betaseron for multiple sclerosis

//www.medhelp.org/posts/Multiple-Sclerosis/DMD-Users-Past--Present---Copaxone--Rebif--Avonex--Betaseron--Tysabri--other/show/1193746 http://www.medhelp.org/posts/Multiple-Sclerosis/DMD/show/1041491 http://www.medhelp.org/posts/Multiple-Sclerosis/DMDs-experiences-please/show/759170 http://www.medhelp.org/posts/Multiple-Sclerosis/For-those-of-you-on-one-of-the-disease-modifying-drugs/show/471258 You may fair well with side affects.

//www.medhelp.org/posts/Multiple-Sclerosis/Gilenya-Users-Past-and-Present/show/1469412 http://www.medhelp.org/posts/Multiple-Sclerosis/Copaxone-users---past-and-present/show/643683 http://www.medhelp.org/posts/Multiple-Sclerosis/Tysabri-Users---Past-and-Present/show/1569374 http://www.medhelp.org/posts/Multiple-Sclerosis/Aubagio-Users-Past-and-Present/show/1946899 http://www.medhelp.org/posts/Multiple-Sclerosis/Our-Tysabri-Users---Past-and-Present/show/658918 http://www.medhelp.

Interferon Drugs for Multiple Sclerosis (Avonex, Betaseron, Rebif)Interferon beta drugs help control the immune system, which helps control MS. Glatiramer Glatiramer helps prevent the body's immune system from attacking nerve fibers. Novantrone Novantrone slows disability and reduces the relapse rate. Tysabri Therapy Tysabri reduces the relapse rate, but is somewhat controversial. Aubagio Aubagio reduces the number of flares in adults with relapsing forms of multiple sclerosis.

Hi Ryan, I want to ask your advice on ativan for longterm treatment of some of the symptoms of MS. I have had Multiple Sclerosis diagnosis since 2001. Took Betaseron for 3 years and quit due to horrible side effects. I have remained stable with not much changes since 2001 except for severe anxiety panic attacks that the specialists feel are connected to the brain lesions I have. I take beta blockers and also 1/2 to 1 mg of Ativan daily.

Please be careful gleaning information from articles based on study that involved 26 patients. Not posting my thoughts here to discredit what they have learned. Just pointing out the size and scope of this initial study.

org/posts/Multiple-Sclerosis/DMD-Users-Past--Present---Copaxone--Rebif--Avonex--Betaseron--Tysabri--other/show/1193746 -Shell

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15 Dec 2008 - 0:00 PST www. medicalnewstoday .com/articles/132947. php "FTY720 (fingolimod), an experimental oral drug for relapsing MS is more effective than current treatments according to new research reported today. The trial, called TRANSFORMS, is the first of three studies of FTY720 to report. TRANSFORMS was a one year study involving 1,292 participants receiving either 0.5 mg or 1.25 mg FTY720 or interferon beta-1a (Avonex).

My Dr. wants me to start the new oral meds after the baby is born. I was on Betaseron for one year before we conceived. In that year, I had three relapses that required steroids. He said that ment that the Betaseron was not effective. One of the relapses really does not caount against the treatment because it was the 10th week of the treatment. I guess I am ok with trying the new meds. What do you all think? Would you try it? Do you think that it is a good idea?

Multiple Sclerosis (MS) Drugs | Avonex | Betaseron | Betaferon | Copaxone | Rebif | I happened to see this the other day, it was listed on http://www.themcfox.com/multiple-sclerosis/ms-drugs/avonex/avonex-blood-counts.htm updated 2004, it might be worth finding out if your having a negative reaction and need to change DMD.

I am a 31 yr old female who was diagnosed w/multiple sclerosis in 2005. I have had a couple of relaspes since,however,I have full recovered. Two months ago,I was rushed to the hospital in excruciating just to be diagnosed again. Only this time it was tmj. My question is is tmj more severe to a person with ms as to a person without? The pain from the ms is pretty bad,however,can be managed. Where as the pain in regards to the tmj is unbarable! It literally takes my breath away.

org/posts/Multiple-Sclerosis/DMD-Users-Past--Present---Copaxone--Rebif--Avonex--Betaseron--Tysabri--other/show/1193746 Welcome, and tell us how you feel comfortable to share.

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Hi and welcom to the forum, I have never heard of anyone being on Medrol for that long, what are your reasons for being on it for such a long period of time? Seems to me that being on it for that long could be very problematic but I could be wrong, I am sure others will chime in. As for the DVT I don't believe that is related to MS that is more of a blood disorder if I am correct and MS is a CNS disease.

my sister (24) was diagnosed Multiple Sclerosis in 2010, responded to steroid. now she suffered sudden & complete loss of vision in her left eye. she has been put on SOLUMEDROL. please suggest any available treatment modalities world over ? chances of return of vision ??

Betaseron for multiple sclerosis

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