He is 94. Sleeps most of the day, eats a fraction of what he used to eat, but still insists on going with me on outings even though he finds them confusing and tiring. I’m willing to take each day as it comes, but wondering when it’s time to ask for additional help.
Palliative Care can help. Palliative care is specialized medical care focused on relieving the symptoms and stress of a serious illness. It is appropriate at any age and at any stage, and you can have it along with curative treatment. The goal is to improve your quality of life.
In the meantime, if you're needing help with bathing(as that is all hospice pretty much does as far as hands on care, along with a nurse coming once a week to start to check your vitals,)then you will have to hire aides to come assist you.
I wish you well in finding joy in the time you have left here on this earth.
No one knows when someone will pass, so people are on hospice for varying lengths of time. If a patient continues to decline they can stay on hospice; if the patient improves, hospice is discontinued. While there can be exceptions, hospice means no more trips to the hospital...your care is managed at home.
She also has stage 3-4 kidney disease, and has dementia.
It was in the hospital that a hospice dr came in to tell her that she qualifies for hospice.
So I called hospice to get her set up.
A hospice nurse came to her house to evaluate her, and while there, she noticed that my dad would qualify also for hospice, because of his dementia.
I was told that dementia is considered a terminal illness.
My dad was on hospice for four months (sadly he passed earlier this month). My mom is still on it. She will be reevaluated at the end of October.
In my experience, it does sound like it's time for you to ask for additional help.
I called hospice when Mom became bedbound, eating very little and did not speak. She was in hospice for 18 months.
If his condition improves, then Hospice may terminate their services, but can re-evaluate again at a later time.
I recently did this for my husband. It provides more services for him and more help for me. He seems to be pretty stable for now, but I'm going to accept the extra help from Hospice for as long as they will provide it.
Wishing you and your loved ones well.
Hospice mostly benefits those who already need help with toileting or bathing. Chux, Depends, diapers, lotions, powders are all free. Bath aides come 2-3 times a week for free. If he’s still independent and not in pain, I wonder what hospice might do for him.
Hire a caregiver occasionally if you need a break....and you will need a break.
Respite care was available that hospice pays for.
Our mother was in hospice 4 years. The first months, we didn't think she had months to live. Our family gave 24 hour care and it was her strong will to live, our incredible family and the hospice care that kept her with us. She was reevaluated every 90 days.
Our mom recently passed at 97 and the support of the hospice staff has been a blessing.
Wishing you the best!
1- I thought “perking up” was a thing the dying did just before death
2- My brother was discharged from the hospital with a promise that needed (vital) medical equipment would be delivered and was actually enroute.
It never arrived ( machine for breathing treatments for COPD).
We were able to get the medicine for the machine the next day, but it took weeks and another doctor to get the machine needed to actually do the treatments.
He was not yet on hospice, but it scares me to think of them yanking necessary equipment and me( or anyone) having to do the kind of running around , fighting for needed supplies and maybe having to find a doctor and get the LO ( apparently the lady had been on hospice for some time) to the office somehow, in order to suddenly spend large sums of money to replace needed supplies like with my late brother).
Maybe I am missing something?
We have people coming on here crying that Hospice hastened a LOs death. And what they complain about is part of the process. Your nurse should be available 24/7 by phone. She orders any equipment needed, meds and Depends, wipes ect. If you don't care for a certain nurse or aide, you can call the agency and ask for replacements. If you don't like the Hospice, you can fire them and hire another. And remember, they are coming into your home. We had a OP complain about a Nurse who seemed to take over. They are there to guide you thru. If you feel they are overstepping you have a right to complain.
My Dad had hospice in the home. They were good to him and Mom. His last day was Thanksgiving and his family was there. He could not talk but he ate his dinner and watched Football with my brothers. Sometime during the night he passed. Mom called the Nurse about 8am. She was there finishing up what she needed to when .I got there and then called the funeral home who was out in no time, but then they were just down the street. Equipment was picked up the next day.
Explains a lot of changes in the last months of life.
Let me know if you cannot find I will post few important points.
My opinion is that the sooner you call in Hospice the better.
The improved attention, the improved care from the Nurse, the CNA and the rest of the Team is immeasurable.
After my Husband broke his hip I happened to be passing by a Hospice and I stopped in to ask questions. I spoke with a Nurse, she asked me who my Husbands doctor was, she had me fill out some papers while she made a few phone calls. She came back and said after talking to his doctor he was approved for Hospice. He died almost 3 years later all the while on Hospice.
So...yes the standard is 6 months or fewer BUT as long as there is a documented decline that meets Medicare standards a person can be recertified and remain on Hospice.
So
Make the call to Hospice. If your LO does not meet the criteria for Hospice Palliative Care is an option and in many cases the Palliative Care Team will let you know when Hospice criteria has been met and the transition to Hospice would be easy.
The caregivers, and the patient if they are still aware enough, have to understand that they are accepting comfort care in place of curative care.
https://www.nia.nih.gov/health/hospice-and-palliative-care/frequently-asked-questions-about-hospice-care