Hospice while in MC
Before I ask the people here at MC, can anyone comment on the benefits of having hospice while your LO is in MC? I’m not sure yet if he’ll qualify but wondering if it’s worth trying. He’s in late Stage 6. I don’t know how it works between hospice and the current staff nurses and caregivers. Just looking for some comments before pursuing it.
Comments
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I have not walked this path yet, but last winter when my LO in MC was very ill, I asked the MC director of nursing to tell me about hospice. That facility works regularly with a couple of different hospice organizations. The MC director spoke well of “having more eyes” on the resident. Hospice would mean regular visits from hospice staff as well as access to chaplains, additional nurses, etc. I had the impression that they are all used to working together.
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It was a benefit for my wife and my mother. Further, it was covered by Medicare and cost me nothing. I am even receiving chaplain services for a year after my wife's death, so it helps me too.
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My DW is in an MCF and has now been on hospice for over two years. She is very, very near the bitter end, Stage 7f, of this awful disease. The primary benefit has been additional nursing oversight and the hospice doctor who is very familiar with dementia patients. They provide aides with useful expertise in bathing and feeding. Hospice also provides incontinence supplies and some end-of-life medications. They also provide additional services, like a music therapist, and a social worker, which is nice but not essential to her care. All at no cost if they are on Medicare.
But of course hospice also means that you agree that your LO will generally not be provided with restorative medical care, just palliative care for medical conditions that could lead to your LO’s passing. This is the only real downside, but only if you’re not ready to forgo “saving” them in case they have a life threatening issue. But of course you can just take them off hospice in that case if you want.
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My mom and step-dad both had hospice while in an AL. Doing so gave them more 1 on 1 care, a visiting nurse dedicated to them during the visit, shower help, incontinence supplies, a hospital bed, meals in their apartment rather than the dining hall, and so forth. I got lots of support from the visiting nurse too. It also allowed them to stay in their AL apartment until their death rather than be sent to a higher care facility.
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We were helped tremendously with extra visits and attention while my mom was in MC. I encourage you to have him assessed.
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This was my experience too. If I had to do it all over again, I would have had my sister evaluated sooner - I'm pretty sure she would have been accepted as she was in the first stages of stage 7 when she passed away. Peggy was too young for everything to be covered by medicare (she was 64 when she passed away), but her regular health plan covered hospice, which was a relief.
I found that hospice wanted to know about Peggy, her likes, her dislikes, her interests, etc. Being a musician, the music therapist was very helpful to her. I had told the therapist that Peggy had been in a college production of Paint Your Wagon, so the next time he came by, he came with Paint Your Wagon show tunes. Peggy perked right up. it was really nice to see.
The one-on-one care Peggy received from hospice was also nice - and they kept me informed. I really appreciated that. And like Quilting said, hospice came with incontinence supplies, a better hospital bed, a better wheelchair - seriously, I could have cried when I saw everything they came with. And, Peggy was able to stay in memory care rather than have to move to a snf. That was huge.
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I was advised by many on this forum to get hospice involved when my husband was late Stage 6. I was in denial and thought I could do it later. I was wrong. He progressed rapidly and one weekend he aspirated. Although the MC facility implemented hospice protocols, it would have been better for me if he was with hospice when he passed. Don’t wait. They offer so much. 💜
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Thank you all for your responses and for sharing your experiences. I will certainly look into it.
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Hospice was a wonderful extra layer of services in mom's memory care facility. They worked with the facility staff to care for her. Facilities are used to it, happens all the time. It meant more visits for mom, more eyes on her, more supplies and equipment and the whole thing was designed to make her more comfortable. They sent a chaplain and music therapist. Her hospice nurse was wonderful and had more time that the facility nurse to really guide me and answer questions. Once you are ready to forego trips to the emergency room and extreme interventions and just focus on the quality of their remaining days, there is no downside to hospice in my experience. It doesn't hurt to have your loved one evaluated. They have their metrics, and if he doesn't quite qualify now they will track him and check back every few weeks to re-assess. Not all hospices are the same, they all spend their resources a little differently so you can shop around and find one you like.
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Commonly Used Abbreviations
DH = Dear Husband
DW= Dear Wife, Darling Wife
LO = Loved One
ES = Early Stage
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FTD = Frontotemporal Dementia
VD = Vascular Dementia
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AL = Assisted Living
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