Tuesday we had a visit with the Neurologist. Doc confirmed my suspicion that mom has had a pretty significant decline in the last 6 months. She needs assistance with everything. She can feed herself, after she has been served, but I am beginning to notice the fork going into the glass of water more often! She has these random seizures (supposedly Mioclonic seizures) that seems to be happening everyday, several times. Although Doc says they do no damage to the brain, I think they are. In any case, I asked the doctor if he thought Hospice Care would be appropriate or even available for my mom, to my surprise he said he thought it would be the best course of action at this time.
So, if anyone has had experience with Hospice for Alzheimer's let me know. What should I look for and what questions should I ask? I live in South Florida and there are basically 3 Hospice organizations in our are; Vitas, Catholic Hospice and Hospice Care of South Florida. I anyone has any experience with any of these groups please enlighten me.......
A bit of history; My mom has lived with me the last 3 years. I am the primary caretaker with 4 brothers that I squeeze what I can out of them. She was my best friend. Presently I have a CNA that helps me approximately 25 hours a week but mom will not let anyone bathe her other than me. Bottom line, she is fading away relatively quietly. She is a healthy woman that only takes 1 pill, every so often for her seizures and that is it. She hates going to the doctor and will deny if she is not feeling well or has a any kind of pain (has alway done that) that is a big issue!!
Thanks in advance......bh