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Copaxone
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Copaxone
Hi all, Im out of meds, my dr has switched me off
copaxone
and i want my old friend. I really could do with help. If anyone has spare please let me know its urgent. Thanks E
Hi all, Im out of meds, my dr has switched me off
copaxone
and i want my old friend. I really could do with help. If anyone has spare please let me know its urgent. Thanks E
SunnyDays202
in
My MSAA Community
2 months ago
Possible Anaphylaxis with Glatimirer Acetate
But the gist of this post is that in Europe they are putting a warning on generic
copaxone
that it can cause a life-threatening allergic reaction. Something to ask your neurologist about if you are using a generic version of
Copaxone
.
But the gist of this post is that in Europe they are putting a warning on generic
copaxone
that it can cause a life-threatening allergic reaction. Something to ask your neurologist about if you are using a generic version of
Copaxone
.
CatsandCars
in
My MSAA Community
2 months ago
Autoinjector
Is there another to use with
Copaxone
40mg? Read about the WhisperJect but not sure it can b used for
Copaxone
. Anyone know or is using it? Thank you all!
Is there another to use with
Copaxone
40mg? Read about the WhisperJect but not sure it can b used for
Copaxone
. Anyone know or is using it? Thank you all!
Christopher04
in
My MSAA Community
4 months ago
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Smile, and you get through it...
So my next move is Kesimpta or back to
Copaxone
.... Any info on Kesimpta would be awesome! Missed you guys!, 🤗💕🌠
So my next move is Kesimpta or back to
Copaxone
.... Any info on Kesimpta would be awesome! Missed you guys!, 🤗💕🌠
Jesmcd2
CommunityAmbassador
in
My MSAA Community
8 months ago
This is a day of winning 💪
Promise I'm not proud of that 😅).For the MS, I was on
copaxone
, tried on tysabri (couldn't continue, high JCV titre), so back on
copaxone
until the 1st of my status epilepticus events, then ocrevus, and I'm now on kesimpta. I don't think the kesimpta is working well for me.
Promise I'm not proud of that 😅).For the MS, I was on
copaxone
, tried on tysabri (couldn't continue, high JCV titre), so back on
copaxone
until the 1st of my status epilepticus events, then ocrevus, and I'm now on kesimpta. I don't think the kesimpta is working well for me.
Cwright170994
in
My MSAA Community
8 months ago
Medication Bureaucracy-“ So Tired of it.”
Lastly, approved
Copaxone
for a $4000.00 Co -Pay; why because I take the Brand instead of the generic - “ Ancillary differential “ or so they call it! Now, I’m told to have my doctor write a letter stating the generic makes me ill.
Lastly, approved
Copaxone
for a $4000.00 Co -Pay; why because I take the Brand instead of the generic - “ Ancillary differential “ or so they call it! Now, I’m told to have my doctor write a letter stating the generic makes me ill.
stepsforNeeC
in
My MSAA Community
8 months ago
Copaxone dropped from formulary
I take the daily, and going forward the formulary will cover the generic; the 3-times-a-week
Copaxone
isn't listed as an alternative, so I assume they're dropping that, too. Of course there is NO collusion between the drug manufacturers and the insurance companies! Hmmmm
I take the daily, and going forward the formulary will cover the generic; the 3-times-a-week
Copaxone
isn't listed as an alternative, so I assume they're dropping that, too. Of course there is NO collusion between the drug manufacturers and the insurance companies! Hmmmm
MrStripey
in
My MSAA Community
11 months ago
Insurance Disaster!
Found that Glatopa (a generic of
Copaxone
) had a copay assistance that I qualified for. It was a maximum of $9,000 annually. That would cover 6 months of the copays. I actually had a 3 month supply of extra med so I figured that I would only need to pay the $1500 3 times.
Found that Glatopa (a generic of
Copaxone
) had a copay assistance that I qualified for. It was a maximum of $9,000 annually. That would cover 6 months of the copays. I actually had a 3 month supply of extra med so I figured that I would only need to pay the $1500 3 times.
elaineinqueens
in
My MSAA Community
8 months ago
Well, rats
I haven't been seen by a neurologist for a couple of years after stopping
Copaxone
. I've enjoyed not being tied to a medication and especially not dealing with insurance and specialty pharmacies (horrors!).
I haven't been seen by a neurologist for a couple of years after stopping
Copaxone
. I've enjoyed not being tied to a medication and especially not dealing with insurance and specialty pharmacies (horrors!).
greaterexp
in
My MSAA Community
9 months ago
25 Nov 2023 Read the whole article before YOU comment.
Where does
Copaxone
come from, who makes it? Think about this. No more nee3 be said. Rest and relax through this and all holidays from now on. Take it very slow. YOU are fighting an incurable unknown illness. YOU may be bulletproof, but we have aa chink in our armor now.
Where does
Copaxone
come from, who makes it? Think about this. No more nee3 be said. Rest and relax through this and all holidays from now on. Take it very slow. YOU are fighting an incurable unknown illness. YOU may be bulletproof, but we have aa chink in our armor now.
RoyceNewton
in
My MSAA Community
10 months ago
Is it Just Me????
