First, the cuteness!
Here we have David the Magnificent, formally known as F****d Up Dave, due to the eye problems he had that led to him being brought indoors. He is snuggling with Ghosty, curled up in his belly and using Mitsy. At least I think that’s Mitsy. Mitsy is using Clarence as a pillow.
Partially visible behind David is Tiny, The Beast, next to a small carboard box that is a favourite bed for many of the cats. Beside David’s head you can see part of Peanut Butter Cup.
What a bunch!
I didn’t get any pictures of the outside cats this morning. I headed out earlier than usual – it was just starting to get light – to tend to the outside cats and do my morning rounds. Once those were done, I messaged with my SIL, then headed out to my mother’s town to meet her. We were early enough that when we drove to the pharmacy, we had to wait a few minutes for the doors to open.
I was afraid I would be too early, but my mother’s updated bubble packs were ready and waiting. Once we saw the packs, we knew without a doubt that they would never fit into the lock box! Especially not 4 week’s worth.
From there, we head to the the hospital in the town nearer to our place. When we got there, we found my mother was all dressed and ready. We gathered up her stuff, including a lovely orchid and succulent pairing she got as a gift. My SIL took everything to her car and was going to move it closer to the doors, while I went to the nurse’s desk.
One of the staff came back to my mother’s room with me and we went over the paperwork. One page was ensuring that my mother’s stuff was accounted for, including that I’d already taken her old bubble packs, earlier. We went over her prescriptions list that was faxed to the pharmacy, with special attention to the new or changed medications. There were notes about my mother needing to have monthly follow ups with her doctor to monitor her kidney function, now that she’s back on water pills, and with the person in home care to keep in touch, in regards to supportive living.
This was all stuff for us to keep. Normally, it would go to my mother’s but she isn’t able to read or understand most of it. I took them home with me, and made sure to get photos of each page to send to my brother, just like I got a photo of the medication list in my mother’s bubble packs and sent it to him, after we picked them up. This way, we will all have at least digital copies of everything.
Once going over the paperwork was done, it was time to head out. We took it slow, and my mother had to stop to rest a few times. When we got to the lobby near the doors and gift shop, she stopped to rest longer in one of the comfortable arm chairs.
My mother says she is feeling a lot better now, which tells me she was feeling really bad the day she went into emergency! The last time I saw her, after doing some grocery shopping for her, she was not having as hard a time as she was, just today, after 2 weeks of hospital care!
She did have an easier time getting into the car than when I last drove her somewhere, while using my brother and SIL’s other car. She needed a stool to get in, that time. I’d brought it along today, just in case, but she was able to manage without it.
From there, it was straight to her apartment. The spot I usually park at, by a sidewalk to a door closer to her apartment, was blocked by a fire inspection vehicle, so we had to stop at the loading zone near the main doors. I had found a notification under her door during one of the times I checked on her place, about the annual fire and safety inspection. The date range was from the 6th and the 10th, but I had no way of knowing if they’d done her building yet. Seeing the truck, it seemed we got my mother home, just in time to miss it!
I went with my mother into the building while my SIL moved the car out of the loading zone, so she could bring everything in after parking. Some of my mother’s neighbours were in the common room, and they were quite happy to see my mother coming home. My mother also got introduced to the new building manager. After confirming which apartment was hers, he said they had just finished doing the inspection there. I don’t think she quite heard him, though, which is good, because she would have gotten quite angry. She is still convinced the exterminator guy stole a jar of change and dug through her boxes of papers to steal 80 year old passports. She now thinks anyone that goes into her apartment – whether it’s the exterminator, or safety inspectors, or any other official entrance – is there to go through her stuff and steal things.
After a brief conversation, we continued to her apartment, and my SIL caught up to us soon after.
Once my mother was settled comfortably into her chair, we went through some stuff with her. She wondered what the lock box was and we explained it, but my SIL took it with her. They should be able to return it. The new, larger one will arrive in a couple of days. So my mother’s medications will not be locked up until then. They’ve been left in the pharmacy bag and my mother is under strict instructions to leave them, and only home care can touch them.
Oh! I almost forgot.
While I was walking around the yard, doing my rounds this morning, I got a phone call. (It seems my “new” phone is much, much better and getting phone signals than my old phone!)
It was home care, letting me know that they did not have someone available for my mother’s morning medical assist today.
…
I said, that’s good, because she’s still in the hospital.
I did confirm that she would be getting her usual visits for her evening and before bed pills.
While it worked out today, I’m rather displeased. This was her first day back on home care visits, and they were already calling me about not having anyone to do a it! Her morning assist now included getting dressed and emptying her commode, too, not just her med assist.
