Lockdown Favourites – Week 7

Hello again! I hope you’re continuing to keep safe and well – and also staying alert, as is the new watchword here in England.

As I see it, the current small changes to our lockdown, as part of the government’s long term recovery plan, are basically urging people to use their common sense, as the virus is still circulating. We must continue to stay at home and work from home if at all possible, avoid other people’s homes, wash our hands and disinfect surfaces often, and stay 2 metres away from everyone. But provided those rules are adhered to, we have a bit more freedom – people in selected industries can go back to work, we can use outdoor spaces like parks more freely, we can walk or cycle or drive further to exercise, and face coverings are advised if social distancing isn’t possible (to protect others in case you’re asymptomatic).

So I hope people will continue to be careful and sensible, as we’re nowhere near out of the woods yet. And obviously for disabled people things are more complicated – it’s impossible to socially distance if you can’t see, for example, so you have to rely on others around you to stay away. Lucy Edwards has chatted with a couple of her fellow blind activists in a recent video about the new rules, if you want to hear their reactions to the new rules.

As for me though, my mother and I are still doing fine, touch wood. Last week I went out for the first time in over 5 weeks, as a couple of essential items were missing from our online shopping delivery. So I was very pleased to find that there were hardly any people and very few cars about, and that I was able to use the priority hour for disabled people at the supermarket, which was fully stocked and had social distancing measures very well enforced. So my risk of exposure was hopefully minimal.

But otherwise I’m still staying at home for the safety of my mother as well as myself, and I’ve continued to keep myself entertained in various ways. So let’s crack on with this week’s post and video to update you on my latest discoveries. As usual nothing is sponsored and all opinions are my own. So I hope you enjoy!

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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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Journal – Christmas 2016 (Moving To London)

Finally, after nearly 120 journal posts – and thank you so much for reading if you’ve gone through some or all of them – my mother and I have now moved away from Devon into my Nan’s house in London, which we inherited when she passed away.

So in this post you’ll find out how we’ve settled in over the festive period, sorting through various bits and pieces, having problems with BT, going shopping and taking some nice walks. I also got to see my best mate and his wife who were visiting the city, signed up for some social events in January, watched a lot of TV, and was shocked to hear about the deaths of 3 very popular entertainers.

Going forward, I’ll be sharing my (hopefully many) adventures in London in a monthly roundup format, as I’ll explain at the end. But for now, I hope you enjoy this bumper post about my long-awaited arrival in the capital!

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Journal – January 2016 (Guernsey Holiday)

So here we go with another year – hopefully my final one in Devon, as we feel determined to make the move to London happen now after all the delays.

But to start with, 2016 has got off to a fun start, because I’ve visited my best mate in Guernsey again, the first time I’ve seen him since I was Best Man at his wedding last September. These are my first journal entries since that event, as there was nothing else of interest to write about for the last few months of 2015.

So I hope you enjoy reading about my little holiday – including an awkward bus trip, the latest Star Wars film and a games night, among other things – plus a few other updates.

Continue reading “Journal – January 2016 (Guernsey Holiday)”
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