The PT report
Apr. 23rd, 2025 07:41 am![[personal profile]](https://www.dreamwidth.org/img/silk/identity/user.png)
We got Dana settled at the new place. It is located in part of a smallish hospital. I've been a patient there (hip number one) but she has never so they were creating an entire medical record for her. This is a med system different from the one we normally use. Our usual one does not have a local in patient rehab facility. And, of course, there is no sharing of records. If congress were going to do something useful that would be it. Mandate that med groups share med histories with each other. Everything we do with this one will disappear (or would without me) from record when we return to our normal system. If there were only somewhere in the world with oh, I don't know, a National Health System. Why doesn't someone invent that?
Anyway, back to reality. She got there OK in a transport and I met her there an hour or so later. This place is MUCH closer and easier to get to so I don't mind shuttling back and forth. They don't allow visitors until 3PM so there is no inteference with PT. That is a good idea, I think.
I managed to break into her record at the new place and have their app installed so I can track what is going on. Communication is the last thing that health systems worry about. Especially communication with the caregiver. I went to the web site to see if I could find a contact, a case worker kind of thing, but there is no phone number at all on the entire system's web site. Zero. They do not give a way to contact them. Amazing.
What I did find, buried in her online record was:
So early next week. I'm thinking I need to get the bed problem solved, a fait accompli, before she comes home.
I'm going to try to take Toby to see her today when we visit. She should be able to roll out in a chair and meet him. He has been really sad to be without her and she would get a huge mental boost from having him in her lap for a bit.
I was scheduled for pickleball this morning and we got rained out. I just signed up for a 10:30 group. I really need to get outside and run around and have a couple of hours not thinking about anything. And I can stop by the Mattress place on my way back.
This morning was bordering on depression. It is a strange feeling to be in the house by myself (ok, me, Toby and Zoe) for any more than a couple of days. I'm fairly sure that I'd adjust over time but for the moment I've lost the anchor. And I've got four days of meals for two staring me in the face. The food box came yesterday. On the bright side it means I won't live on cereal like I normally would do. But I've got to cook it all up and freeze the portions so it doesn't go to waste. And decide whether to cancel the one coming next week or roll the dice that Dana will be back.
And the weird thing about all of this is the cost of the in hospital to us will be zero. I can't imagine going through this and having to have all the debt involved. It would be crushing.
Anyway, back to reality. She got there OK in a transport and I met her there an hour or so later. This place is MUCH closer and easier to get to so I don't mind shuttling back and forth. They don't allow visitors until 3PM so there is no inteference with PT. That is a good idea, I think.
I managed to break into her record at the new place and have their app installed so I can track what is going on. Communication is the last thing that health systems worry about. Especially communication with the caregiver. I went to the web site to see if I could find a contact, a case worker kind of thing, but there is no phone number at all on the entire system's web site. Zero. They do not give a way to contact them. Amazing.
What I did find, buried in her online record was:
DC Plan: Return home with spouse. Patient is Ind at baseline, now with ongoing gait deficits r/t periprosthetic hip fracture. Patient will benefit from an intense rehab program with physician oversight, 24 hr rehab nursing, pain and medication management, precaution education, as well as a comprehensive inpatient therapy program including three hours of skilled therapy intervention 5/7 days in order to return to prior setting safely at a reduced risk for medical complication, falls, and hospital readmissions.
She is willing and able to participate in 3 hours therapy/day, 5 days/week and is expected to make sustainable, functional gains.
So early next week. I'm thinking I need to get the bed problem solved, a fait accompli, before she comes home.
I'm going to try to take Toby to see her today when we visit. She should be able to roll out in a chair and meet him. He has been really sad to be without her and she would get a huge mental boost from having him in her lap for a bit.
I was scheduled for pickleball this morning and we got rained out. I just signed up for a 10:30 group. I really need to get outside and run around and have a couple of hours not thinking about anything. And I can stop by the Mattress place on my way back.
This morning was bordering on depression. It is a strange feeling to be in the house by myself (ok, me, Toby and Zoe) for any more than a couple of days. I'm fairly sure that I'd adjust over time but for the moment I've lost the anchor. And I've got four days of meals for two staring me in the face. The food box came yesterday. On the bright side it means I won't live on cereal like I normally would do. But I've got to cook it all up and freeze the portions so it doesn't go to waste. And decide whether to cancel the one coming next week or roll the dice that Dana will be back.
And the weird thing about all of this is the cost of the in hospital to us will be zero. I can't imagine going through this and having to have all the debt involved. It would be crushing.