rebif copay assistance

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.

m thinking that maybe REbif has a monthly $50 copay max for patients with private insurance. You can always call them and talk to them about their program before you make your final decision. You are so right - another 1-2 months won't make much of a difference.

Well I am again left hanging by Teva copay assistance. I went through being accepted to SS discount program never to have them come through. Then they suggested I apply for needs based through the Chronic Disease Fund in July they accepted me a day after I refilled even though I faxed in the paperwork asap. They would not honor it until my next three month refill in October. I sold my mother's gold necklace to pay the three hundred dollars.

Caring for yourself is the most important thing. Most drug companies have copay assistance if you have insurance.

I'm on tecfidera and am on Biogen's copay assistance. I don't pay more than 10 for each refill. It was very very easy to join the copay assistance for me...

One is a financial assistance program that helps you with the cost of your copay - for example, my copay was $90, and they helped me out with $40 of it. When I had problems affording the $50, I talked to my neurologist, who helped me with a complete financial assistance program that would allow me to get it for free. However, Aetna is a complicated mess. I have to get all my medication through their Specialty Pharmacy, not their mail-order pharmacy, which is confusing.

the next day i had a reimbursement specialist calling me from the betaplus program and we discussed my situation and i was required to fax her my notice of assessement of how much i make and it is low so she told me if i had a spouse because she needed his net income as well because of both patners and i said i am divorced with 2 kids so she said thats fine when i faxed her the documents she called me back witin 2 days and i said i was approved for financial assistance with the whole copay 100%

Laura, aka Lulu54 mentioned that there may be copay assistance programs available. I went to the Genentech website and found a wealth of information about assisatance for payments associated with many conditions. None of these were MS. I have a call in to them. but sustpecty that since Rituxan for MS is off label there is no program at Genentech. Does anyone know of any fiancial assistance programs for Rituxan?

does anyone know of any copay assistance programs that would help with copayments .for my osteoarthritis?

Hello. I have been on Rebif now for just over three years after nine and a half years taking Avonex. Have been very consistent in making sure to take my shots. Having a short term memory moment, realized the other day while taking my 2nd to last shot of my current distribution; This being true, tomorrow will be my last shot with a schedule to take the first of a new packet on Saturday, Dec 22nd. Many thanks if you can supply me with the appropriate phone number to order a next batch.

My copay is $100 a month but I applied for needs based copay assistance from the drug maker and they help me out. I realized it would be more expensive in the long run for me not to be on my DMD. Try not to dwell on costs at the beginning. I freaked myself out so bad I decided it was better for my family if I did not treat my MS. If you had cancer you would find a way. We have just as much right to health care as anyone.

They have copay assistance if you have insurance. They sent me a letter to reapply and the deadline for 2012 was December 5 2011. I am not sure if that deadline is for reapplying. You have to reapply every year. The Copay assistance is a separate arm of TEVA I believe not for profit. It is a limited amount per year of assistance. You send in your tax returns or pay stubs, etc. to show your income.

These drugs are expensive. My chemo is $50,000 and infusion multiplied by six. But with the MS drugs and chemo I think of how much money the drugs save me. If we did not have the MS drugs there would be more disability. Disability is way more expensive. Wheel chairs, vans, converting the house, nursing care, hospitalizations, nursing homes, etc. I can't afford any of that if it comes to it. Pharmaceuticals often save people money in the long run by lessening the time we spend in hospitals.

I have Blue Cross/ Anthem insurance but have a 30% copay for the injections and 40% copay for the pills, which will be about $900 a month out of pocket expence. since this is a non elective tretment i dont have a choice but to get the treatment, but i do need help paying for it. Is there any kind of program that will help me offset the copay cost for this program?

Please do not despair about this glitch - if nothing else, there are patient assistance programs from all of the pharmaceutical companies that will also help with the drug cost. If I'm remembering correctly, betaseron has a $0 copay program for folks with insurance and very good help for those who don't. Again, I'm sorry for the reasons you've joined us.

Vertex does have a copay help program which give a 20% copay help. After a 20% copay card from Verrtex, my out of pocket, roughly $14,000 for a 12 week treatment. I just cant afford this. Is anybody working on a drug coverage appeal for Incivek or have you found other means of assitance?

The pharma companies could all take a clue from Bayer Health and work this out. A copay assistance program for EVERYONE would be wonderful. OR maybe all of us should make the switch to rebif? Believe me when I say this is something I am considering.

Does anyone know about any financial assistance programs? I'm in Arizona. My neurologist wants me to take Tecfidera and just found out that I'm not eligible to get the $10 copay because I'm on MEDICARE. Been on SS disability since 1992 and have take four of the injectables for MS. Had to stop all of them because of side effects.

Darn! I just wrote a very lengthy indepth reply and hit enter and it was lost! Argh!!! i'll try this again - welcome to the club no one wants to belong to. immesceo hit the key points and it is especially great you are being proactive and learning more BEFORE you go to the doctor so you can have an informed conversation and know the right things to say. The CRABs - copaxone rebif, avonex and betaseron were the only drug choices we had for quite a while.

There are other drugs approved for treating MS - copaxone is not the only one available (I am on copaxone) and one, I believe it is Rebif, covers the copay for everyone who wants to take it. BUT The rules how they apply to people on government assistance (medicare/medicaid) are often different and I hate to speak out of line about it. You should contact your neurologist and the local NMSS chapter for advice, too.

Rebif copay assistance

Common Questions and Answers about Rebif copay assistance

rebif