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Copaxone
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Done!!
My real thrill is that my doctor agreed that it's time to stop the
Copaxone
! I'm progressing slowly, but not having any relapses and show no sign of changes in my MRIs.
My real thrill is that my doctor agreed that it's time to stop the
Copaxone
! I'm progressing slowly, but not having any relapses and show no sign of changes in my MRIs.
greaterexp
in
My MSAA Community
2 years ago
Post injection reaction to copaxone
Has anyone had a reaction to
copaxone
where after injecting it your chest felt like it was being squeezed along with dizziness and followed by cramps in the chest. What did your doctor instruct you to do? Been on
copaxone
for about 15 years and this never happened before.
Has anyone had a reaction to
copaxone
where after injecting it your chest felt like it was being squeezed along with dizziness and followed by cramps in the chest. What did your doctor instruct you to do? Been on
copaxone
for about 15 years and this never happened before.
Blue000
in
My MSAA Community
2 years ago
MRI Thursday
I really don't want to go back to
Copaxone
cuz the injections were leaving hard knots on my hips and belly & sinking my arms as if it was deteriorating the tissue. I've used Rebif(6mos), Techfedera(2yrs),
Copaxone
[7 & 3](12yrs) & Ocrevus(2yrs). I have a month to research & decide.
I really don't want to go back to
Copaxone
cuz the injections were leaving hard knots on my hips and belly & sinking my arms as if it was deteriorating the tissue. I've used Rebif(6mos), Techfedera(2yrs),
Copaxone
[7 & 3](12yrs) & Ocrevus(2yrs). I have a month to research & decide.
hairbrain4
in
My MSAA Community
2 years ago
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Anyone using Copaxone here?
Looking to learn from your experiance
Looking to learn from your experiance
EmmaHar132
in
MS Society
2 years ago
Covid anyone?
So i was on solumedrol 1000 mg once a month and PT(My DMT
Copaxone
). This was working for me. On December 20th another intravenous solumedrol. I became fatigued and had post nasal drip. I thought I was coming down with cold or getting sinus infection.
So i was on solumedrol 1000 mg once a month and PT(My DMT
Copaxone
). This was working for me. On December 20th another intravenous solumedrol. I became fatigued and had post nasal drip. I thought I was coming down with cold or getting sinus infection.
TonyiaR7
in
My MSAA Community
2 years ago
Greetings!
After using
Copaxone
, Rebif and now Ocrevus I'm back in the search for an MS med that’s ‘right for me’.
After using
Copaxone
, Rebif and now Ocrevus I'm back in the search for an MS med that’s ‘right for me’.
Peddler
in
My MSAA Community
3 years ago
Is anyone on Copaxone and how are you doing on it?
But i was also told about
Copaxone
.. I know it's a self injection but if anyone is on this one, how are you doing and what type of side effects, if any, are you having? I just cannot go thru another low white count situation like i did with the Mayzent.. It was a nightmare. never again.
But i was also told about
Copaxone
.. I know it's a self injection but if anyone is on this one, how are you doing and what type of side effects, if any, are you having? I just cannot go thru another low white count situation like i did with the Mayzent.. It was a nightmare. never again.
wolfmom21fl
in
My MSAA Community
3 years ago
NEW HERE - Choosing a medication and lost.
I was told to choose a medication and I have it narrowed down to Ocrevus, Tecfidera or
Copaxone
. Truthfully I am scared on going on any medication but I am strongly urged to do so. Can anyone provide any tips on choosing which medication and how you made your way through this journey?
I was told to choose a medication and I have it narrowed down to Ocrevus, Tecfidera or
Copaxone
. Truthfully I am scared on going on any medication but I am strongly urged to do so. Can anyone provide any tips on choosing which medication and how you made your way through this journey?
Greatful25
in
My MSAA Community
3 years ago
MRIs
At my last Neuro appt when the decision was made to go off
Copaxone
and switch to Aubagio, neuro ordered new MRIs w/wo contrast. I go in tomorrow for the scans. I am scared.
At my last Neuro appt when the decision was made to go off
Copaxone
and switch to Aubagio, neuro ordered new MRIs w/wo contrast. I go in tomorrow for the scans. I am scared.
Tulip77
in
My MSAA Community
3 years ago
Fatigue
I’ve been on
Copaxone
but am to start Aubagio Friday. I am a little scared of aubagio so we will see how that goes.
I’ve been on
Copaxone
but am to start Aubagio Friday. I am a little scared of aubagio so we will see how that goes.
Tulip77
in
My MSAA Community
3 years ago
DMTs- what are you on and how are you doing on it?
I am on
Copaxone
. I have appt with neuro tomorrow to talk about why that choice was made and what are the other options. I know there are several others but they never talked to me about it and gave any explanation.
I am on
Copaxone
. I have appt with neuro tomorrow to talk about why that choice was made and what are the other options. I know there are several others but they never talked to me about it and gave any explanation.
Tulip77
in
My MSAA Community
3 years ago
Better days!
