On Aug. 13, I joined other members of the kidney care community for Voices of Dialysis: Protecting Access to Care—a Google+ Hangout discussing the government’s proposed funding cut for dialysis care. In this interactive video chat, the other speakers and I shared our concerns about the Centers for Medicare & Medicaid Services (CMS) plans to cut dialysis funding by 9.4 percent and elaborated on the potential impact for hundreds of thousands of Americans who rely on dialysis for life-saving treatments.

In case you missed the live Google+ Hangout, watch the complete 45-minute recap of Voices of Dialysis: Protecting Access to Care.

Speakers:
Eric Edwards, Dialysis Patient,
Dialysis Patient Citizens Board President

Allen R. Nissenson, MD, Chief Medical Officer,
DaVita

Robert J. Kossmann, MD, President,
Renal Physicians Association (RPA)

Diane Wish, President and CEO,
Centers for Dialysis Care

Join representatives from the kidney care community myself on Tuesday, Aug. 13, at 4 p.m. PT/ 7 p.m. ET for Voices of Dialysis: Protecting Access to Care—an important Google+ Hangout discussing the government’s proposed funding cut for dialysis care.

What’s a Google+ Hangout?
It’s a 45-minute interactive video chat that’s free to join and open to anyone. Participants will watch as a panel of speakers discuss a particular topic. All you need to participate is internet access.

Speakers to include:

Eric Edwards, Dialysis Patient,
Dialysis Patient Citizens Board President

Allen R. Nissenson, MD, Chief Medical Officer,
DaVita

Robert J. Kossmann, MD, President,
Renal Physicians Association (RPA)

Diane Wish, President and CEO,
Centers for Dialysis Care

“July and August will be critical months to take our message to Washington: no more cuts for dialysis patients and their providers.”

The recent proposal from the Centers for Medicare & Medicaid Services (CMS) to cut reimbursement for dialysis treatments by 9.4 percent has made me think hard about where dialysis has been, where it is now and where it might be headed. When I began my internship and residency at Michael Reese Hospital in Chicago (now gone, unfortunately), the Medicare entitlement for dialysis had not yet been enacted. Michael Reese had a long connection with pioneers in dialysis dating back to the 1920s. During my internship I rotated on the nephrology service. We had converted a hospital room to a dialysis ward and built Kiil dialyzers each time we wanted to do hemodialysis. We created Scribner shunts for blood access, and each treatment was an exciting challenge to get through without hypotension, clotting or other misadventures. We also had more than 40 patients on intermittent peritoneal dialysis (IPD). They would be admitted to the hospital each week, have a peritoneal catheter inserted and receive 48 hours of IPD. As the intern on the service, I admitted each patient, drew blood and then ran a set of electrolytes in a dedicated lab on the ward. I prescribed the peritoneal dialysis regimen for the 48 hours based on the physical examination and laboratory values. The Medicare entitlement for dialysis was enacted in the first year of my residency, 1972, and implemented in 1973. It changed everything.

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