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Rebif
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Living with MS
I was on the Medication
Rebif
and had to change because it was not working for me. Now I'm on Gilenya and it seems to be working for me. My neurologist put me on Ampyra to help with my walking also. It seems that the Ampyra assistance program was terminated Dec. 31, 2017.
I was on the Medication
Rebif
and had to change because it was not working for me. Now I'm on Gilenya and it seems to be working for me. My neurologist put me on Ampyra to help with my walking also. It seems that the Ampyra assistance program was terminated Dec. 31, 2017.
SBLinda
in
My MSAA Community
6 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
Ocrevus News from ECTRIMS
http://www.businesswire.com/news/home/20171026006738/en/New-OCREVUS-Ocrelizumab-Data-ECTRIMS-Advance-Clinical There is a bit of good news for RRMS people in that there is new data showing Ocrevus significantly prevented progression over
Rebif
when measured by a new measurement (PIRA).
http://www.businesswire.com/news/home/20171026006738/en/New-OCREVUS-Ocrelizumab-Data-ECTRIMS-Advance-Clinical There is a bit of good news for RRMS people in that there is new data showing Ocrevus significantly prevented progression over
Rebif
when measured by a new measurement (PIRA).
Raingrrl
in
My MSAA Community
7 years ago
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Gilenya
I was diagnosed in 2012 and have been on
Rebif
for the last 5 years. I am switching because recently I have been feeling really wiped out the day after my shots. Thank you🌻
I was diagnosed in 2012 and have been on
Rebif
for the last 5 years. I am switching because recently I have been feeling really wiped out the day after my shots. Thank you🌻
Vallie02
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
Joe R
I've been on
Rebif
for the better part of 11 years, Until I started OCREVUS 2 years ago, after first dose it seemed to be helping but not so much anymore. The Dr diagnosed me with secondary progressive MS about 6 1/2 years ago.
I've been on
Rebif
for the better part of 11 years, Until I started OCREVUS 2 years ago, after first dose it seemed to be helping but not so much anymore. The Dr diagnosed me with secondary progressive MS about 6 1/2 years ago.
Russso
in
My MSAA Community
7 years ago
Medicine
Me just started tecfidera 2 days ago after Using
rebif
for a while
Me just started tecfidera 2 days ago after Using
rebif
for a while
Lay24
in
My MSAA Community
7 years ago
Stopping My MS Therapy
I stopped taking the
Rebif
. My last injection was 12/12/2016 and in just this little bit of time I have noticed a difference in my abilities.
I stopped taking the
Rebif
. My last injection was 12/12/2016 and in just this little bit of time I have noticed a difference in my abilities.
amyshif1
in
My MSAA Community
7 years ago
Introduction
Went back to Copaxone then changed later to
Rebif
. My liver didn't like
Rebif
so went back on Copaxone. I have changed since to Aubagio and haven't had issues since starting more than a year ago. Currently into motorcycles, astronomy and flying quadcopters.
Went back to Copaxone then changed later to
Rebif
. My liver didn't like
Rebif
so went back on Copaxone. I have changed since to Aubagio and haven't had issues since starting more than a year ago. Currently into motorcycles, astronomy and flying quadcopters.
megraham
in
My MSAA Community
7 years ago
GODFIDENCE!
.🍷 January 2012 I started the medication Avonex once a week injection, and after two relapses within the year I was then prescribed
Rebif
three times a week injections. At that time I decided to discontinue taking the medication and pray on it and leave it in GODS! hands.
.🍷 January 2012 I started the medication Avonex once a week injection, and after two relapses within the year I was then prescribed
Rebif
three times a week injections. At that time I decided to discontinue taking the medication and pray on it and leave it in GODS! hands.
Kimlovesshoes
in
My MSAA Community
7 years ago
I'm new here. A little bit about me...
I am on the
rebif
MS treatment and the 12th of this month had an MRI and that shows no new lesions. Why do I seem to be getting worse? Each day is becoming more of a challenge. I am married to a wonderful man and he helps me with everything. Sometimes he is too helpful.
