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Copaxone
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Working with MS
I started on
Copaxone
, then Tecfidera, and am now on Tysabri. I have only 3 lesions in my brain. Lesions in my spinal column are my major problem.
I started on
Copaxone
, then Tecfidera, and am now on Tysabri. I have only 3 lesions in my brain. Lesions in my spinal column are my major problem.
Juleigh21
in
My MSAA Community
8 years ago
40 years of adapting
He was on
Copaxone
until he turned 62 when the neurology studies showed that by that age it was fairly useless to continue DMD therapy. He enjoys telling people we do everything we want to do just often in a different way than the norm.
He was on
Copaxone
until he turned 62 when the neurology studies showed that by that age it was fairly useless to continue DMD therapy. He enjoys telling people we do everything we want to do just often in a different way than the norm.
kjc1951
in
My MSAA Community
8 years ago
New to this forum and not used to reaching out...
I began
Copaxone
injections one year ago even though I'm scared silly of needles! :) My husband gives them to me. I have a first cousin who also has RRMS. We have the same symptoms except hers are on the L.
I began
Copaxone
injections one year ago even though I'm scared silly of needles! :) My husband gives them to me. I have a first cousin who also has RRMS. We have the same symptoms except hers are on the L.
cindyrn68
in
My MSAA Community
8 years ago
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ALASKA GIRL/MS WORLD
I've been on
Copaxone
since the very beginning and really haven't had any flares To speak of, so I just hang in there and pray, pray, pray!
I've been on
Copaxone
since the very beginning and really haven't had any flares To speak of, so I just hang in there and pray, pray, pray!
Happykp56
in
My MSAA Community
8 years ago
New to this
I will start
Copaxone
injections 3x a week soon. I'm a Registered Nurse, a wife, and a mother.
I will start
Copaxone
injections 3x a week soon. I'm a Registered Nurse, a wife, and a mother.
KimberlyPenningon
in
My MSAA Community
8 years ago
Recently diagnosed in the last few years?
Now two years later I have a bunch of symptoms, but all mild to moderate enough to live with without need for medication (other than my
Copaxone
).
Now two years later I have a bunch of symptoms, but all mild to moderate enough to live with without need for medication (other than my
Copaxone
).
Kokomo26
in
My MSAA Community
8 years ago
My name is Jim and I have MS
I am currently taking
Copaxone
as my DMT. I hate the shots but I think that it does help, even though overall my symptoms are progressing.
I am currently taking
Copaxone
as my DMT. I hate the shots but I think that it does help, even though overall my symptoms are progressing.
JimAndMS
in
My MSAA Community
8 years ago
Introducing myself
I have been on Betaseron,
Copaxone
(twice - 7 & 3 day), Rebif and Tysabri. Getting ready to start Tecfidera. I also now have Type 1 Diabetes, Hashimotos, Fibromyalgia, Arthritis and Celiac. MS stinks. It was the beginning of a very challenging adulthood and took a lot of "normalcy" from me.
I have been on Betaseron,
Copaxone
(twice - 7 & 3 day), Rebif and Tysabri. Getting ready to start Tecfidera. I also now have Type 1 Diabetes, Hashimotos, Fibromyalgia, Arthritis and Celiac. MS stinks. It was the beginning of a very challenging adulthood and took a lot of "normalcy" from me.
April-1995MSWarrior
in
My MSAA Community
8 years ago
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