My daughter was initially diagnosed with gastroparesis, this was 4 years ago. Unfortunately, due to the specific, gastrointestinal, affiliated consultants, Caitlin had been left with no means of being fed or helped. Caitlin has already lost too much of her young life to this illness and lack of support from these people. We, as a family have and had managed to assist Caitlin in attaining accurate diagnosis and nutritional support through the provate secyor, because we had no other options. Caitlin was granted a make a wish, ehich due to her failing health, has to be restricted to within the Uk. Caitlin would like to be able toblive a life where she is not receiving fluids via IV, for up to 8 hours a day. Further private sppointments are required which all come at a cost, due to blockages from these consultants. Many thanks for your understanding