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Speakers

Somer Love

Moderator | Adult with CF

Luisa Palazola

Speaker | Adult with CF

Rebekah Kraemer

Speaker | Adult with CF

Amy Mueller

Speaker | CF Care Center Social Worker

Megan Park

Speaker | Adult with CF | Fitness Instructor

Rebecca Shook

Speaker | Adult with CF | Actor

Bobby Shook

Speaker | CF Spouse | Actor

Elizabeth Amber

Workshop Host | Adult with CF

Tara Goodwin

Workshop Host | Adult with CF

Sarina Sandstrom (she/her)

BreatheCon 2021 Co-Chair | Adult with CF

Olivia Clark (she/her)

BreatheCon 2021 Co-Chair | Adult with CF

Jenny Livingston (she/her)

Moderator | Adult with CF

leah Schwanke

Moderator | Adult with CF

Bradley Poole

Speaker | Adult with CF

Tiffany Rich

Speaker | Adult with CF

Nicholas Kelly (he/him)

Speaker | Adult with CF

Lauren Ortiz

Moderator | Adult with CF

Christopher Jones (He/Him)

Speaker | Adult with CF

Aaron Stocks

Speaker | Adult with CF | CF Foundation Compass Operations Manager

Marissa Benchea (she/her)

Moderator | Adult with CF

Neema Chandel (she/her)

Speaker | Adult with CF

Gabriela Castillo

Speaker | Adult with CF

Natalie Wasserman Kingston (she/her)

Speaker | Adult with CF

Michelle Herpolsheimer

Speaker | Adult with CF

Lara Govendo

Speaker | Adult with CF

Hosted by

Cystic Fibrosis Foundation

The mission of the Cystic Fibrosis Foundation is to cure cystic fibrosis and to provide all people with CF the opportunity to lead long, fulfilling lives by funding research and drug development, partnering with the CF community, and advancing high-quality, specialized care.

Booths

Advocacy

The cystic fibrosis community is small but powerful. Volunteer advocates drive our legislative and regulatory agenda forward at every level of government. Together, we are improving access to high-quality, specialized care so people with CF can live longer, healthier lives.

CF Peer Connect

CF Peer Connect is a one-to-one peer support program for people with cystic fibrosis and their family members age 16 and older. Talk with and learn from someone who is also affected by CF and has gone through similar experiences.

Community Voice

People with cystic fibrosis and their family members know CF better than anyone, and Community Voice provides opportunities for you to actively shape research and programs for the CF community.

Compass

Cystic Fibrosis Foundation Compass is a personalized, one-on-one service that provides people living with cystic fibrosis, their families, and their care teams with a partner in dealing with challenges related to life with CF.