Search
Search
About
Log in
Join
Experiences with
Copaxone
Posts
Communities
227 public posts
Filter results
Hanging by that familiar thread again
I still don’t have any
Copaxone
. My mom passed away, left the life insurance to my brother (she thought that I would be a successful lawyer- so I wouldn’t need my half.) My brother has only visited her once since 2007.
I still don’t have any
Copaxone
. My mom passed away, left the life insurance to my brother (she thought that I would be a successful lawyer- so I wouldn’t need my half.) My brother has only visited her once since 2007.
TracyBelle
in
My MSAA Community
5 years ago
Goals goals goals
She who must be obeyed is on
Copaxone
and her 3 a week schedule screws her up a lot. She has RRms twenty-three years I believe. She never forgets her RRms anniversary, it was near a cousins wedding, but she has a habit of doing her shoot really late instead of early.
She who must be obeyed is on
Copaxone
and her 3 a week schedule screws her up a lot. She has RRms twenty-three years I believe. She never forgets her RRms anniversary, it was near a cousins wedding, but she has a habit of doing her shoot really late instead of early.
RoyceNewton
in
My MSAA Community
5 years ago
Medication change
So has anyone medication has been changed from
copaxone
to glatopa??
So has anyone medication has been changed from
copaxone
to glatopa??
Mrsfig
in
My MSAA Community
5 years ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
Do you see the possibilities around "YOU"?
The next year I believe Avonex then
Copaxone
came along. Rebif was next, it meant fewer needles so of course, I went for it as soon as it came on the market.
The next year I believe Avonex then
Copaxone
came along. Rebif was next, it meant fewer needles so of course, I went for it as soon as it came on the market.
RoyceNewton
in
My MSAA Community
5 years ago
Update on Dermatology appt :)
Most likely it is from when I was on the
Copaxone
injections and I nicked a vein. The weird part is that after the biopsy was done and it started to heal the pain on the side of my leg has gone away! She laughed about it and said 'I cured you' lol It's weird but I'll take it.
Most likely it is from when I was on the
Copaxone
injections and I nicked a vein. The weird part is that after the biopsy was done and it started to heal the pain on the side of my leg has gone away! She laughed about it and said 'I cured you' lol It's weird but I'll take it.
bxrmom
in
My MSAA Community
5 years ago
Making "Lemonade Out of Lemons" - and trying to stay positive!
Many headaches too as I just found out my pharmacy doesn't want to cover
Copaxone
and removed it from a Tier 2 -5 Category giving me an outrageous patient co - pay! The BATTLE IS ON as well as Shared Solutions. NeeC
Many headaches too as I just found out my pharmacy doesn't want to cover
Copaxone
and removed it from a Tier 2 -5 Category giving me an outrageous patient co - pay! The BATTLE IS ON as well as Shared Solutions. NeeC
stepsforNeeC
in
My MSAA Community
5 years ago
Just the facts, nothing but the facts
Copaxone
) or Tec (Tecfidra) is. Make things smaller easier to handle and come to terms with. I do not start at 150 kilogram (300 pounds) weight at the gym. I start lower and work my way up. This is how “YOU” should handle your RRms.
Copaxone
) or Tec (Tecfidra) is. Make things smaller easier to handle and come to terms with. I do not start at 150 kilogram (300 pounds) weight at the gym. I start lower and work my way up. This is how “YOU” should handle your RRms.
RoyceNewton
in
My MSAA Community
5 years ago
Insurer dumping Copaxone, now what?
I have been on
Copaxone
for 13 years, with a short break to try the generic version (which did not agree with my body). Insurance will no longer cover
Copaxone
, so I need to switch to something else. Suggestions? I have very "mild" MS with few issues.
I have been on
Copaxone
for 13 years, with a short break to try the generic version (which did not agree with my body). Insurance will no longer cover
Copaxone
, so I need to switch to something else. Suggestions? I have very "mild" MS with few issues.
LakeshoreGreys
in
My MSAA Community
6 years ago
Massage & yoga- calling experienced MSers
It’s been a little bit more than a year since I’ve been diagnosed with RRMS & on
Copaxone
, which my dr. Thinks is not strong enough (another topic another day) My symptoms go from my rib cage on the right to my knee on the right.I’m still learning my new body.
It’s been a little bit more than a year since I’ve been diagnosed with RRMS & on
Copaxone
, which my dr. Thinks is not strong enough (another topic another day) My symptoms go from my rib cage on the right to my knee on the right.I’m still learning my new body.
Rileymom
in
My MSAA Community
6 years ago
Knees feel numb but I can feel them ? Also approved for rituxan!
