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Welcome to Joyce Lamberson's Page

Joyce Lamberson

Joyce Lamberson

I will soon be honored by the Cystic Fibrosis Foundation at a special event recognizing outstanding young professionals in my community. In accepting this distinction, I have committed to raise money to help the Foundation realize its mission of controlling and curing cystic fibrosis (CF).
I fight in honor of my brother, Charlie. Charlie passed away from cystic fibrosis at the age of 16 in February of 2002. It was a long and hard fight for him and my family. Charlie seemed to be the textbook definition of CF with a barrel chest, digital clubbing, weight gain issues, salty skin, and chronic cough. I remember his mucus being so thick, colorful, and foul smelling. He required oxygen at times and would be limited to his home oxygen concentrator or weighted down by a mobile oxygen tank. Charlie seemed to understand how terminal his disease was but that never stopped him from living. He was a great big brother to me. We would try to stay up all night watching wrestling, eating snacks, and playing video games. We created secret clubs with themes like Pokemon. When the final months came near, he was so brave when he got the news and made sure to cherish every lasting moment with his family. I fight CF for my brother Charlie!
Please help me meet my fundraising goal by making a donation. Your generous gift will be used efficiently and effectively to help support vital CF research, medical and education programs. Making a donation is easy and secure! Just click the Donate button on this page to make a donation that will be credited to my fundraising efforts. Any amount you can donate will be greatly appreciated! Cystic fibrosis is a devastating genetic disease that affects the lungs and digestive system. More than ten million Americans are symptomless carriers of the defective CF gene. Advances continue to be made in finding a cure, but your help is needed now -- more than ever -- to help keep up the momentum of this life-saving research. Sixty years ago, children with CF usually did not live long enough to attend elementary school. Today, because of Foundation-supported research and care, the median survival age of people with CF is about 40. This is remarkable progress, but not good enough. We continue to lose precious lives to CF every day. To learn more about CF and the CF Foundation, visit cff.org. Together, we can make a difference in the lives of those with cystic fibrosis. Thank you for supporting the mission of the CF Foundation!


raised of $5,000 goal

Recent Donations

1. CF T-Shirt Fundraiser
2. Rusty Bull Brewing Co.
3. Gary Lamberson
4. CF 50/50 Raffle
5. Jennifer Deraney
6. Rita Barber