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Welcome to Christina Simms's Page
Christina Simms
Christina Simms
I am being honored by the Cystic Fibrosis Foundation at a special event recognizing outstanding professionals in my community. In accepting this distinction, I have committed to raise money to help the Foundation realize its mission of curing cystic fibrosis (CF) and providing all people with CF the opportunity to lead long, fulfilling lives. My personal goal is to celebrate my best friend, Nancy, and the entire Sinegal Family. They lost Tammi to CF two years ago. Tammi spent her entire life raising awareness and funds for the CF Foundation. I want to continue Tammi’s legacy and help reach the goal where ‘CF stands for Cure Found’.
Please help me meet my fundraising goal by making a donation. By supporting my fundraising efforts, you have an opportunity in your lifetime to be part of ending this disease. Please consider joining us and help make medical history.
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.
To learn more about CF and the CF Foundation, visit www.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!
Please help me meet my fundraising goal by making a donation. By supporting my fundraising efforts, you have an opportunity in your lifetime to be part of ending this disease. Please consider joining us and help make medical history.
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.
To learn more about CF and the CF Foundation, visit www.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!
AUG
20
20
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AUG
14
14
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Swags Poker Run 5K. We donated to Toys for Tots and dressed up as our favorite toys!
JUL
31
31
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Bake Sale Campaign! Are you team cookie or cake pop?
JUL
28
28
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Christmas In July campaign winning costume. Thank you for voting Frosty into the number 1 spot!
JUL
21
21
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Swags Midnight 6k #CooperrunsforCF
JUL
18
18
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Swags Ice Cream 5K #CooperrunsforCF
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Independence Day 5K #CooperrunsforCF
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ParkRun "I'm Feeling 22 on tutu Saturday" #CooperrunsforCF
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