Most of you may know that Wade Miller has Cystic Fibrosis. He was diagnosed during his routine newborn screening. Never did it cross our minds that we would get this sort of news. As parents, this rocked our world! Taking our newborn, fragile, baby boy, Wade home from the hospital, we knew as parents from that very moment we had to be strong for our little man. Wade has been healthy and we want to keep him that way. Everyday we keep him in a routine, this routine consist of enzymes mixed with applesauce (this helps him absorb the nutrients he needs), his vest treatments (to break up mucus), and additional vitamins and supplements. The most important part of keeping our boy strong and healthy is keeping a positive attitude! I have to let everyone know Wade is one of the most happiest and smartest little guys. We are so lucky he is ours. Below are more details about what your donation will do and what Cystic Fibrosis is:
Cystic Fibrosis is a progressive, genetic disease that affects the lungs, pancreas, and other organs.
There are approximately 30,000 Americans living with cystic fibrosis. They are moms, dads, sisters, brothers, daughters, sons, and friends who struggle every day just to breathe. I am walking for our son, Wade Miller. Will you join me and support my fundraising goal?
Real progress has been made for those who have CF, but there is still no cure for this devastating disease and many lives are cut far too short. We've come so far, but there's still so much work to do. I will not stop striding until all those with cystic fibrosis have a cure. We will not leave anyone behind.
Please support me!
We are at a pivotal moment in the history of cystic fibrosis and your support matters. With your help, we can invest our resources in research today, while raising funds for tomorrow, to ensure we have what it takes to reach the finish line. Together, we can make CF stand for Cure Found. Please help me reach my fundraising goal!