Medicare Part D major disaster for chronically illOnce able to get help with medical bills, residents now caught in gray area as their health declinesBy Liz Freeman naplesnews.comTuesday, November 28, 2006They are at wit's end when medical bills arrive in the mail that Medicaid used to pay.There is no way many of the 38,000 chronically ill Florida residents who once were part of the state's Medically Needy program can pay the bills for their visits to specialists, for laboratory tests or dialysis, given that they struggle to live on disability income of about $800 a month. ...
When England was just emerging from the disastrous expenses of World War II, it introduced a national healthcare plan which not only covered all doctors' bills, hospital expenses, and diagnostic tests, but also provided full coverage for all dental care and for all prescription medications.
When England was just emerging from the disastrous expenses of World War II, it introduced a national healthcare plan which not only covered all doctors' bills, hospital expenses, and diagnostic tests, but also provided full coverage for all dental care and for all prescription medications. But why the world's richest nation, the United States, today has to impose such financial burdens on its chronically ill population is inexplicable.
Way to go jbeany and Zach... Stauffenberg you appearto be a most negative person - unfortunately - I'll bet you always see your glass as half empty...too bad - from us Americans hope always springs external...
The Marshall Plan was utterly selfish and just a method to keep the devastated nations of non-Communist Europe plus Turkey from becoming communist themselves. If the U.S. was going to keep markets open for its manufacturing industry to make profits, the taxpayer had to contribute to keeping other nations within the sphere of the market economy.
And by the way, I'm an American citizen, though I live outside the country because I don't like American policies and because the only way I can get full health insurance is through a public healthcare system.
Quote from: stauffenberg on December 02, 2006, 02:32:23 PMAnd by the way, I'm an American citizen, though I live outside the country because I don't like American policies and because the only way I can get full health insurance is through a public healthcare system. Nature or nurture? Where you born a U. S. citizen or a naturalized U.S. citizen? You were in your forties when you became ill, didn't you have your own health insurance? Didn't you work?I'm in the U.S., and when I started hemodialysis I was just a few years out of college in 1982. My HMO covered the treatment until Medicare kicked-in, which at that time took perhaps three to six months. For over twenty-four years, U. S. Medicare Insurance has paid most of my healthcare costs, with my private supplemental insurance paying the difference.For those who don't work, the New York State-run Medicaid Insurance program covers the difference. Of course it's not a perfect system, but hardly what you make it out to be.
I'm in the U.S., and when I started hemodialysis I was just a few years out of college in 1982. My HMO covered the treatment until Medicare kicked-in, which at that time took perhaps three to six months. For over twenty-four years, U. S. Medicare Insurance has paid most of my healthcare costs, with my private supplemental insurance paying the difference.
I'm looking at this thread late, but have a question for Zach, so I hope you check this thread! I've been on dialysis since 1989 and lost my secondary insurance in 1996 when I moved from Colorado to Texas. I didn't stop working but the company I worked for didn't offer health insurance and now I'm self-employed. I've never been able to buy a supplemental Medi-gap policy because I've been told that because I started dialysis prior to 1992, I'm not eligible. You mention private supplemental insurance.......through an employer or is it a Medicare supplement?
