The end of Chronic Disease Month is near — make sure your voice is heard: chronicdiseasecoalition.org/take-action/co…

Texas family scrambles after their disabled child loses Medicaid | The Texas Tribune ⁦Chronic Disease Coalition⁩ #ptsafety #childhealth texastribune.org/2023/07/28/tex…

Chronic Disease Coalition Did You Miss The Broadcast With Cynthia Infante, 2x Kidney Transplant Recipient, Mentor and NKF Kidney Advocate? Catch the Instant Replay Here! Cynthia Has A Very Compelling Kidney Story! m.facebook.com/story.php?stor…

Check out this awesome work from IU School of Medicine and CDC ambassador Curtis Warfield!

#PBMs are making patients pay way too much for vital meds! Chris Holden, let's support #SB873 and reform the state’s rebate system. It's time to put #PatientsBeforeProfits! shorturl.at/mzFK3

… I’m looking for some info on foods that have either been gentle or exceptionally hard on ppls stomach’s before & after surgery. Not to be too whiny, I’m very over 🤢🤮 multiple times a day. (2/2) Chronic Disease Coalition Crohn's & Colitis Foundation #rheum #chronicillness

Chronic Disease Coalition Did You Miss The Broadcast With Our Guest David Perchinsky, Dialysis Patient, Former Coach and Teacher, Currently Seeking a Kidney Transplant? Catch The Instant Replay Here! m.facebook.com/story.php?stor…

Rare disease patients often face a variety of representation obstacles, but the rarity of their condition doesn't make the impacts of bad health care policy any less real. In fact, it can easily exacerbate it.

Hear from rare disease patients and advocates about what you can do to elevate rare disease voices and protect patient access in legislatures across the country. Register at: chronicdiseasecoalition.org/chronic-univer…

Grateful to @cdcgov for including this new #RSV immunization for infants. #RSV can lead to serious chronic conditions, and we were proud to advocate for this inclusion in the Vaccines for Children program. Read the press release: cdc.gov/media/releases…

@AverysHope1 Chronic Disease Coalition Too late, darn it!

ICYMI: Alzheimer’s advocates traveled to Capitol Hill to ask Congress to push CMS for full access to FDA approved Alzheimer’s treatments. Thank you Ron Wyden for urging CMS to speed up access to Alzheimer’s therapies koin.com/news/health/de…

"This latest proposal compounds the challenges that many dialysis providers are facing across the country, especially in rural areas." Thx to our partners Chronic Disease Coalition Dialysis Patient Citizens RenalSupportNetwork for raising this issue! chronicdiseasecoalition.org/news/80-years-…

Dialysis is a health care innovation that was first invented back in 1943. While we celebrate 80 years of lives saved, our country is facing more kidney disease than ever, and we are still fighting for access to this essential treatment. chronicdiseasecoalition.org/news/80-years-…

#CHRONICUNIVERSITY: Thursday, August 24 — Chronic disease impacts nearly half, or 133 million, Americans—with only 1 in 10 having a rare disease. chronicdiseasecoalition.org/chronic-univer…

Rare disease patients often face a variety of representation obstacles, but the rarity of their condition doesn't make the impacts of bad health care policy any less real.

In fact, it can easily exacerbate it. Hear from rare disease patients and advocates about what you can do to elevate rare disease voices and protect patient access in legislatures across the country.

This Thursday our co-founder Joshua Henderson will be joining a Chronic Disease Coalition panel discussion on Representation for #RareDisease! RSVP today: chronicdiseasecoalition.org/chronic-univer…