Cooperating Hands

CF Services Pharmacy...

COMMUNITY PARTNERS

A Walgreens Alliance Pharmacy

Community Partners

Community Partners receive recognition on the Cystic Fibrosis Services Pharmacy website, with a logo and link to their partner website. In exchange, we ask our Community Partners to cross link to the Cystic Fibrosis Services Pharmacy website and assist us in making contacts with others who are interested in information about cystic fibrosis and the Cystic Fibrosis Services Pharmacy.
There is no financial contribution required. The Cystic Fibrosis Services Pharmacy is the only
Pharmacy that is a wholly owned subsidiary of the Cystic Fibrosis Foundation.
Thank you for your support!
 

CFF Logo

Since 1955, theCystic Fibrosis Foundation has been the driving force behind the pursuit of a cure for cystic fibrosis. Thanks to the dedication and financial backing of their supporters--patients, families and friends, clinicians, researchers, volunteers, individual donors, corporations and staff, the Cystic Fibrosis Foundation is making a difference, adding tomorrows every day. 

New CFPAF Logo

TheCystic Fibrosis Patient Assistance Foundation (CFPAF) is a non-profit organization that helps patients and their families living with cystic fibrosis afford the medications and devices they need to manage pulmonary complications of their disease. The CFPAF offers the only national patient assistance program designed specifically for the cystic fibrosis community.

Cytsic Fibrosis Lifestyle Foundation

TheCystic Fibrosis Lifestyle Foundation (CFLF) assists in providing avenues toward healthy and active lifestyles through recreation, thereby educating people with CF on the critical psychological, social, and emotional connections between their lifestyle and their health. Recreation grants are offered for up to $500 for activities such as classes, camps, lessons, memberships, horseback riding, or other interests that help work the lungs, build self esteem, and better quality of life. A "Peer Support" or "Recreation Mentor" may also be requested for up to an additional $500. "Living Stronger! Living Longer!" Read more...

 Visit The Boomer Esiason Foundation Here!

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.

 Visit Club CF Here!

The Boomer Esiason Foundation'sClub CF is an online “club” for individuals with CF of various ages who are LIVING, BREATHING and SUCCEEDING, and for caregivers who are the true warriors in their support and fight against CF.CLUB CF features individuals with CF who are an inspiration to the CF community.

 Visit Jerry Cahill's Cystic Fibrosis Podcast Here!

Jerry Cahill's Cystic Fibrosis Podcast “LIVING. BREATHING. SUCCEEDING.” Podcast/Vodcast series is a collection of podcasts made possible through and unrestricted educational grant from Genentech to The Boomer Esiason Foundation.

Visit The CF Legal Information Hotline Page Here!

The CF Legal Information Hotline provides free information about the laws that protect the rights of individuals with cystic fibrosis (CF). It serves as a resource for Cystic Fibrosis Care Centers, individuals with cystic fibrosis, and their families.

Visit The Cystic Fibrosis Reaching Out Foundation Here!

TheCystic Fibrosis-Reaching Out Foundation, Inc. is an all-volunteer 501(c) 3 benevolent organization to help Cystic Fibrosis patients and families by providing financial and educational resources to assist them. 

Visit Cystic Fibrosis Worldwide, Here!

Cystic Fibrosis Worldwide reaches out globally focusing on countries where little is known about CF, to aid people with CF living without access to medication, treatment or equipment. CF Worldwide works to bring long term solutions via educational conferences, capacity building programs, clinical development, international lobbying efforts and creating a global network.

Visit The Power Of Two, Here!

The Power Of Two is a documentary, interactive web community and international call-to-action around organ donation and transplantation, cystic fibrosis (CF) awareness and related health causes. The Power Of Two, inspired by the unique story of Anabel and Isabel Stenzel, identical twins who have endured a life long battle with CF, and their 2007 memoir of the same title, will engage and inspire people around the world by conveying a fundamental truth: There is a miracle in every breath.

Visit The USACFA CF Roundtable Here!

Visit The USACFA CF Roundtable Here!

USACFA is the United States Adult Cystic Fibrosis Association, Inc USACFA publishes CF Roundtable, a quarterly newsletter for adults who have cystic fibrosis. CF Roundtable is a newsletter published four times a year by USACFA. USACFA, a nonprofit corporation, was formed to provide a source of information and education for adults who have CF. USACFA provides a network and a forum for communication among adults who have CF, their families, and medical professionals.

Visit The Blooming Rose Foundation For Cystic Fibrosis Here!
FOUNDATION
for CYSTIC FIBROSIS

The Blooming Rose Foundation was created to give hope to families immediately following diagnosis with cystic fibrosis, offering an online resource for individuals, families, and friends to find up-to-date research, links to encouraging websites and blogs. The Blooming Rose Foundation will talk with families about raising a child who is thriving with cystic fibrosis about the positive outlook and breakthrough treatments available now and on the horizon. Read more...

Visit The Bonnell Foundation Living With Cystic Fibrosis Here!

The Bonnell Foundation is about living with cystic fibrosis and building relationships between parents who have children with cystic fibrosis, especially parents who have children newly diagnosed. They are working with the media to help raise awareness, funds to donate to CF research and scholarships. They hope to be part of finding a cure for CF so that one day no CF parent will experience the pain and loss of losing a child to the disease. Read more...

Think Alive Foundation
Foundation

Think Alive Foundation, founded by Tim Enfield, is dedicated to providing a financial means for disabled achievement. We hope to provide the community's youth members with added confidence that comes from succcess by financing lessons, equipment and other expenses associated with activities and passions of all kinds. Read more...

 
Visit Cystic Fibrosis Services Pharmacy Community Outreach
 

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