

Welcome to McCall Casas's Page
Mccall Casas
McCall Casas
Hi!! My name is McCall Casas. I am proud to once again be sitting as a committee member for this year’s DC Finest.
My connection to CF started as a baby: my older sister and nephew have CF. She’s almost 3 years older than me and my nephew is 3 years younger. They were both diagnosed before the age of one, so I mean what I say when I say it’s been a part of my life from the beginning. I’ve been participating in fundraisers for over 30 years.
I had the honor to be selected as one of DC’s Finest in 2022, and have been working with the foundation since!
I look forward to networking within the CFF family and learning new inventive ways connect with the professional communities and enhance my ability to impact CFF. Fundraising and research are paramount to finding a cure
Please consider helping me meet my fundraising goal of $2,500 by making a donation. By supporting my fundraising efforts, you have an opportunity in your lifetime to be part of ending this disease.
More CF info below: Nearly 40,000 people in the United States have cystic fibrosis: a progressive, genetic disease that affects the lungs, pancreas, and other organs. 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 over 50. Working alongside the CF community, the CF Foundation has fostered the development of more than a dozen CF treatments and helped add decades of life for people with CF. Yet, many people with CF do not benefit from existing therapies. Our vision is a cure for every person with cystic fibrosis – a life free from the burden of this disease – and we will not leave anyone behind.
My connection to CF started as a baby: my older sister and nephew have CF. She’s almost 3 years older than me and my nephew is 3 years younger. They were both diagnosed before the age of one, so I mean what I say when I say it’s been a part of my life from the beginning. I’ve been participating in fundraisers for over 30 years.
I had the honor to be selected as one of DC’s Finest in 2022, and have been working with the foundation since!
I look forward to networking within the CFF family and learning new inventive ways connect with the professional communities and enhance my ability to impact CFF. Fundraising and research are paramount to finding a cure
Please consider helping me meet my fundraising goal of $2,500 by making a donation. By supporting my fundraising efforts, you have an opportunity in your lifetime to be part of ending this disease.
More CF info below: Nearly 40,000 people in the United States have cystic fibrosis: a progressive, genetic disease that affects the lungs, pancreas, and other organs. 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 over 50. Working alongside the CF community, the CF Foundation has fostered the development of more than a dozen CF treatments and helped add decades of life for people with CF. Yet, many people with CF do not benefit from existing therapies. Our vision is a cure for every person with cystic fibrosis – a life free from the burden of this disease – and we will not leave anyone behind.
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