Help Fund slice of Twisha's US treatment cost. She's braved 20 surgeries in Australia, that failed to give her Food-pipe

Please Help Save my only child, Twisha, 3, who is born with very rare birth defect called – Long Gap Esophageal Atresia. This means she is born with an incomplete esophagus, hence unable to eat. She has undergone around 20 major and minor operations in Australia to cure her condition, but all in vain. She is left with G-feeds and Esophagostoma. The only medical treatment in the world that can give Twisha a fair chance of living a normal healthy life is the Foker Treatment at the Boston Children’s Hospital, MA, USA. The cost of this treatment is estimated to be 1.17M USD, which is beyond my reach. I'm single mother; we both were abandoned by Twisha's father. I've managed to raise 720K USD so far. Please help fund remaining cost of her treatment. More info on www.twishamakwana.com.
Thank You