A cystic fibrosis community for patients, families and caregivers offering news, messageboards, daily living, associations, cf centers, fund raisers, books and treatment information ...

Cystic Fibrosis Canada's mission is to help people with cystic fibrosis (CF). Cystic Fibrosis Canada: - funds research towards the goal of a cure or control for cystic fibrosis - supports high quality CF care - promotes public awareness of cystic fibrosis, and - raises and allocates funds for these purposes.

Large collection of information and tips on living with cystic fibrosis, written by a patient.

The Cystic Fibrosis mutation database.

Cystic fibrosis (CF) is the most common fatal, inherited disease in the US. CF causes the body to produce abnormally thick and sticky mucus in several different parts of the body, most prominently the lungs and other parts of the respiratory system.

CYSTIC-L is a free email service dedicated to the exchange of information and support specific to cystic fibrosis. Members include people with CF and those who share their lives: medical professionals, scientists, researchers, parents, grandparents, spouses, siblings, friends and significant others.

CFRI was founded in 1975 as an independent, nonprofit volunteer organization dedicated to saving the lives of children and adults who have cystic fibrosis. What sets us apart from other cystic fibrosis organizations is our commitment to offering educational and personal support to families living with cystic fibrosis.

This site intended for U.S. residents only. Contents 2001 Chiron Corporation. U.S. patent issued April 1996. ...

The Canadian Cystic Fibrosis Foundation is the world's second largest non-governmental granting agency in the field of CF research. In 1998, the Foundation awarded close to $6 million in grants to CF scientists to conduct an extensive range of investigations.

The 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.

Hi, My name is Yancee Mathews. I have Cystic Fibrosis. I was diagnosed when I was born (1978). I created this web page for everyone to come and view my thoughts on living with CF. If you can't find what your looking for here, feel free to E-mail me, yanc@velocity.net. You are visitor since February 28, 1998. Login to CysticFibrosis mail User Name: Password: Technical Support Help Password ...

Medical news, information, community message boards and chat rooms, free email, free homepages, books, newsletter, links directory and more on AIDS and HIV ...

Current information on Cystic Fibrosis, Cystic Fibrosis Victoria the organisation, online chat room, message board, '65 Roses Magazine', SSL Secure Online Shop and donations, events ...

Online presentation.

About Us | Beaver Bulletin | CARE | Culture Club | Lung Transplant | Membership | Scholarships ...

Online children's story about life with cystic fibrosis. Also available in French.

Jake's Cystic Fibrosis Page Cystic Fibrosis Page with the CFAM newsletter.

Article discusses using pulsatile irrigation for the treatment for cystic fibrosis and sinusitis.

This site contains information about cystic fibrosis ...

Cysticfibrosis, cystic fibrosis, cf, sixtyfiveroses, 65roses, sixty5roses, sixty five roses, 65 roses, sixty 5 roses, cff, gene, genetic, tobi, pulmozyme, pancrease, lung, children, great strides, cure, gene therapy, therapy, chat, messages, message board, calendar, events, fundraisers ...

The following statements test what you know about cystic fibrosis. Fill out the test by choosing true or false, then press the submit button. True False 1. Cystic fibrosis (CF) is a hereditary disease. 2. CF is more common in white children than in children of other races. 3. As many as 30% of Americans of European descent carry the gene which is responsible for CF. 4. The lungs are the only ...

Cystic Fibrosis Our twelve year old son, James, has Cystic Fibrosis - CF This page is devoted to the understanding and cure of this debilitating disease. Cystic Fibrosis Foundation CF and CF Research The Transplant Sharing Exchange 65 Roses HHCS Health Care Love Puppy Program Michigan Pulmonary Disease Camp Cystic-L Cystic Fibrosis Caregiver Community - Web of Care Camp Funshine CysticFibrosis.

BUPA health information factsheet - cystic fibrosis (CF) is an inherited disease that affects the lungs and causes chest infections...

Foundation-supported researchers have reported the results of a high-dose ibuprofen study in The New England Journal of Medicine, March 30, 1995. Ibuprofen slowed the rate of pulmonary decline over a four-year period in patients with cystic fibrosis (CF).

This site contains information relating to Cystic Fibrosis with a worldwide mandate.

Forum for research, experiences, and synthesizing information with respect to ameliorating the conditions of cystic fibrosis.

For the first time, investigators are focusing on the development of treatments based on the underlying cellular defect. In this article, we review advances in genetics and molecular biology, as well as in clinical care, during the past decade. We also discuss the significance of the inflammatory response in CF lung disease and new and experimental CF therapies.

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Big Brother is Watching Ben Greasley (CF) bumped into a couple of familiar faces at the Titans V Tigers basketball match recently. Blair and Ben who were the last 2 house members that survived the full term in the Big Brother house. ...

Collection of statistics from Canada, the U.S., Denmark, and Finland.

Patient information sheet covering the basics of cystic fibrosis.

Providence Hospital's Cystic Fibrosis Center for Adult and Adolescent patients represents 1 of only 76 accredited programs by the Cystic Fibrosis Foundation nationally. This is the site of the adult program developed at Sinai Hospital of which Dr. Pichurko assumed directorship in 1988.

Gene symbol and name, locus information, map information, Homo sapiens CFTR RefSeq, GenBank Sequences.

This is an omnibus protocol for studying patients with cystic fibrosis and other familial pulmonary and pancreatic disorders. The main purpose of the study is to expand knowledge of the natural history, clinical manifestations (phenotypes) and the genetic variants (genotypes) of cystic fibrosis. A well-characterized population of patients with cystic fibrosis will be invited to provide appropriate specimens for laboratory research and to participate in clinical trials of therapeutic agents for cystic fibros