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Copaxone
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New here and love the positivity
I have PT, OT, and ST twice weekly and have started
copaxone
. I miss my "real life" and am trying to adjust to my new reality. Just want to say hello and thanks to everyone for sharing! Kim
I have PT, OT, and ST twice weekly and have started
copaxone
. I miss my "real life" and am trying to adjust to my new reality. Just want to say hello and thanks to everyone for sharing! Kim
latellama
in
My MSAA Community
8 years ago
Auto-injector, Copaxone, wasting a syringe
Over the past 16+ years my wife, a PWMS, has benefited from
Copaxone
. For 15 years, every day (20 ml), since early 2016, three a week (40ml). In all those years I bet I could count the number of wasted syringes on one hand but it still galls me when it occurs.
Over the past 16+ years my wife, a PWMS, has benefited from
Copaxone
. For 15 years, every day (20 ml), since early 2016, three a week (40ml). In all those years I bet I could count the number of wasted syringes on one hand but it still galls me when it occurs.
BUZZ1397
in
My MSAA Community
8 years ago
Starting Copaxone Monday. Any advice?
The Shared Solutions nurse is coming Monday to get me started on the 40 mg of
Copaxone
. I'm not at all nervous about injections, but not excited about potential side effects. I've never taken anything remotely like this. If anyone has advice, I'd love to hear it.
The Shared Solutions nurse is coming Monday to get me started on the 40 mg of
Copaxone
. I'm not at all nervous about injections, but not excited about potential side effects. I've never taken anything remotely like this. If anyone has advice, I'd love to hear it.
greaterexp
in
My MSAA Community
8 years ago
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Happy New Year
I have been on
Copaxone
and look and feel like a human pin cushion after all these years. I have been retired for 9 years and and have limited mobility. I am new to this site and look forward to being here.
I have been on
Copaxone
and look and feel like a human pin cushion after all these years. I have been retired for 9 years and and have limited mobility. I am new to this site and look forward to being here.
BigMar7
in
My MSAA Community
8 years ago
Hi, I am Aliciab523
He takes
Copaxone
3x a week and it has not many side effects, except a reaction when he takes the shots. It has kept his MS stable, thank God. His MRI's are stable and no new lesions. Yea! He does deal with fatigue, brain fog and numbness, too.
He takes
Copaxone
3x a week and it has not many side effects, except a reaction when he takes the shots. It has kept his MS stable, thank God. His MRI's are stable and no new lesions. Yea! He does deal with fatigue, brain fog and numbness, too.
aliciab523
in
My MSAA Community
8 years ago
Introduction
I started on
Copaxone
immediately after the diagnosis. Changed to Tysabri and had one infusion then they took it off the market. Went back to
Copaxone
then changed later to Rebif. My liver didn't like Rebif so went back on
Copaxone
.
I started on
Copaxone
immediately after the diagnosis. Changed to Tysabri and had one infusion then they took it off the market. Went back to
Copaxone
then changed later to Rebif. My liver didn't like Rebif so went back on
Copaxone
.
megraham
in
My MSAA Community
8 years ago
New to this site but not new to MS
I am currently on the high dose of
Copaxone
3x week. I do not really like it but I tried Abagio and had major side effects from it despite my neurologist saying my symptoms were not from the Abagio. Oh well, what can you do? Enough about me. How is everyone doing after the holidays?
I am currently on the high dose of
Copaxone
3x week. I do not really like it but I tried Abagio and had major side effects from it despite my neurologist saying my symptoms were not from the Abagio. Oh well, what can you do? Enough about me. How is everyone doing after the holidays?
Susan219
in
My MSAA Community
8 years ago
Foxy
I was diagnosed in 2009 with Multiple Sclerosis.I have been on
copaxone
and blessed with a great support system.To me it is 5% disease, and 95% mental attitude. I am still working every day and refuse to let this minor stumbling block keep me from being me.
I was diagnosed in 2009 with Multiple Sclerosis.I have been on
copaxone
and blessed with a great support system.To me it is 5% disease, and 95% mental attitude. I am still working every day and refuse to let this minor stumbling block keep me from being me.
lilfoot57
in
My MSAA Community
8 years ago
New here but not to MS
I was on
Copaxone
until it stopped working for me and have been on Tysabri the last 5 years despite being JVC+. A few months ago my Neuro started me on the extended infusion schedule so I'm now going every 56 days instead of every 28 days.
I was on
Copaxone
until it stopped working for me and have been on Tysabri the last 5 years despite being JVC+. A few months ago my Neuro started me on the extended infusion schedule so I'm now going every 56 days instead of every 28 days.
Raingrrl
in
My MSAA Community
8 years ago
New to Aubagio
Been on
Copaxone
for ten year my doctor change me to Aubagio it is nice of having any shots,
Been on
Copaxone
for ten year my doctor change me to Aubagio it is nice of having any shots,
Hidden
in
My MSAA Community
8 years ago
My (our) official Intro...
