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To all friends and family:
Wow! I can’t believe it has been an entire year since the last Great Strides fundraiser! Last year I was blown away with how many friends and family, near and far, took the time not only to view Asher’s page and send prayers, but generously donate to this cause that is so very important to us!
For those that are new to this page or were not aware, Asher was born on July 1st, 2017. Six days later, I received a phone call stating that, what we thought to be a beautiful, healthy baby boy was actually not the case. We were told that his newborn screening and further testing revealed that Asher had received 2 genetic mutations, 1 each, from Kevin and I. These mutations further indicated that Asher has Cystic Fibrosis. This news absolutely crushed our world and broke my heart.
Many of you may not know what Cystic Fibrosis is and I don’t blame you for not knowing, because until that day I received that crushing phone call, I had no idea! In short, Cystic fibrosis is a progressive, genetic disease that causes persistent lung infections and limits the ability to breathe over time. Not only does Cystic Fibrosis affect the lungs, it can also affect the Pancreas and Liver.
Since birth, Asher has been doing pretty well and is mainly experiencing issues with his pancreas and digestion. We have a daily and vigilant routine that includes Pancreatic enzymes with every feeding (6 capsules per meal and 3 with snacks), a special vitamin that he takes, 2 additional medications that aid in the absorption of his pancreatic enzymes, an inhaler twice daily, a nebulizer, and respiratory therapy (vest) twice daily. I thank God everyday that we haven’t had any hospital stays thus far.
Since last year, Asher has grown tremendously . The doctors say that weight and lung function go hand and hand, so we want our big boy to continue growing at this excellent rate!
There is no cure, as of yet, for Cystic Fibrosis which is why research is so important. Please help us in prolonging our sweet baby Asher's life by donating to Cystic Fibrosis research to find a cure, hopefully someday soon! We love and appreciate all of you!
Great Strides walk, supporting Cystic Fibrosis Foundation is on May 6, in Memphis, TN, at Shelby Farms! I know many of you won’t be able to make the walk, but any donation small or large is very much appreciated. And if you can’t donate or participate, we appreciate prayers!
Much love and thanks!
Heather, Kevin, Asher and family
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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.