I will read as much as I can to understand what goes on now. But, if anyone has anything to add, I could use it. I do know we will have more services now. There are volunteers that will come twice a week if I need them. He will get a massage when he wants one now and then and they even said I could have one. He will no longer be going to ER or to his doctor. Lucky for us, our doctor is the head doctor for Hospice. He knows my Partner and it will be easier.
What did you find that was NEW about Hospice that helped your patent and yourself. I know one thing that will be new and that is diapers. He will be difficult to allow this. I also need to get some loose fitting sleeping clothes. It is SO difficult to dress him everyday.
For his pain, he will either have drops under his tongue or pills. He is having trouble swallowing and I THINK I was told this is part of Parkinson. What foods do you recommend I make? Any recipes???