The Sunshine Blogger Award

I enjoy doing Q&A tag posts, whether they’re disability related or on other topics, as they’re a nice way to connect with other bloggers so we can get to know each other better, and it’s also lovely to be invited to participate in them.

And this time around, appropriately for summer, I’ve been very kindly nominated for the Sunshine Blogger Award. This award is given by bloggers to other bloggers, to recognise and celebrate the creativity, positivity and inspiration in their work. And the rules are simple:

  1. List the rules and display The Sunshine Blogger Award badge in your post.
  2. Thank the blogger who nominated you and link back to their blog.
  3. Answer the 10 questions that the person who nominated you asked you.
  4. Nominate up to 12 other bloggers to receive the award and ask them 10 new questions.

So to be nominated just once by anybody is a great honour. But over the last few weeks I’ve been nominated THREE times, which is extremely flattering! So thank you very much indeed to Holly (Life of a Blind Girl), Luke Sam Sowden & Carol (The Invisible Vision Project), it’s very generous of you all to nominate me! They’ve all asked completely different questions too, which is wonderful. So I hope you enjoy reading my answers to them all.

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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.

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.

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.

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

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September 2017 Favourites

Hello again, nice to have you back for my next roundup. It’s been my most significant and eventful month of the year so far, with my first ever public speech, a holiday overseas, a walking tour and a meal with a fellow blogger, audio described tours of an art exhibition and a few special buildings, a day trip to another town, and a music and drama workshop. So I hope you enjoy!

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Preparing For My First Public Talk

This weekend I was invited to attend the Nystagmus Network Open Day in Birmingham. Although I’ve been to things like Sight Village before, where I got to meet a handful of people with aniridia, I’ve never been to a large, dedicated conference for people with the same eye condition to network and find out information. So that in itself was going to be interesting.

But I wasn’t just a regular attendee – I was going to be one of the speakers! So that meant doing another first – publicly talking about myself and my life. This was naturally a daunting prospect, but exciting too. So I agreed to give it a go, it was worth a try.

And I wanted to write in detail about my experience, which I’m going to split over a couple of posts so it doesn’t get too long. I’m then going to publish a written article version of my speech here, and a video version on my Youtube channel, so you can see what I said, and maybe it will give you some inspiration and reassurance too. So I’ve got quite a bit to share!

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