Medicare Part D major disaster for chronically illOnce able to get help with medical bills, residents now caught in gray area as their health declinesBy Liz Freeman naplesnews.comTuesday, November 28, 2006They are at wit's end when medical bills arrive in the mail that Medicaid used to pay.There is no way many of the 38,000 chronically ill Florida residents who once were part of the state's Medically Needy program can pay the bills for their visits to specialists, for laboratory tests or dialysis, given that they struggle to live on disability income of about $800 a month.With the launch of the Medicare Part D drug program this past Jan. 1 by the federal government, many of the Medically Needy no longer qualified for the state program. That meant the state's Medicaid program quit picking up the tab for their medical expenses."We figured a lot of people were going to take a hit but we didn't realize how many," said Karen Paladino, a social worker at dialysis centers in Bonita Springs and Naples owned by Fresenius Medical Care.When Medicare Part D moves into its second year this coming January, more chronically ill patients now covered by the Medically Needy program will be in the same bind when they are required to have Part D drug plans.A petition is circulating around the state for patients, their families and any concerned citizens to sign that asks the Florida Legislature to address the life-and-death quagmire that many of the Medically Needy are facing when they lose Medicaid assistance."We can't get sick people to Tallahassee but now they can get there on paper (the petition)," said Mary Ellen Ross, executive director of the Florida Transplant Survivors Coalition in Delray Beach. "What we would like to do is open a dialogue with the Florida Legislature and look at Part D and income levels."At issue is the structure of the Medically Needy program, started in 1986 to provide temporary Medicaid coverage for residents who face a catastrophic medical condition but whose incomes are too high, often by a meager amount, to qualify for traditional Medicaid.They must qualify every month for Medically Needy coverage by meeting their "share of cost," when their total medical expenses for the month would add up to 75 percent of their monthly income. At that point, Medicaid kicks in for the rest of the month.Traditionally, the patients would reach their share of cost when they totaled up their monthly drug expenses. They or their social workers would submit their total drug bill for the month to the state. Medicaid then would cover the drug bills and all other medical expenses for the month.That all changed when Medicare Part D came into being this past Jan. 1. Many of the Medically Needy are "dual eligibles" with Medicare. They were automatically enrolled in Part D plans and that meant they could no longer count their drug expenses toward their share of cost each month.So they no longer qualified for the Medically Needy program and immediately were left with bills for doctor visits, lab tests or dialysis. Some have reacted by not going to doctors' appointments or for laboratory tests and their health is declining. Others are tapping the compassion of their physicians for free care or for payment plans, Ross said."Our illnesses are not getting better," Ross said. "We are not here for a free ride but honestly when you are given a certain amount of money to live on and can't get care, we will be forced into hospitals. Share of cost is a very large issue."Paladino, with the local dialysis centers, said her Medically Needy patients were facing enough stress in their daily lives because of their illnesses, so the impact of Part D has been tremendous."People who were (medically) stable are not stable anymore," she said.Physicians are helping out by billing them but not actively pursuing payment, she said. Her dialysis centers are not turning the patients away even though the centers know Medicaid isn't picking up the bills anymore, Paladino said.Lifelink Foundation in Tampa, an organ procurement and transplant program, saw numerous transplant recipients lose their Medically Needy coverage."It was unbelievable. The outcry was enormous and justifiably," said Rebecca Arsenault, Lifelink spokeswoman.Statistics for how many Southwest Florida residents lost their Medically Needy coverage this past January weren't readily available from the state Department of Children and Families. Last November, 776 individuals from Lee County and 338 people from Collier County were in the program.The petition asks state lawmakers to revise the Medically Needy share of cost by using a sliding scale formula according to federal poverty guidelines. That would helpThe petitioners will collect signatures through the end of December. Supporters can sign it at dialysis centers, transplant hospitals or online at www.floridachain.org."The more we get the word out, the better we are going to be," said Bette Luksha, another member of the survivor transplant coalition.At the same time, Luksha realizes that homeowners' insurance reform and immigration are priority issues next spring for the state Legislature."I believe we will be coming in with open minds and other options to the sliding scale (proposal)," Ross said. "I would like to see some hearings, to tell people exactly who we are and how by the third week of the month don't have any money to live on."Lifelink representatives are backing the petition and have met with elected officials from the Tampa region to inform them of what is happening, said Arsenault, of Lifelink."It's heartbreaking," she said. "It flies in the face of everything we try to accomplish here."•••A grassroots petition in Florida asking the Legislature to restructure the state's Medically Needy program can be seen and signed at www.floridachain.org.original story: http://www.naplesnews.com/news/2006/nov/28/petition_asks_legislature_look_medically_needy/