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!
I took Forteo for 10 months. and i can barely walk. i took Tymlos for the first 6 months and was fine, and then Forteo for 10 months. my strength is gone, my feet hurt wearing shoes, i have stomach pain when exercising, and ave thigh muscle cramps, neck pain, and can't sleep. I had confusion when driving, so i told my doctor i'm done with this. I know where i'm going these days, but I now use a walker around the house, elastic knee braces to walk on my own.
I have severe osteoporosis and am trying to take Forteo. I started out with half dose and have worked up to a full dose. The full dose 2 days in a row was disabling. My doctor suggested every other day. So I let the previous trial work its way out of my system for 5 days and tried another full dose. This is three days after the dose and I am weaker each day. I move in slow motion. My doctor is puzzled. Anyone had a similar experience?
I have worked with this site for many years assisting people to get the medicines that they need. You should check and see if you qualify for the Forteo assistance program: http://www.needymeds.org/drug_list.taf?_function=name&name=Forteo
Good luck! I am a breast cancer patient in a drug study taking the osteoporosis drug, Zometa. There is some promising data that suggests osteoporosis drugs may help prevent breast cancer patients having recurrances of cancer as bone cancer.
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.
I had a BMD issue a couple of years ago (suffered 3 hip fractures over 2 years) and after seeing 7 different doctors my Primary Care seemed to put a ton of things together and believed I was not absorbing calcium and may estrogen levels were super low and virtually non existent. I was put on Ogestral and Forteo and knock on wood- no more injuries and a BMD increase of 22% in 1 yr. However, I started having what I thought was food allergies.
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.
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.
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?
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.
My 20 year son has severe chronic bone pain, osteoporosis and has had multiple fractures. We have also had bone biopsy with showed a mineralization defect(focal osteomalacia) and high turn bone turnover but these do not lend themselves to a diagnosis. His blood levels of calcium and vit D are normal. He received a Pamidronate infusion in October 2004 and that is when the pain began. He was completely debilitated at that time as he is now.
In the summer, when I take a hot shower or just when I wake up, my foot becomes red and swollen. It has evolved to the point that both my feet and hands have this condition. My injured foot is worse.
I live in a cold, winter climate and my feet turn purple as well. I have lost feeling in my left foot and it is becoming scary. Meds (to increase circulation) have aggravated the problem). RSD was ruled out as I had a nerve block which aggravated the problem. I have had all blood tests.
When standing after a long period of time sitting I experience symptoms beginning with pressure and pain to the center of my forehead. The pressure generates into my sinus and ears, making my ears pop as if in a plane. My vision becomes blurry and my legs feel as if they are going to collaspe from up under me. I have actually had to crawl on several occasions as my legs would not support me. This has been a consistant problem for about two months. It may occur 1-5 times a week.
I have now been without insurance for a year and need the medicare. I am 56 years old, so it should be obvious that I am not trying to "work" the system. I have an excellent work history, and believe me it is much easier to work if you can than to fight the social security team. Anyone else out there with similar issues?
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