Cystic Fibrosis Foundation/Tampa Chapter

www.myspace.com/cffoundation_tampa
  • CF foundation Tampa

  • 39 / Female
  • TAMPA, Florida, US
  • Last Login: 4/23/2009

429803913|39|11111|http://c2.ac-images.myspacecdn.com/images02/38/m_536adf9e218f4b0e976809c873dd3759.jpg

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    Photobucket Photobucket CureFinders® is the CF Foundation's school fund-raising program for grades K through 12. The CureFinders® program provides students with the opportunity to compete with one another to see who can raise the most money in their school to help support CF research and care. **Nominate a Student Today** We are accepting the nominations of middle and high school students to serve on a CureFinders® Student Youth Board. Students appointed to this prestigious panel will be responsible for recruiting schools in their communities to participate in the CF Foundation's CureFinders® program. Nominees should exhibit strong leadership skills and have the desire to make a difference in their community. Student Youth Board members will organize and lead other students and volunteers in activities throughout their community to help raise awareness and money to support vital cystic fibrosis research.
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    Photobucket GREAT STRIDES: Taking Steps to Cure Cystic Fibrosis is the Cystic Fibrosis Foundation's largest national fund-raising event. Tens of thousands of co-workers, friends and family come together each year as one community for one cause…to help find a cure for CF. In 2008, nearly $37 million was raised to support vital CF programs. Photobucket ***GREAT STRIDES 2009*** March 14th-Siesta Key, Sarasota***//March 28th-Fort De Soto Park, St. Petersburg***//April 4th-Walsingham Park, Largo***//April 25th-Lakes Regional Park, Ft. Myers***//May 2nd-Munn Park, Lakeland***//May 3rd- East Bay, exact location TBA***//May 16th- Lowry Park Zoo, Tampa***//October 31st- Lake Park, Carrollwood!! **Please continuously check the Tampa chapter home page for information regarding new walks, dates and times, and locations!!http://www.cff.org/Chapters/tampa/

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About me:

Photobucket *** What Is Cystic Fibrosis?*** Cystic fibrosis is an inherited chronic disease that affects the lungs and digestive system of about 30,000 children and adults in the United States (70,000 worldwide). A defective gene and its protein product cause the body to produce unusually thick, sticky mucus that: clogs the lungs and leads to life-threatening lung infections; and obstructs the pancreas and stops natural enzymes from helping the body break down and absorb food. In the 1950s, few children with cystic fibrosis lived to attend elementary school. Today, advances in research and medical treatments have further enhanced and extended life for children and adults with CF. Many people with the disease can now expect to live into their 30s, 40s and beyond. ***Symptoms of Cystic Fibrosis*** People with CF can have a variety of symptoms, including: very salty-tasting skin; persistent coughing, at times with phlegm; frequent lung infections; wheezing or shortness of breath; poor growth/weight gain in spite of a good appetite; and frequent greasy, bulky stools or difficulty in bowel movements. ***Statistics*** About 1,000 new cases of cystic fibrosis are diagnosed each year. More than 70% of patients are diagnosed by age two. More than 40% of the CF patient population is age 18 or older. The predicted median age of survival for a person with CF is more than 37 years. Photobucket Volunteers are the key to our success, and we encourage you to get involved! Whether you join a committee and help get sponsors for an event, recruit companies to put together walk teams or volunteer time in our office, you help us achieve our mission—curing and controlling cystic fibrosis. Take a moment to see what a difference you can make by supporting events throughout the year. Together, we can continue adding tomorrows every day to the lives of people with CF.

Who I'd like to meet:

About 65 Roses® "65 Roses" is what some children with cystic fibrosis (CF) call their disease because the words are much easier for them to pronounce. Mary G. Weiss became a volunteer for the Cystic Fibrosis Foundation in 1965 after learning that her three little boys had CF. Her duty was to call every civic club, social and service organization seeking financial support for CF research. Mary's 4-year-old son, Richard, listened closely to his mother as she made each call. The Weiss brothers, Richard, 5; Arthur, 7 and Anthony, 16 months. After several calls, Richard came into the room and told his Mom, "I know what you are working for." Mary was dumbstruck because Richard did not know what she was doing, nor did he know that he had cystic fibrosis. With some trepidation, Mary asked, "What am I working for, Richard?" He answered, "You are working for 65 Roses." Mary was speechless. He could not see the tears running down Mary's cheeks as she stammered, "Yes Richard, I'm working for 65 Roses." Since 1965, the term "65 Roses" has been used by children of all ages to describe their disease. But, making it easier to say does not make CF any easier to live with. The "65 Roses" story has captured the hearts and emotions of all who have heard it. The rose, appropriately the ancient symbol of love, has become a symbol of the Cystic Fibrosis Foundation. 65 Roses® is a registered trademark of the Cystic Fibrosis Foundation.

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Cystic Fibrosis Foundation/Tampa Chapter has 51 friends.
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Comments

Displaying 2 of 2 comments
  • Jan 14 2009 3:16 PM

    Hi Laura :)
    Glad you found me.....Lets make it BIG this year!!!!

    EXCITED

    Allisha
  • Nov 23 2008 4:31 PM

    Keep up the great work CF.
    It's people like yourselves that
    are making this world alittle
    better each and every day.
    Let me know if theres anyway to
    help raise money or anything I
    have a bunch of volunteers willing
    to help.

    -God Bless
    -SamiGumbo♥