Scripting the Conversation, Part 2: The provider-patient dialogue

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My last post —  Scripting “the Conversation” — discussed scripted dialogue at the national level.  It demonstrated how a few academics, so-called health policy experts, special interest groups, and foundations can stage a national dialogue — frame a conversation — with the help of their media allies.

The same group of academics and foundations have been at work on the micro level, generating scripts — literally word-for-word scripts — to be used by providers when they encounter difficult situations with patients and families, mostly in the context of patients and families who want life-sustaining treatment. Continue reading →

Scripting “The Conversation”

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They’re at it again. NPR hosted another sham debate. On the left we have Ira Byock, hospice and palliative care advocate; and on the far left we have Compassion & Choices, the radical pro-assisted suicide/euthanasia group.

They are debating a subject that no one would have noticed if it weren’t for well-coordinated media hype from MSNBC, People Magazine and the like.

This is a staged “dialogue” on assisted suicide. Compassion & Choices presents the thesis (assisted suicide should be legal), then Ira Byock comes in with a straw man antithesis (traditional medicine will let you suffer) and then the synthesis: palliative care.

Here’s the dirty little secret: Ira Byock is, himself, a euthanasia advocate. Continue reading →

Time for an Antidote

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Take this, all you purveyors of evidence-based, biopsychosocial, deconstructed, social-engineered medicine and new age spirituality:

Mozart’s Great Mass in C Minor, K. 427.

Performed in the Grand Chapel of the Séminaire Saint-Sulpice in Paris.
Laurence Equilbey (her bio here) conducting the Accentus Choir and Insula Orchestra.

[NOTE: Unfortunately ads come with the video.  Close them by carefully clicking the x in the corner of the ad, not by clicking within the ad, or you might find unwanted programs loaded onto your computer.]

Behind-the-scenes audio from the Patient Quality of Life Coalition training session

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Last month I wrote about the Lobby Day hosted by the Patient Quality of Life Coalition (PQLC) and American Cancer Society’s Cancer Action Network (ACS-CAN). Title-Slide The Coalition invited representatives of a variety of non-profits and professional organizations to Capitol Hill to lobby for two pieces of legislation:

The legislation would focus federal money on marketing palliative care to the public, educating teams of professionals in Continue reading →

Progressives lobby for end-of-life funding “to change health care delivery”

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On July 23 a new pro-Obamacare coalition called the Patient Quality of Life Coalition (PQLC) lobbied on Capitol Hill for “two bills to change health care delivery.”

The bills (H.R. 1339 / S. 641; and H.R. 1666) would authorize (to start) roughly $300 million for advertising to the public, training navigators, educating health professionals, establishing a national supervisory board, and promoting research, all with the goal of replacing standard care with palliative care (symptom treatment and hospice) for sick people, in lieu of costly life-saving treatments.

Dick Woodruff -- former chief of staff to Rosa DeLauro; former legislative advisor for Alliance for Justice -- gives the PQLC lobbyists some final instructions.

Dick Woodruff — former chief of staff to Rosa DeLauro; former legislative advisor for Alliance for Justice — gives the PQLC lobbyists some final instructions.

Veteran lobbyist Dick Woodruff explained why the urgency:  “Because these people who have these illnesses . . . are the ones who are driving healthcare costs more than anybody else . .  if we can figure out a way to manage their care, we can make life better for them, but then save the system money. . . .  [These bills] could have major returns over the next 25-45 years.” [my emphasis]

Woodruff, who served as chief of staff for Rosa DeLauro (of EMILY’s List fame), and later as senior Continue reading →