October 2020 Favourites

Here we go again. It’s time for Lockdown 2: Electric Avenue, so the cases don’t get higher. It’s not quite as severe as the first one, with education settings remaining open in particular, but there are still very tight restrictions nonetheless. And it had been inevitable for some time. The use of different ‘tiers’ to set regional rules was keeping the infection rate lower than it otherwise would have been, but it wasn’t quite doing enough to drive cases down. So we didn’t have a choice, sadly, as many other countries have found.

There are still lots of reasons to be optimistic, thanks to the ever-improving knowledge about the virus, the better treatments now available, the developments of mass testing, and the very promising results of vaccine trials. But right now we have to be vigilant to get through the winter safely, and it’s important to take care of ourselves and look after our mental health during this time.

I feel relatively calm about it thankfully, as I’m fortunate to have a steady job, priority grocery deliveries, family support, regular contact with friends, blogging projects, local walks, entertainment, etc to help pass the time. And we’ve pre-ordered our meat for Christmas from a farm we like, so that gives us peace of mind too. I still greatly miss seeing friends in person and visiting interesting places of course, nobody wants this. But right now my mother and I feel safe and comfortable, which is the important thing. We’re more prepared than the first time around, when the uncertainty and panic buying made it really difficult to begin with. So we know we can get through it, having done it once already.

But for many other people it’s going to be a lot harder, due to physical and mental health issues, loneliness, loss of employment and business, financial worries, family and domestic problems, the loss of loved ones from the virus or other causes, and so on. So please do help others if you can, either by direct support or by charitable donations, because every little bit helps. And do also sign the petition by Mind calling on the Government to invest in a Winter Mental Health Support Package.

And if you’re in a position where you’re struggling, then my thoughts are with you, and please know that you’re not alone. And don’t be afraid to seek help or support, there’s absolutely no shame in that. If you’re unable or too anxious to talk to someone you know, then there’s lots of advice and support available from the Samaritans, counsellors, mental health charities, other charities relevant to disabilities and health conditions, support groups on social media, etc. I know it’s easier said than done – I’ve had to confide in friends about difficult things in the past, most of us have to at some point in our lives. But having any kind of support network, even if it’s just one person you can reach out and talk to when you need it, is a massive lifeline. Use it.

And to my American friends, who are going through a stressful period with their election right now, we’re all thinking of you too. You’ve had enough to deal with in 2020 on top of the pandemic as it is, without this in the mix as well. At the time of publishing this post, the outcome is still not clear, but I sincerely hope that common sense and decency prevails in the end. Stay safe out there.

But anyway, with all that said and done, let’s get into my latest monthly update, which is what you came here for in the first place. In this post and video for October there’s plenty to mention as usual, including my latest appearance on national radio, my walks out and about, and the various bits of entertainment I’ve been enjoying. None of it’s sponsored or gifted as usual, and I hope you find it interesting!

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September 2018 Favourites

Time for another monthly update, and it’s fair to say that September was very busy and productive, as well as throwing up one or two surprises, which in turn are paving the way for a very interesting October. There is of course a video to go with this post, and I hope you enjoy this little catch-up as usual!

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June 2018 Favourites

Time for another monthly favourites post and video, this time looking back over June. It was a significant month on social media for a few reasons, plus I also got to see 2 theatre shows, went out to a few museums and did a few walking tours in the nice weather. So there’s plenty to mention.

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May 2018 Favourites

May was a lovely month. The weather’s been gorgeous lately, for the most part, and with no major events going on it’s been quite a relaxing few weeks .But there are still various bits and pieces I’ve enjoyed, and want to mention in this latest post and video update. So I hope you find this interesting.

To start with though, I just quickly want to plug a couple of upcoming events in June that will interest some of you. They’re for people all over the world to join in with, not just the UK. The more the merrier really, as it will help to spread vital awareness in both cases.

Sue Ricketts talking to a lady at the Nystagmus Network table ,with a tall poster next to it giving details of the charity.June 20th will be Nystagmus Awareness Day, which is its new permanent date, having moved from November. This year’s theme is Nystagmus In The Open, where people are being encouraged to do outdoor activities to raise funds and generate awareness. Sue, who runs the Nystagmus Network, is opening her garden for people to visit, for instance. People are also being invited to submit their stories online to show how amazing people with nystagmus are.

The Aniridia Day logo is a cartoon style image of the Earth, wearing sunglasses, smiling and giving a double thumbs up. Curving over the top, in yellow text with black outline, are the words “Aniridia Day”. Below the Earth in bold black text is 21 June, and below that the address for aniridiaday.org.June 21st will then be Aniridia Day. This is the second time it’s been held, as it was a big success last year. This year’s awareness campaign is called Aniridia Sight, where we want people with aniridia to share a photo or video of a scene, and describe how they see it through their eyes. So the more people that get involved, the more we can show how varied the vision of people with aniridia is. And then there will hopefully be live webinars too, for people to discuss aniridia related topics e.g. doctors, researchers, people with aniridia, etc. If you’d be interested in doing a webinar on the day, please fill out the form to sign up.

So now that’s out of the way, let me tell you what I’ve been up to in May.

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