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Rebif
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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
7 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
9 months ago
Not for me.
She went on and on about how great Octevus was to her which led me switch to it from
Rebif
. Bad move on my part. The Ocrevus not only did not work but seemed to make my symptoms worse. Because of that my neurologist convinced me to use nothing. That isn't doing much good either.
She went on and on about how great Octevus was to her which led me switch to it from
Rebif
. Bad move on my part. The Ocrevus not only did not work but seemed to make my symptoms worse. Because of that my neurologist convinced me to use nothing. That isn't doing much good either.
Peddler
in
My MSAA Community
2 years ago
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Greetings!
After using Copaxone,
Rebif
and now Ocrevus I'm back in the search for an MS med that’s ‘right for me’.
After using Copaxone,
Rebif
and now Ocrevus I'm back in the search for an MS med that’s ‘right for me’.
Peddler
in
My MSAA Community
2 years ago
MRI Thursday
I've used
Rebif
(6mos), Techfedera(2yrs), Copaxone[7 & 3](12yrs) & Ocrevus(2yrs). I have a month to research & decide. I have RRMS any suggestions? I really appreciate y'all.
I've used
Rebif
(6mos), Techfedera(2yrs), Copaxone[7 & 3](12yrs) & Ocrevus(2yrs). I have a month to research & decide. I have RRMS any suggestions? I really appreciate y'all.
hairbrain4
in
My MSAA Community
2 years ago
Unnumbered post Learn from your mistakes 23 Feb 2021 2
I learned that
Rebif
hurt upon injection so I changed back to Beta. I learned that I may get headaches post-injection. So I took Ibuprofen and ate a meal beforehand. I paid attention to my mistakes. I listened to others then ignored them and made my own mistakes. BUT I always learned.
I learned that
Rebif
hurt upon injection so I changed back to Beta. I learned that I may get headaches post-injection. So I took Ibuprofen and ate a meal beforehand. I paid attention to my mistakes. I listened to others then ignored them and made my own mistakes. BUT I always learned.
RoyceNewton
in
My MSAA Community
3 years ago
How long does it take Rebif to kick in?
How long does it take
Rebif
Rebidose to work if you continue to relapse on a titration pack?
How long does it take
Rebif
Rebidose to work if you continue to relapse on a titration pack?
Mamawolf23
in
MS Society
4 years ago
Life update
My neuro said if there’s no change he may reduce the frequency I take
Rebif
injections. Can’t complain about that! I don’t mind the noise or enclosed space of an mri but I hate how bad my legs ache from holding still so long!! I had an appointment to get evaluated for lasik. Big waste of time.
My neuro said if there’s no change he may reduce the frequency I take
Rebif
injections. Can’t complain about that! I don’t mind the noise or enclosed space of an mri but I hate how bad my legs ache from holding still so long!! I had an appointment to get evaluated for lasik. Big waste of time.
StacyHayward
in
My MSAA Community
4 years ago
MS diagnosis vs CIS Diagnosis
Hey guys....my neurologist diagnosed me with RRMS a few weeks ago... i have been waiting on my
rebif
... the doctor put on the paper work CIS... probably because I’ve only had one episode... so lifeline assistance said RRMS is a requirement for them... my doctor never told me he changed my diagnosis.
Hey guys....my neurologist diagnosed me with RRMS a few weeks ago... i have been waiting on my
rebif
... the doctor put on the paper work CIS... probably because I’ve only had one episode... so lifeline assistance said RRMS is a requirement for them... my doctor never told me he changed my diagnosis.
Newlyfe
in
My MSAA Community
4 years ago
Successful 1st injection
My
Rebif
treatment finally came and yesterday was my first injection! It was very easy. I never felt the needle or burning a sensation or flu like symptoms...All smiles... I’m praying you all are doing alright!
My
Rebif
treatment finally came and yesterday was my first injection! It was very easy. I never felt the needle or burning a sensation or flu like symptoms...All smiles... I’m praying you all are doing alright!
Newlyfe
in
My MSAA Community
4 years ago
Unnumbered post DMT, YES I am on it 9 Feb 2020
Rebif
hurt and hated me so back to beta. The logic was less injections and that is all. Tecfidera came on the market and of course no injections so I was on it. It is a DMT, NOT a Disease Stopping therapy or Disease Curing Therapy.
Rebif
hurt and hated me so back to beta. The logic was less injections and that is all. Tecfidera came on the market and of course no injections so I was on it. It is a DMT, NOT a Disease Stopping therapy or Disease Curing Therapy.
