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Avonex and medicare

Common Questions and Answers about Avonex and medicare

avonex

2015036 tn?1332997788 Some of you probably received the same email I did. Biogen sent me an email saying they could now help people get financing, even if you're on a Medicare plan. So far, only Biogen is working with Medicare patients. There's a lot of paperwork involved, but it look like I'm finally going to start a DMD again. All of Biogen's MS meds are available for the program: Avonex Plegridy Tysabri Tecfidera It's worth calling about.
645390 tn?1338555377 2 MS nurses lead it, and there was a MS advocate, who is a social worker that also brings information. It has been going strong for 12+ years, really good group. They also had muffins, candy and bottles of water, need I say more LOL. Anyway, they told us that Betaseron, the company that makes it, I cant remember the name, will be doing away with co-pays. They will accept what the insurance gives, and will not expect any more from the patient.
198419 tn?1360242356 SarahL asked for a good list for patient medicine assistance sites. I came across pparx and tried it out. Type the name of your medicine you need help in the box (link should bring you to page with a box - I typed in Provigil in the search term using drug name), and it brought up the company's program, and I also tried it with Avonex.... Quicker than linking a whole host of individual websites! http://www.pparx.
5681139 tn?1372268736 My Tysabri cost, after Medicare and United Health Care AND getting Tysabri assistance for the drug (I could get it for $10) ended up being over $600 PER INFUSION. I asked and asked and asked what the charge would be before I started - and they said after insurance probably $50-60. They would NOT give me a number. They didn't bill me for the first infusion until I had gotten 3. Therefore owing almost $2,000. HORRORS for someone on disability. Fighting it. Plus, I stopped taking it.
Avatar f tn Hi, the test for neutralizing antibodies is done only by a few labs in the country and not all of them give reliable results. My neuro will only use Athena Laboratories in Boston. The test costs $800 (as of last August). Sometimes insurance won't pay for it. I am on Medicare and had no problem. The test is not done routinely, but should be run if there is a suspicion that a medication has stopped working.
198419 tn?1360242356 have been on in order, avonex, rebif, avonex again, betaseron, copaxone and tysabri. Currently not on any, but will be on gileyna in january. Tysabri worked the best for me, but because of the very high risk for me to get PML, I decided not to chance it any more.
Avatar f tn Are you including government health insurance, such as medicaid and medicare in your list? There are so many different types of insurance as well. Policy coverage can range from excellent to minimal. The out-of-pocket expenses might be an intersting poll for you to put together as well. This is a great question.
587890 tn?1295473081 I have had MS for 10 years and I just stopped my AVONEX so I can try and get pregnant I know it sounds stupid but there is no studies on avonex and pregnancy so I just thought I would ask if any one else has been on some treatment or off to get pregnant? and how long were you off your meds ?
Avatar f tn ) and still have a safe and fulfilling sex life. Your best bet is to discuss this with your doctors and possibly and Infectious Disease Doctor. The doctors may recommend vaccinating your partner. They may also consider the risk of contracting HPV to be a low risk exposure and do nothing. Most people with MS can be vaccinated with "non-live virus" vaccines. Gardasil is a VLP (Virus Like Partials) vaccine (so it is safe) protecting against infection by HPV types 16, 18, 6, and 11.
2015036 tn?1332997788 ve had a several episodes of what were probably relapses over the last several years, (including mild optic neuritis, left sided weakness/numbess, shaking, twitching, and some outright jerking and flopping (clonus?), and multiple other odd sensations) but I didn't always know what they were.
211940 tn?1267881266 I am sorry you are having this problem. It must be frustrating. As for missing the rebif injections my neurologist had to stop mine for a month due to illness and he said it wouldn't make that big of difference and not to worry. Hope this helps and hope you get approved soon.
Avatar f tn If you have Medicare and Medicaid, you will usually get your drugs covered by the Medicare prescription drug benefit (Part D) and the Extra Help program. Extra Help is the federal program that pays for most of the costs of Medicare drug coverage if you meet the eligibility requirements. In some limited cases, Medicaid may cover drugs that Medicare does not cover. As long as you have Medicare Part D your drugs will be covered. Call Medicare if you have questions.
Avatar f tn This is already the situation for me and my Medicare coverage, so be prepared if you are going onto Social Security Disability Income and then Medicare. I have to pay $4000 out of pocket before going to 10% of my (now $1715 Avonex). Right now I am in my "donut hole" where Medicare doesn't pay a thing. Our legislators really screwed us with the Medicare Drug deal!
