The Boomer Esiason Foundation - The Boomer Esiason Foundation is a dynamic partnership of leaders in the medical and business communities joining with a committed core of volunteers to heighten awareness, education and the quality of life for those affected by cystic fibrosis, while providing financial support to research aimed at finding a cure.

Breathe California – Through grassroots education, advocacy and services, Breathe California fights lung disease, advocates for clean air and advances public health.

Breathing Room – Facilitates candid and open communication between adults with Cystic Fibrosis, supports the development of a community of adults with CF and provides education and insight for families, caregivers, and medical professionals who impact our lives.

California Transplant Donor Network – Saves and improves lives through organ and tissue donation for transplantation, concentrating efforts on the recovery and placement of vital organs in northern/central California and northern Nevada.

Cystic Fibrosis Research, Inc. – A community of families, professionals and volunteers committed to funding Cystic Fibrosis research and improving the quality of life for children and adults with CF.

Cystic Fibrosis Worldwide – Cystic Fibrosis Worldwide (CFW) is dedicated to improving quality of life and life expectancy for persons living with cystic fibrosis globally. CFWW reaches out to its 52 member countries by working to help develop effective cystic fibrosis treatment and care.

Donate Life America – Assists in mobilizing the transplant community to educate the American public on the need for organ, eye and tissue donation and motivating the public to make an actionable donor designation.

Donate Life California – A nonprofit Organ and Tissue Donor Registry dedicated to saving the lives of thousands of Californians awaiting life-saving transplants.

Donate Life Hollywood – A film festival celebrating the entertainment industry’s inspiring and accurate organ and tissue donation storylines.

The Elizabeth Nash Foundation – Honors and perpetuates Liz Nash’s lifelong example of giving and to continue her fight against Cystic Fibrosis by making focused investments in CF research and scholarships for individuals with CF.

Japan Transplant Recipients Organization – Serving the Japanese transplant community.

Miracles for Life - A non-profit dedicated to inspiring teens and children recovering from life-saving tissue and organ transplants to be their greater selves by offering them an outdoor educational experience that revitalizes their heart, their minds and their spirit.

Oakland Fukuoka Sister City Association – The Oakland Fukuoka Sister City Association helps to foster and promote cultural awareness, understanding, and friendship between the people and cities of Oakland, California and Fukuoka, Japan.

One Legacy – The nonprofit, federally designated transplant donor network serving 18 million people in seven Southern California counties.

Second Wind Lung Transplant Association, Inc. – Second Wind Lung Transplant Association, Inc. was formed in 1995 by a small group of people who wanted to provide information about lung transplantation to others. Today, Second Wind is an international organization with over 400 members scattered throughout the United States and in Australia, South Africa, the United Kingdom, and Germany.

Transplant Buddies – Established in 1999, the TransplantBuddies site provides information about the transplant process, resources covering drugs and side effects, and daily discussions about living life as a transplant patient. The site also includes members Photos, Life stories while covering experiences of both transplant recipients and donors.

Transplant Recipients International Organization - TRIO is an independent, not-for-profit, international organization committed to improving the quality of life of transplant candidates, recipients, their families and the families of organ and tissue donors.

United Network for Organ Sharing (UNOS) – A non-profit scientific and educational organization that administers the United States’ only Organ Procurement and Transplantation Network (OPTN), and advances organ availability and transplantation by uniting and supporting our communities for the benefit of patients through education, technology, and policy development.

The United States Adults Cystic Fibrosis Association, Inc. - An independent, non-profit organization that provides a source of information for CF adults regarding the basis, nature and progression of the disease, as well as the latest treatments and research to fight it and to provide a forum for CF adults to communicate to each other.

Interested in becoming a Community Partner?

Click here for more information on becoming a Community Partner.