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Betaseron and medicare

Common Questions and Answers about Betaseron and medicare

betaseron

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.
Avatar f tn My husband has been on Betaseron, IVIG, and Tasabyri. He built up antibodies on the betaseron and tasbryi.
233622 tn?1279334905 I have been off of Betaseron for about 2 weeks now and my eyes are back to being very uncomfortable. Before I started Avonex eye pressure and pain was a huge problem. Now it is is starting again.
338416 tn?1420045702 re taking your Coumadin for the positive serology for a positive serology of aCL IgG/IgM and Reynauds and taking Betaseron for your MS (even prophylactically while waiting for a diagnosis) that it can cause a little anxiety. It's one medication counteracting another. I would be concerned too. Are you going to talk to your doctor about this?
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 at first it was just like spotting but now its aot like a period (as of today). I am on betaseron and I didn't know if it could mess with your period like tha or make your breasts sore.. (fatigue is a normal ms symptom tho so that doesn't concern me except its been worse lately). Plus.. I have been noticing that its harder for me 2 hold it when I have to pee and smetimes it leaks (which again could be ms related). I'm just worried and really can't do a test yet..
Avatar f tn I've been on Betaseron since a year after I was diagnosed in 2000. On August 20th, I quit taking Betaseron cold turkey when I finally received my new oral medication Tecfidera. For the last few days I have been dealing with horrible body aches, diarrhea, cold sweats & the inability to eat (not feeling sick, just not being hungry or interested in eating). I do not have a fever, a cough, allergies or anything else I can conclude to be at fault for these annoying symptoms.
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 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 I'm three weeks into Betaseron . . . and am pleased to hear all of the positive news.
Avatar m tn d be getting your dr to sort out this problem for you. To me its part of his/her job to get you what you need and if Betaseron is what you need, he/she should hopefully know how to get it (back) for you. Cheers.........
Avatar f tn The specialist at UCSF is switching me to Tysabri and has told me to go ahead and stop my Betaseron. It has now been 2 shots that I missed (well didn't take) and for the past 2 days I have been feeling like someone beat the crud outta me. My husband is insisting it is cuz I am not taking my shots. I don't see how that can be. We went to UCSF Monday night (4 hr drive), had my Dr appt Tues which took 4 hrs.
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.
338416 tn?1420045702 Well, as some of you guys may remember, I had a blood clot in my leg last October. This was right behind my right knee, which is the knee with all the problems - weakness, numbness. I also have phlebitis in my left leg. I also have Reynaud's, apparently since 2009. Well, I hadn't been taking my Betaseron, because I'd read some anecdotal evidence that indicated there was a connection between blood clots, reynaud's, and Betaseron.
1967803 tn?1325679473 ve been trying to figure out what to do about health insurance. My neurologist and I were discussing Betaseron and gawking at the out-of-pocket cost. Luckily he was nice enough to waive the fee for my next visit, but we haven't figured out a solution for the medication. He told me to come back when I got insurance so I could get a proper diagnosis and a prescription. Does Medicaid cover Betaseron?
Avatar f tn Hi there, I'm glad they are keeping an eye on your liver enzymes since you are on betaseron. They should run a CBC and thyroid too every so often. Sometimes they don't run the thyroid panel though as a general rule and you may have to request it. Doesn't seem they ranges are extremely out of the average, but none the less it's good Dr. is keeping a watch - though they should have called you and not the other way around. Seems to be the norm these days for many, unfortunately.
Avatar f tn I have been on Betaseron for 2 years with no side effects and am happy with it. Obviously with the NHS I have no choice about the change. Any insight would be greatly appreciated.