RoyceNewton
in
My MSAA Community
4 years ago
Post 585 Take your time 8 Jan 2020
I switched from Beta once to
Rebif
. fewer needles and we all know how much I dislike needles. Within two injections, I knew something was wrong, but I still followed through for a month, I think. I gave it time, I let my body adapt. These are powerful medicines, and I was not designed to need them.
I switched from Beta once to
Rebif
. fewer needles and we all know how much I dislike needles. Within two injections, I knew something was wrong, but I still followed through for a month, I think. I gave it time, I let my body adapt. These are powerful medicines, and I was not designed to need them.
RoyceNewton
in
My MSAA Community
4 years ago
Hello everyone I'm new to this!
I'm started out with
Rebif
for 6 months. Too much flu like symptoms. Now I take Avonex and so far doing alot better.
I'm started out with
Rebif
for 6 months. Too much flu like symptoms. Now I take Avonex and so far doing alot better.
Ladybriars
in
My MSAA Community
4 years ago
Post 536 side effects 8 Oct 2019
Even worse for my month on
Rebif
Interferon Beta 1A. None on Tecfidera, and it is a tablet so no needles. Yaay as I have a needle phobia. There are side effects with pretty much everything, especially this condition. Have "YOU" noticed that birth has a guaranteed side effect?
Even worse for my month on
Rebif
Interferon Beta 1A. None on Tecfidera, and it is a tablet so no needles. Yaay as I have a needle phobia. There are side effects with pretty much everything, especially this condition. Have "YOU" noticed that birth has a guaranteed side effect?
RoyceNewton
in
My MSAA Community
4 years ago
Neuro appointment today
Ampyra has been my miracle drug and
Rebif
continues to work well. I am going to try a sleeping pill. Bad sleep and increased fatigue were my only complaints today. On a side note...my tomatoes are taller than I am!
Ampyra has been my miracle drug and
Rebif
continues to work well. I am going to try a sleeping pill. Bad sleep and increased fatigue were my only complaints today. On a side note...my tomatoes are taller than I am!
StacyHayward
in
My MSAA Community
5 years ago
I'm a fighter.. I'm a Conqueror.. I'm a winner...
I'm currently taking
Rebif
but I don't see a difference. I am having very bad muscle spasms in my legs when I sit up. I open for any suggestions..
I'm currently taking
Rebif
but I don't see a difference. I am having very bad muscle spasms in my legs when I sit up. I open for any suggestions..
Msbeauty01
in
My MSAA Community
5 years ago
Vaccines FYI
For example, Copaxone,
Rebif
, Avonex, and Betaseron don't prevent you from building immunity, and they don't make you more likely to become sick from any vaccines.
For example, Copaxone,
Rebif
, Avonex, and Betaseron don't prevent you from building immunity, and they don't make you more likely to become sick from any vaccines.
sashaming1
in
My MSAA Community
5 years ago
Long term
I switched from Beta to
Rebif
a few years back and I could not cope with
Rebif
. It just hurt too much, so I went back to Beta. I did not stop DMT altogether, I just changed back. When Tecfidera became available I started that. My bony body was very tired of every other day injections.
I switched from Beta to
Rebif
a few years back and I could not cope with
Rebif
. It just hurt too much, so I went back to Beta. I did not stop DMT altogether, I just changed back. When Tecfidera became available I started that. My bony body was very tired of every other day injections.
RoyceNewton
in
My MSAA Community
5 years ago
14 year old daughter starting Ocrevus
The one Ocrevus vs
Rebif
trial that I read said that that there was no difference in results between the highest dose & lowest dose that they gave. She weighs 105 pounds. Thanks for any and all input! You guys are wonderful! Cher
The one Ocrevus vs
Rebif
trial that I read said that that there was no difference in results between the highest dose & lowest dose that they gave. She weighs 105 pounds. Thanks for any and all input! You guys are wonderful! Cher
LorenzoOilMom
in
My MSAA Community
5 years ago
Neuro appointment
Interestingly, I asked him his go to med if I just can’t stand taking
Rebif
anymore. (I don’t have side effects and it’s working great, but hate shots). He said unless
Rebif
stops working he’s hesitant to change because it could change how my MS is doing.
Interestingly, I asked him his go to med if I just can’t stand taking
Rebif
anymore. (I don’t have side effects and it’s working great, but hate shots). He said unless
Rebif
stops working he’s hesitant to change because it could change how my MS is doing.
StacyHayward
in
My MSAA Community
5 years ago
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