This is a real potential problem. I live the closest, but it still takes me about a half hour to get to my mother’s, if I am able to leave right away. If we have a situation like a few weeks back, where all home care is cancelled because of a storm, it would be too dangerous for me to do the drive. Since my mother’s medications will now have to be in a lock box, she can’t even take them herself (which she shouldn’t be, due to her habit of messing with her prescriptions). It’s not like we live in the same town and I’m just blocks away!
My SIL and I were talking about this while waiting for the pharmacy to open, and agree that this could become a real issue. They’ve called me quite a few times since she’s been on med assist, letting me know that no one could make it.
We’ll do the best we can to manage things, but it’s just one more thing to stress how badly we need to get my mother into supportive living!
I went through the cupboards and fridge to show her what what my brother and SIL had picked up for her, and where they were. She asked about Meals on Wheels, as they would normally come on Mondays. I told her they would not be coming today, as I didn’t know what time we’d be getting her home, so I would be calling them later to get it started for Wednesday.
My mother told us she hadn’t had her lunch yet (which we knew, since discharge time is an hour before lunches are served at the hospital), and we assured her, we would take care of that.
Once we got everything worked out and organized, my SIL gathered up the lock box and I went out with her to her car, transferring stuff to my own vehicle that I would be taking home, before we said our good byes.
That done, I went back inside and made a lunch for my mother. Once that was ready and she was starting to eat, I said my good byes and headed home. I had lots of phone calls to make!
The home care coordinator is now aware of the situation with the lock box. I’d already called her this morning to give them the combination. The new one will have the same combination.
I had to call the clinic at the hospital near my mother’s place. She was wanting to change doctors to the local clinic, and seemed to think that the nurse practitioner that saw her was now her primary caregiver.
He isn’t.
In fact, while talking to the receptionist, she told me there’s even a note saying that he can’t see her as a patient, because she already has a family doctor.
The one my mother doesn’t want to see, because she’s female, black and has a strong accent.
So I had to call the clinic in the town that’s about half way between my mother’s town and the city. I explained things to the receptionist there a bit, and suggested a telephone appointment with my mother’s doctor might be more efficient. She agreed. I now have a phone appointment for this Friday. Her doctor should have all the files, notes and test results sent to her by now, but she wouldn’t have any reason to look at them, yet.
The receptionist I spoke to also does home care, privately, so when I mentioned my concerns about getting my mother to monthly appointments, and that I wasn’t happy she was sent home from the hospital, she totally understood. There are so few supportive living places, and they all have long waiting lists.
While I was at it, I asked about getting my own files transferred. I had the same doctor as my mother, as an interim doctor, after our regular doctor moved to another clinic. Now that the doctor my daughter is seeing has accepted me as a new patient, I have to get my files transferred.
I can show up at the clinic at any time they’re open, with $35 cash or check. They’ll print out my files, and I would deliver them to my new doctor’s clinic myself.
This province’s system is so antiquated.
Once I was done with that call, I called my new doctor’s clinic. I need to talk to her about my prescription pain killers. After explaining things to the receptionist, she was able to book me in right after my daughter’s appointment, next week. The appointments are in the afternoon, so if we leave early, we can go to my old clinic, get my files, then take them to the new clinic before our appointments.
After I was done all the phone calls, I updated my siblings, and then called my mother to update her. I had to explain about her doctor situation. She wasn’t happy. In her mind, the doctor that is at the clinic in the hospital next to her place should take her as a patient, just because she wants him to – even though she claims that “everyone” doesn’t like this doctor. They should get rid of that doctor and get a new one. She doesn’t understand that there’s only so many patients a doctor can take on, and that if they got rid of this one, a new doctor would just be taking on the other doctor’s patients, not taking in new ones. That clinic needs more doctors, and there just aren’t any. All the rural clinics need more doctors, but even among the doctors we have, few want to live and work in the boonies.
What I’m hoping is that, since my mother needs to have bloodwork done to monitor her kidney function every month, her doctor can send her a requisition and my mother can get it done in the lab, locally. She’d still need to make the trip to see the doctor in person, but hopefully not every month!
Hopefully, this won’t be for very long, and a space for supportive living will be found. We’ve already stressed with my mother to take any space that comes up, even if it’s in one of the towns she doesn’t want to live in. She just needs to get into the system as soon as possible. Once she’s in, it will be easier to get her transferred to where she would prefer – though where she would prefer is long term care, not supportive living!
It’s not very often they have someone who actually wants to be in a nursing home!
Well, it is what it is.
For now, my mother is home. We just need to go from there!
The Re-Farmer
The Re-Farmer 