81. Cystic Fibrosis NIDDK Cystic Fibrosis. The Cystic Fibrosis Research Program supports investigatorinitiated research grants encompassing both fundamental and clinical studies of the etiology http://www2.niddk.nih.gov/Research/ScientificAreas/GeneticGeneTherapy/CFXX.htm

82. Nederlandse Cystic Fibrosis Stichting Verenigd (ouders van) pati nten met Cystic Fibrosis (CF) en geeft informatie over CF en verwijzingen naar andere nuttige websites. http://www.ncfs.nl/

83. Cystic Fibrosis Cystic fibrosis, Cystic fibrosis (CF) is a chronic, progressive, and frequently fatal genetic disease of the glands that produce or secrete sweat and mucus. CF primarily http://www.umm.edu/altmed/articles/cystic-fibrosis-000045.htm

Information For Referring Physicians Nurses Health Care Professionals ... Connect With UMMC Connect with UMMC Email this page Print this page Home Home Medical Reference Complementary Medicine Note: The resources listed in this guide are not intended to be fully systematic or complete, nor does inclusion here imply any endorsement or recommendation by The University of Maryland or the Center for Integrative Medicine. The University of Maryland and the Center for Integrative Medicine make no warranties, express or implied, about the value or utility for any purpose of the information and resources contained herein. Related Content Center for Integrative Medicine Physicians and Staff Cystic fibrosis Introduction: Cystic fibrosis (CF) is a chronic, progressive, and frequently fatal genetic disease of the glands that produce or secrete sweat and mucus. CF primarily affects the respiratory, digestive, and reproductive tracts in children and young adults. On average, individuals with CF have a lifespan of around 37 years. According to the Cystic Fibrosis Foundation, about 30,000 Americans have CF. The disease occurs mostly in whites whose ancestors came from northern Europe, although it cuts across all races and ethnic groups. About 3,500 babies are born with the disease each year in the United States. Moreover, about one in every 30 Americans are unaffected carriers of an abnormal CF gene.

84. 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

85. What Is Cystic Fibrosis? Cystic fibrosis is an inherited disease that causes thick, sticky mucus to build up in the lungs and digestive tract. It is the most common type of chronic lung disease in http://www.medhelp.org/medical-information/show/156/Cystic-fibrosis

cystic fibrosis Information, Symptoms, Treatments and Resources Overview Information Treatments Posts ... Health Videos Table of contents Definition Causes, incidence, and risk factors Symptoms Signs and tests ... Next Definition Cystic fibrosis is an inherited disease that causes thick, sticky mucus to build up in the lungs and digestive tract. It is the most common type of chronic lung disease in children and young adults, and may result in early death.   Causes, incidence, and risk factors Cystic fibrosis (CF) is caused by a defective gene which tells the body to produce abnormally thick and sticky fluid, called mucus. This mucus builds up in the breathing passages of the lungs and the pancreas, the organ that helps to break down and absorb food. This collection of sticky mucus results in life-threatening lung infections and serious digestion problems. The disease may also affect the sweat glands and a man's reproductive system. Millions of Americans carry the defective CF gene, but do not have any symptoms. That's because a person with CF must inherit two defective CF genes one from each parent. An estimated 1 in 29 Caucasian Americans have the CF gene. The disease is the most common, deadly, inherited disorder affecting Caucasians in the United States. It's more common among those of Northern or Central European descent. Most children are diagnosed with CF by their 2nd birthday. A small number, however, are not diagnosed until age 18 or older. These patients usually have a milder form of the disease.

86. 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.

87. CF Pulmonary Treatment Research Center The UNC Cystic Fibrosis Pulmonary Research and Treatment Center is a large, multidisciplinary group focused on the pathogenesis and therapy of cystic fibrosis and other lung diseases. One of the largest clinical programs in the country with over 500 patients in our pediatric and adult programs. http://www.med.unc.edu/wrkunits/3ctrpgm/cystfib/CFcent.htm

88. AMA - Cystic Fibrosis Testing Information on genetic testing to identify people who carry the mutation associated with this condition. http://www.ama-assn.org/ama/pub/physician-resources/medical-science/genetics-mol

89. About Recipes For Kids With Cystic Fibrosis Learn to make these high-calorie recipes, like cheesecake squares, cheesy mashed potatoes, and baked creamy chicken. http://www.kidshealth.org/kid/recipes/cf_recipes/about_cf_recipes.html

90. Cystic Fibrosis: Diet And Nutrition Learn what CF teens need to eat more of, supplements that help, and a sample diet. http://www.kidshealth.org/teen/diseases_conditions/digestive/cf_diet.html

91. Esiason.org - Fighting Cystic Fibrosis of the symptoms of CF, causes, treatments, and current research....... http://esiason.org/index.php/site/cysticfibrosis/