I've been on
Copaxone
and Aubagio. Just got word that insurance has approved Rituxan after a 6 month denial and appeal. Good thing since I've had the oddest sensation that my knees are numb, but I can feel when I touch them. Have any of you experienced this? Maybe a new exacerbation?
I've been on
Copaxone
and Aubagio. Just got word that insurance has approved Rituxan after a 6 month denial and appeal. Good thing since I've had the oddest sensation that my knees are numb, but I can feel when I touch them. Have any of you experienced this? Maybe a new exacerbation?
latellama
in
My MSAA Community
6 years ago
Aubagio?
Anyway, so my doc is talking abt switching me from
Copaxone
to Aubagio. I balked at the mention. I rather like my side effect free
Copaxone
. I already feel relatively crappy on any given day and I dont want to have to deal with side effects from meds.
Anyway, so my doc is talking abt switching me from
Copaxone
to Aubagio. I balked at the mention. I rather like my side effect free
Copaxone
. I already feel relatively crappy on any given day and I dont want to have to deal with side effects from meds.
cassielynn71
in
My MSAA Community
6 years ago
Teva Teleconference
I've never done one of these through Teva, so I can't comment on its content, but I don't think one has to be taking
Copaxone
to join.
I've never done one of these through Teva, so I can't comment on its content, but I don't think one has to be taking
Copaxone
to join.
greaterexp
in
My MSAA Community
6 years ago
Rx switch
My health insurance is making me switch to the generic
Copaxone
, has anybody used it yet and if so any feedback?
My health insurance is making me switch to the generic
Copaxone
, has anybody used it yet and if so any feedback?
MadMaxx93
in
My MSAA Community
6 years ago
Stopping DMT
When I saw my neurologist 2 weeks ago, I mentioned it to her and she agreed that I could stop my
Copaxone
. I have been on it for 15 years and have not had a significant relapse since 2007. I have had minor ones, though.
When I saw my neurologist 2 weeks ago, I mentioned it to her and she agreed that I could stop my
Copaxone
. I have been on it for 15 years and have not had a significant relapse since 2007. I have had minor ones, though.
Mssailor
in
My MSAA Community
6 years ago
Ooncrevus
My neuro and I have decided to forget O and go back
Copaxone
since my condition had gotten worse since starting O. Not looking forward to needles again but maybe will keep me from declining more.
My neuro and I have decided to forget O and go back
Copaxone
since my condition had gotten worse since starting O. Not looking forward to needles again but maybe will keep me from declining more.
judymax
in
My MSAA Community
6 years ago
Copaxone and hair
Anyone who has been on
Copaxone
have hair loss/thinning due to drug? My neurologist & Shared Solutions staff say “it was not reported in clinical trials.” If anyone has experienced this, did anything help? I’m on 5,000 mcg of Biotin to see if that helps. 😊 thank you
Anyone who has been on
Copaxone
have hair loss/thinning due to drug? My neurologist & Shared Solutions staff say “it was not reported in clinical trials.” If anyone has experienced this, did anything help? I’m on 5,000 mcg of Biotin to see if that helps. 😊 thank you
Rileymom
in
My MSAA Community
6 years ago
Home from physical today
I am getting a referral to get a mammogram again this year with a history of breast cancer (my mom) and see a dermatologist because I have a mark on my toe that looks suspicious to be possibly melanoma and scar tissue from when I was doing my
Copaxone
injections.
I am getting a referral to get a mammogram again this year with a history of breast cancer (my mom) and see a dermatologist because I have a mark on my toe that looks suspicious to be possibly melanoma and scar tissue from when I was doing my
Copaxone
injections.
bxrmom
in
My MSAA Community
6 years ago
Injection fatigue
I have been on
Copaxone
since 2002. I inject three times a week.
Copaxone
seems to be working very well for me so I am reluctant to switch to a new medication. But it is getting harder and harder to inject. Has anyone switched from
Copaxone
to an oral medication with little or no trouble? Thanks!
I have been on
Copaxone
since 2002. I inject three times a week.
Copaxone
seems to be working very well for me so I am reluctant to switch to a new medication. But it is getting harder and harder to inject. Has anyone switched from
Copaxone
to an oral medication with little or no trouble? Thanks!
GildaS
in
My MSAA Community
6 years ago
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
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
1
...
4
5
6
...
12
Next page
10
Filter results
Clear filters
Posted in
All communities
My MSAA Community
224 results
Functional Neurological Disorder - FND Hope
1 result
MS Society
1 result
View top 10 communities
Sort by
Most Relevant
Newest