does avonex work

Does anyone know of long-term side-effects of Avonex? I've had about 8 or 9 injections so far - was diagnosed a few mos. ago. I will see the (MS) dr. in 2 days, a 3 month follow-up visit. Does anyone know of any questions I should ask her? Thank you very much! I appreciate any feedback.

In addition, he works in a very high pressure job and I am concerned that this may leave him sidelined from work (in an environment that he does not want to open up to about the situation yet).... I know many have had similar concerns but really just looking for some support. THANK YOU!

Like MS everyone does not get every side effect. Tecfidera does not work there are other options which is great. I hope things work out. For gastro issues there are medications.

Hi I am new to MS. My doctor prescribed Avonex. I have little to no drug insurance. I went to a site which offered discount coupons. I called them to ask them if this is a come on price or is this within reason the price every month. They would not give me an ansewr. Does someone here have any experience with this?

Just curious - was the prednisone prescribed because of the reaction to Avonex, and does the prescription provide a dosage range to work within so you can adjust as needed? I agree with contacting your neuro and/or nurse, a month is a long time to wait if you are in a lot of discomfort, especially if it is avoidable or could be at least minimized. Re: the prednisone, your pharmacist is also a great resource for you.

Hi - I am starting on Avonex next week and of course am concerned about side effects but like the once a week part of the treatment. Those that are on Avonex how do you handle the side effects any tips you can give me?

I was dx in January & started Avonex in February. Prior to this I have always been known as very easy going. I work in a highly stressful job, but have for 15 years and I have always rolled with the punches. After my dx & starting Avonex I noticed myself becoming a bit testy. Now 8 months later I believe I am no longer able to roll with those punches. So my 2 parted question would be, does this sound remotely familiar to anyone and any suggestions to controlling emotions?

I have been on Avonex for the last 15 years and have finally reached my limit. I am taking a 6 week break from the Avonex and will be starting Copaxone at the end of April. I actually have two questions: 1) Has anyone taken a break from their medication for that long (and if so, any consequences) and 2) Has anyone switched from Avonex to Copaxone, and if so, how did you do?

To counteract the damage the drug does I did some research and take supplements to counteract the issues caused by the very thing(s) that are supposed to help. Question is, would a complete stoppage of pharmaceutical meds be a smart thing to do? I will say that progression has been slowed.....who's to say it's because of the pharmaceuticals? I am 55 yrs old, the mother of four raised primarily solo. Have endured much strife in life as have all others.

s possible connection with the GB issues-I will find out next week. Neuro doc has all the blood work from the last year and it will show high levels if the avonex caused it. I will keep you informed, but he did tell me Avonex has a tendancy to raise you liver enzimes. Which to my ears means Pancreatitis at the least! I know he will pull new blood levels which include liver, will keep you informed after I know for sure the outcome. By the way-the rep's at Avonex will not leave me alone...

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.

thanks guys, :) Laura, we did talk the Tecfidera, but not Gilenya, she did not mention that. The chemo drug she talked about was talked to me from another specialist in Vancouver, and she did not want to jump to that. I had taken in a list of some drugs, and tried to be prepared for the appt. and go in with some knowledge....

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.

i HAVE BEEN ON THE AVONEX FOR 8 MONTHS. I DONT GIVE MYSELF THE INJECTIONS EACH WEEK, MY HUSBAND DOES BUT THEY ASSISTANCE PROGRAM AVONEX HAS IS GREAT. WE PAID 10 A MONTH AND WHEN HE CHANGED JOBS AND WE LOST INSURANCE I HAVE BEEN GETTING IT FOR FREE. I DO STILL GET ACHY, EMOTIONAL BUT FEEL LIKE I AM ADJUSTING TO THE MEDICATION. GOOD LUCK WITH YOUR CHOICE. HOPE THINGS GO WELL WITH YOUR INSURANCE.

Hi, I was wondering if anyone who has taken both Avonex and Rebif could give some input here. I have been taking Rebif since this past June, but have started to wonder about how Avonex would compare side-effect-wise. As they are both interferons, I would think they would be similar, but I'm not certain. The idea of once a week sounds nice in comparion though, so I would like some actual first-hand knowledge. Thanks!

Hello All... I'm turning to you all for some advices! Burbandude started another flair-up this Monday. He has blurred vision and balance issues. We raced off to see his neuro who was not pleased that he was having another attack only 6 months after beginning treatment with Avonex. His recent MRI from last week showed "significant improvement" lots of the lesions he had were not visible and the ones that are were much lighter than his first MRI.

i wish i could choose a day like that but i work shift work and rotation so no matter what day i choose i will still have to work it.....

well at 11am today will be my first shot of avonex..... i am scared...... not so much with the needle ..... just the possible side affects .... i am supposed to go camping lol..... and just in general..... anyone have stories of there first injection with avonex?????

It is good to know Avonex does not work in the same way.

Does avonex work

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