101. Cystic Fibrosis Cystic Fibrosis Links and Information http://www.goodgulf.com/cystic.html

Cystic Fibrosis Our fifteen year old son, James, has Cystic Fibrosis - CF This page is devoted to the understanding and cure of this debilitating disease. Cystic Fibrosis Foundation Canadian CF Foundation Cystic Fibrosis Victoria - Australia Cystic Fibrosis Resource Centre ... sci.med.diseases.cysticfibrosis newsgroup - not very active, how about some action here? Return to Home Page Questions, suggestions, links ? e-mail us Dudley Leaphart Billings, MT

102. Breathing Room: The Art Of Living With Cystic Fibrosis Guidance about the art of living with cystic fibrosis. http://www.thebreathingroom.org

Home News and Info Looking Glass Caregiver Stories ... Contact Join our newsletter list! Enter your email address: Organ Donor Awareness! Breathing Room has lots in store for the year. If you would like to share your personal stories, news items or poetry with us, please contact: us at: info at thebreathingroom.org. Stories, Poems and opinions of participants are their own, and not necessarily those of the Breathing Room organization. Please visit cfmessageboard.com to connect with members of the CF community online. 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. Shaping Our Choices We take a look at how Cystic Fibrosis has shaped other choices (career and family spring to mind). photo from Caregivers' Collection Through the Looking Glass An ongoing multimedia project showcasing the emotional journey traveled by adults living with this genetic disease. Image index Featured Image Hidden Agenda "Me discovering the giant tailpipes in the sky,

103. The Annual North American Cystic Fibrosis Conference Information on program and location. http://www.nacfconference.org

104. Canadian Cystic Fibrosis Foundation Support and resources. Located in Toronto, Ontario. http://www.cysticfibrosis.ca/

105. Cystic Fibrosis -Lungs For Life Foundation -Organ Donation Transplant Provides financial assistance to cystic fibrosis and lung transplant patients. http://lungsforlife.org/

Welcome About LFL Cystic Fibrosis Raise Awareness ... View Your Cart JOIN THE DISCUSSION Ask questions, exchange ideas, share your stories. View LFL Message Boards Celebrating 9 years of: assistance, education and support! Welcome The Lungs for Life blog, Breathe , has moved. Check out our new location at http://lungsforlifeblog.blogspot.com Support the mission of the Lungs for Life Foundation Lungs for Life (LFL), an all-volunteer 501c3 organization dedicated to assisting individuals and families affected by cystic fibrosis Our primary goal is to provide necessary assistance * to meet the daily living and medical needs of those with cystic fibrosis. We improve the quality of life for cystic fibrosis individuals as they await a cure and we help to ease the burdens they face as they battle their disease. The LFL website is a resource for both the cystic fibrosis and transplant communities. We provide important links to cystic fibrosis information sites, transplant information sites, outside organizations, individuals and a host of other resources that share or further our mission. *At this time, our assistance program extends only to U.S. citizens of Monroe County, New York State. We hope to re-open nationwide assistance at some point in the future.

106. Sarah Yourman: An Inspiration Site by a girl with CF and Diabetes. http://www.yourphotoservice.com/sarah/

Please sign my guestbook View My Guestbook Sign My Guestbook Recent Articles Click on the links below Presidential Debate JDAC Volvo for Life Park City Record ... Shopper News THIS I BELIEVE The highlight of all my achievements was the honor of being presented with the Michael Brennan Courage Award by the Boomer Esiason Foundation in March. It was an incredible experience!! Many thanks to the Boomer Esiason Foundation for all they do for patients living with cystic fibrosis. To view my acceptance speech, Click here College!!!! Wow! I finished my Freshman Year of CollegeDean's List! I made the adjustment to college very easily. I was able to manage my classes and my medical treatments with only a few minor bumps. This summer I traveled to England and Germany and had a great time! I am exploring the idea of going on a clinical drug trial for cystic fibrosis this year. I will talk to my doctors to see if this would be the right choice, since the trial is being done at a different CF Center than the one I normally go to. JDAC Thanks to my friends and the nurses, I initiated a club called the Juvenile Diabetes Awareness Club (JDAC) my freshman year in high school. Together with members of the community, and the

107. Living With Cystic Fibrosis Site by a young man with CF. http://frontpage.velocity.net/yanc/

Hi, My name is Yancee. 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 IMPORTANT ARTICLE about FDA approval and pancreatic enzymes! You are visitor since February 28, 1998. Thanks for visiting! Come back again.

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