Organizations (15)

• A Wish for Wendy Softball tournament benefiting Cystic Fibrosis research in honor of Wendy Carol Lipman who died 15 days after birth from cystic fibrosis.

• About TOBI and the Management of Cystic Fibrosis Information on Tobramycin Solution for Inhalation (TOBI) for pseudomonas infection, by pharmaceutical agency.

• Ambry Genetics Testing for CF mutations. Offers a comprehensive screening of CF mutations, plus Poly T Variant analysis, and direct DNA sequencing of exon.

• Billycook.com Billy Cook battled cystic fibrosis and died. The site generates funding for patients of this deadly disease.

• Cindy's Friends Information about the disease, progress being made towards a cure, and fundraising efforts in Tennessee.

• Cute Petite Chic - A Cystic Fibrosis Web Basic information with good description of sweat test, memorial page for a girl lost to CF at age 9, details of her last days and link to give in her memory through Great Strides.

• Cystic Fibrosis Medicine Provides free information to professionals involved with the treatment of cystic fibrosis. An open access section is also available to both patients and family

• Cystic Fibrosis Research Inc. News about CF research. Site also has a newsletter available.

• Cystic Fibrosis Resource Centre A source of information for cystic fibrosis patients, parents, doctors and other carers.

• Cystic Fibrosis Services A subsidiary of the Cystic Fibrosis Foundation and a national pharmacy that specializes in providing medications to individuals with cystic fibrosis (CF).

• Cystic Fibrosis Symptom Cystic Fibrosis Information and Resources.

• Cystic Fibrosis Western Australia Includes a calendar of events, information for people with CF who travel to Australia from other countries (what their healthcare entitlements are), pointers for teachers of children with CF, and a list of services and support.

• Cystic-L Cystic fibrosis information and support, including a vibrant on-line community, via email, a Handbook of information and resources, photos of CFers, a CF Shop and bookstore.

• CysticFibrosis.com Internet community for cystic fibrosis patients, families and loved ones.

• Kate McCloughan Krzyzak Obituary site.

• Michigan Pulmonary Disease Community, Inc. Organization dedicated to enhancing lives of children and adults with Cystic Fibrosis.

• MyCysticFibrosis.com Personal management tools to help track important health measures, together with in-depth articles and personal support from site specialists. Members can share data with caregivers and their healthcare team.

• North American Cystic Fibrosis Conference in New Orleans Information on program and location.

• Providence Cystic Fibrosis Center Ran by Dr. Bohdan Pichurko. Includes staff biographies, contact information, events, and latest developments in treatment.

• Sharktank.org Dedicated research for a cure for cystic fibrosis.