Benjamin was diagnosed with cystic fibrosis shortly after birth, and since then a day hasn't gone by for him without his treatments and medications. Twice each day he is hooked to a vibrating vest to help shake mucus from his lungs, and takes in three inhaled medications that help thin and break up mucus and keep him healthy. He takes around 30 other pills each day so he can digest the fat in his food, grow, and live a healthier and longer life. When sick, treatments increase to 3-4 times per day usually with more medication, and thankfully it has only led to hospitalization with IV antibiotics once! He has had a very healthy year overall, but has recently test results have earned him the label prediabetic. CF-related diabetes is a still a common occurrence for many, but thankfully we're told this doesn't mean he will be diabetic in the near future, it is just something to keep an eye on.
We are so thankful for all the medical research and treatments currently available that have changed the prognosis for CF patients dramatically. The newer medication Trikafta has been a game changer and it's looking more and more like CF patients can expect a normal lifespan which is just amazing! There is so much promising new research being done, and scientists who don't plan to stop until a cure is found. All of this is made possible through generous donations to continue funding these groundbreaking medical advancements. 90% of donations to the Cystic Fibrosis Foundation go directly to lifesaving research!
We're excited to be walking again this year on May 18th at Outlets of Des Moines! We'd love to have you join us for the walk!
By becoming a member of our team, you are joining a growing group of people committed to finding a cure for cystic fibrosis. Together, we are adding tomorrows to the lives of people living with CF by supporting the search for a cure. We're so thankful for donations of any amount, it's amazing what we can accomplish when we all work together for a common goal!
As always, we are so thankful for your prayers and support! God is so good and we're grateful that we can fully trust Him as the one who holds Ben's future in His mighty hand!!!
Love,
The Kline 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.