Copaxone
Injection 😪. I think when I take my injection it makes me "hyper sensitive" - in other words: I can be "cry baby.". A little sensitive and don't like to feel like I have to explain myself all the time.
Copaxone
Injection 😪. I think when I take my injection it makes me "hyper sensitive" - in other words: I can be "cry baby.". A little sensitive and don't like to feel like I have to explain myself all the time.
GratefulNeeC
in
My MSAA Community
10 months ago
MS Treatments
Doctor started me on Rebif but had to switch to
Copaxone
due to liver enzymes escalating. I have been using
Copaxone
since 2012 with very little side effects but my Doctor feels my MS might be progressing so she switched me to Abaigio.
Doctor started me on Rebif but had to switch to
Copaxone
due to liver enzymes escalating. I have been using
Copaxone
since 2012 with very little side effects but my Doctor feels my MS might be progressing so she switched me to Abaigio.
Caste19
in
My MSAA Community
1 year ago
Autoject for Copaxone discontinued—ARGH!!
Does anyone know whether there's another device that could handle
Copaxone
needles? I am simply not able to mentally face the prospect of sticking myself with a needle daily.
Does anyone know whether there's another device that could handle
Copaxone
needles? I am simply not able to mentally face the prospect of sticking myself with a needle daily.
MrStripey
in
My MSAA Community
1 year ago
Ocrevus
I have been on Ocrevus for 6 years, after being on
copaxone
for 5 years. I use a walker and need to self cath. Two years ago I was diagnosed with microscopic colitis. I’m not sure if this is a side effect from the infusions. I am debating about stopping the Ocrevus.
I have been on Ocrevus for 6 years, after being on
copaxone
for 5 years. I use a walker and need to self cath. Two years ago I was diagnosed with microscopic colitis. I’m not sure if this is a side effect from the infusions. I am debating about stopping the Ocrevus.
Linda3579
in
My MSAA Community
1 year ago
Vumerity
Switching from
Copaxone
40MG soon, which has been amazing for me, but skin needs a break. Any tips or things to be aware of when taking this? Really scared to make a switch. Side effects seem horrible for all the DMT’s. Trying to pick the one with the least potential issues.
Switching from
Copaxone
40MG soon, which has been amazing for me, but skin needs a break. Any tips or things to be aware of when taking this? Really scared to make a switch. Side effects seem horrible for all the DMT’s. Trying to pick the one with the least potential issues.
SGL33
in
My MSAA Community
4 months ago
Been away for a bit...depression hit hard
Been on Avonex, Rebif,
Copaxone
, Tecfidera, Vumerity, and Kesimpta. Each drug had its pros and cons, some side effects were more bearable than others. The Kesimpta, which I hoped would work for me, made me very sick and I stopped after six months.
Been on Avonex, Rebif,
Copaxone
, Tecfidera, Vumerity, and Kesimpta. Each drug had its pros and cons, some side effects were more bearable than others. The Kesimpta, which I hoped would work for me, made me very sick and I stopped after six months.
Helpmeup
in
My MSAA Community
1 year ago
Hello Everyone, Your Feedback is Welcome!
I take
Copaxone
because for me with other health issues it's the best option. After very careful thought and pray 🙏 I decided to stick and stay with my current Neuro.
I take
Copaxone
because for me with other health issues it's the best option. After very careful thought and pray 🙏 I decided to stick and stay with my current Neuro.
stepsforNeeC
in
My MSAA Community
1 year ago
13 Oct 2023 G'day
I hope none of the Teva (
Copaxone
) scientists were murdered this week. An ugly display of our species cruelty., Try not to be too upset. Cry a little, that is okay. Think of yourself. YOUR ms. There is little that we can do about this horror.
I hope none of the Teva (
Copaxone
) scientists were murdered this week. An ugly display of our species cruelty., Try not to be too upset. Cry a little, that is okay. Think of yourself. YOUR ms. There is little that we can do about this horror.
RoyceNewton
in
My MSAA Community
11 months ago
Its been awhile...
My Neuro is going to put me back on
Copaxone
... Why, you ask? Cause its all l can take!! Remember the last time l was on
Copaxone
? I ended up with Black Holes in my brain. Yes, its a thing... He knows this, I know this. He is sending me to Neuropallitive Care, I have my 1st appt in bout 2 wks.
My Neuro is going to put me back on
Copaxone
... Why, you ask? Cause its all l can take!! Remember the last time l was on
Copaxone
? I ended up with Black Holes in my brain. Yes, its a thing... He knows this, I know this. He is sending me to Neuropallitive Care, I have my 1st appt in bout 2 wks.
Jesmcd2
CommunityAmbassador
in
My MSAA Community
1 year ago
Tysabri for me
After my diagnosis only the ABC drugs—avonex, betaseron and
copaxone
—were available and I had intolerable symptoms. My doctor recommended Tysabri which was new at the time and it was recommended to be used only—not in combination with any other interferon or MS drug.
After my diagnosis only the ABC drugs—avonex, betaseron and
copaxone
—were available and I had intolerable symptoms. My doctor recommended Tysabri which was new at the time and it was recommended to be used only—not in combination with any other interferon or MS drug.
disconcerting
in
My MSAA Community
1 year ago
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