Hello all,
It is the start of Disability History Month here in the UK. The theme for this year is life and death. How fun.
It is interesting that this theme would be the topic when the government have been having conversations around Euthanasia. I’m not going to get into that here because it is a very difficult topic.
My point is this topic alongside the current conversations surrounding our benefits system seem to fit in with this theme of life and death.
When you then consider the long waiting lists within the NHS for services such as mental health support this years theme seems quite interesting.
I’m going to focus more on the life side of this years theme, lets focus on giving Disabled people a quality of life which enables us.
Disabled people have a right to exist. We have a right to life.
We should not be looking to go backwards in terms of Disabled peoples access needs. Just because someone is Disabled does not mean they are lesser than.
Disability is a group which anyone of us can join at any time. Often as people get older they will develop some form of Disability. We need to ensure all Disabled people have access to dignity at every stage of life. We, as a society, also need to start seeing mobility aids as items which empower us. Which give us independence.
One of the sections on the DHM website shows you the themes since 2010. I would urge you to go back and see what some of those themes were. I know I will be revisiting those themes to see the journey the movement has been on.
I think there is importance surrounding the topic of death, but I do not have the spoons to cover it. Just remember to respect everyones opinion on this topic and remember to ensure Disabled people are included in this conversation.
Everyone deserves respect, dignity and choice.
Thank you for reading.
Monthly Archives: November 2025
CVI
Hello all,
A few weeks ago we went to a conference specifically for one of my conditions. CVI- Cerebral Visual Impairment. While it does have the term Visual in the title it is important to note that your brain is the part which interoperates what you see.
The best way I can explain it to people is imagine you’re looking at some writing in a language you don’t understand. You can see the writing but you can’t understand it.
That’s the best way for me to describe CVI.
It can be quite confusing and scary at times, for example if I’m crossing a road I may think it is clear, start to cross then a car ‘appears’.
I think it is difficult for people to comprehend this and that’s why it’s difficult for people with CVI to feel like people get our condition. There is no way to show people how we see the world exactly as we do.
Things can just magically appear because we can’t always interpret what we’re looking at. The brain struggles with this process.
But this conference was wonderful because you’re in a room full of people who get it. They’re all there to learn something and create a community for CVI. It was great hearing people who have CVI explain similar things to what I have experienced.
It was also great because those with CVI were explaining things from their perspectives.
One of the things which is hard to fix is the ability to reduce visual stress. This is probably because the world is so busy and there is always something which is trying to catch your attention. Whether it’s a loud advert, or people rushing around going about their day. This creates a lot of anxiety which makes it more difficult for me to process what is going on.
And no- don’t ask if new glasses will help. They will not magically allow my brain to suddenly interpret what is going on around me.
I do wear sunglasses a majority of the time when out and about because light hurts my eyes.
Here is a link to the CVI society. They are wonderful and a place to find a community for those of us with CVI. I would recommend checking them out and using their resources. CVI can be very difficult to explain, so being able to connect with people who have CVI or their allies is really important.
We had a great day meeting some amazing people who were sharing their stories and information around CVI. I had never met anyone else with CVI before so it was brilliant.
Have a great day!
Christmas
Hello all,
It is coming up to Christmas time. Which means everything will be getting busier and there will be more going on around us. Which can be great but for those of us who are Visually Impaired or Blind it can be a bit more difficult.
There are lights going up and Christmas trees being decorated, shops are filling up with more of their Christmas stock. This can all feel quite festive. I do enjoy Christmas and giving presents to people. It is nice to get together with family and friends and to have a catch up.
What can be difficult is the Visual Clutter. At home we have everything where we normally put it so it’s not something new in a new spot.
I don’t really enjoy shopping as it’s busy, so we go when it’s not a weekend day. This makes it easier as there are less crowds. Shops will often have a move around of their stock at Christmas to utilise space. But when you go in and nothing is where it was before it’s quite disorientating.
This is another reason to go when it is not busy as you can take your time and not feel rushed. Top tip for the Visually impaired and Autistic shopper, go when it’s not busy so you are not feeling rushed.
Christmas can be great from a sensory perspective, that’s why it’s important to get it right for yourself as a Visually Impaired or Autistic Person. Take the time to not feel overwhelmed and to do it at your own pace.
Once all our decorations are up I’ll try make a post with you showing what it can look like if you have Nystagmus.
I find when shops have a lot out it can be very overwhelming. I find there’s too much stuff. I get it, it’s commercialisation, but sometimes there’s just too much going on.
Enjoy your Christmas season and all the merriment it can bring. If Christmas is hard for you, then make time for yourself and do what you need to get through. It can be hard this time of year.
Thank you for reading.
I’m on Threads @VisuallyImapiredPip