cf-reachingout.blogspot.com

randysnider.com

Thomas Randall "Randy" Snider | Cystic Fibrosis Foundation | 65 Roses

http://www.randysnider.com/index.html

The Randy Snider Memorial Website. Cystic Fibrosis Foundation, 65 Roses. Today is the day we lost you, Randy. August 19, 2005. We miss you and love you. But you are not alone now. Your Faw Faw is with you. Randy Snider and his "Faw Faw" together again. RIP. In 1992, two year old Randy Snider and his Grandfather shared some fun. He loved Randy so much and Randy was always so affectionate and loving. Now they are both together again in heaven. RIP. Then visit The Thomas Randall Snider Memorial Channel.

reachingoutfoundation.org

Cystic Fibrosis-Reaching Out Foundation

http://www.reachingoutfoundation.org/aboutus.htm

Tell A Friend About Us. Cystic Fibrosis-Reaching Out Foundation, Inc. is sensitive to the needs of patients and families with Cystic Fibrosis and provides financial and educational resources to assist them. Healthcare professionals and social workers familiar with the unique financial and social needs of CF families identify families that qualify for Cystic Fibrosis-Reaching Out Foundation support. The Foundation provides funds to pay for prescribed nutritional supplements for Cystic Fibrosis patients&#4...

reachingoutfoundation.org

Cystic Fibrosis-Reaching Out Foundation - Lung Transplantation

http://www.reachingoutfoundation.org/lungtransplantation.htm

Tell A Friend About Us. Susan Burroughs is the founder of the Cystic Fibrosis-Reaching Out Foundation, Inc. Below is her personal story. She is now 48 years old and is doing extremely well eight years after her double lung transplant. If you want to communicate with her about cystic fibrosis or transplant, please email her at susan@reachingoutfoundation.org. Susan Burroughs- Double Lung Transplant Story 5/23/2000. My Double Lung Transplant Story. By: Susan C. Burroughs, CPA. TO LIST OR NOT TO LIST? I am ...

reachingoutfoundation.org

Cystic Fibrosis-Reaching Out Foundation - Cystic Fibrosis Support and Information

http://www.reachingoutfoundation.org/index.htm

Tell A Friend About Us. Cystic Fibrosis (CF) is the most common, fatal hereditary disease in the U.S. CF is a disorder of the cells that line the lungs, small intestines, sweat glands and pancreas. Sticky, thick mucus contributes to the destruction of lung tissue and impedes gas exchange in the lungs. It also prevents nutrient absorption in the small intestine, and blocks pancreatic ducts from releasing digestive enzymes. To Donate in honor of or in memory of. Click here. Or continue to the form below.

randysnider.com

Randy Snider | Thomas Randall Snider | Cystic Fibrosis Foundation | Randy Snider Site Map

http://www.randysnider.com/randy-snider-sitemap

Randy Snider Site Map. Living with Cystic Fibrosis. 800) FIGHT CF (344-4823). CF Reaching Out Foundation. CF Reaching Out Blog. Cystic Fibrosis on YouTube. CFF Video Podcast: Cassalina family. CFF Video Podcast: Frank Deford. Emory CF Center, Atlanta. Financial Assistance and Patient Support. Authorized Distributors for KALYDECO. Vertex Guidance and Patient Support. Microsoft Research and CF. Cystic Fibrosis Lifestyle Foundation. Cystic Fibrosis Scholarship Foundation. Miles for Cystic Fibrosis.

randysnider.com

Randy Snider | Thomas Randall Snider | Cystic Fibrosis Foundation | Randy Snider Site Map

http://www.randysnider.com/randy-snider-sitemap.html

Randy Snider Site Map. Living with Cystic Fibrosis. 800) FIGHT CF (344-4823). CF Reaching Out Foundation. CF Reaching Out Blog. Cystic Fibrosis on YouTube. CFF Video Podcast: Cassalina family. CFF Video Podcast: Frank Deford. Emory CF Center, Atlanta. Financial Assistance and Patient Support. Authorized Distributors for KALYDECO. Vertex Guidance and Patient Support. Microsoft Research and CF. Cystic Fibrosis Lifestyle Foundation. Cystic Fibrosis Scholarship Foundation. Miles for Cystic Fibrosis.

reachingoutfoundation.org

Cystic Fibrosis-Reaching Out Foundation

http://www.reachingoutfoundation.org/orderthecd.htm

Tell A Friend About Us. About the 2000 Music CD-. This music is dedicated to the thousands of individuals affected by Cystic Fibrosis (CF). CF is a genetic disease that overcomes the lungs and other vital organs. Treatments for CF patients include an intensive regimen of breathing treatments, medications and frequent hospitalizations. Often, through caring for a friend or loved one with CF comes love and compassion in its purest form. These songs express some of those feelings of love. The Cystic Fibrosi...

reachingoutfoundation.org

Cystic Fibrosis-Reaching Out Foundation - Thank you notes

http://www.reachingoutfoundation.org/yourmoney.htm

Tell A Friend About Us. Below are just a few of the thank you notes. Dear Cystic Fibrosis-Reaching Out Foundation,. I'm writing you to thank you for assisting me with my rent payment. I'm in a financial bind and it is deeply appreciated. Thank you very much, for your support it really has made a difference in my life. Dear Cystic Fibrosis-Reaching Out Foundation:. Thank you for your generous assistance with equipment need for the repair of my IPV machine. It is greatly appreciated. Mother of a 2-year-old.

reachingoutfoundation.org

Cystic Fibrosis-Reaching Out Foundation - Cystic Fibrosis - The Disease

http://www.reachingoutfoundation.org/cfinfo.htm

Tell A Friend About Us. What Is Cystic Fibrosis? How Is Cystic Fibrosis Treated? How Common Is CF? How Do You Know If You or Your Child Has CF? What Can You Do If You Have CF? What Does Cystic Fibrosis-Reaching Out Foundation, Inc. Do? How Can You Assist Cystic Fibrosis-Reaching Out Foundation, Inc? What Is Cystic Fibrosis? Cystic Fibrosis (CF) is the most common, fatal hereditary disease in the U.S. (Source:. CF patients exhibit some or all of these symptoms to varying degrees:. Middot; Clubbed fingers.