My Great Strides Story
Please visit my blog to read my story:
We're raising money again for Cystic Fibrosis Foundation for our son, Fawkes. Here's his daily regimen now (this is considering he's healthy):
~20 enzyme pills per day (5 with each meal 2-3 with snacks). Imagine not being able to eat without taking medicine.
2 doses of Zantac to help with heartburn due to gastric imbalance
2 doses of fat-soluable vitamins due to malabsorption
2 airway clearance treatment sessions (total 1.5 hours) consisting of inhaled albuterol via nebulizer and chest percussion therapy through his VEST.
CFF is doing everything they can to fund research to develop medications and other therapies and has a low 6.3% administrative rate. They use the money raised to develop drugs that add tomorrows. Please donate, so that my baby can grow up and have a full life!