have a diagnosis. It took about 6 years to get a diagnosis. I’m losing some weight and taking care of myself.
Girl50
in
My MSAA Community
6 years ago
DMT for those who work with kids?
I take
Copaxone
. My neurologist wants to put me on something stronger, but I am afraid stronger medication lowers my immune system and I will be sick all the time. I’ve had breast cancer, so I know one medication is out.
I take
Copaxone
. My neurologist wants to put me on something stronger, but I am afraid stronger medication lowers my immune system and I will be sick all the time. I’ve had breast cancer, so I know one medication is out.
Rileymom
in
My MSAA Community
6 years ago
copaxone vs ocrevus
I'm thinking of going back on
copaxone
. After my two 1/2 and two whole doses of ocrevus I still feel like I'm going downhill!
I'm thinking of going back on
copaxone
. After my two 1/2 and two whole doses of ocrevus I still feel like I'm going downhill!
judymax
in
My MSAA Community
6 years ago
I want off my Copaxone
I'm seriously considering going off
Copaxone
, and I may very well not want to be on ANY meds. I need to know if any of you know anyone who's gone off their meds...successfully. I'm an avid health guru, and I've never been big on "traditional medicine".
I'm seriously considering going off
Copaxone
, and I may very well not want to be on ANY meds. I need to know if any of you know anyone who's gone off their meds...successfully. I'm an avid health guru, and I've never been big on "traditional medicine".
laurenhc
in
My MSAA Community
6 years ago
Beyond frustrated
One doctor wants me to hold off on the
copaxone
injections till I’m on Prozac for a couple weeks. The neurologist says Prozac isn’t important right now.
One doctor wants me to hold off on the
copaxone
injections till I’m on Prozac for a couple weeks. The neurologist says Prozac isn’t important right now.
Jeremyhess1980
in
My MSAA Community
6 years ago
Back to whining
I had my
Copaxone
shot last night with no reaction. But today my muscles feel like I had Avonex. I feel sore as if I had worked out (I didn’t). My head hurts and I hurt ALL OVER. If I take more muscle relaxers then I will be DEEPLY DEPRESSED tomorrow and I am very sad already.
I had my
Copaxone
shot last night with no reaction. But today my muscles feel like I had Avonex. I feel sore as if I had worked out (I didn’t). My head hurts and I hurt ALL OVER. If I take more muscle relaxers then I will be DEEPLY DEPRESSED tomorrow and I am very sad already.
TracyBelle
in
My MSAA Community
6 years ago
Anyone else losing teeth?
I also heard yesterday that
Copaxone
can damage teeth. I was on
Copaxone
for 20+ years. I saw an oral surgeon yesterday to get the rest of my teeth taken out and he agreed steroids can do this. For the rest of my life go to scooterjon58.com.
I also heard yesterday that
Copaxone
can damage teeth. I was on
Copaxone
for 20+ years. I saw an oral surgeon yesterday to get the rest of my teeth taken out and he agreed steroids can do this. For the rest of my life go to scooterjon58.com.
scooterjon58
in
My MSAA Community
6 years ago
New Here...
Was on
Copaxone
for years and just moved to Ocrevus. Had my first half infusion last Tuesday with moderate side effects. The itching was the worst, but I got through it! Also had some fatigue and body aches, but they didn't last but a couple of days.
Was on
Copaxone
for years and just moved to Ocrevus. Had my first half infusion last Tuesday with moderate side effects. The itching was the worst, but I got through it! Also had some fatigue and body aches, but they didn't last but a couple of days.
miwido
in
My MSAA Community
6 years ago
My introduction
Been on
Copaxone
, Rebif, then began in the clinical trial for Fingolimod... Began taking Gilenya (aka Fingolimod) as soon as it was approved by FDA for release.
Been on
Copaxone
, Rebif, then began in the clinical trial for Fingolimod... Began taking Gilenya (aka Fingolimod) as soon as it was approved by FDA for release.
