rebif canada

I was just wondering what devices other people use to inject their DMD. I'm on rebif and I use the RebiSmart injector. That's what they sent me and no one asked me what I wanted, but I'm glad because it's very easy to inject with.

I started rebif Nov/12 since being on this medication I have not felt normal,it is like the flare up that will not go away. Prior to Oct.

It is true that the four drugs currently approved in Canada for modifying the progression of MS (Avonex, Betaseron, Copaxone and Rebif) must be injected. These drugs are ineffective if taken orally, as they become inactivated or destroyed in the gastrointestinal system before taking effect, or becoming absorbed into the bloodstream." http://www.msanswers.ca/QuestionView.aspx?

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.

Is there anyone on here who is or has breastfed while taking interferons. I was diagnosed with ms last week and my dr. has prescribed Rebif. If the diagnoses wasn't bad enough, I found out that I will no longer be able to breastfeed my son due to the medicine. Through online research it looks like the interferon molecule is too big to get into the milk and would be destroyed in his digestive track anyway. It also looks like interferons are naturally occuring in the milk.

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.

Copaxone since June 2008 after an unsuccessful 8 or 10 week try with Rebif. The latter drove my liver enzymes up and I never even made it up to the full dose. I had picked Rebif mainly due to the lesser frequency of injections, but I don't actually mind the Copaxone daily. In fact i think I'm less likely to forget a shot when I do it every day rather than trying to keep track of whether I did one yesterday or the day before. I've had one very mild IPIR in five years.

Hi all, I have been on Rebif for about 18 months now and it makes me constantly feel like ****, sorry for the expression! What I mean is I just never feel normal. I came off it for 2 months in Jan to try for a baby, I have never felt so great, I had a relapse after 6 wks so my neuro said trying for another child was a bad idea for me and my family, so I went back on the Rebif. I was just thinking should I try another dmd to see if it makes me feel better or are they all gonna be the same?

Alas, the accompanying journal and information package is entirely in French. I know Canada is a bilingual country, but I must admit, I haven't taken a French class since the 6th grade. No harm done, though... I mentioned it when I called "Multiple Support" (get it? :P) to schedule the in-home nurse visit, and the very nice lady I spoke with told me that this little packaging mistake had been happening a lot as of late, and they'll send me the English version ASAP.

For help with the Rebif I'd call the LifeLines number. They advertise being available 24/7. The number is 1-877-447-3243. I would think you still need a doctor to prescribe your Rebif. Do you still have a doctor willing to treat your MS and general medical needs now that your coverage has been cancelled? There was a topic recently with info about financial assiatance for drugs. I'll see if I can find that one. Otherwise I'm not sure what your options are.

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 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.

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.

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

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.

I have been on Rebif for four months now, and I am not going to do another shot, I can't handle the side effects. I've tried premedicating and nothing seems to work. How many of you are in the same situation? and what did you do?

I took my first shot of Rebif today. I gave myself the shot and i thought this is great no stinging, no redness, no lump like i had with Copaxone. Then WHAM!!!! I had abdominal pain about an hour after the shot it lasted for about 6hrs The only thing i could compare it to was a 6hr nonstop labor pain. We will see what happens Monday when i take the next shot. Does anyone else get this abdominal pain on Rebif.

Is there anyone using Rebif for MS? if so how are you getting on with this treament?

Is anyone currently taking Rebif? And does anyone know anything about it? I was just (finally) diagnosed with MS, though my Neuro wouln't say which kind it was... and is planning on putting me on Rebif. It's been 2 years since my symptoms started, and haven't had any kind of relapse or relief in any symptoms, they just keep coming.

Common Questions and Answers about Rebif canada

rebif