I am on the
rebif
MS treatment and the 12th of this month had an MRI and that shows no new lesions. Why do I seem to be getting worse? Each day is becoming more of a challenge. I am married to a wonderful man and he helps me with everything. Sometimes he is too helpful.
amyshif1
in
My MSAA Community
7 years ago
CharlesHH
I was on copaxone for 2 years
rebif
for 1 year and currently on retuxin every 6 months. I have tried every thing to slow the progression but have not found anything to slow it (i.e. diet,exercise,drugs,herbal). My walking has gotten a lot worse even when I keep pushing myself hard.
I was on copaxone for 2 years
rebif
for 1 year and currently on retuxin every 6 months. I have tried every thing to slow the progression but have not found anything to slow it (i.e. diet,exercise,drugs,herbal). My walking has gotten a lot worse even when I keep pushing myself hard.
CharlesHH
in
My MSAA Community
7 years ago
MS has met "its" match !
I have used Copaxzone,
Rebif
: Tysabri; Tecfadera & now I in March of this yr. I had the Lemtrada infusions. So far I have noticed some positive results, my gait doesn't make me look like a drunk & my "word finding" is not happening as much.
I have used Copaxzone,
Rebif
: Tysabri; Tecfadera & now I in March of this yr. I had the Lemtrada infusions. So far I have noticed some positive results, my gait doesn't make me look like a drunk & my "word finding" is not happening as much.
Me63
in
My MSAA Community
8 years ago
Hi from Texas
I went from
Rebif
to Tysabri to Techfidera back to Tysabri and now on Techfidera again. I am getting weaker again so I talked to my Dr about going back on Ty since I seem to do better on it. Just wanted to say Hi to everyone.
I went from
Rebif
to Tysabri to Techfidera back to Tysabri and now on Techfidera again. I am getting weaker again so I talked to my Dr about going back on Ty since I seem to do better on it. Just wanted to say Hi to everyone.
Justrubl
in
My MSAA Community
8 years ago
New to community
I was diagnosed with MS in February 2004 & have PPMS; I was diagnosed while living in NY & MD was great; tried
Rebif
initially, (no help-he didn't think it would work, but tried it anyway).
I was diagnosed with MS in February 2004 & have PPMS; I was diagnosed while living in NY & MD was great; tried
Rebif
initially, (no help-he didn't think it would work, but tried it anyway).
letselia
in
My MSAA Community
8 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
Rebif
I am starting
Rebif
on Monday. Just want to know experiences others have had, either positive or negative. Side effects etc. Thank you.
I am starting
Rebif
on Monday. Just want to know experiences others have had, either positive or negative. Side effects etc. Thank you.
dar58
in
My MSAA Community
8 years ago
Aubagio
My husband switched to Aubagio a few years ago from
Rebif
and has been satisfied with it. I haven't met anyone else who takes it. Anyone out there?
My husband switched to Aubagio a few years ago from
Rebif
and has been satisfied with it. I haven't met anyone else who takes it. Anyone out there?
Joalyn
in
My MSAA Community
8 years ago
New to this site
Dr put me on
Rebif
to slow progression and I don't know if it is working or not but I try.
Dr put me on
Rebif
to slow progression and I don't know if it is working or not but I try.
Mark1193
in
My MSAA Community
8 years ago
REBIF 1st shot yesterday UPDATE
I know it was just my 1st injection and I was so worried about the pain from more injections and the flu-like symptoms. I was on Avonex years ago and they were painful because I had to put the meds right into the muscle. I also have been on Lovenox shots so many times for my blood clotting disorder,
I know it was just my 1st injection and I was so worried about the pain from more injections and the flu-like symptoms. I was on Avonex years ago and they were painful because I had to put the meds right into the muscle. I also have been on Lovenox shots so many times for my blood clotting disorder,
dar58
in
My MSAA Community
8 years ago
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