Shannondixon
in
My MSAA Community
6 years ago
10 Multiple Sclerosis Travel Tips
Received this email from Shared Solutions (
Copaxone
). A lot of the tips still apply to those on a pill form of meds: https://liftms.com/education/travel-tricks-and-tips?into_cid=em-copaxcons-julyem-40mgsat-traveltips6
Received this email from Shared Solutions (
Copaxone
). A lot of the tips still apply to those on a pill form of meds: https://liftms.com/education/travel-tricks-and-tips?into_cid=em-copaxcons-julyem-40mgsat-traveltips6
bxrmom
in
My MSAA Community
6 years ago
My neuro says don't need DMT since no changes in MRI in 2 years
I was on
Copaxone
for 7 years and did great with it, until I didn't. Balance, fatigue, etc. So previous neuro had me going to PT, Ampyra, etc. Current neurologist, we think he needs his own neuro! tells me 2 years ago I'm moved on to Secondary Progressive.
I was on
Copaxone
for 7 years and did great with it, until I didn't. Balance, fatigue, etc. So previous neuro had me going to PT, Ampyra, etc. Current neurologist, we think he needs his own neuro! tells me 2 years ago I'm moved on to Secondary Progressive.
purpletustin
in
My MSAA Community
6 years ago
Has anyone experienced tooth loss after taking Copaxone?
https://www.ehealthme.com/ds/
copaxone
/tooth-loss/
https://www.ehealthme.com/ds/
copaxone
/tooth-loss/
dogdaddy
in
My MSAA Community
6 years ago
Diagnosed in 1987 three years after my PhD defense and beginning R&D in biotechnology Industry.
I had been taking
Copaxone
since 1992 and hope it reduced the rate demyelination. After 2000 I started taking Avonex with the same hope, then after switch to Tysabri which I just discontinued this year of 2018, and now I'm back on Avon again.
I had been taking
Copaxone
since 1992 and hope it reduced the rate demyelination. After 2000 I started taking Avonex with the same hope, then after switch to Tysabri which I just discontinued this year of 2018, and now I'm back on Avon again.
DavidMaskalick
in
My MSAA Community
6 years ago
G'day Newbies
Back in the olden days we had the A B Cs Avonex Betaseron and
Copaxone
, lucky you you have a lot more to choose from these days, BUT YOU and only YOU have to Choose which one and You have to take it as prescribed.
Back in the olden days we had the A B Cs Avonex Betaseron and
Copaxone
, lucky you you have a lot more to choose from these days, BUT YOU and only YOU have to Choose which one and You have to take it as prescribed.
RoyceNewton
in
My MSAA Community
6 years ago
MS giving flu like symptoms
I’m currently not taking any meds as I had a really bad reaction to
Copaxone
2 months ago. I’m scheduled to see my neurologist on Thursday. I just hope I start to feel better soon, I really don’t like the solumedrol (steroid) treatment. 😔
I’m currently not taking any meds as I had a really bad reaction to
Copaxone
2 months ago. I’m scheduled to see my neurologist on Thursday. I just hope I start to feel better soon, I really don’t like the solumedrol (steroid) treatment. 😔
Eveliz
in
My MSAA Community
6 years ago
Gilenya experience?
Unfortunately
Copaxone
does not seem to be working. Thanks!
Unfortunately
Copaxone
does not seem to be working. Thanks!
cgladdin
in
My MSAA Community
6 years ago
Migraine meds
I currently take Topamax which it worked in the beginning but it doesn't seem to be really working any more and I just read that a side effect is weight loss which could explain my continued weight loss after being off of
Copaxone
now for a year and being on Tecfidera.
I currently take Topamax which it worked in the beginning but it doesn't seem to be really working any more and I just read that a side effect is weight loss which could explain my continued weight loss after being off of
Copaxone
now for a year and being on Tecfidera.
bxrmom
in
My MSAA Community
6 years ago
1
...
5
6
7
...
12
Next page
10
Filter results
Clear filters
Posted in
All communities
My MSAA Community
225 results
Functional Neurological Disorder - FND Hope
1 result
MS Society
1 result
View top 10 communities
Sort by
Most Relevant
Newest