
Dear Friends, Family & Colleagues:
I hope you are staying well and taking care. I am reaching out to you today in an effort to raise money for the Cystic Fibrosis Foundation once again. Cystic Fibrosis is a genetic disease that limits a person's ability to breathe and impacts every organ that secretes something. Over time, it shortens the lives of those it affects. When the CF Foundation first began in 1955, people with CF seldom lived to see elementary school, but today more than half of the CF population are adults and are reaching major milestones. Because of the money donated to research to find a cure, the life expectancy is now 50!!
As a lot of you already know, Alex was first diagnosed when he was 6 months old. He has had to live with this disease and all of its implications since. We are fortunate that Alex has been able to stay healthy so far from Covid and continues to enjoy working out and making music. He will be turning 29 this summer. He also continues to assist my mom in caretaking duties for his dad.
The mission of the Cystic Fibrosis Foundation is to find a cure for cystic fibrosis and to provide all people with CF the opportunity to lead long, fulfilling lives by funding research and drug development, partnering with the CF community, and advancing high-quality, specialized care. Nearly every CF-specific drug available today was made possible with the financial support of the CF Foundation.
Here's where my special request comes in. I am participating in a the Great Strides Walk at the new Austin FC Q2 Stadium on May 14. I am also considering doing another 65 mile ride as well. My personal goal is to raise $3,000. My team goal is to raise $4,000. Here are several ways to helpsupport my goal:
Donate to my page! Any amount of money is much appreciated.
Help me raise funds by signing up for Alexander's Army and participate in the Great Strides Walk on May 14 and come see the new soccer stadium!
Best Wishes,
Connie Adams
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