It is getting round to that time of the the year again when I need to remember to take a hat with me when I go out.
The sun is causing a lot more glare than what I’d like.
I do enjoy summer, the warmer weather is better for my back pain. But the brighter sunshine is not good for my vision.
Hats are the best way for me to be able to move safely when I’m out, they cut down the amount of glare I’m having to put up with.
Otherwise I have to close my ‘good eye’, which means I’m left with less than 3ft of vision to see where I am going. Yes I have my cain, but I’m in pain when I’m using the very little vision in just the one eye.
It feels like someone is jamming their fingers into my eyes. That’s how much it hurts.
By wearing a hat I don’t have to worry about the glare, meaning there is less chance of me pain from the sun.
Please remember that when you see a visually impaired person, or anyone who is using a mobility aid, give them room. Be patient and let them do what they need to. We appreciate not being rushed.
Kindness goes along way.
Have a great day,
How are we all doing today?
Normally I do not go out alone as I struggle to get to new places independently. Getting to work I do alone as it is a familiar route.
When getting on and off trains it can be quite difficult for a few different reasons, one of which is when the platform and trains are busy.
It can be very helpful when someone asks me if I need help. My preferred way of people asking is if they say ‘hello’ rather than touching my arm to get my attention. This is just because I don’t like people in my personal space.
If I say yes to you your help then please let me take your arm and the guide me onto the train. Then help me to find a seat. Once we have found one I will say thank you and that I am happy for your help.
People will ask me if it is OK to ask a Disabled person if they need help. My response is always, please ask if you are unsure. The reason I say this is because it is always nice to be asked and if we do not need help we will politely say no.
Things I do not appreciate as a White Cane user are people assuming I have no site at all and using this to think it is ok to push past me.
This week in one train journey the following happened:
The train pulled up and I was about to get on when someone got on in front of me. Then another person decided to the same. The second person did so as my cane was helping me navigate the train step. My cane caught in between his feet and he could have fallen over or I could have misjudged the gap and hurt myself. This is all because people are arrogant and want to get on first.
The train is not leaving any quicker because you got on first.
Then getting off the train I stood waiting to go through the doors from the carriage into the exit. My cain was stuck out and I was ready to move through the door. Then someone stepped round the side of me and pushed through the door before me. These doors are quite narrow. My cain got stuck between their feet as they continued to walk off the train. Once again this could have ended up in injury to myself or them.
If an injury were to occur, it would not be my fault. I have a cain for a reason, if you chose to ignore it and you fall over it is not my fault at all. You may think that’s a bit harsh, but it is not. My eyes don’t work well, which is why I have the cain, your eyes work, so please use them.
Please be respectful of Disabled people, well everyone really. Personally I think if you were to ask if someone needs help it is OK to do so. As long as it is coming from a good place then it is all good.
Thank you for reading.
I have decided this weeks post will be all about Scoliosis. Recently I have adjusted the exercises I do so I can try get a better balance, strengthen my core and shoulders. How exciting.
Doing physio exercises is very tiring. Normally when you go to a physio via the NHS you get exercises to do and they will, if necessary do a sport massage to release some of the tension. This is not normally the case though.
I do my exercises and then I have sport massages separately. Yes they are costly however I think it is really worth it. The sport massage releases the tension and helps you to start again. Then you can do the exercises to rebuild your strength and reset your muscles.
All of this does not stop my need to take painkillers on a daily basis. Right now for example, I am sat in my comfy chair but I have had to take pain killers. I am also wearing layers to keep my back muscles warm.
Scoliosis is very hard to live with and there is no cure. Even if you have the surgery you still have scoliosis. You still have days when you are in pain.
If you have any questions around scoliosis please feel free to drop a comment a below. Also check out SAUK.org.uk
Thank you for reading.