rebif uk

I have MS and have been taking Rebif foe 7 years. It has worked very well. I just learned that my current drug insurance plan from Humana will not cover Rebif in 2015. What plans cover at least some of the Rebif cost? My copay with Humana was about $300 per month. Would like not to exceed this amount.

Hello! I've just been diagnosed with MS and am wondering which drug is better. I've read the material for Copaxone, Rebif, Avonex, and Betaseron. I've narrowed it down to two -- Rebif or Copaxone based mainly on side effects. Which drug is the best?

Anyone here one with a diagnosis of MS and is having trouble getting disease modifying drugs, such as Copaxone or Rebif, due to lack of insurance, insurance company unwilling to pay or trouble with pharmaceutical company please tell your story as to why.

I was working alot on our new house and I think that and the fact that I was off medication for a few months (the switch from copaxone to rebif took a few months) resulted in the attack. When I went for my Drs appointment with the neuro in April, he noted some weakness on my left leg. Around may time the spasms went away and my leg started to feel like its normal self. It's not completely back to normal, but I can only tell in Karate. I just can't kick as high or fast with my left leg.

s work about the same and the choice you have to make depends on your personal preferences. Copaxone is one class of drug while Rebif, Avonex, and Betaseron are all interferons. The British UK site has one of the best walk-throughs on picking a drug that I have seen. It discusses in depth each DMD and its side-effects and injection schedule/technique. Just pretend you live in the UK and spend about 45 minutes working through their presentation and you will feel so much smarter.

ve kicked around the CRABs here, a lot. Copaxone, Rebif, Avonex, and Betaseron are the primary four. Your doctor didn't offer Tysabri as your fifth, did he? I like the Decision Maker tool in the uk that walks you through the drugs and helps you figure what is important for you. You can access this at http://www.msdecisions.org.uk welcome to the world of drugs aand bills. I'm glad to hear you are getting treatment for your CIS. Congrats on that one.

Just trying to get my head around starting drugs have known had MS since 06 listed as proable until next relapse although they were sure I had it two weeks ago half head went numb now have to decide which I want to take I am leaning towards rebif any would be great .

There is a favorite website I always refer people to with your question - it is a DMD (disease modifying drug) decision making tool put out by the UK MS Society - ignore the part about having to be in the UK to use it and walk through the site. It will help you understand the choices. http://www.msdecisions.org.uk/ It seems all the neuros put this choice back onto the patient. Remember there is no real difference in the DMD/s - my msologist talks about it as the pepsi/coke challenge.

I was wondering if anyone new a website where I could go and see comparisons in the different MS drugs, Avonex, Copaxone, Rebif,and Betaseron. I am interested in the success, side effects and anything that would be beneficial in helping us to decide which drug to choose.

While talking to my rebif rep about the possibility of having both the Rebismart injector and some pre-filled syringes on hand, (ty Shell for the suggestion), he told me there is a new device available called the Rebislide. Well...first he laughed nervously and said he's never heard of someone wanting to us syringes instead of the Rebismart. He said it was crazy that I was using syringes without having had the training. I got a real kick that he was so surprised with my request.

s and reading other forums, I have narrowed it down to Rebif or Betaseron due to the strength of the meds. My Neuro is leaning towards Rebif for me. I just need a thorough explanation as to why. My last two meetings with him where with me laying on the floor because I couldn't sit down due to lumbar puncture headaches! I will keep you all posted. Thanks again and God Bless you all!

//www.msrc.co.uk/index.cfm?fuseaction=show&pageid=1695 I went to this site several times and worked through their information to see which drug might fit my lifestyle needs best - this is an interactive quiz that helps you... http://www.mssociety.org.uk/just_diagnosed_pathway/ I hope these help.

This is another IMPORTANT survey for Canadians with MS. Make your voice is heard, to ensure those conducting this survey understand how critical our DMDs are to maintaining our health and functioning. Every provincial and territorial government in Canada has programs in place to provide Canadians with MS access to DMDs, in keeping with the spirit and intent of the Canada Health Act. Please provide your input to help ensure we retain funding for access to these important medications.

My doctor gave me the choice of Avenox and Rebif. I picked Rebif for the size of the needle. When it comes to needles I am a baby. The first month on Rebif my husband had to give me the shots but now I am able to do them myself. When I started I was having spacity in my legs and that has stayed the same or gotten better on some days. I do not think my spacity is getting any worse. I don't have flu like symptoms from Rebif.

Hi all Just wanted to share how I am getting on with the Betaferon. First a bit of history: I was diagnosed with "mild" MS 15 years ago - (Good old UK neuros an their mild diagnoses!) Until 2 years ago I had only a few relapses is that time, and sensory symptoms that never really went away. Then early 2007 I started to get one relapse after another, about every couple months and mostly leaving me with sime residual effects.

Yes, I am on rebif for 11 months and must take advil liquid gels To stave off headache fever that wakes me up!

This is a thank you rather than a question but about 18 months ago I posted with my concerns about possible MS after 10 years of symptoms and 2 previous generations of my family with MS. I got practical and concerned comments that gave me the courage to change my doctor (who would not refer me to a neurologist), present a detailed list with dates to my new doctor who referred me straightaway to a Neurologist.

Hi Footsie, Absolutely do NOT store your Rebismart in the fridge! It will kill the batteries and could cause moisture to damage the machine. Only store the multi-dose cartridges that haven't been loaded into the machine in the fridge. The cartridge in the machine should be fine for the week outside of the fridge. Rebif can be kept at room temp for up to a month, maybe longer, I can't remember, but for sure at least a month.

So, I'm now onto my 5th shot of Rebif and so far I hate it! I'm only on a mini dose (due to titrate on Sunday) but I feel rubbish and I just hate the thought of what I'm injecting plus having to take painkillers on top of the Rebif. I'm told it gets better with time but I think I may one of the minority on here who would prefer not to take a dmd. How did you all decide which drug to try and have you switched much? I tried copaxone first but had an adverse reaction.

So the ins company wont pay for Copaxone or Gilynia until my daughter first tries Rebif (i guess because its cheaper for them.) I have a concern with her being on an interferon due to the possible mental health side effects. She is already on Lexapro for anxiety and mild depression. I dont want anything adding to the issue. We have dr app tomorrow to discuss Rebif but I dont want her on it. Anyone have bad side effects with Rebif??? Any advise for me?? Thank you.

Hello. Does anyone take Rebif for MS? Is it helping? How long before any improvement? Does anyone think that it's just a false hope with nasty side effects? Thanks.

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