She's been on most of the injectable A-B-C drugs and has been on
Copaxone
for many years now. Except for the slow progression of the disease, we are mostly happy with her medication. She is, also, on many meds to help with the MS symptoms.
She's been on most of the injectable A-B-C drugs and has been on
Copaxone
for many years now. Except for the slow progression of the disease, we are mostly happy with her medication. She is, also, on many meds to help with the MS symptoms.
Hidden
in
My MSAA Community
8 years ago
Aubagio
Diagnosed June 2015, went on
copaxone
and recent MRI showed new lesions. Nuero suggested Aubgio. I start in couple of days and honestly I am pretty scared of the side effects. Can anyone tell me about thier experince with it?
Diagnosed June 2015, went on
copaxone
and recent MRI showed new lesions. Nuero suggested Aubgio. I start in couple of days and honestly I am pretty scared of the side effects. Can anyone tell me about thier experince with it?
masontimesfour
in
My MSAA Community
8 years ago
About the Shingle and pneumonia vaccine
Since you are on
Copaxone
, which doesn't suppress your immune system, I don't think you need to get it at this time unless otherwise indicated by your primary care provider. As for the shingles vaccine, we recommend M.S.
Since you are on
Copaxone
, which doesn't suppress your immune system, I don't think you need to get it at this time unless otherwise indicated by your primary care provider. As for the shingles vaccine, we recommend M.S.
Jesmcd2
CommunityAmbassador
in
My MSAA Community
8 years ago
CharlesHH
I was on
copaxone
for 2 years rebif for 1 year and currently on retuxin every 6 months. I have tried every thing to slow the progression but have not found anything to slow it (i.e. diet,exercise,drugs,herbal). My walking has gotten a lot worse even when I keep pushing myself hard.
I was on
copaxone
for 2 years rebif for 1 year and currently on retuxin every 6 months. I have tried every thing to slow the progression but have not found anything to slow it (i.e. diet,exercise,drugs,herbal). My walking has gotten a lot worse even when I keep pushing myself hard.
CharlesHH
in
My MSAA Community
8 years ago
Copaxone
Just out of curiosity, what time of day do you take and/or recommend taking your
Copaxone
shot? I take mine in the morning. :)
Just out of curiosity, what time of day do you take and/or recommend taking your
Copaxone
shot? I take mine in the morning. :)
Jesmcd2
CommunityAmbassador
in
My MSAA Community
8 years ago
Anyone with ROOT CANALS?
I also just found out yesterday that
Copaxone
causes tooth decay. I am still convinced it is the safest DMT so I won't switch anyway. It did make me feel less guilty somehow though to know that the tooth problems come from the medicine and are not somehow my fault.
I also just found out yesterday that
Copaxone
causes tooth decay. I am still convinced it is the safest DMT so I won't switch anyway. It did make me feel less guilty somehow though to know that the tooth problems come from the medicine and are not somehow my fault.
TracyBelle
in
My MSAA Community
8 years ago
Ongoing reactions to copaxone
I posted my reactions to
copaxone
a few months ago and now that I've been using
copaxone
my reactions seem to be getting a bit worse. I'm wondering if anyone else is having this issue or has dealt with this type of thing? I cannot see my doctor until January.
I posted my reactions to
copaxone
a few months ago and now that I've been using
copaxone
my reactions seem to be getting a bit worse. I'm wondering if anyone else is having this issue or has dealt with this type of thing? I cannot see my doctor until January.
37kf80
in
My MSAA Community
8 years ago
Medicine switch
I have been taking
copaxone
three times a week. It used to be every day till it was changed. My doctor says I've become immune to it so she has changed my med to trecfidera. I start this Saturday when my hubby will be home in case something happens.
I have been taking
copaxone
three times a week. It used to be every day till it was changed. My doctor says I've become immune to it so she has changed my med to trecfidera. I start this Saturday when my hubby will be home in case something happens.
Momjules
in
My MSAA Community
8 years ago
Hi y'all! I'm Katie from Texas...
I currently take
Copaxone
to help manage the disease. I'm a General Manager for a major clothing retailer. Overall I've been able to handle working but have had a few times that I've needed STD. The last couple of years in the spring I seem to have an exacerbation.
I currently take
Copaxone
to help manage the disease. I'm a General Manager for a major clothing retailer. Overall I've been able to handle working but have had a few times that I've needed STD. The last couple of years in the spring I seem to have an exacerbation.
meowmix915
in
My MSAA Community
8 years ago
Tysabri
I was diagnosed two years ago and have only been on
Copaxone
. My neurologist wants to put me on Tysabri because I had a legion this summer on my MRI. Has anyone been on this? What was your experience if you were?
I was diagnosed two years ago and have only been on
Copaxone
. My neurologist wants to put me on Tysabri because I had a legion this summer on my MRI. Has anyone been on this? What was your experience if you were?
Pbargal
in
My MSAA Community
8 years ago
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