We have spent the last week in hospital and we have seen multiple pediatricians, dieticians and psychologists, the ED doctors and the first dietician we saw mentioned possibly getting starting with a NG tube and then getting a peg down the track (which I feel is the best permanent solution), but they keep saying we have to go through our pediatrician who doesn't even want to talk about it with me.
We went to our GP tonight after getting discharged this morning, he doesn't want to talk about it until he gets the discharge paperwork (they are sending it out) but he does agree with my theory of it being behavoural as apposed to what the pediatrician thinks - reflux (but I am open to any suggestions and open to try anything that may help, it just needs to happen now, she cant afford to loss weight) It may be something rare or it my simply be the autism in her.

I just don't know, and i don't know how long I can keep doing it, I don't ask for there help very often but now I am reaching out for medical support and they don't seam to want to do anything about it.