Need Help to my TOF Baby and babies need medical aid

Tracheo-Oesophageal Fistula or Oesophageal Atresia. (rare congenital malformaltions of the gullet and windpipe). Immediate neonatal surgery is a treatment, not a complete cure. My Baby  has a birth defect(TEF/EA(Tracheoesophageal Fistula - Esophageal Atresia)) ,Immediately I joined my baby in another hospital on 16th Feb. 2015,Doctors said they should do surgery for my newly born baby until then baby cannot drink and eat. So they did surgery on 19th Feb. 2015.My baby discharged from hospital on 10th march 2015(After 23 days),but now My baby had feeding and breathing complications.I am asking this fund for not only for my baby,Now i decided to help all the children who are suffering with this type of diseases.Based on this fund i will approach all children hospitals and give some amount of this fund to needy children.If i succeeded in this fund raising event ,I will start a charity.Please make a hope in poor children life. Tof/oa children endure many surgical procedures , some more than others.They all have difficulties with eating, reflux, reacurring chest infections and various other complications. What causes Tofs is still unknown and yet it occurs in  1 in every 3500 . Please dig and help donate.