Hi everyone. I’m joining #WeekendCoffeeShare again. I apologize for not having commented on anyone else’s posts last week. As I write this, it’s 5:15PM, so I’ve just had dinner. I won’t have my next cup of coffee until 7PM, but at least I’m not writing that it’s too late at night for coffee for me. Let’s have a drink and let’s chat.
If we were having coffee, first I’d talk about the weather. It’s quite chilly, though most days the daytime high is still above normal. Most days, it’s been around 10°C, but yesterday the temperature didn’t climb above 6°C. We haven’t had more than a slight drizzle of rain.
If we were having coffee, I’d share that I’ve been doing okay in the health and wellness department. I walked everyday, though not as far as I’d have liked. I also downloaded the FitOn app onto my iPhone and did a workout on it yesterday. My eating has been okay and I lost half a kilogram over the past week. Sleep has been all over the place though.
If we were having coffee, next I’d share that this week has been tough. You might remember that I shared several months ago about the improvements to my care that would take effect in mid-October. Some did happen indeed, while others didn’t and the end result is that my quality of life isn’t improving.
Part of the problem is the fact that half the team rigidly shove the new rules down my throat and the rest do as they please regardless of what my new day schedule says. For example, in my new day schedule, there are now shift codes assigned to times my staff are with me, so that it’s hopefully clearer for everyone who will be supporting me. Some staff have been rigidly following the rules, while others changed things up, sometimes at the last moment. Most staff also don’t tell me who has which shift a day in advance, yet when I am supported by a staff one day who rigidly follows the rules, they’ll tell me that so-and-so will be supporting me half an hour in advance and not care that I didn’t know the day before because their coworker didn’t tell me. And they’re unwilling to change things up because the day schedule says they can’t. This means I’ve had to deal with new-to-me temp workers three times this week and, at least once, I wasn’t told the day before that they’d be supporting me. This led to me having an outburst and telling my staff that I didn’t want the temp worker. I wasn’t demanding someone else, for clarity’s sake, but the temp worker refused to leave me alone too, despite the fact that I’m not under involuntary care.
There were other things discussed at the meeting that these rules were decided at, but I don’t see these being implemented at all. For this reason, my trust in my support coordinator and behavior specialist has suffered again.
If we were having coffee, finally I’d share that I had a phone appt with an independent client supporter on Tuesday. This appt had been on the calendar for months and I originally intended to say it’s all fine here and to close my file at her agency. That’s not how it went: I was honest that, while I do see my staff have good intentions, it’s still proving hard to figure out the care I need and to make it work with the way the home works. She recommended involving the Center for Consultation and Expertise (CCE) again. This is an organization that helps care agencies and clients when they’re stuck.
I have mixed feelings about this. On the one hand, I am hopeful that an external organization can shed new light onto the situation or, if not, I’m able to accept that my home are doing all they can. On the other hand, I feel slightly guilty for not being able to suck it up when things seemed so positive at the meeting. Hope is the dominant feeling though.
If we were having a cuppa I would share that after six good nights of sleep I had a really bad one, I would share that thankfully the following night that being last night I slept straight through. I would also share that I get up to find a message from daughter number 3 telling me her toilet is blocked, over flowing and leaking and could I please ring and lodge a maintenance request, which I did I would add she is 35 and at times useless. Lastly I would share that I hope you have a good day and generally feel loved and appreciated.
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Thanks for stopping by. I’m sorry your daughter’s toilet is blocked and that she cannot call for help herself. If I remember correctly, she has an intellectual disability though and I, even though I’m of above-average intelligence, wouldn’t be able to solve this problem either. It doesn’t make it any easier on you, of course.
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It is her sister who has the disability and oddly enough it is that sister who often makes the phone calls for Jess
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Ah okay, thanks for clarifying.
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It is very frustrating for you to be the last person to know day to day what you will be doing or if things have changed.
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True. Well actually, my day schedule isn’t structured at all, it’s up to me to decide what I’ll do. This is quite hard for me, being that I’m autistic.
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Glad you still have hope, and that it is the dominant feeling, glad too that your doing pretty well in the health department. X
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Thanks so much for your kind words.
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Glad to read that you’re doing OK in the health and wellness department. I hope you have a nice weekend and a great week ahead. Thank you for your weekend coffee share.
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Thanks so much for stopping by. I’m glad I’m doing okay health-wise too.
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If we were having a cuppa, I’d tell you how sorry I am that your caregivers do not respect your needs.
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Thanks. That being said, like I’ve said a few times before, they have good intentions but lack the knowledge and skills to truly support me.
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Hope is very important to hang onto. Glad it is the dominant feeling. Sorry the staff isn’t being consistent, hopefully the CCE can help you out, if you decide to involve them. Thanks for the coffee, stay warm and have a great week!
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Thanks for your kind words. Unfortunately, the decision to involve CCE or not isn’t mine to make.
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You’re welcome.
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Hopefully things clear up and you can really get the care you need without always having to worry about it. That would be hard. My sleep is often all over the place.
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Thanks for your kind comment. I really hope we’ll figure out a way to help me either get better care or accept that I can’t.
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