Life in the Twilight Zone - Damn Rona

Firstly I just want to explain Rona, in case you are wondering that is. Rona stands for Corona Virus or Covid-19, shortened to Rona, cause I'm Aussie lol. Secondly, shout out to my cousin Robyn, I won't go into details, but she messaged me today, and it reminded me that I hadn't written for quite some time, and as it helps me feel better when I write, here goes. Fair warning, this probably won't contain as much humour as usual, in my 'Life in the Twilight Zone' missives, although it's rather presumptuous of me to think anyone actually laughs at my musings lol. 

We've all been living in isolation, socially distancing ourselves, some of us have been wearing face masks, and we've all been busy washing our hands (although one would like to think we do that normally anyway). There's been ads on TV about how to act and what we can do, one that comes to mind is a shot of a grandparent sitting in a chair outside a window reading to grandkids who are all sitting inside. Or people face timing family and friends, even just talking on the phone makes an appearance. But what we don't see is what do we do if it's not possible to sit outside a window, face time or call. Just to be clear, it's not impossible to face time or call, but I'll explain what I mean and why I added them. 

I work from home, which I'm sure I've said before, so am used to isolation. I like it, I hate when I have to go to the office, sitting on a couple of crowded trains for 2 hours each way, is not my idea of a fun time, and the city is dirty and loud. I can live without it, easily. In a normal week, I would go out twice, once to shop and once to visit Mum. Of course, there are times when I'm out more, visiting family or friends, but normally it's just the twice. Now it's once a week and I'm getting antsy. 

Mums nursing home has been in lock down for over a month. A staff member who worked there, tested positive for Rona, they say she wasn't working while sick, but just because she didn't feel sick, doesn't mean she wasn't. So into lock down they go, totally understandable and glad they did. They followed the guidelines from the Health Department, and ran tests on all. Luckily all tests have shown negative results. They've sent texts each day to ensure we know all is fine. And I love that, they are a great group of people and I'm so confident that they will do everything they can to keep all the residents safe. They've looked after Mum so well, since she's been there. 

Because Mum has Alzheimers she really has no idea what's going on, what day it is, and when she last saw anyone lol. So she would just be coasting along, in her own little world. I was told that I could face time her, or call anytime, which is great, but......... Even before Mum was diagnosed she was technologically challenged lol. She had bought herself a computer, and would call me to find out why it wouldn't turn on, she wouldn't have clicked the power button, or had unplugged from the wall. She'd forget her password constantly, and lose the paper it was written on lol. She had a pretty good flip phone, but decided she wanted a new one that had larger buttons. Okay, it's easier with the larger buttons. But, she'd have the phone in her bag, and bump it or something, and bam, she'd be calling me, with no idea she had actually made a call. It had a lock on it, to stop that from happening, but she never remembered how to do it (it was a switch, up or down, on the side, easy as lol). She had trouble operating remote controls too, and know this, all of this was way before her diagnosis, it was just her. Not everyone has to get it, so that's okay. 

I've called Mum at the home before, or she's had them call me, it doesn't go well. She will ask me when I'm coming to get her, or when is her Mum and Dad coming. It's like she thinks she doesn't live there, has just been there for a holiday or as if she's been in hospital. And of course her Mum and Dad have been dead for years so they aren't ever going to come lol. She always ends up in tears, or starts the conversation in tears, and is unsettled for days after wards, which doesn't do her any good. There's been times she's been so unsettled she has needed medication to calm her down and I don't want her to be constantly medicated. I figured since I was off work I could give face time a try, I wasn't overly confident but determined. To do this, I had to make an appointment, and she was sitting with a staff member in control of the tablet. It was great to see her, but so frustrating. She didn't get it, kept trying to touch the tablet, which of course might have hung up or minimised or something lol. She also didn't understand why I didn't just pop up for a visit rather than talking to her like this, 'was I sick?' lol. 

I got a text from the home today, they are going to Tier 3, which is you can visit, but have to make an appointment and it has to be office hours Mon - Fri. On top of that, you have to have proof that you've had a flu shot, and they do a temp check (temp check is fine). I haven't had a flu shot, ever, so not sure I want to have one. When they get to Tier 4 it will all be back to normal, I can visit whenever and no checks. I'm not complaining, I want them to ease into it, I want Mum and the others to be safe, it's just frustrating. 

Regardless of how often I tell myself she is fine, they'd tell me if there was a problem, it doesn't ease the worry, the anxiety and the guilt. Sure I shouldn't feel guilty, nothing I can do about Rona, I didn't have anything to do with it's spread. I don't need to worry or feel anxious as I know she's fine, but that doesn't stop me from doing either lol. Mum having Alzheimers has basically taken a grown, independent, capable and intelligent woman, and stripped her down to the basics. I know that despite my worrying, when it's all over and we can resume life after Rona, she probably won't even realise it's been ages since I've seen her, I could tell her I saw her the previous week, and she'd believe me lol. 

Life hasn't been the same for us, since Mum was diagnosed, It's been a roller coaster ride, and this is just another part of it. As the saying goes 'it is what it is'. There is nothing that can be done about it, life will go on and we will get back to normal, or as normal as our lives are. The best thing about the Alzheimers at the moment is the fact that Mum has no clue, I won't have to worry about trying to explain it to her, because she'll forget it in no time. The worst thing is that she forgets stuff all the time, will this go on so long that she'll forget me? 

Catch yas
Cathy