The DPC Board of Directors is pleased to announce that Jack Reynolds will serve as Interim President, effective immediately. Reynolds chairs the Board’s Policy Committee and previously served as Vice President. Few have the firsthand experience Reynolds does, having been on dialysis over 40 years. He took on the new role to allow former President Eric Edwards to take an extended leave of absence. Click here to read Reynold’s biography, along with that of the other DPC Board Members.
By Jack Reynolds, DPC Board Member and Patient Ambassador As it is Ground Hog Day, I thought I would come out of my winter hole and blog once more. March is only four weeks away, and it will be time to visit Washington, D.C. and another chance for Dialysis Patient Citizen Ambassadors to bring our issues and concerns to our elected Congressional Representatives and Senators. Although I have made this journey many times since 2005, I am not a “natural” political advocate; and in fact, if not for a social worker, I may have never become a dialysis citizen at large [...]
The National Association of Insurance Commissioners (NAIC), a membership organization for the nation’s chief insurance regulators, recently named 30 consumer liaison representatives for 2015. Through these representatives, who are committed to the public interest, consumers can interact with NAIC’s membership, the insurance industry and other interested parties. “Our consumer liaison representatives play an integral part in helping the NAIC and regulators protect U.S. insurance consumers,” said Monica J. Lindeen, NAIC President-Elect and Montana Commissioner of Securities and Insurance. “This partnership program is an important component of our mission to protect the public interest and facilitate the fair and equitable treatment [...]
DPC was saddened to learn of the recent passing of two of our previous board members, Robert (Bob) Mize and William (Bill) Litchfield. Robert Mize was one of three patients who served as a founding board member. He was instrumental in laying the groundwork for the successful advocacy and education programs we produce today. He frequently made trips to Washington, D.C. to elevate the patient voice and his dedication to promoting kidney disease awareness and education will surely be missed. Robert Mize on the steps of the Supreme Court. William Litchfield also served on the board of DPC [...]
Join us in welcoming our new Government Affairs Director Jackson Williams. Hailing originally from Chicago, Jackson brings with him an impressive list of advanced degrees including: a Bachelor's degree in political science, a Juris Doctor, a Master's of Public Administration along with Ph.D. coursework in public policy analysis. Jackson has taught law and health politics at several colleges and universities. He couples his impressive educational background with extensive real world professional experience. Jackson actually just left the Center for Medicare and Medicaid Innovation in order to help us further elevate the kidney patient voice. Previously he served as a Senior [...]
By Hrant J., DPC Executive Director With the creation of the DPC Education Center, it became increasingly apparent that Dialysis Patient Citizens (DPC) needed to do some internal realignment of its staff. Our goals for this process were to ensure: 1) we maximize DPC’s limited resources, 2) we secure the sustainability of the DPC Education Center, and 3) we continue to prioritize our advocacy efforts and the work we do to elevate the patient voice with policy makers. As a result, I am pleased to announce that DPC has hired a Government Affairs Director. Since his departure from the Center [...]
By Tony B., Director of Research and Information Today we are excited to announce the creation of a new sister organization The DPC Education Center (The Center). The new organization, which is incorporated as a 501(c)(3) non-profit, will work together with DPC to advance their shared mission of improving the quality of life of all kidney disease and end-stage renal disease (ESRD) patients. The Center is dedicated to improving kidney patients’ quality of life and reducing the occurrence of ESRD through education and by developing awareness of dialysis and kidney disease issues, improving the partnership between patients and caregivers and [...]
If you are reading this, we all survived the Mayan apocalypse or you had a well-stocked shelter with built in internet access. Either way, all of us here at DPC and with the Patient’s Voice want to wish you happy holidays. Our office will be closed until January 2nd, and new posts (hopefully sent in by Voice readers) will resume shortly after.
An icebreaker activity at the recent board meeting. Can you tell what it is? By Sage B., Grassroots Manager Hi Voice readers! My name is Sage and I recently joined DPC as the Grassroots Manager, which means that I will work with many of you personally to influence state and national kidney disease policies. Each month I will keep you up to date on what we are doing at the local level and share inspiring stories of our patients in action. Thank you for joining me here today, and I hope to see you again next month! Coming to [...]