[Warning for family: This post is about Nana’s hospice care. You may prefer not to read it.]
I got an unexpected call this week from my mom’s (Nana here at TJCM) hospice social worker. She wanted to set up a family meeting with her and the hospice nurse. It was a bit unusual to have a formal meeting time set up, but we agreed to meet in my mom’s room at Mercy House, the hospice residence where she moved in May. We were fortunate that my older sister was here visiting, so she was able to join in, too.
What I hadn’t suspected was that the meeting was about re-certification issues. In most hospices, acceptance means that life expectancy is six months or less. With some diagnoses, that determination is relatively clear, but, with heart failure, as my mom shows, it isn’t so clear.
Nana was re-certified at three months, at six months, and then every two months since. We are now at fourteen months. There have been lots of ups and downs, but, sadly but not unexpectedly, the overall direction has been one of decline with continuing weakness and fatigue that has worsened significantly over the course of this year.
Therefore, we were shocked that the social worker told us that the medical director was considering de-certifying Nana. I guess I shouldn’t have been shocked, as there had been a couple of other times that the medical director has questioned re-certification, but it seemed so clear that symptoms were worsening that I never thought there was a possibility that he would think Nana didn’t meet the criteria to remain in hospice care.
As I understand it, there are two basic issues. One is that the medical director only has access to data points collected during visits from the hospice personnel, perhaps two or three hours a week and always during the day. Second, the criteria to stay under hospice care have to do with rate of decline, so, even though Nana would easily qualify to enter hospice care in her current condition, it doesn’t necessarily follow that she would be re-certified to remain under hospice.
So, on hearing the news from the social worker, I freaked out a bit. Well, not outwardly. But losing hospice care at this point would be very complicated. In order to be in residence at Mercy House, one has to be under hospice care, so de-certification would have meant having to move Nana, which would be complicated and exhausting. We had a preliminary plan in place, but we hoped not to have to implement it.
What we could do was give the social worker more information of what we were seeing when we were there visiting, which covers about nine hours most days. Nana was also able to give us some more information about night-time issues.
The social worker took the additional information we were able to provide and the medical director was able to see how it fulfilled the criteria for Nana to be re-certified. We were very relieved. From now on, though, I will be more deliberate about noting changes in case we need to fill in the blanks again.
Through it all, we are grateful for the care hospice has been able to provide. If it were not for their expertise in managing symptoms, it is likely that we would already have lost Nana. As it is, we continue to have the hope of more time with her.
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Linda’s prompt for Stream of Consciousness Saturday this week is “call.” Join us! Find out how here: https://lindaghill.com/2018/08/03/the-friday-reminder-and-prompt-for-socs-august-4-18/
I’m sorry you had to go through that stress. It reminds me of when I worked in addictions care and we had to document and regularly re-certify the severity of each individual to justify the use of state funds at different levels. It took more and more of my time over the years. Very frustrating. I’m glad Nana’s care is still good and that administration agreed. Good job, Joanne! I hope you’re taking care of you, too. ❤
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Thanks for your thoughts, JoAnna. I am trying to be more deliberate about self-care, but circumstances have made things more difficult lately.
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Sending angel hugs.
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❤
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Hospice is such a complicated medical “space” to occupy. I’m so sorry for the intense anxiety and so grateful with you for the outcome that feels right and good. 💜
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Thanks, Pat. I realize that most hospice patients never need re-certification, as, even after all these years, the average length of time under hospice care is only eleven days. It’s unfortunate, given that the philosophy and services are beneficial for the patient and family over a much longer period. Sometimes, when someone is de-certified, it is because their condition and life expectancy have improved; if that had happened with my mom, we would have been grateful to be able to take her back to GSV, but, sadly, that isn’t where we are.
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How very unsettling. I am so glad you were able to communicate with them and establish her condition. It sounds like she’s been getting excellent care, which is so important.
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Thanks, Ellen. Part of the irony is that, without hospice care, I’m sure we would have lost her months ago. When she entered hospice, there was still fluid in her lungs from pneumonia months before. Because hospice knew what to do to relieve her cough, she was able to do some respiratory therapy that cleared her lungs, which are still clear nine months later.
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