DD was born with gastroschisis, ended up with short bowel syndrome and TPN Liver Disease, got on Omegaven, and now is better and 100% orally fed (still has her g-tube though). Her Intestinal Rehab team wants her to start drinking Pediasure, now that she is taking her nutrition orally. But, our insurance won't pay for it! They will pay for formula through her tube, but not by mouth...
Has anyone found a good homemade alternative? It needs to have at least 30 calories/oz, and be lactose free and no nuts (DH has anaphylaxis w/ nuts). TIA!
Has anyone found a good homemade alternative? It needs to have at least 30 calories/oz, and be lactose free and no nuts (DH has anaphylaxis w/ nuts). TIA!












