cfvancouver.ca
Cystic Fibrosis in Canada
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EQA - Biomedical Quality Assurance KU Leuven
Pulmozyme® (dornase alfa) is a nebulized cystic fibrosis (CF) treatment option to help manage CF symptoms. See full safety for more information.
A non-profit dedicated to educating the world about cystic fibrosis and giving those living with CF the tools to lead healthy lifestyles.
Normal breathing provides oxygen for body cells to treat chronic diseases and restore health
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.
My life with cystic fibrosis.
Chi (Qi) Healing
Airway is developing a new class of biologics to break the cycle of injury and inflammation for patients with respiratory and inflammatory diseases.
Cystic Fibrosis Canada is a national charitable not-for-profit corporation committed to finding a cure for cystic fibrosis (CF). We invest more in life-saving CF research and care than any other non-governmental agency in Canada.
Workers' compensation blog for Powell & Denny, P.C., in Birmingham. We have the experience to help. Call 205-978-2051 or 800-227-0882 for more info.
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Nathan Charles
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
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Innovative eHealth systems; integrated, cross-sector cloud-based clinical information solutions.
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.
Doing our part in the battle against cystic fibrosis...