The latest information for July 9, 2020
The latest information for July 9, 2020

Thursday, July 9, 2020

COVID-19 Q&A Updated to Address Reopening

Our COVID-19 community Q&A has been updated. The update focuses on reopening and includes new and revised questions regarding attending work and in-person clinic visits, travel, and participating in summer activities
View our COVID-19 Q&A »

Save the Date for NACFC

We're excited to share that NACFC will be held virtually from October 21 to 23. The online program will be made available when registration opens in early August. There will be a registration fee of $125 per person, which includes access to live and on demand sessions, including Q&A, as well as hundreds of posters, chat conversations, the supporter showcase, and networking opportunities.
Learn more »

CF Foundation Leadership Provides Patient Perspective During Global Antibiotics Initiative Launch

Today, the Foundation’s president and CEO, Dr. Michael Boyle, participated in the launch of the AMR Action Fund, a collective venture that expects to invest more than $1 billion into the development of novel antibiotics to address the growing threat of antimicrobial resistance. Speaking on a panel discussion to more than 600 online attendees, Dr. Boyle shared the challenges people with cystic fibrosis face with chronic infection and stressed the need for novel antibiotics as superbugs and antibiotic resistance continue to be a global health concern.
Learn more »

Nearly 200 Teens Gather Virtually for Teen Advocacy Day

On June 24 and 25, nearly 200 teen advocates from across the country – half whom are living with cystic fibrosis – participated virtually in the Foundation’s 12th Annual Teen Advocacy Day. This year, due to the COVID-19 pandemic, the teen advocates gathered virtually, marking the first time that people with CF were able to attend the advocacy event along with their loved ones.
Read how teens participated »

Hurricane Season is Here

Having a disaster and emergency preparedness plan during a natural disaster or emergency is especially critical when living with a chronic illness like cystic fibrosis. Review the Foundation’s guide to learn what you or your loved one with CF can do to prepare for a disaster or emergency, and how Compass can support people with CF and their families.
View our guide »
  We will not rest until we find a cure  
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