@import "http://esiason.org/index.php?css=site/site_css_tb.v.1248455264"; Home Cystic Fibrosis Donate About Us ... FAQ Cystic fibrosis Cystic fibrosis is a fatal genetic disorder that affects more than 30,000 Americans, usually the most vulnerable among us: our children. Although CF is not yet curable, the situation is not hopeless. Every day since the CF gene was discovered in 1989, the pace of CF research has greatly accelerated, and scientists continue to find ways to help those who live with the disease. Today, many people with CF now live into their late-30s and have fuller and more comfortable lives. Treatment There are a variety of drug therapies available to CF patients, and there also are a number of non-medical treatments that can help relieve the symptoms of the disease. Research The Boomer Esiason Foundation isn't the only organization working to find a cure for cystic fibrosis. Here are some links to other organizations that are leading the fight against CF, as well as advice from Dr. Jamie Wells, BEF's in-house medical expert. Resources The Boomer Esiason Foundation isn't the only organization working to find a cure for cystic fibrosis. Here are some links to other organizations that are leading the fight against CF, as well as advice from Dr. Jamie Wells, BEF's in-house medical expert.

92. 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. http://www.mycysticfibrosis.com

93. Cystic Fibrosis Medicine Provides a place to search various databases for Cystic Fibrosis articles, links to other CF sites, a message forum and a wide variety of information on management of the disease. http://www.cfprescriber.com/

CLICK HERE FOR FREE DOMAINS CLICK HERE FOR FREE DOMAINS

94. The Spirit Of Lo - One Family's Extraordinary Journey Of Raising A Child With Cy Book about Cystic Fibrosis and the effects on the family. Tells the story of an ordinary family and their struggle with having a chronically ill child. http://www.spiritoflo.com

Home Orders Endorsements Excerpt Readers Reviews ... Speaking Engagements YOU NEED The Spirit of Lo if: You want to triumph over adversity Someone you know has a disease or chronic illness, a crisis of faith or family You want to make a difference through: volunteerism education family life parenting " I think, your book is by far the best thing I have read dealing with Cystic Fibrosis." Jonathan Dailey, 25-year-old CF patient "Even though I had known a CF patient for years, I really had no idea.Your book has given me new insights and inspiration." - Fred Fleischner, Friend of CF family ORDER copies of The Spirit of Lo (There are many ways to order the book) Purchase The Spirit of Lo Online By Mail or Call Toll-Free 1-877-222-2095 Order through these online stores ...or Order from your Local Bookstore READ an Excerpt from The Spirit of Lo After checking in and enduring the insertion of an IV catheter into Lo's wrist, Don and Jane left for the night. Read More CONSIDER the Detrichs for your next keynote speech "Your speech impacted the practice of medicine for an entire community..."

95. A-Z Directory Of Cystic Fibrosis Resources Biomedical directory with listings of hospitals, charities, research, and information by topic and location. http://www.cellscience.com/CFmain.html

96. Clayton Bates CF Support Site - Home For family, friends, and other supporters to find out about the disease and offer support for Clayton. http://www.claytonbates.org

@import "raised.css"; Skip Navigation Clayton Bates Cystic Fibrosis Support Site Menu Home News CF Data Links ... Share Change Styles Default Alternative 1 Introduction Clayton was born on July 6, 2000. Clayton was diagnosed with Cystic Fibrosis at 18 months old. Some of his favorite things: His puppy, a Shetland Sheepdog named Tubby Boating/Swimming Playstation 3 / PC / XBOX Gaming Bowling This site is for family, friends, and other supporters to find out about CF and offer support for Clayton. FB.init("5b18acf1c1b89619f47e5c6d4a80266e"); Visitors since February 1, 2005

97. Cystic Fibrosis Therapeutic Options For Co-management Illustrated article details causes, symptoms, treatment, prognosis, and other effected systems. http://www.thorne.com/media/cysticfibrosis.pdf

98. Welcome To The International Cystic Fibrosis Support Group. Provides information about CF and its effects on the lungs, liver, and pancreas. Includes complications, bacteria, medication, nutrition, and bulletin board. Board requires free registration. http://cf.conncoll.edu

THOSE WHO POST AND/OR READ POSTS TO THE CONNCOLL CYSTIC FIBROSIS SUPPORT LIST AND WEB PAGE AGREE TO SAVE HARMLESS CONNECTICUT COLLEGE FROM CIVIL AND OTHER LEGAL LIABILITIES THAT COULD ARISE FROM POSTS SENT TO THE LIST AND WEB PAGE. INFORMATION SENT TO THE LIST AND WEB PAGE SHOULD NOT BE CONSTRUED AS MEDICAL ADVICE. PARTICIPANTS SHOULD GET MEDICAL INFORMATION ONLY FROM MEDICAL PROFESSIONALS

99. Cystic-L - Cystic Fibrosis Info & Support 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. http://cystic-l.org/

What's New The CF Shop Thunder-Bay Productions What's New The CF Shop Thunder-Bay Productions

100. Official Site For CFF Jack Buck Book Event Jack Buck, A Collection of Poems and Stories , by Jack Buck. 100% of the proceeds from the sale of this book go directly to Cystic Fibrosis Foundation. http://www.jackbuckbook.com/homepage.asp

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