Blogger Interview – Amanda Gene

This is a new type of post for me – an interview exchange with another blogger! Amanda Gene came to me with the idea, having interviewed some other bloggers already, and I was of course very flattered and happy to take part! Amanda has already published her interview with me, so do go and check that out too.

I’d love to do more posts like this too. I think it’s a really nice way to learn about other people, for the same reason that tag posts are so enjoyable. Plus it’s very important to support and promote each other in the blogging community, especially as disabled bloggers get overlooked somewhat (which is why I’ve created lists of bloggers who post about sight loss, disability, London & entertainment). So if anybody wants to do an exchange of Q&As like this, feel free to contact me.

Anyway, here is the interview I did with Amanda. I hope you enjoy it. Do give her a follow if you can, all of her social links are at the end of the post. Thank you so much to Amanda for featuring me on her blog and for answering my questions here as well! She gives great advice on blogging and interacting with disabled people, and it’s really interesting to get an insight into her disability and the things she enjoys.

Continue reading “Blogger Interview – Amanda Gene”

July 2018 Favourites

Time for another monthly favourites post and video, looking back at July. Things were very busy and successful on the blog and social media this month, I enjoyed some fun social events, museum visits and other entertainment, and I even got a bit sporty for once, all while enjoying the sweltering heatwave. So it was a pretty good month, and I hope you enjoy my review of it.

Continue reading “July 2018 Favourites”

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.

Continue reading “The Sunshine Blogger Award”

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.

Continue reading “June 2018 Favourites”

Yoocan Do It

“My impairment’s just a dropped stitch in life’s rich tapestry. I’m successful, independent, it’s no barrier to me.”

I’m rather proud of that motto, which I came up with this week. It’s adapted from a quote in my favourite sitcom (Only Fools And Horses). Del Boy and Rodney are trapped in a lift, with Rodney understandably distraught about his wife Cassandra’s miscarriage, and Del Boy tells him “it’s just a dropped stitch in life’s tapestry”. It’s a line that’s stuck with me ever since for some reason, I just think it’s lovely.

I created the quote to go with a guest post this week, which has had a massive reaction, way beyond what I could have expected. So I wanted to do a post to explain it and give it a bit of a plug, especially for those who haven’t seen it yet.

Continue reading “Yoocan Do It”

Aniridia Day – My Aniridia Sight

Happy Aniridia Day! Following the shining success of last year’s launch event, this year it’s back and there’s loads going on today.

For starters, there are hours of live webinars taking place all day, with talks and Q&A sessions by patients, parents, doctors and researchers from all over the world. And I’m involved in one of them, because myself and James Buller will be discussing living with aniridia. So do join us if you can!

But the other major part of the day is the Aniridia Sight campaign, where people post a photo of a scene, and then describe how they see the same scene from the same position – i.e. when they take the place of the camera, what can they see with their own eyes?

So in this post, I’m going to share my contribution to the Aniridia Sight campaign. And you can do the same, by sharing your Aniridia Sight photos and descriptions to the Aniridia Day Facebook group, or posting on social media with hashtag #AniridiaSight and tagging @AniridiaDay. I hope you all have a great day, and you find the following description about my sight interesting.

Continue reading “Aniridia Day – My Aniridia Sight”

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.

Continue reading “May 2018 Favourites”

April 2018 Favourites

Time for another monthly favourites post, and April was very busy for me. There were a couple of big important events, a couple of interesting museum visits, vanother theatre trip, and a few nice walks now that the weather’s improving. So I hope you enjoy this little post and video recap of what I got up to.

Continue reading “April 2018 Favourites”

Naidex 2018

On the 25th and 26th of April I went to the Naidex show for the first time, which was held in the Birmingham NEC. It’s Europe’s biggest event dedicated to disability and independent living, and is full of companies showcasing the latest technology, products and services they have to offer, along with seminars and panel discussions, a mobility test track, a sporting arena for people to try out different activities, a moving and handling lab offering training for healthcare professionals, and more. And it’s completely free to attend, which makes it very worthwhile going to check it all out.

I’d never heard of the event before, so I was very intrigued to see what it was all about. I became aware of it because I was one of various bloggers contacted by Cláudia from the Prysm Group marketing team. As well as telling me about the event, she asked if I wanted to be an ambassador for it – which basically involved me giving them a plug on my social media channels, and they would promote my blog in return. I was happy to do that, given my interest in the event, so that’s what we did. Hence you will have seen me mentioning them every so often over the past month, and they did indeed share the link to my blog on Facebook and Twitter a couple of times as well. I didn’t receive any payments or gifts for it, we were literally just exchanging posts to promote each other.

And the event itself was great, I really enjoyed exploring it over both days. So I want to give you a comprehensive review of the event, and tell you about the various companies, products and services that I became aware of. As a result, this is quite a long post, but it is divided into headings with a contents list if it’s helpful. So I hope you enjoy reading about it!

Note: Footage from the event can be seen in my April Favourites video. I also discussed my Naidex visit with Fern Lulham on AMI Audio‘s Kelly & Company show on 24 May 2018.

Continue reading “Naidex 2018”

The Wallace Collection

Last weekend I took my first ever visit to The Wallace Collection, which is a museum full of paintings, sculptures and furniture collected by multiple generations of the same family. When I was younger I had no idea this was just behind Oxford Street, and a lot of shoppers in that area have probably been blissfully unaware of its existence. Of course, even if I had known back then, I wouldn’t have been interested, as I was never into art as a child, and didn’t pay it much attention for a while as I got older.

However, since moving to London, I’ve been able to start exploring and developing an appreciation for artworks and visiting galleries, particularly thanks to guided tours and other interactive and accessible methods of exploring such spaces. As very much an art novice, I am enjoying learning about it and seeing some of the delights on offer. It’s like a fascinating new world, more so than I’d initially expected perhaps. So that was one reason I was looking forward to this visit.

This was also the third and final outing I was doing as part of a PhD study into museum accessibility for the visually impaired, being worked on by Rafie Cecilia. Our previous visits were at the Victoria & Albert Museum last year, and the Museum of London in February. I also met her again during the ultrahaptics testing at the V&A earlier this month, but that was for a different study. It’s always a pleasure meeting her, and it’s wonderful that she’s putting so much time and effort into this work, to support people like myself who find it harder to explore museums compared to normally sighted people. And now she and her colleague Maryam Bandukda have set up the Disability Innovation Research Society, bringing together researchers to discuss disability innovation and accessible technology, which is great. So I was glad to be meeting Rafie again.

And talking of accessibility, that sounded really good in this museum as well, with the website stating that they had an audio guide for the visually impaired, plus Rafie had recommended a special app I could use to find out more about the artworks. So that was another big reason for me to go. I’d heard very good things about the Wallace Collection, and getting information about the various exhibits sounded like it would be pretty easy. So now I want to tell you how it all went.

Continue reading “The Wallace Collection”