Joens' Journey Great Strides Walk 2024
This will be our 17t h year participating in the Great Strides walk. It's hard to beleive Tarryn was just a year old when we started this. Tarryn was 7lb at her 3 month check up, which led to multiple tests and blood work where she was finally diagnosed with Cystic Fibrosis. Now it is apart of the newborn screening so thankfully Savannah's was caught right away. They have countless doctor appointments, blood draws, throat swabs and pulmonary funtion tests. Add to that the multiple medications and treatments they do everyday at home, they don't lead a "normal" life for a kid. The girls get up 40 min. earlier just to get their treatments in before school. Even though they look healthy on the outside CF continues it's attack on the inside.
Tarryn is 17 years old and She's thrilled to finally be driving and enjoys cross country. Tarryn still has CFRD (CF related diabetes) so sees an Endocrinologist along with her CF team. Thankfully she has been mangaing her diabetes without insulin. Her liver enzymes contine to get higher every year when they do a full blood panel so they are constantly monitoring that. CF not only affects the lungs and pancreas but also the liver as the mucus that builds up can cause blockage of the liver ducts. If they continue upward she will have to go on another medication to help lower those levels. She has been on Trikafta for 4 years and recently they took one of her nebulized medications away since her pulmonary function tests continue to be over 110%. So some good things have come about since starting this medication. It's the most recent drug that helps correct the defective gene. It doesn't reverse the damage that's been done but is supposed to help with the progression of Cystic Fibrosis.
This year the walk will take place Saturday June8th, 10am at Riverdale Park in Sioux Falls and everyone is welcome to join us. Our goal this year is $3,000! Please help us and show your support by going to fightcf.cff.org click on the Great Strides link. Go to menu and there you will see donate to walker or register to walk and enter either my name or Phillips. You can also send your donations made out to the CF Foundation to: Amber and Phillip Joens--18539 Lais Ave in Reading MN 56165
Thank you for your continued prayers and donations as we could not do this without you. The CF Foundation is not federally funded so all donations come from people like you and me. We will not stop until a cure is found.
Phillip, Amber, Tarryn, Brandt and Savannah
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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.