CF Relief Fund Launched for Those with CF Impacted by Hurricanes.

Isabella Passamano, daughter of Beth Sufian and James Passamano, has launched the CF Relief Fund to provide direct relief to children and adults with CF affected by Hurricanes Harvey and Irma. Continue reading CF Relief Fund Launched for Those with CF Impacted by Hurricanes.

Boomer Esiason Wants You… to Run the TCS NYC Marathon!

NOVEMBER 5, 2017
STEP 1: REGISTER
To run for Team Boomer

STEP 2: INTERVIEW
with Team Boomer staffer Katie

STEP 3: RUN NEW YORK CITY! Continue reading Boomer Esiason Wants You… to Run the TCS NYC Marathon!

Sign up for BreatheCON Sept 8th and 9th!

By Jeanie Hanley MD, President of USACFA and
John Mercer, BreatheCon 2017 Co-Chair

Sign up today for this FREE virtual event for adults with cystic fibrosis.

Our USACFA director, Mark Levine, is a featured Keynote Speaker on Friday and our CF Roundtable columnists, Aimee Continue reading Sign up for BreatheCON Sept 8th and 9th!

The Cystic Fibrosis Reproductive & Sexual Health Collaborative (CFReSHC) Patient Task Force Meeting is on September 18th!

By Kelly Gilmore

On Monday September 18th from 12:30pm PST- 2:30pm PST we are having a virtual discussion with CF women, and you’re invited! We need your help in understanding what aspects related sexual and Continue reading The Cystic Fibrosis Reproductive & Sexual Health Collaborative (CFReSHC) Patient Task Force Meeting is on September 18th!

USACFA’s Fall 2017 Lauren Melissa Kelly Scholarship Winners

The US Adult CF Association (USACFA) is excited to announce our recipients of the Lauren Melissa Kelly Scholarship: Congratulations to Jacob Greene and Elizabeth Shea! They will be awarded $2500 each. Continue reading USACFA’s Fall 2017 Lauren Melissa Kelly Scholarship Winners

Boomer Esiason: In search of a breakthrough for my son’s cystic fibrosis

http://www.cincinnati.com/story/opinion/contributors/2017/05/31/search-breakthrough-my-sons-cystic-fibrosis/346681001/

Just over 24 years ago, my son Gunnar was diagnosed with cystic fibrosis, a debilitating and unrelenting disease for which there is no cure. At the time of his diagnosis, CF was akin to a death sentence – there were no FDA-approved Continue reading Boomer Esiason: In search of a breakthrough for my son’s cystic fibrosis

Vertex Grants $1 Million to Non-Profits for Cystic Fibrosis

http://www.raredr.com/

Earlier today, Vertex Pharmaceuticals Incorporated – a corporation designed to fund scientific innovation to create transformative medicines for people with serious and life-threatening diseases – announced the grant recipients for its 2017 Cystic Fibrosis (CF) Circle of Care program. Continue reading Vertex Grants $1 Million to Non-Profits for Cystic Fibrosis

Maxing Out Your Strides – Mark A. Levine

By Mark Levine

Here we are again, on the precipice of another Great Strides Walk season. Not sure about you but I have already sent out my second email, a gentle reminder, to my entire list to increase the size of my team and boost my donations. It’s an exciting time of the year and a great event to be a part of that fulfills a lot in my Continue reading Maxing Out Your Strides – Mark A. Levine