Lungs for Life Foundation -Cystic Fibrosis Organ Donation Transplant Lung Transplant
Lungs for Life is dedicated to providing assistance and resource information to individuals and their families affected by cystic fibrosis and/or organ donation and transplantation.
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The Kidney Foundation of Canada is committed to achieving excellent kidney health, optimal quality of life, and a cure for kidney disease.
United Network for Organ Sharing (UNOS) is the private, non-profit organization that manages the U.S. organ transplantation system under contract with the federal government.
Donate Life America is a nonprofit organization increasing the number of donated organs, eyes & tissue available to save & heal lives through transplantation.
Register to be a blood donor, give blood and save lives. Find out more about blood donation.
The Official website for the Original Lungs for Life; the Lungs for Life Foundation; www.lungsforlife.org and new lungs information.
30 million people in the U.S. have kidney disease but only 10% know it. NKF is a lifeline for all people affected by kidney disease-the largest public health issue you'll ever hear about.
You may know us from our head-shaving events, but in the bigger picture St. Baldrick's Foundation is leading the way in funding the best in childhood cancer research. Help support the cause. Every donation counts.
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Southern Ontario group uses Elaine Gottschall`s Specific Carboydrate Diet (SCD) found in her book, Breaking the Vicious Cycle, to treat Inflammatory Bowel Disease (IBD, Crohn`s disease, ulcerative colitis, celiac disease, diverticulitis, cystic fibrosis and irritable bowel syndrome (IBS). Resources and support.
EQA - Biomedical Quality Assurance KU Leuven
My life with cystic fibrosis.
Pulmozyme® (dornase alfa) is a nebulized cystic fibrosis (CF) treatment option to help manage CF symptoms. See full safety for more information.
Chi (Qi) Healing
Normal breathing provides oxygen for body cells to treat chronic diseases and restore health
A non-profit dedicated to educating the world about cystic fibrosis and giving those living with CF the tools to lead healthy lifestyles.
In 1992, best friends Mike Cassidy and Sid Keay discussed the idea of holding a small golf tournament to raise money for Cystic Fibrosis. Mike suffered from CF and Sid had relatives that were affected as well. The idea was simply to get friends and business acquaintances together for a fun day of fund raising. 18 years later that idea was spawned the largest private source of funds for Cystic Fibrosis in British Columbia raising over $2.5 million. With the generous assistance of long time sponsors from
Cystic Fibrosis in Canada
Airway is developing a new class of biologics to break the cycle of injury and inflammation for patients with respiratory and inflammatory diseases.
Doing our part in the battle against cystic fibrosis...
Cystic Fibrosis is Ireland's most common genetically inherited disease. With 1100+ CF Patients, Ireland has the highest proportion of CF people in the world. CF Ireland was established by a small dedicated group of parents in 1963 with the first meeting in Crumlin Children's Hospital. 2013 marks the 50th anniversary of the Association.
Innovative eHealth systems; integrated, cross-sector cloud-based clinical information solutions.
Nathan Charles