DinkyKt's Blog

My First Blog Post

Katie Wearing • April 25, 2018

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Hello everyone!!
This is the first post of my brand new website and I’m hoping you are enjoying my new site?!? On this site, you will find not my blog, but my DinkyKts EDS Diaries posts and there will be much more added as I get to grips with having my own website.
You may be wondering why I’ve decided to set up this site and the new home for my blog? Well it’s because I wanted to start a new and to have everything that I work so hard on in an accessible place together. Obviously by clicking on widgets etc, they will Take you to my social media and you can follow me on those but for me it will be easier and more organised to have everything in one place. Please bear with me as I continue to work on the finishes touches of this site but don’t be afraid to share your thoughts, advice and just to say hi with me!!
So who else is excited for this new and exciting adventure? I know I am for sure! See you in my next post xxx

Hello my lovely peeps!!

As sad as I am about leaving worldofdinky.blogspot.co.uk behind, I’m very excited to have this new website up and running. My life has suddenly got busier and I feel more inspired to write and post more so this makes lots of blogging to be done. I know that I don’t really fit into any particular niche within the blogging world as I write not only about beauty, fashion, reviews and my life as a person with Ehlers-Danlos Syndrome. So if you like who I am and what I’m about, then that’s what is important. You’ll see that I’m an all rounder when it comes to blogging and the same goes for my YouTube channel.
So that’s all I’m going to say in this post and I can’t wait to see what awaits us on this new journey, and to see what your thoughts are on this new site.
Tske care and make sure you subscribe so you don’t miss anything! There’s links to all of my social media platforms so there’s no excuse for not following me EVERYWHERE 😀❤️ xxx

By Katie Wearing April 30, 2025
Because being a Bluebird isn’t just for one season — it’s for life.
By Katie Wearing April 4, 2025
Navigating dental trauma, healing, and care with classical Ehlers-Danlos Syndrome
By Katie Wearing March 15, 2025
Navigating Uncertainty: How the NHS Reforms Could Impact Those of Us with Rare and Complex Conditions
By Katie Wearing March 13, 2025
“Speaking up about cEDS and medical care—raising awareness, not negativity.”
By Katie Wearing March 8, 2025
The Power of Lyrics, the Strength of a Story
By Katie Wearing March 4, 2025
“A personal account of medical neglect, pain, and the lasting consequences of being failed by the system.”
Katie with her thumb up on her birthday!
By Katie Wearing June 10, 2024
It's been a while!
By Katie Wearing January 2, 2024
My Summary of 2023!
Left side is a wine tumbler. Right side is a bright blue ladies t-shirt. Both have World of Dinky on
By Katie Wearing February 14, 2023
Discussing the pricing.
By Katie Wearing January 19, 2023
Hi everyone! As many of you who follow us over on our Facebook page Dinkykts EDS Diaries, you will be aware that we are coming up to 10 years since we began, back in February 2013. So slowly, we are looking back on the positives of our campaign work. I believe in celebrating these milestones and why not?!! While the odd bit of Dinkykts EDS Diaries has received bits of help from various individuals, the majority has been done by myself (Katie) so anything that has been done is incredible. I know that we haven't done huge things, what we have done is wonderful and I am proud. Looking back, we never did manage to organise a family fun-day and that was one of the reasons why we began this campaign but due to the nature of having a rare disease like Ehlers-Danlos Syndrome, you just never know what life throws at you. Perhaps in the near future, we can actually organise a family fun-day? Hopefully this time, I won't end up in hospital (twice) haha! I have always wanted to go out in the community, whether it's going into schools, colleges, medical panels or having a stall where I meet random members of the public and raise awareness, and hopefully fundraise at the same time. I did get a taster of going into classes at college when I attended my local sixth form college and I really enjoyed it. We will be showcasing whatever we do on our YouTube channel as that's our main focus of awareness work. We also have the whole month of May to do lots of things as that's EDS Awareness Month and we want your ideas/suggestions! So definitely more highlights to come in 2023 and beyond!! Love DinkyKt
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