My Great Strides Story
On this very date 58 years ago
An angel was born with a pure heart and pure soul
When she entered the world, her future was bright
Her smile so wide and eyes that could brighten the night
But the cloud of cystic fibrosis reared its cruel head
She won't make it long the doctors all said
But Tena was a fighter. She wouldn't give in
She gave it her all so CF wouldn't win
Over the years her battles were tough
Most people would say enough is enough
But my big sister never complained
She just kept on fighting through all of her pain
The time finally came when she could fight no more
Her time to meet Jesus on that Heavenly shore
Fifteen years here with me
Was not nearly enough but at least she was free
Her pain was over. Her suffering done
She fought the good fight but CF finally won
So I write this today to honor that girl
And the effect she had on those in this world
If you knew her, you truly were blessed
To see how she fought through every test
You see, she wasn't here long, but her impact was mighty
After 46 years gone, I still miss her nightly.
Nearly 40,000 people, like my sister and brother, in the United States have cystic fibrosis: a progressive, genetic disease that affects the lungs, pancreas, and other organs. They are moms, dads, sisters, brothers, daughters, sons, and friends who face the sobering prospect of a shortened lifespan. I walk for them.
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.
You can support me!
By supporting my fundraising goal, you have an opportunity in your lifetime to be part of ending this disease. Please consider joining us and help make medical history.
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IMPORTANT NOTE ON ATTENDANCE AT FOUNDATION EVENTS:
Updated July 5th, 2023
The CF Foundation is committed to ensuring the health and wellbeing of individuals attending Foundation events. Individuals attending CF Foundation events must abide by the Foundation's Event Attendance Policy www.cff.org/attendancepolicy, which includes guidance for event attendees living with cystic fibrosis.