Blogger Interview – Chelsey (VI Blind Resources)

Last month I was very kindly featured on the blog VI Blind Resources, after Chelsey interviewed me about being raised by visually impaired parents. It’s not something I’ve really written about here on my blog, so do go and give it a read to find out a bit more about me.

In exchange for that, I’m delighted to feature an interview with Chelsey here on my blog. She regularly posts on her blog and YouTube channel and across social media, and she even makes the effort to provide written descriptions for images and audio descriptions in her videos. So do go and check her out, and I hope you enjoy this little interview with her. Thank you to Chelsey for featuring me and answering my questions!

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Raised by Visionally Impaired Parents: An Interview with Glen from Well Eye Never!

Here’s my most recent guest post to share with you all. This time I was interviewed by Chelsey from VI Blind Resources about what it’s like for me to have visually impaired parents. I hope you enjoy reading it! This brings me up to date at the moment, but I have another interview with another blogger coming soon, so keep an eye out for that.

While I’m here, thank you so much to everyone who has donated to my charity abseil and/or shared my tweets about it. It’s all very much appreciated. I’m now up to £765, thanks in particular to an astonishing £250 (plus £62.50 Gift Aid) donation from TV’s own Richard Osman this morning, which I’m still in shock about! That is extremely generous, so massive thanks to you sir! Everyone who has donated is credited on my Thank You page, including quite a few fellow bloggers now.

There are still 3 days to go before the abseil takes place, so if you want to give me your support before then, you can donate at JustGiving.com/WellEyeNever, or in the UK you can also text WENA80 plus a space and your amount to 70070 (e.g. WENA80 £5). You can donate £1, £2, £3, £4, £5 or £10 by text message. Thanks for your support! 🙂

VIBlindResources

by Chelsey Zumpano

Glin is a fellow Blogger and YouTuber, he’s also visionally impaired, but unlike me he has been raised by parents who also happend to be visionally impaired. So I asked him some questions about what it was like growing up.

1 Do you have the same visual impairment as your parents and either way what is the name/names of it?

I have the same conditions as my mother – aniridia and nystagmus. Aniridia means I don’t have an iris (the coloured circle) in my eye, so my eyes don’t adjust to changes in light properly. As a result, I’m very sensitive to glare and I find it hard to adjust in the dark. Nystagmus means my eyes shake and wobble all the time. This makes it harder for me to focus on things, unless they’re close up or enlarged.

My mother’s sight got a lot worse over…

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An Interview with Glen Well Eye Never (Guest Blog Post #3)

Yesterday’s reblog of a guest post went down very well, so here’s another – an interview with me on Amanda Gene’s blog, the first time I’ve been interviewed by another blogger (but already not the last). So do check that out, and Amanda’s blog in general. And in return I’ve also done an interview with Amanda on my blog too, so do give that a read as well. Thank you to Amanda for featuring me! 🙂

P.S. While I’m here, there’s just a week to go until my charity abseil for nystagmus research. So if you can sponsor me it would be very much appreciated, while I try and psyche myself up for the big leap!

Amanda Gene

Hi Everyone, I got the pleasure of interviewing my friend Glen. He is the fantastic blogger and YouTuber who runs Well Eye Never. Many thanks to Glen for allowing me to interview him and for allowing him to interview me in return. Don’t forget to check out his website 🙂

  1. What is your name?
    Glen Turner
  2. Age?
    In a few days time I’ll be 35 years old.
  3. Who has inspired you the most in life and your blogging?
    My parents also have sight loss like myself, and have always encouraged and supported me to achieve whatever I want to do. At the school for the visually impaired I went to, the teachers there were also very supportive and really helped me to grow in confidence. My friends also mean a lot to me and inspire me, of course. And the blogging community has been so welcoming and supportive of my…

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Celebrating Diversity Amongst Bloggers — Post 6

Recently I’ve been invited to do a number of interviews with other bloggers, which has been very flattering. I’ve promoted them on social media and in my favourites posts, and linked to them on my blogger collaborations page, but it occurs to me that I should reblog them as well, to help draw attention to them and give a bit more promotion to the lovely bloggers in question.

So this is the first post, one in a series running on Kel’s wonderful blog Consider Yourself Warned. Check out all the posts in his “Celebrating Diversity Amongst Bloggers” series, as there are a great mix of people featured. Thank you Kel! 🙂

Consider Yourself Warned...

Post 6 comes from Glen. I actually found Glen on Twitter when reaching out for people to partake in this project — I guess it’s working!! Despite not being a blogger, Glen is very active on Twitter, and I felt that his story, told in the below post, is very apt for this project.

*NOTE* After scheduling this post, I realised that Glen does in fact have a blog, which I have taken some time to read and enjoy. For whatever reason, I didn’t amend this article to reflect this; the post was updated on 21st July to include his blog link.

My name is Glen, I’m 34 years old, and I live in London, having moved here a year and a half ago.

I am visually impaired as a result of 2 conditions. Aniridia means I have no iris, the coloured part of my eye, and so I’m unable…

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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:

An Interview With Glen

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 get in touch, either via Facebook or Twitter messages, or emailing welleyenever@icloud.com

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.

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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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February 2018 Favourites

Well, what a way to start a new month, with snow all over the place! Winter has seemed very reluctant to let Spring take over, but hopefully things will warm up in the coming weeks now.

And the cold weather didn’t stopped February from being an eventful month. Following on from my January 2018 Favourites, it’s now time to look through what I’ve been enjoying in February. And even though it’s the shortest month, I seem to have packed quite a bit in! So I hope you enjoy this post and video for February.

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