rebif patient assistance

I am also on Copaxone - can I suggest that you talk with them again at Shared Solutions and ask what criteria they use for patient assistance? They fund for people without insurance or underinsured through NORD - national organization of rare disease. Unfortunately it sometimes takes more than one phone call to connect with the right people at SS to get help. If you can't work it out with SS you might talk to your neurologist about other options.

Not sure about insurance, but most drug companies have a patient assistance program to help people with cost. They require financial information. All they can say is no. Give it a try.

http://www.pfizerhelpfulanswers.com/pages/application/Application.

could anyone give me ideas as to where or who i would contact to get some patient assistance for acute hep c treatment? I am not working, cannot wait on s.s. disability. I try to do some construction work when available, but it is really rough.

All of the CRAB (copaxone/rebif/avonex, betaseron) drug companies have patient assistance programs, if they are needed. I recommend calling your insurance first though, to see what their preferences are- because with mine, they wanted me to try certain ones first, before they would agree to pay for the others. I have know idea why, and neither did the agent I was speaking to. There aren't any generics available for these drugs. With a prescription from your doctor, you should be okay.

They will accept what the insurance gives, and will not expect any more from the patient. The nurse said, the rest of the injectables will follow (Copaxone, Rebif, Avonex). They "always" follow each other to stay competitive. That is a GREAT thing.I hope she was/is right.

t afford to fill his copaxone rx. Can any of you give me some hints to share with him? Does TEVA offer any patient assistance programs?

What is usually the cost of these meds? ( I am considering trying Rebif or Avonex) I have heard they run about $1500/month. I have to meet a $3000 deductible which means I may have to pay for my first dose. I don't have an extra $1500 floating around. I am really starting to freak out! But then again part of me figures I have probably had MS for 15-20 years an I am fine so far. I guess waiting another 1-2 months to start taking DMDs can't hurt. Can it?

They have a program that offers the best assistance for those in financial need. There are two kinds of assistance programs...one there is no need for any financial forms to be filled out. They make sure to keep your cost at thirty or forty dollars (I don't remember the exact amount) per month. The other requires you to fill out financial forms...If you are in need you will be approved and they move quickly. I wish you the best.

Rebif has a very good assistance program, ms lifelines -- -- no income verification etc. & will work with or without insurance. It's just a short phone call to get it set up.

http://www.mslifelines.com/rebif/guide/side-effects.

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.

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 used to take Copaxone, and had to quit because of an allergy. I now take Betaseron - I'm evidently one of the lucky ones that doesn't have a flu-like reaction. Both of these are sub-cutaneous, which means really short thin needle. I think both Rebif and Avonex are intramuscular. Both of these medications have patient assistance programs, so it's worth looking into. I think that Rebif and Avonex are for a more progressive course.

I was reading the post about suboxone prices ,someone wanted to know if the was any assistance for the cost . I did some research this is what I found RECKITT BENCKISER suboxone patient assistance programs 1-866-512-2216 I don't know what are the guidelines but its worth a call . Any little bit I am sure would be very helpful. If I find anything else I will post it.

I have been taking Rebif injections, since January 2010, and I have never missed a single one, until now. Up until January 1, 2012, I have received my Rebif injections, free of charge, due to the fact I had no health insurance. I became eligible for Medicare, on January 1, 2012, and so I have had to wait for MS Lifelines to decide whether I'm still eligible for their "free of charge" program.

I take Rebif for RRMS and I am having severe Right thigh pain & low back pain I have severe degeneration of my entire spine and my Orthopaedic Surgeon who is also a Pain management specialist wants me to try the injections. He believes that the leg pain is coming from my back not my hip. Is there any problem associated with taking Rebif and getting the steriod injections? I am scheduled to start the injections on May 5th. This discussion is related to <a href='http://www.medhelp.

Hi Jen, We've not met. I'm Shelly and I'm on Rebif. You'll be contacted to receive your Rebif script, and a nurse covering your area will contact you to find a time to come visit (will also make sure you received the meds - which you'll keep in the fridge). He or she will teach you and whoever else you want to learn the injection techniques. The nurse will also talk to you about your MS, the meds and possible side affects, etc.

For instance, what are the monthly costs for medication (e.g. Rebif or others)? What is the official go to info source in Singapore? Looking forward to your feedback. All the best!

Rebif patient assistance

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