Braylen Zayne Lewis Clubbed Feet Campaign

Braylen zayne Lewis was born November 25th 2016 with spina bifida, heart defects, bilateral clubbed feet, chiari malformation, digeorge syndrome and many other things that has challenged his health within these 2 short years. He has been casted from kc childrens hospital to Iowa city hospital so about 50 times total in his short 2 years. He currently is scheduled at cmh for a bilateral talectomy and me as his mother been having doubts about not only the doctor but that specific surgery! It will cause future issues and I'm so scared to allow him to get it done and feel bad later on for the back lash it will cause. Moral of the story we have been trying to raise money to get to st Louis to Dr. Mathew Dobbs one of the best clubbed foot doctors in America. He don't take out of state insurance such as kancare is what braylen has. With the kindness of my heart I'm running out of time before his bones get hardened and he will probably be deformed the rest of his life. He currently cant wear braces because his feet are so turned in that he walks on his ankle bone. As his mom I'm terrified and just want his feet fixed. I been through hell and back trying to do what's right. It's about time we get to St. Louis and get things done correctly. Anything will help us. The total of things to fix both feet is 14,000 I'm raising money in all ways possible while still working to survive at my house with my other 2 kids. update: we have raised 4,000 so far and working very hard to get the remaining!! thankyou for all your current donations. share share!!