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Betaseron
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Very very interesting, mshope.org
I took
Betaseron
\Betaferon and take Tecfidera now, Merely that it will not hurt "YOU" to add some healthy eating principles to your lifestyle. Some exercise is great as well, getting the endorphins flowing and feel better within yourself. This is a multi-factorial condition.
I took
Betaseron
\Betaferon and take Tecfidera now, Merely that it will not hurt "YOU" to add some healthy eating principles to your lifestyle. Some exercise is great as well, getting the endorphins flowing and feel better within yourself. This is a multi-factorial condition.
RoyceNewton
in
My MSAA Community
6 years ago
This is sort of obvious
msers, good Monday morning. YOU have a CHRONIC medical illness. Now that we have that clear what are YOU going to do about it? Something or nothing? If YOU pick nothing, then ignore this message it is not for YOU. On the other hand, being YOU and wanting to be in the best possible shape for
msers, good Monday morning. YOU have a CHRONIC medical illness. Now that we have that clear what are YOU going to do about it? Something or nothing? If YOU pick nothing, then ignore this message it is not for YOU. On the other hand, being YOU and wanting to be in the best possible shape for
RoyceNewton
in
My MSAA Community
6 years ago
I am here to learn how others cope with the everyday living of MS.
I know that because after taking
Betaseron
for about 8 years I was told I was moving on to Secondary Progressive and because I was "so" educated about what was then the "ABC"s" of disease-modifying drugs I chose to go off even though the doctor wasn't as sure as I was that
Betaseron
was only for R/R
I know that because after taking
Betaseron
for about 8 years I was told I was moving on to Secondary Progressive and because I was "so" educated about what was then the "ABC"s" of disease-modifying drugs I chose to go off even though the doctor wasn't as sure as I was that
Betaseron
was only for R/R
Hidden
in
My MSAA Community
6 years ago
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It really is YOUR choice
I and others will suggest and show you options for you to take, & yes you most certainly do have options. 20 years ago I had
Betaseron
and that was it, Before that people had nothing, Today you have many many more. WILL you take an option and live better than I ever dreamed of?
I and others will suggest and show you options for you to take, & yes you most certainly do have options. 20 years ago I had
Betaseron
and that was it, Before that people had nothing, Today you have many many more. WILL you take an option and live better than I ever dreamed of?
RoyceNewton
in
My MSAA Community
6 years ago
Dr's give me no hope. I need help!
Everson at UCH CO. 5 rounds of interferon A, pegalated interferon and riboviran and
betaseron
and my genotype 2 didn't respond. Dr.
Everson at UCH CO. 5 rounds of interferon A, pegalated interferon and riboviran and
betaseron
and my genotype 2 didn't respond. Dr.
TaraRae
in
Hughes Syndrome APS Forum
6 years ago
G'day Newbies
Back in the olden days we had the A B Cs Avonex
Betaseron
and Copaxone, lucky you you have a lot more to choose from these days, BUT YOU and only YOU have to Choose which one and You have to take it as prescribed.
Back in the olden days we had the A B Cs Avonex
Betaseron
and Copaxone, lucky you you have a lot more to choose from these days, BUT YOU and only YOU have to Choose which one and You have to take it as prescribed.
RoyceNewton
in
My MSAA Community
6 years ago
Anyone on Tysabri?
I have been on
Betaseron
for 15 years with not much change in my symptoms until a little weakness last year for a couple weeks and just recently.
I have been on
Betaseron
for 15 years with not much change in my symptoms until a little weakness last year for a couple weeks and just recently.
cats3
in
My MSAA Community
6 years ago
OCREVUS - I NEED INFO
I went on
Betaseron
with no success. Went on Tysabri and it worked very well but because of the JC virus, was only able to have 24 treatments.
I went on
Betaseron
with no success. Went on Tysabri and it worked very well but because of the JC virus, was only able to have 24 treatments.
SueStu
in
My MSAA Community
6 years ago
Itchy Welts After Injections
I am on
Betaseron
injections every other day. I do alright with them with the exception of itchy welts. Any ideas for dealing with them?
I am on
Betaseron
injections every other day. I do alright with them with the exception of itchy welts. Any ideas for dealing with them?
MrsDenny17
in
My MSAA Community
6 years ago
I'm new here
I have been on
Betaseron
and Gilenya. I am currently on Tysabri for the past two years. My neurologist is suggesting that I go on Ocrevus? Anyone out there on Ocrevus? How is it working for you?
I have been on
Betaseron
and Gilenya. I am currently on Tysabri for the past two years. My neurologist is suggesting that I go on Ocrevus? Anyone out there on Ocrevus? How is it working for you?
alleynyberg
in
My MSAA Community
7 years ago
Starting Meds ~ Any opinions?
Injectables: Avonex;
Betaseron
; Rebif; Copaxone Oral: Aubagio; Tecfidera Your thoughts ... Thank you, Carrie
Injectables: Avonex;
Betaseron
; Rebif; Copaxone Oral: Aubagio; Tecfidera Your thoughts ... Thank you, Carrie
Daring_Greatly
in
My MSAA Community
7 years ago
Introducing me
Over the years, I have been on
Betaseron
, Avonex, and Tysabri. I fell and broke my left hip (Nov. 2015).Because it did not heal, I had two additional hip replacement surgeries All 3 surgeries within 7 months of each other.
Over the years, I have been on
Betaseron
, Avonex, and Tysabri. I fell and broke my left hip (Nov. 2015).Because it did not heal, I had two additional hip replacement surgeries All 3 surgeries within 7 months of each other.
DebbyLou
in
My MSAA Community
7 years ago
M.A.S. Multiple Autoimmune Syndrome
Diagnosed with MS in 2000, I injected
betaseron
then rebif then finally avonex for 9 years. My body began rejecting the interferons, injection sites were even leaking. I had no place left to poke. I then opted to stop treatment and go as healthy natural as I could.
Diagnosed with MS in 2000, I injected
betaseron
then rebif then finally avonex for 9 years. My body began rejecting the interferons, injection sites were even leaking. I had no place left to poke. I then opted to stop treatment and go as healthy natural as I could.
Sierranne
in
My MSAA Community
8 years ago
It's about time!
I tried
Betaseron
, then Copaxone, then Aubagio and finally Tecfidera, which is what I take now, along with duloxetine and modafinil.
I tried
Betaseron
, then Copaxone, then Aubagio and finally Tecfidera, which is what I take now, along with duloxetine and modafinil.
Ashirva
in
My MSAA Community
8 years ago
intro.
i was dg. in 2001 right after graduating college. was on
betaseron
for years in combination w. chemo. at 35 was in a nursing home and went to northwestern to see dr. burt about hsct. i could barely walk and was treated off study and only wish i had it sooner! ~nadine
i was dg. in 2001 right after graduating college. was on
betaseron
for years in combination w. chemo. at 35 was in a nursing home and went to northwestern to see dr. burt about hsct. i could barely walk and was treated off study and only wish i had it sooner! ~nadine
nes78
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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