Not sitting around like a zombie I can actually have a good brain function clear headed I actually feel normal in my head and except for my symptoms that I have a tremors and I can’t walk very well without a walker I don’t know I don’t seem to have any MS symptoms kind of odd isn’t it I was taking
copaxone
Not sitting around like a zombie I can actually have a good brain function clear headed I actually feel normal in my head and except for my symptoms that I have a tremors and I can’t walk very well without a walker I don’t know I don’t seem to have any MS symptoms kind of odd isn’t it I was taking
copaxone
Tracelr
in
My MSAA Community
3 years ago
New lesion
I took Tecfidera 1st, then because my WBC went so low switched to
Copaxone
. Been on that 8 yrs. so now it seems like either i become disabled, or die from a deadly disease. Can anyone please help me to feel better about this?
I took Tecfidera 1st, then because my WBC went so low switched to
Copaxone
. Been on that 8 yrs. so now it seems like either i become disabled, or die from a deadly disease. Can anyone please help me to feel better about this?
Neworleanslady
in
My MSAA Community
3 years ago
Copaxone users??
Twice now when I got to inject (I inject manually), the plunger does not want to “plunge”. I try to wiggle it around thinking it is not lined up correctly? I don’t know. Nothing helps. I end having to pull the needle out of myself and the restick in another area within the location. This has been in
Twice now when I got to inject (I inject manually), the plunger does not want to “plunge”. I try to wiggle it around thinking it is not lined up correctly? I don’t know. Nothing helps. I end having to pull the needle out of myself and the restick in another area within the location. This has been in
Tulip77
in
My MSAA Community
3 years ago
Better days!
Not sitting around like a zombie I can actually have a good brain function clear headed I actually feel normal in my head and except for my symptoms that I have a tremors and I can’t walk very well without a walker I don’t know I don’t seem to have any MS symptoms kind of odd isn’t it I was taking
copaxone
Not sitting around like a zombie I can actually have a good brain function clear headed I actually feel normal in my head and except for my symptoms that I have a tremors and I can’t walk very well without a walker I don’t know I don’t seem to have any MS symptoms kind of odd isn’t it I was taking
copaxone
Tracelr
in
My MSAA Community
3 years ago
Severe spasms and rigidity - say a little prayer for me ...
Copaxone
is the safest DMT with Covid Pandemic, I have been toldd. Yes, I am beyond the Tin Women of my unpredictable world. May be my spine and tail bone is the source of my pain from traveling traveling back forth to Long Island NY - 3 hour trip. I helped and tried to guide my younger brothers.
Copaxone
is the safest DMT with Covid Pandemic, I have been toldd. Yes, I am beyond the Tin Women of my unpredictable world. May be my spine and tail bone is the source of my pain from traveling traveling back forth to Long Island NY - 3 hour trip. I helped and tried to guide my younger brothers.
TonyiaR7
in
My MSAA Community
3 years ago
Would you dare admit to “going freestyle”??
😅 I stopped
Copaxone
for financial and ethical reasons, but also because I got to a point where my life was absolutely OVERTAKEN by “being an MS patient”. ...I was sick of it.
😅 I stopped
Copaxone
for financial and ethical reasons, but also because I got to a point where my life was absolutely OVERTAKEN by “being an MS patient”. ...I was sick of it.
HensTooth
in
My MSAA Community
3 years ago
Now What?
I think I will speak to my neurologist about moving to something else, but none really have the few side effects that
Copaxone
does for me. Has your neurologist allowed/encouraged a switch based mainly on being weary of the needles and lipoatrophy?
I think I will speak to my neurologist about moving to something else, but none really have the few side effects that
Copaxone
does for me. Has your neurologist allowed/encouraged a switch based mainly on being weary of the needles and lipoatrophy?
greaterexp
in
My MSAA Community
3 years ago
Holiday Greetings and Blessings to All!
Friday's are "injection day" for
Copaxone
and Melatonin tabs aren't working; my Neuro prescribed Zolpidem PRN (as yes they help tremendously) even though I don't want to rely on them. I mailed off my Christmas gifts to my three grandchildren in Delaware; I miss them so much!
Friday's are "injection day" for
Copaxone
and Melatonin tabs aren't working; my Neuro prescribed Zolpidem PRN (as yes they help tremendously) even though I don't want to rely on them. I mailed off my Christmas gifts to my three grandchildren in Delaware; I miss them so much!
stepsforNeeC
in
My MSAA Community
3 years ago
Copaxone and other stuff
Hi everyone! This past few weeks when I inject, I get a little bit of chest tightness. It is mild and lasts 5-10 minutes and then it’s gone. With my Friday night injection, I had the same thing but with a rush of metallic taste in my mouth. It lasted a little bit and then went away. I can deal with
Hi everyone! This past few weeks when I inject, I get a little bit of chest tightness. It is mild and lasts 5-10 minutes and then it’s gone. With my Friday night injection, I had the same thing but with a rush of metallic taste in my mouth. It lasted a little bit and then went away. I can deal with
Tulip77
in
My MSAA Community
3 years ago
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