
, Ember. I know this is tough for you.
My FIL is dying of pancreatic cancer, and DH is basically his primary caregiver, although his sisters come as often as they can. FIL is still living at home, which presents different challenges. As much as he wants to live at home, he is very very lonely and very very afraid of dying, so much that he sometimes refuses to go to sleep for fear he won't wake up.
DH went with FIL to his doctor's appointment yesterday and the doctor and the palliative care team are going to do some things to help him. They are making the arrangements for everything, which is a godsend since DH and I both work full time. Here is the latest plan:
They are giving him a small dose of an anti-depressant. He has been exhibiting signs of depression, which really throw him off with everything else. He is very clingy and weepy, and has no energy.
They instructed him to take his anti-anxiety meds to help calm him down before bedtime instead of his pain medication. That should help him be more alert, less sleepy all the time, and more able to function on a daily basis.
They are making arrangements for a Visiting Nurse to come by periodically (she called this morning and will make her first visit today). She can help him with his personal needs and help him get his meds straightened out. I think she can also reassure him that he is o.k. medically for the moment. I hope he can also ask her questions that he might not be comfortable asking the doctor in front of DH.
They are making arrangements for Meals on Wheels to deliver to him. I think that it will make sure he is eating well, and give him something to look forward to when they come.
There are so many services available through palliative care and it is their goal to help. So take advantage of it.
Here are a couple more hugs, you need them.

Denae