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Welcome to Rachel Mains's Page

Rachel Mains

Rachel Mains

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).

Giggleblossom Boutique is partnering with me in my fundraising goal. The store is located in downtown Littleton at 5654 S. Prince St. Unit B. You can round up your purchase or buy a discount punch card to support the campaign. Visit Giggleblossom on their website at giggleblossomboutique.com.

You can also help me meet my fundraising goal by making a donation here. 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. Anonymous
2. Anonymous
3. Anonymous
4. The Strickler Family
Thank you Rachel for helping raise awareness. We’re so grateful for you!
5. Anonymous
6. Melissa Macdonald
Always hoping for a cure! All my best to those and their families and friends who are affected by this disease.