Avatar f tn Hello Everyone :) I haven't been around on the forum or a while due to a string of horrible bad luck, but things are starting to look up so here I am :). I have a question about DMDs I have been on Avonex now for 5 weeks and have noticed a huge difference in my muscle spasms. It's as if the off switch got flipped! I went from having them literally 24/7 literally. My neuro said she hadn't really seen anything quite that severe she could see muscle spasms everywhere during my exams.
233622 tn?1279334905 Does Avonex cause a lot of leg weakness and aching? Or is that something more associated with MS itself?
462771 tn?1358355843 The sole purpose of Copaxone, Rebif, Avonex and Betaseron is to slow the progression of the disease and reduce the number of relapses. If you look at the studies, people on these CRAB's still have relapses, they just don't have as many relapses as people who are not on a CRAB. So it should not be a surprise to any of us on a DMD when we do have a relapse. The CRAB should be making it less intense and shorter in duration, hopefully.
Avatar n tn Besides Liver Transplant Centers (where you MUST be treated to have your cirrhosis and portal hypertension managed) usually take both Medicaid and Medicare for payment so there is no advantage to Medicare. In fact Medicare is very expensive. You say you have one doctor. Any one doctor can NOT treat all of your health conditions and certainly not your liver disease. You will have to make sure the liver transplant center takes Medicaid. This should be the first think you do.
Avatar m tn Well Avonex is a lot like beta. Got a fever of 102 and feel like death. It hit me within 3hrs after the shot. Well at least it's just once a week.
Avatar f tn 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.
Avatar f tn People in Raleigh were very rude and said i need to stop being lazy and deal w my case worker...my caseworker told me to call Raleigh. So am i just pretty much **** out of luck. I just wanna have this baby and never turn to medicaid again.
7827642 tn?1396958758 For my last pregnancy I applied at 7 weeks when I found out I was pregnant and I didn't hear from them at all. I called my case worker and everything and nothing. I lost my baby because I couldn't go to the doctor and I still didn't hear from them. It was so hard.
Avatar m tn I have medicare in California I will enroll in it next month,I have liver transplant with hcv and cirrhosis ,I need to find out how medicare and if medicare pay for sovaldi and olysio.
Avatar f tn This is random i know. So i faxed over my new adress and stuff for medicare and its been literally almost a month since and still waiting for approval and i was just wondering if im not sure if i have it yet that i can just go into the hospital in the outpatient section for treatment because im literally almost 4 months preg and still have not seen a doc. even for an ultrasound for christ sake.... can somebody tell me how i can get immediate care?
Avatar f tn //www.rxlist.com/avonex-drug.htm) and, like other proteins, can only work within a very small range of conditions (ie pH, temperature). As the stomach is a fairly acidic environment, proteins will denature (fall apart) and so Avonex would be rendered useless. That said, there is a therapy available in pill form (http://www.sciencedaily.com/releases/2009/04/090429205613.htm). Called "cladribine", it may very well be the first treatment for MS that does not involve regular injections.
Avatar f tn I am close to Medicare age, and have a low viral load, so my doctor says my insurance won't cover Harvoni. Anyone know what Medicare's guidelines are? Do I have to be sympomatic to qualify? It's pretty frustrating knowing that there is now an easy cure, that I can't get. So I'm hoping the cost will come down soon, or Medicare will be more generous than my insurance!
Avatar m tn I have CIDP (Chronic Inflammatory Demylinating Neuropathy) this is the chronic form of Guillan Barre. I will be going on Medicare in April and I need to know if they will cover my IVIG treatments. The drug is Gamunex. I can't get any answers from Medicare.
Avatar f tn I called Gilead and the person there told me that Gilead will NOT give any financial assistance to ANYONE on Medicare Part D. I did some research and found out that most Part D plans DO NOT cover Solvadi and even if you do get approved through an appeal, you will still be responsible for 5% of the total cost which is exceedingly high (5% of $84,000). PAN will only pay at most $7500 of this total.
97654 tn?1214348650 t affect your spirits, even though I think depression is listed as a side affect. I have been on Avonex for about a year and a half and have found that my right side reacts better when injected than my left. I also inject in the early evening, then take 2 tylenol and two naprox about an an hour later. Usually I wake up pretty free of the yucks next morning.