BlackPhx
Posts: 3432
Joined: 11/8/2006 Status: offline
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I would have to say you are among the Lucky ones Nueva..I know more than a few who have had to file Medical bankruptcy. One was an ex dominant of mine who was in a motorcycle accident before I met him... the time spent in the hospital, sepsis, prosthesis, PT and other ancillary expenses were not completely covered by his insurance, auto coverage and the other persons insurance. His co pays and limitations even with all of the insurances kicking in left him thousands in the red, and he ended up losing his job as he could no longer perform it and was out so long. But he isn't the only one...http://blogs.wsj.com/health/2007/11/29/even-with-insurance-hospital-stay-can-cost-a-million/ is an example of what can happen as Insurances cap out. http://www.sfgate.com/cgi-bin/article.cgi?file=/c/a/2004/06/22/MNGB87A0J71.DTL is another article regarding HMO's who deny medically necessary health care and your limitations on suing them. Some of this has slowly been changed over the years, state by state, but it is far from a problem solvedh n I have diabetic retinopathy. I had cataracts. Before the cataracts were removed, due to their placement I was unable to drive as under certain conditions I could not SEE an F-350 and in fact didn't one morning until just before I hit it. I had BCBS with vision and dental coverage and it was one of their top of the line coverages due to the company my ex was working for, and I also had medicare as I am disabled. Neither would cover cataract surgery until I lost almost 50 % of my vision. Of course by that point I had to have some drive me where ever I needed to go and BCBS was outta there. They were no longer my secondary insurance..Medicare is always primary, and what they DON'T pay ( I am still trying to figure out their math) is phenomenal..you can only hope any secondary insurance will pick it up. Once the cataracts reached that certain point they replaced the lenses of my eyes. Yes both of them and while my co-pay was only $100 per eye that is a lot when your income is limited. The Logic of waiting until the cataracts were so bad that your life is badly impacted eludes me. When I was diagnosed I had a 25% vision loss already. Since they replace the lens completely and cataracts do not resolve on their own, why the wait? As I said I have diabetic retinopathy http://www.nei.nih.gov/health/diabetic/retinopathy.asp Intermittently my vision blurs so that I cannot read until the blood is reabsorbed or I have to angle and tilt my head to have clear vision. Eventually it may become bad enough that they will treat it with more than just eye exams to track it. Currently my right eye is the worst one and I am back in glasses instead of just having them for reading. I fight to keep my blood sugars under control but, the disease is progressive and anytime I am ill even on tight BG control my sugars will spike. Since the only coverage I have medically now is a Medicare Advantage plan..my vision problems will have to wait until they reach the badly deteriorated stage before it is handled. I am scared to death of going blind. But medicare (Advantage plans are Privatized Medicare Administration (read as insurance companies and HMO's)) is penny wise and pound foolish, instead of dealing when a problem is small..they wait for catastrophic which invariable costs more to correct if it can be. Of course by that point, you can be blind, deaf, have complications that will require MORE medications, home health care, hospitalizations etc. For the millions of people on Medicare there is a 2700$ cap on their drug plan. When you reach 2700$ then you are under a second tier where you pay 100% of the cost until you accumulate 4500$ in payments (starting again at 1$), at that point you become eligible for catastrophic drug coverage and they once again pick up paying a large percentage of the cost. To those who are elderly or disabled and living on a limited budget, that middle point is very hard to pay for and can often mean they have to make a choice between medications and food or other necessities of life. that initial cap can be reached extremely quickly under some conditions..Cancer drugs can max that out in a week. But what happens if you don't have the money to cover the Gap? Many on Social security or disability are living UNDER the poverty line. Something has got to give. A friend of my M-I-L has leukemia, her chemo and drugs are eating up her savings at a rate of nearly $6k a month. She did everything right, saved for retirement, banked money against job loss, kept her bills within her means, and now because she is ill she is looking at losing everything she worked her entire life for just trying to keep up with her medical costs. She will soon file for Disability and medicare and that will take a year to kick in AFTER she gets disability. She is still struggling to work to stave off that point, but her job at the Space Port is going away. She has excellent coverage right now and she is STILL paying out of pocket $$$$ and that will vanish with her job. She has already maxed several benefits under her health insurance trying to survive. Something needs to give in this country. Medical costs are out of line $25 for an aspirin is not unheard of..Doctors charging for reading the wrong chart, Insurance companies that insist on waiting until a condition becomes chronic or catastrophic, drugs that never make it to generic or cause more problems than they treat (read your side effect inserts) are breaking the backs of the people who are paying them for coverage. I am still paying the price of drug side effects. Long ago and far away they wanted to give me Methotrexate a cancer drug to wean me off of a year of steroids (prednisolone) prescribed to treat highly brittle asthma. The steroid had it's own side effects of suppressing my adrenal gland, triggering a genetic predisposition to diabetes and a few other joys in my life. The Methotrexate was experimental at the time for steroid withdrawal. The possible side effects can include anemia, neutropenia, increased risk of bruising, nausea and vomiting, dermatitis and diarrhea. A small percentage of patients develop hepatitis, and there is an increased risk of pulmonary fibrosis.The higher doses of methotrexate often used in cancer chemotherapy can cause toxic effects to the rapidly-dividing cells of bone marrow and gastrointestinal mucosa. The resulting myelosuppression and mucositis are often prevented (termed Leucovorin "rescue"- as this is the folic acid based drug used). I would have had to have monthly liver tests, blood tests, etc to insure that none of the side effects occurred. I said HELL NO. The result, I kicked the steroid cold turkey and my sons spent 3 months helping me move a body that had turned to stone to the bathroom and back to the bed. It had suppressed my own corticosteroid production among the other side effects. Something has to give..Private Insurance is out of control and out of reach for far too many people. poenkitten
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