Mom has Parkinsons and is not eating well. Shes very weak and needs max assistance to stand and transfer. I am thankful for all the services Hospice provides and I know Mom's condition will most likely not improve drastically, but want her to have the help so she be the best she can be. We had a great PT person working with her (paid by Medicare) but now that hospice is on board they are saying we cant use our therapist anymore and we have to use theirs. Is the only way we can use our PT person is if we private pay? Why won't hospice allow our PT agency to continue?