HHS announced a $32 million initiative with the @American_Heart, a NASDOH member organization, to improve COVID-19 related health outcomes by addressing hypertension among racial and ethnic minority populations. Read more: https://t.co/DJik7jqmpD
The Improving Social Determinants of Health Act was introduced today! On behalf of @healthyAmerica1 & 350+ groups, thank you @SenTinaSmith & @SenMurphyOffice for your leadership in improving #healthoutcomes & addressing health inequities. #SDOH https://t.co/Zi7Sve4H92
Check out this upcoming SDOH webinar put on by @Bree_WA featuring Sara Singleton and discussing how we can impact moral and social determinants of health.
Check out the new report from the @Surgeon_General. The report includes an afterword penned by @NASDOH_Alliance co-convener @GovMikeLeavitt which explores the link between a community's healthcare and economic resources. https://t.co/LJWfn7YnSo
The approval of the triple-combination modulator represents a truly transformational milestone in the fight against #cysticfibrosis. We could not be more excited about this pivotal moment in the history of CF.
We were honored to receive the Paul G. Rogers Distinguished Advocacy Award from @ResearchAmerica! The awards program was established by Research!America’s Board of Directors in 1996 to honor outstanding advocates for medical, health, and scientific research. #CFadvocacy
Amazing to spend time with @RepShalala discussing @CF_Foundation and access to affordable, adequate healthcare. Thanks for joining the CF Caucus! It’s All About The 🙌🏻! Delaney is so lucky to have you in her corner! #cfadvocacy
CF advocates are in Albany today to educate their lawmakers about CF and the importance of adequate, affordable health insurance #CFadvocacy@CF_Foundation
Superstar extraordinaire, @MaryDwight 🙌 Leads the charge to get our voice as a CF community to those who need to hear it. We need adequate, affordable and available healthcare. ‘Can’t treat CF at the Minute Clinic’ #CFFVLC
Today is finally here! Advocates from 47 states are going to Capitol Hill to speak with lawmakers about the best story in medicine — and why access to affordable, adequate care is so important. #CFadvocacy#ProtectPatientsNow
Ensure the voice of the #cysticfibrosis community is heard by lawmakers on Capitol Hill. Learn how you can participate in our online Day of Action on March 15! https://t.co/VhaiwoVy5W #CFadvocacy
We're headed to Capitol Hill for March on the Hill later this month! You can get involved too by participating in our online Day of Action. https://t.co/LjicsVZfBY #CFadvocacy
Thank you, Lt. Gov @SpencerJCox, for meeting with us this week to talk about the needs of people with #cysticfibrosis at our first Utah State Advocacy Day! #CFadvocacy
Wonderful to meet with Utah’s Senate Majority Leader @RalphOkerlund today.
Thank you for taking the time to hear from the CF community about access to affordable, specialized CF care! #CFadvocacy
Thank you @JaniIwamoto for giving the Cystic Fibrosis Foundation a few minutes of time to discuss the needs of people affected by #cysticfibrosis in your Minority Caucus Meeting today at our first annual #CFAdvocacy day at the Utah State Capitol!