Team August
August Schuster was born on April 8, 2024. At eight days old he was diagnosed with Cystic Fibrosis through the heel prick newborn screening. From that moment August has been endured a lot, but he continues to persevere everyday.
Cystic Fibrosis is treated mostly through medications, and routines such as chest percussion therapy, and nebulizer treatments. The Cystic Fibrosis Foundation has been a huge part of these treatments and medications being what they are today. The fight against Cystic Fibrosis is not done yet, we still have a long way to go in treatments being available for all patients with Cystic Fibrosis.
Thank you for your support!
--The Schuster Family
We invite you to take part in Great Strides by joining our team. We promise, you belong here! This event promises to be a fun-filled day where you can help advance the care and research needed to cure cystic fibrosis. By walking with us, you’ll enjoy not only the natural camaraderie (yes, lots of laughter!), but the important impact we are making together.
While the CF Foundation has made incredible progress, not everyone with CF can benefit from existing therapies and we still need a cure. This will require time, funding, and persistence – but with you on our team – we are ready to go the distance.
Our team is committed to providing every person with CF the opportunity to live a long, healthy life. Will you join us?
Cystic Fibrosis is treated mostly through medications, and routines such as chest percussion therapy, and nebulizer treatments. The Cystic Fibrosis Foundation has been a huge part of these treatments and medications being what they are today. The fight against Cystic Fibrosis is not done yet, we still have a long way to go in treatments being available for all patients with Cystic Fibrosis.
Thank you for your support!
--The Schuster Family
We invite you to take part in Great Strides by joining our team. We promise, you belong here! This event promises to be a fun-filled day where you can help advance the care and research needed to cure cystic fibrosis. By walking with us, you’ll enjoy not only the natural camaraderie (yes, lots of laughter!), but the important impact we are making together.
While the CF Foundation has made incredible progress, not everyone with CF can benefit from existing therapies and we still need a cure. This will require time, funding, and persistence – but with you on our team – we are ready to go the distance.
Our team is committed to providing every person with CF the opportunity to live a long, healthy life. Will you join us?
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