Thread by me.
In recent weeks one of the many problems Americans have had with plans for the federal government to take over the health care industry has had to do with life and death issues such as rationing, euthanasia and “death panels.”
The socialists pushing government health care have tried very hard to whitewash these concerns, but to little avail. Even the elderly (who are often solid Democrat supporters because of their addiction to the government largess they already enjoy in programs like Social Security and Medicare) are deserting the Temple of Government in droves; apparently the thought of euthanasia and rationing scares them more than the blessings of the Government god draws them.
Despite those attempts to whitewash this very real concern, the information continues to come in to substantiate those fears...
Thread by Scanian.
First, the bad news. For the first time since 1975, Social Security recipients are being told they won't be receiving an annual cost of living increase in their monthly benefits. At the same time, their Medicare premiums will go up, so monthly checks will actually shrink next year. Not to worry, though. Here's the good news. Seniors may not have to live on such meager funds for long because the government is going to help them plan how they want to die.
This benevolent plan is in Section 1233 (p. 424) of the health care reform bill known as "America's Affordable Health Choices Act of 2009" (HR 3200). It didn't just show up on the doorstep of health care reform, but was packaged and delivered by Compassion & Choices (C & C), the assisted-suicide advocacy group previously known as the Hemlock Society.
Under Section 1233, a doctor would be paid for having an "advance care planning consultation" with a patient. The consultation wouldn't be mandatory, at least for now. But if the doctor wants to get paid for it, the consultation's contents are very specifically prescribed. For example, each consultation "shall include" an explanation of legal documents such as living wills and durable powers of attorney, and information about the "continuum of end-of-life services." Patients need not be ill but, because they are over a certain age, their doctors will suggest that it's time to talk about death.
So, if George, a healthy 70-year-old marathon runner, goes to the doctor because of tendonitis, his doctor will have the all-important discussion with him, reminding him that he's not getting any younger and that it's time to decide how he'll die. Sure, George may or may not be adversely affected by this. But consider Clara, an 84-year-old widow who needs a hip replacement. If the doctor tells her that the government health plan won't pay for her surgery but will pay for pain pills, and then tells her it's really time to discuss her end-of-life options, what message is she getting? Isn't it likely that Clara will acquiesce, if her doctor suggests that she "choose" to forgo treatment for any future illnesses so she won't be a burden on her family?
To hear proponents of Section 1233 talk about it, one would think that people have no access now to information about advance directives. But for years, federal law has required that patients be provided with general information about advance directives. . .