rebif financial assistance

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.

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.

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.

If Shared Solutions thinks you won't qualify for any kind of assistance, I'm not sure what to tell you. They have two kinds of financial assistance - partially funded and completely funded assistance. I'm on the 100% assistance plan, but then, I'm broke!

My doctor has given me options for medications for MS. These are expensive since they are considered specialty drugs. Tecfidera seems to be my safest choice for now, but I was told my insurance would only cover 50% and my payment would be about $3600. I don't have that kind of money to spend every month. I'm on unemployment. I know some of the drug companies have financial assistance....has anyone had experience with the financial assistance they provide?

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.

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.

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.

If you do not have insurance or if you need help paying for Copaxone, Shared Solutions can refer you to other financial assistance programs. To speak with someone at Shared Solutions, call 1-800-887-8100.Your doctor's office or the local chapter of the National Multiple Sclerosis Society should also be able to assist you in determining financial options for affording treatment. More Information: Copaxone is made by Teva Pharmaceutical Industries Ltd.

hate to be the bearer of bad news but they are mostly Tier 4. Many of the drug companies have financial assistance, some more than others. Then, unfortunately, there are people who don't take anything either because they don't want to or can't afford to. MS is not a cheap date, for sure but can be a demanding one. Wish I could have given you better news!

My neurologist was furious at the cavalier attitude with the county attending physician, but suggested that Shared Solutions may have a financial assistance program. I am going to go on Feb. 11th in Los Angles to see if I can get some help. This last week I have been experiencing an exacerbation that is affecting my balance...I keep falling to the right and my legs are very weak. The fatigue is overwhelming. I am hopeful that this will help my overall health.

I wanted to share some encouraging news for people who have Chronic Hep B and have financial difficulty affording Baraclude. I contacted Brystol Myers Squibb and applied for the Patient Assistance Program. The website and application is here: http://www.bms.com/products/Pages/programs.aspx It took about a week and they have approved me to receive the medication and are shipping it to my home.

If you make lower then your cities standard income for families you can do to your local family services and sign up for temporary assistance for needy families. (Tanf) you can also apply for food stamps and child care costs if your wanting to find a job they provide child care as well at least that's how it is in mo. Good luck hope u figure something out!

Okay, these might sound like stupid questions but I am so worried about the financial ramifications of this disease. 1. When I get my DMDs will I get them filled at a regular pharmacy? 2. Do insurance companies usually fight with you on trying to pay for them since they are so expensive? 3. What is usually the cost of these meds? ( I am considering trying Rebif or Avonex) I have heard they run about $1500/month.

The injectible MS meds, as well as the new oral meds, are very, very expensive, but most do have good financial assistance, if you qualify (and each pharma company has different rules for assistance). So, there's lots of homework to do. Good luck. Ask if you have more questions.

Hi there, there is a lot of financial assistance available, here is one place, also if you look up Harvoni you can find their site. They not only provide financial assistance but can help you in other ways. i.e. helping find a doctor etc. Here is one place for financial assistance, there are others. http://www.panfoundation.

Does anyone know if there are any statistics showing the effectiveness of Rebif if used only twice a week versus three times a week? My husband will be losing his job come the end of August, and along with that, our benefits. I figure if I start now going to only 2 times a week, between now and the end of August I can make my Rebif last for at least another month. I know this is not the best thing to do, but it appears to possibly be the only solution.

Go get on assistance like food stamps, Medicaid and wic. They may even pay you money because of your situation.

Check the MSAA financial assistance website as well. They have an MRI assistance program that will help folks in the diagnostic process under certain circumstances.

Yes, probably. The manufacturers of HCV meds provide Patient Assistance Programs that you might qualify for if you live in the U.S. I've personally used one, and it helped immensely.

Here's a link to help check for prescription med assistance: http://www.pparx.

Insurance will not cover him as they say it is a pre-existing condition. Where does he get financial aid so he can get medical help with a psychiatrist and councillor.?

Rebif financial assistance

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