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MRI and followup
I remembered that Hurricane Harvey had interrupted my shipment of
Copaxone
for about a week. Maybe that's the cause of the relapse? In any case, dr says Brain MRI is improved and spinal MRI appears unchanged, so DMT change is up to me. I'll take that as good news!
I remembered that Hurricane Harvey had interrupted my shipment of
Copaxone
for about a week. Maybe that's the cause of the relapse? In any case, dr says Brain MRI is improved and spinal MRI appears unchanged, so DMT change is up to me. I'll take that as good news!
latellama
in
My MSAA Community
7 years ago
Have 6 month recheck on Dec 14th with Neuro...
My frequent headaches, dizzy laying on my left side, and the weight-loss after stopping
Copaxone
and starting Tecfidera. Will of course I will update everyone after my appointment. Jessie p.s.
My frequent headaches, dizzy laying on my left side, and the weight-loss after stopping
Copaxone
and starting Tecfidera. Will of course I will update everyone after my appointment. Jessie p.s.
bxrmom
in
My MSAA Community
7 years ago
Banned from Ibuprofen?
I was only on
Copaxone
& Amitriptyline at the time...nothing really says not to take it. I've now been told by 2 Neuro's and my new primary care doc that I can't take it?
I was only on
Copaxone
& Amitriptyline at the time...nothing really says not to take it. I've now been told by 2 Neuro's and my new primary care doc that I can't take it?
cassielynn71
in
My MSAA Community
7 years ago
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Copaxone and weight gain
I have been meaning to look up weight gain with
Copaxone
and found these articles on drugs.com and webmd about a possible side effect: https://www.drugs.com/sfx/
copaxone
-side-effects.html https://www.webmd.com/drugs/2/drug-321/
copaxone
-subcutaneous/details/list-sideeffects It was overtime that I had
I have been meaning to look up weight gain with
Copaxone
and found these articles on drugs.com and webmd about a possible side effect: https://www.drugs.com/sfx/
copaxone
-side-effects.html https://www.webmd.com/drugs/2/drug-321/
copaxone
-subcutaneous/details/list-sideeffects It was overtime that I had
bxrmom
in
My MSAA Community
7 years ago
Year mark and doctor visit
I really wanted
Copaxone
to work for me and allow me to "forget" I have MS. Ah well. Rose colored glasses don't look that great on me. ;) Kim
I really wanted
Copaxone
to work for me and allow me to "forget" I have MS. Ah well. Rose colored glasses don't look that great on me. ;) Kim
latellama
in
My MSAA Community
7 years ago
The Ocrevus roller coaster 🎢
I would also like to state that even so, it's far better than the side effects I dealt with on Tifecdera, Gillenia and
Copaxone
. I am hopefull that the extreme fatigue will pass soon. I am relatively optamistic on that due the vertigo hung around quite a bit longer with my first two infusions.
I would also like to state that even so, it's far better than the side effects I dealt with on Tifecdera, Gillenia and
Copaxone
. I am hopefull that the extreme fatigue will pass soon. I am relatively optamistic on that due the vertigo hung around quite a bit longer with my first two infusions.
Allen5280
in
My MSAA Community
7 years ago
Thank you!
Copaxone
and Aubagio didn't help whatsoever. I'm trying to find out how I can get life insurance. Since my diagnosis, I have had to leave work and lost my life insurance. I applied for a policy and of course was declined....
Copaxone
and Aubagio didn't help whatsoever. I'm trying to find out how I can get life insurance. Since my diagnosis, I have had to leave work and lost my life insurance. I applied for a policy and of course was declined....
lynnkova
in
My MSAA Community
7 years ago
Change from Copaxone to Aubagio
HI all, I've been on
Copaxone
for about a year and although I've had no relapses, I feel I have degraded a bit with my current symptoms. Rather than taking more time to see if the downward trend continues my neuro has suggested moving to Aubagio or Ocrevus.
HI all, I've been on
Copaxone
for about a year and although I've had no relapses, I feel I have degraded a bit with my current symptoms. Rather than taking more time to see if the downward trend continues my neuro has suggested moving to Aubagio or Ocrevus.
pmbevac
in
My MSAA Community
7 years ago
Secondary Progressive
1st diagnosed with RRMS 2009 have used
Copaxone
Rebif and now Avonex. Have been told by doctor that we are now looking at Secondary Progressive. He is not yet changing Medication and I have next appointment in Jan 2018. Currently on Avonex. I feel that Avonex is not a correct Medication.
1st diagnosed with RRMS 2009 have used
Copaxone
Rebif and now Avonex. Have been told by doctor that we are now looking at Secondary Progressive. He is not yet changing Medication and I have next appointment in Jan 2018. Currently on Avonex. I feel that Avonex is not a correct Medication.
chickadee59
in
My MSAA Community
7 years ago
Ovrevus
I think it's going to be worth it not having to have the
Copaxone
injections. At least I have six months before next infusion!
