avonex uk

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.

I have 2 friends in the UK who both have MS (they live together) and I am very concerned about them. Every time I call them they have been smoking MJ or they are seriously drunk. They take DMD's but they don't seem to care - they are both house bound and start drinking beer or whatever after lunch. I spoke with them yesterday and they were so drunk I could barely understand them.

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.

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.

My new Neurologist wants to put me on this med. I don't no much about it i was on Avonex before but it made me really sick and by the time i felt better it was time to take another shot i have kinda a needle phobia anyway i haven't been taking anythig for awhile but i was just wondering what your thoughts were on GILENYA ??

Hello! I hope everyone is doing well! I was diagnosed in November after a few years of symptoms, culminating with me losing motor skills and strength in my arms and hands in October. I have gradually been getting better amd can now write again and hold a cup of tea! I still tingle constantly but reckon I just have to deal with that now. I got flu over Christmas which set me back a bit, then was hit with optic neuritis (I think that's what it is called?) At New year.

//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.

She summed up that I was having more issues with Avonex than MS. She recommended that I switch from Avonex to Gilenya. I like the fact that it is oral, but I would like to hear opinions from others. I don't know much about Gilenya because my old neuro said that it was not for me. I am in the process of reading all the stuff the neuro gave me. Please respond and let me know what you think.

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?

He was happy and happy to see me and reporting doing well with Avonex! He wrote another script for auto injector...so I will be getting that soon... For some reason I am hearing MS everything , everywhere....while if it is not Jack Osbourne's news with Dx. it is a show with celebrities dx. with MS funny it seems to be more prominently discussed and known when it IS infact what is "ailing" you...hmmmmm I was on vacation this week, well sort of...

Hi, I was recently diagnosed with MS and had my first Avonex injection Friday. Friday night was tough (fever, chills, pain and eventually heavy sweating) but I felt pretty good by Saturday morning. Saturday afternoon I started feeling kind of down and by Sunday morning I feel even more so. I can't decide if this is a result of the drug or just the situation as a whole.

Sigh, I have a question from a friend. She would like to know if avonex causes calcium deficiency? She is diagnosed with ms. Not like me.

Is anyone on avonex? My dr. wants to switch me to avonex, but with having lupus, I really don't want to go on an interferon. I'm on copaxone, now but because I have large welts on my arms he wants to switch me. I don't want to switch. Do I have the right to deny a new medication I feel would be detrimental to me?

Flu-like symptoms are a fairly common side effect during the initial weeks of Avonex treatment. It is recommended that you take your Avonex injection before bedtime. Immediately before your injection, and for the 24 hours that follow the injection, patients have found that use of over the counter pain and fever reducing medications can help with this common side effect." You could also get on the Avonex website for further info. good luck. hope that you feel better soon.

I have been on copaxone for little over a year its not working for me so my neuro has asked me to try avonex. My avonex nurse is coming this evening but I am wondering how long you actually gave it to get the symptoms of the shot to calm down. I am crossing everything to hope I dont get the flu symptoms so bad but we will see. I have a husband that works away and 3 small kids to care for, I dont want to be in bed all weekend when its the only time we get to spend as a family.

Hi guys, has anyone not heard from the AVONEX people once they were put on it.??? I have heard from heath nurses, and today, got my WELCOME package, but still no product. I don't know what is going on, and of course the lady or the rep from Avonex is away on holidays till the 2nd. of Dec..... so, I guess we will do it next week ... Just to let you guys know, they stopped my antiobiotic IV today, and said that it was an MS attack. Wherever there are nerves, MS can strike.

Hi Candy, When I was on the Avonex I had terrible itchy skin. I would start scratching and I would well up from the scratching. I also found that it dried out my skin as well. I use pure coconut oil right out of the shower then gold bond lotion right over the top of the oil. It seems to be helping tremendously. The oil soaks in quickly and the lotions seems to seal in the moisture. I hope this helps. Sorry you have this to deal with on top of everything else.

//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've been on Avonex for 2.5 years and it's suited me well but I have just had a 4 week break. I then took my injection on Tuesday night and was strangely fine on Wednesday and Thursday but on Friday, Saturday and today I have lost about 50% of my strength from my left arm and leg. Is this likely to be a side effect from restarting the Avonex (muscle weakness) or a relapse?

After being on Avonex for 1 1/2 years I have developed new side effects?? Red eyes with severe pain (in my eyes & behind my eyes) It started several months ago and now happens with each weekly injection. Has anyone here had to discontinue Avonex due to side effects?

DX on 2/14...started Avonex last week with nurse helping and did fine. This week I thought I did okay but noticed the plunger did not go completely down. It was the 1/2 dose. Since I am inclined to over analyze, trying not to panic. Figure I'll be taking more next week...but since you all seem like you know your stuff...thought I'd ask the experts. Thanks.

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