Our Cycle for Life Story
Join Our Team and help Add Tomorrows!
Thank you for visiting our Team Page!
Living with Cystic Fibrosis is hard. One effect of this terrible disease is like breathing through a straw, all the time, even when exercising or having fun. This is in addition to the enormous amount of medicine that a CF patient needs every day just to be able to do everyday activities that others do normally.
My son Cayleb has CF and we try to add some normalcy to his life, but what is normal about taking multiple enzymes six times a day so you can absorb the nutrients in the food you eat? What is normal about doing treatment 2, 3 or 4 times a day at 30-45 minutes each time? What is normal about seeing the doctors at clinic 4-6 times per year and having to miss school and work to do this because each appointment last 3-6 hours? What is normal about this 9 year old taking more medicine than his parents or grandparents? Unfortunately, this is Cayleb's 'normal.
I am riding in the Cycle For Life to raise money and awareness for Cystic Fibrosis. The money raised helps the Cystic Fibrosis Foundation fund life altering Research and Development for new, improved medication. Money raised also supports patients with financial needs to pay for the medication which can be in the hundreds of thousands of dollars per year. Money raised is helping make CF stand for Cure Found.
We ride to add tomorrow for everyone with CF, for Cayleb, to make CF stand for Cure Found!! Please consider donating to my team through the link below to help Cayleb and others with CF to have more tomorrows. Every Dollar is Another Tomorrow - and every dollar helps us win the fight against this terrible disease. Help us make a difference today and donate. I sincerely appreciate your consideration and support.
Ride Today. Add Tomorrows.