Dialysis and Letter Writing

Writing a LetterFrom the DPC (Dialysis Patient Citizens) Newsletter for August, here’s a very important and practical activity you can do that will have a huge impact and benefit all your fellow dialysis patients.  Write a Letter to your local newspaper.   Your Representatives, Senators, and their staff members read your local papers.   Make your voice heard and make a difference!

LETTERS TO THE EDITOR: As you surely know, The Centers for Medicare and Medicaid Services recently proposed a devastating 9.4 percent cut in reimbursement for dialysis. At the urging of DPC, our members are stepping up and writing powerful Letters to the Editor at their local papers voicing their outrage at this potential reduction.

At last count, there were 25 Letters to the Editor brought to our attention that were published. Newspapers ranged from The New York Times (thank you Eric Edwards, our Board President), to Baltimore Sun (written by Board Member Myron Zayon) , to Brooklyn Daily Eagle (written by Board Member, Christina Esposito . Every letter emphasized the devastating impact that the proposed cuts would have for dialysis patients and dialysis clinics across the nation.

Thanks to all who took the initiative to write a Letter to the Editor. Want to participate but don’t know how or what to do? Email DPC at dpc@dialysispatients.org and we’ll give you step-by-step details. It’s not too late! Join your colleagues and let voters in your area know how these cuts would impact your life.


Eric Edwards’ letter  in the New York Times
Myron Zayon’s letter in the Baltimore Sun
Christina Esposito’s letter in the Brooklyn Eagle
As you read these letters, you can see that it doesn’t take much more than a simple statement of the facts and your opinion of the proposed CMS cuts.  Your letter could make the difference in a member of Congress deciding to support us dialysis patients and send a statement to CMS/Medicare opposing these cuts.  
If you didn’t see all my other posts about these cuts, you may have missed the link to the DPC Action Page on their website.  To access the page where where you can quickly and easily send a letter to your Congress members, CLICK HERE.  All you have to do is neter your zip code and it will walk you through the process.  If your zip code covers more than one Congressional District, you’ll have to enter your address to narrow down exactly who your Representative is. 
Also, here’s another idea.  Let’s let the President know about our opposition to the CMS cuts. There’s a petition at WhiteHouse.gov that you can sign.  CLICK HERE to access that petition on the President’s Web site.  This is important because the CMS is a part of the Executive Branch and the President’s Secretary of Health and Human Services is over CMS/Medicare
Here’s another petition that’s gotten over 57,000 signatures!  Add yours!  CLICK HERE
And a really BIG THANK YOU to everyone that has taken action on this matter.  It’s important to every one of us and especially the most vulnerable dialysis patients who might suffer because of these cuts.  
If you want to know more about these cuts and issues of importance to dialysis patients, contact DPC directly:
Dialysis Patients Citizens
122 C Street N.W., Suite 510
Washington, DC 20001
Toll free: 1-866-877-4242
Fax: 202-789-6935
Email: dpc@dialysispatients.org

About DevonTexas

I am a person with ESRD (End Stage Renal Disease) which means my kidneys don't work. Forty or so years ago that would have been a death sentence but today there is Dialysis which means I could be hooked up to a machine that would clean my blood as the kidneys should. Three days a week, I went to a dialysis center and had too very large needles stuck in my arm to remove and replace my blood as it passed through a process where it was cleaned and the fluid was removed, a process taking a little over four hours each time. In November 2017, I received a kidney transplant from a deceased donor. My life went into overdrive. With a "new" functioning kidney, I no longer had to go to a dialysis center and my days were not open to be lived rather than recovering from dialysis which meant dialyzing for three days and resting for 4 days a week. I work full-time and often 50 hours per week. It is something I never imagined. I highly recommend it! HeeHee I want to advance knowledge about dialysis and transplant so that others can learn from my experience and mistakes. We shouldn't have to reinvent the wheel, eh? There is so much to be learned and experienced about our predicament. There are vast resources available to support us and enrich our lives but many patients don't know about them. There are also many issues that we have to deal with whether we want to or not. So I blog about them in www.DevonTexas.com All comments are confidential until I approve them. If you don't want your comment public, let me know and I will respect that. So, feel free to leave a comment. I also blog in LegacyTales in WordPress if you are interested in the ramblings of a Old Man. Give a peek and let me know what you think. https://legacytales.wordpress.com/ Enjoy.
This entry was posted in activism, dialysis, Dialysis Patient Citizens, DPC, ESRD, kidney, lobbying, Medicare, politics and tagged , , , , , . Bookmark the permalink.

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