rebif for multiple sclerosis

52 year old woman with a severe case of Secondary Progressive Multiple Sclerosis (SPMS). She is around an 8 on the Expanded Disability Status Scale and has been on multiple interferon-beta1a treatments, including Rebif and Avonex and nothing seems to be helping. What course of treatment would you recommend?

My neuro ran test and I was dx with Ms July 2010. I am on rebif and doing well except for knee buckling. I was really ill at first after neuro put me on this med rebif, I am better now.

//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.

Hi all, I pray ya'll are doing well. I'm still having a rough go of it. This latest flare has been going on for almost 6 mo. Actually my doctor told me that since I have PPMS that I wont get better. The muscle weakness that causes me to be in a wheelchair is permanent. That really bites the big one. My question is: Why will none of the current medications that are given for MS (the injections like Rebif) work for PPMS?

Martin, MDApril 15, 2010 (Toronto) -- Nearly 71% of people with early relapsing-remitting multiple sclerosis (MS) treated with the experimental MS drug alemtuzumab showed no evidence of disease activity four years into a study, researchers report. That's twice the percentage of patients treated with the approved treatment, Rebif, says researcher Alasdair Coles, PhD, of the University of Cambridge.

You may be experiencing numbness in the tongue, a common symptom of multiple sclerosis per se. Review with your neurologist if your disease spectrum has changed and for these newer symptoms. He might like to add some muscle relaxant like tizanidine, baclofen or carbamazepine. You are welcome with any further clarifications. God bless.

I have had RR multiple sclerosis since I was 10 ish diagnosed (finally) in 2008. Had routine MRi of head and neck last month, everything is stable for 2 years now. Thank you Tysabri! My question is the impression of my mri stated T1 and T2 disease burden is at least moderate ( written for head and cervical MRI). Also JCV negative this whole time can I stay on Tysabri indefintely as long as I am negative?

http://www.medhelp.

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

http://www.medhelp.org/health_pages/Multiple-Sclerosis/Common-Multiple-Sclerosis-Drugs--Medications--Treatments/show/108?cid=36 It gets to be a habit after a while and we don't really think about it, which is a good thing. And also, many of us have vitamin deficiencies, allergies, and all the general run of ailments that other people do. I'm just grateful for excellent prescription insurance.

The Comparison of Alemtuzumab and Rebif® Efficacy in Multiple Sclerosis (CARE-MSSM) I and II studies are designed to determine the safety and effectiveness of the investigational drug alemtuzumab as compared to the FDA-approved therapy Rebif (interferon beta-1a), in adults with relapsing-remitting multiple sclerosis (RRMS). The studies will look for differences between these drugs on the progression of disability and in the number of relapses (flare-ups) and brain lesions caused by MS.

I just ran a search for "multiple sclerosis night sweats", and I found an article that states that 16-36% of people with ms experience moderate to severe night sweats. The article broke it down better than I just did. All this time I thought it was hormonal, lol! (Who knows, maybe it's both in my case...

) Pharmacokinetics The pharmacokinetics of Rebif® (interferon beta-1a) in people with multiple sclerosis have not been evaluated. In healthy volunteer subjects, a single subcutaneous (sc) injection of 60 mcg of Rebif® (liquid formulation) resulted in a peak serum concentration (Cmax) of 5.1 ± 1.7 IU/mL (mean ± SD), with a median time of peak serum concentration (Tmax) of 16 hours.

ago without contrast) I have been having symptoms for about 9 years and have seen 2 Neuros in the past( in G.R.) ....one that treated me with Rebif for about 3 yrs. and the next one said I didn't fit the "classic" picture of R.R. M.S.and just decided that I would have to live with things as they are, maybe "This is as good as it gets" for me!

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.

Through the MS LifeLines Access Made Simple program, you may be eligible to get Rebif® (interferon beta-1a) at no cost, or for no more than $50 per month, for up to one year of treatment. Best of all, MS LifeLines takes care of all the paperwork.... http://www. mslifelines. com/rebif/insurance/ access-made-simple. jsp?intcmp The following assistance programs info provided by MSAA...msassociation.

I contacted ms lifeline and they sent me an application for assistance with rebif costs. because of my income (or lack thereof) i was granted a year's worth of rebif.

//www.medhelp.org/posts/Multiple-Sclerosis/DMD-Users-Past--Present---Copaxone--Rebif--Avonex--Betaseron--Tysabri--other/show/1193746 Hope to help - please ask anything!

Just wondering if anyone is going to this MS in Balance seminar on "Relapsing Multiple Sclerosis and Its Management" in Carmel (suburb of Indianapolis). It's the evening of Thursday, Dec. 4 and apparently is sponsored by the Rebif people. http://www.mslifelines.com/programs/local-seminars/view/1525.jsp Has anyone ever been to one of these things? Are they likely to be worthwhile?

Hi Cheryl, I did Rebif for about a year prior to going on Tecfidera in May 2014. Rebif was OK but I did have flu like symptoms. Tec was a bugger at the begging but I have felt OK on it. I know a lot of folks do well on Copaxone so it might be worth checking with your neuro as to why they aren't suggesting it. Maybe because it's daily? Good luck!

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.

Rebif for multiple sclerosis

Common Questions and Answers about Rebif for multiple sclerosis

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