I think it's going to be worth it not having to have the
Copaxone
injections. At least I have six months before next infusion!
judymax
in
My MSAA Community
7 years ago
Changing medicine
I told him "I give up .I am just going back on the
Copaxone
" . He goes to the doctors office to find out what is going on. They send him to cardiology. He waits 1 hour to be told the results are in the computer they should have them. He getsa copy and goes back to neurologist. Waits again.
I told him "I give up .I am just going back on the
Copaxone
" . He goes to the doctors office to find out what is going on. They send him to cardiology. He waits 1 hour to be told the results are in the computer they should have them. He getsa copy and goes back to neurologist. Waits again.
cljones
in
My MSAA Community
7 years ago
Copaxone to Ocrevus?
I have been on
Copaxone
since 2001 and have been doing relatively well.
I have been on
Copaxone
since 2001 and have been doing relatively well.
cgladdin
in
My MSAA Community
7 years ago
Fun
Been on
Copaxone
, had tissue damage, swapped to Tysabri and now (October) being swapped to Ocrivus System keeps spelling, I know correct way to spell and say. Am nervous about switching!
Been on
Copaxone
, had tissue damage, swapped to Tysabri and now (October) being swapped to Ocrivus System keeps spelling, I know correct way to spell and say. Am nervous about switching!
Sggmcswain
in
My MSAA Community
7 years ago
Newly diagnosed R&R
I'm on
copaxone
. Feeling pretty overwhelmed. I have horrible balance issues and pain in my right foot and right shoulder blade. Scared of what's to come for myself, husband and our teenager.
I'm on
copaxone
. Feeling pretty overwhelmed. I have horrible balance issues and pain in my right foot and right shoulder blade. Scared of what's to come for myself, husband and our teenager.
suzy20
in
My MSAA Community
7 years ago
I thought I was doing great!
I'm on
Copaxone
for just over a yr. She was concerned. Then as she's reading the results of my psych appt aloud, I was stunned. I did horrible. All noted "as expected for MS". I think that's when the anxiety hit.
I'm on
Copaxone
for just over a yr. She was concerned. Then as she's reading the results of my psych appt aloud, I was stunned. I did horrible. All noted "as expected for MS". I think that's when the anxiety hit.
cassielynn71
in
My MSAA Community
7 years ago
52 Ron
I have been on
Copaxone
for the last 17 years.
I have been on
Copaxone
for the last 17 years.
52ron
in
My MSAA Community
7 years ago
Has anyone gone off their DMTs?
I brought this subject with my MS doctor at my last appointment and he looked at all my MRIs and spinal scans for the past 12 years and we decided I could try going off
Copaxone
which I have taken for 12 years at the end of this month. I will do a MRI in January and follow up with him in February.
I brought this subject with my MS doctor at my last appointment and he looked at all my MRIs and spinal scans for the past 12 years and we decided I could try going off
Copaxone
which I have taken for 12 years at the end of this month. I will do a MRI in January and follow up with him in February.
BigMar7
in
My MSAA Community
7 years ago
Tysabri
I am receiving help on my
Copaxone
but the help I was getting ran out. I have been off my medicine for a week. They are working on getting me more help. I think when I go to my doctor next week he may suggest Tysabri again. So I would like any information available.
I am receiving help on my
Copaxone
but the help I was getting ran out. I have been off my medicine for a week. They are working on getting me more help. I think when I go to my doctor next week he may suggest Tysabri again. So I would like any information available.
cljones
in
My MSAA Community
7 years ago
Still fighting
I am taking
Copaxone
but I don't know if it is helping. I would like to know if steroids has helped anyone. I asked my doctor about them for me and he said won't help. My walking and weaknesses is getting worse. I have alot of balance issuses and have fallen many times.
I am taking
Copaxone
but I don't know if it is helping. I would like to know if steroids has helped anyone. I asked my doctor about them for me and he said won't help. My walking and weaknesses is getting worse. I have alot of balance issuses and have fallen many times.
cljones
in
My MSAA Community
7 years ago
New to this page
In Oct of 2016 i was diagnoused with MS and pit on
Copaxone
. My fatigue can be extreme. My cognition is becoming an issue along with many other symptoms. Trying to learn as much as i can and make good decisions for my family and my future.
In Oct of 2016 i was diagnoused with MS and pit on
Copaxone
. My fatigue can be extreme. My cognition is becoming an issue along with many other symptoms. Trying to learn as much as i can and make good decisions for my family and my future.
Njjack1
in
My MSAA Community
7 years ago
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