I am beyond thrilled!! Thank you so much to everyone who has donated to my page to support the Cystic Fibrosis Foundation. The month of May will be here before we know it and that is Cystic Fibrosis Awareness Month. I have pledged to raise $3,000 and am making great progress at $950 so far! I can’t slow down now!!! Here are just a few ways you can donate to this great cause: Book a photoshoot through our Photoshoot Fundraiser ($100 – further options available) Buy a Virtual Concert ticket, with the option to add craft beer and a Brewery Passport ($25-$150) Explore possible Donation-Match through an employer or business to double your impact. ($$ X2) Listed above are just a few ways… any additional ideas are greatly appreciated! Thank you all so much again!
Thank you for visiting my page and considering a donation to the Cystic Fibrosis Foundation! I am familiar with cystic fibrosis (CF) due to my late classmate Lucy Saladino who passed away from CF in 2009. Lucy’s family and my high school class continue to remember and honor Lucy by supporting and donating to this great cause. I am committed to raising money to find a cure for CF and to educate people on all the life-changing research achievements made possible by this foundation.
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.
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!