Tag Archive for Perception

Feeling Isolated, yet surrounded by others.

Although I am a VIP, I pride myself on being independent and when I am within environments that I know or at least understand I am able to achieve this.

But move me away from my comforts and I struggle. I have often linked asking for help and needing support as a weakness and laughed it of as me being silly not being able to do things because of my eye condition.

After all,  lazy, I don’t like to just sit back and get others to do things for me while I am able to do it for myself.

A recent bought of bad health has seen me admitted to hospital. Which I am sure you will agree without adding in my eye condition is quite a daunting and scary thing.

But starting with the travel in the ambulance to get here, to moving from emergency medicine, to medical assessment to the current ward, I am feeling very low and lost.

The ambulance crew were fantastic, very descriptive and explained what they were doing and even where we were on our journey especially when we were travelling down the corkscrew of a slip road off of the motorway, which whil laying down and travelling backwards felt like a roller coaster ride!

Emergency medicine was very busy and nurses and doctors were rushing everywhere, I was really looked after and treated brilliantly, every time a nurse came passed my bed they asked if I needed help to get to the bathroom as they were all aware of my sight or lack of it.

Following hospital guidelines on time etc ( the politics of the nhs) I was moved to a medical assessment unit for further looking at. The handover on this ward was detailed about my eye condition, but sadly not passed over clearly to the next staff that took over, so having buzzed for assistance to go to the bathroom I was advised that if I couldn’t walk I was to use a commode…. So I corrected them that I was able to walk, but couldn’t see, which she argued over as I wore glasses, surely I knew where the bathroom was (don’t worry, the compaint went straight in to the staff the next day and the bed allocator who spoke with me about my preferences before I moved to the ward I am on now)

The porter that took me between the two wards was unaware and grumpy that she had been apparently stood by the side of my bed being ignored for 5 minutes, so she got a firm explanation of my eye condition and how it was polite to make people aware of her presence!

The ward I am on now was not able to accommodate me in, but I was given the next best thing. The ward I Amon with just 3 other ladies has a bathroom directly opposite me. The layout of the room was thoroughly explained as was the location of the bathroom, the rails and most importantly the help call buttons.

The odd slip up with cleaners moving my table or my glass from one end to the other has occurred, but the ladies on my ward have helped greatly, although immobile they have always explained the new location of the table or the glass perfectly. Just this morning they advised me of a wet floor sign just at the side of my bed that I would have kicked into.

Hospitals are not my favourite place and I know how busy the staff are, so hate to feel that I am making a nuisance of myself when taking up their time with silly little things.

The reaso sharing this with you is because, just this morning I had a great chat with the nurse. I explained my condition, my worries and had a really good chat, she then helped me sort out my clothes within the locker so I would find things easier. She briefed her staff about me and even got one of the assistants to help me plait my hair to cheer me up. She told me that all of the things I needed, whether that was medication or being told where food was on my plate wa all part of my care, nothing silly, nothing was because I was being stupid. She said that she would expect everyone on the ward to receive the care that they required with all of their needs, not just the medical issue that had bought them into hospital.

I sometimes need reminding of that. Just because I see my disability as a failing on my independence, others don’t and they would be failing within the job they were assigned to do if they did.

Fun Fairs

Lots of blogs this week, but I get to break from the usual boring home, study routine when my two children are home.  As I said before, I won’t let me being a VIP affect them or the fun they get to have.

So, on Sunday as a birthday treat we went to the fun fair at Hayling Island, I have never been there before, but friends had raved about it & how much fun the kids could have (big & small!)

They weren’t wrong.

With a 3 and 7 year old it is often difficult to find the balance on somewhere they can both have fun and do things together or with me.  Of-course my faithful GD came along too although she didn’t partake in much of the fun, just the run along the beach afterwards.

For me, I got to drive! only on the bumper cars, but didn’t I make the most of it, first with my son, then with my daughter and then they had their own car and I got to go alone.

 

We went on the halter skelter, the log flume, the balloon ride, even the rickettly old roller-coaster (I didn’t want to ask if it was part of its design or age that made it that way)

I know many people do these sorts of rides with their eyes closed, so most can guess what that feels like, but how about if your eyes were a blurry haze?

It makes things seem there that aren’t, it makes it feel that you will hit your head or that the cart your in will come off of the rails.

Also with no depth perception I have no ability to judge the hieght of a climb or the steepness of a drop….. But for me that adds to the excitement.

So to say that I had just as much if not more fun as the kids would be an understatement …….. We loved it!

The weather was just right and like all good funfairs I got to enjoy an old family tradition of having my bucket of pennies and playing on the slot machines too, dropping the coin at just the right time to not fall on top of the pile, put to push some of the coins down into the winning bit.

Who says sight loss has to make you miss things, it just makes it a different experience, but having never had brilliant sight I can’t say is it were a better or worse experience, my children had a fabulous time and that was the whole point of the day.

Me getting to join in so much was an added bonus!

What’s in a saying?

We all have little ways of saying things, little phrases that we all use every day, without thinking.

The most common of these are:-

” Have you seen this?”

“Look at this.”

“did you see that?”

my response to aloof these is no, but I have never, nor will I ever take offence to them.  I myself usually end a conversation with ” See you again soon,”

They are common sayings and I even do it, if I’ve been to a film having listened to the audio description, I still say ” I saw that…….film the other night, have you seen it?”

I also say that I’ve read a great book book lately, even though I listen to it.  “I’ve just listened to a great film/book” just doesn’t have the same ring to it!

The reason I am writing this blog about this is because yesterday when out with a good family friend and all our kids, he went to show me a photo on his phone and stopped dead and then apologised for saying the classic “look at this”

As the day went on he continued to say ” come look at this” again apologising after each time.

This unsettled me, not because he had said these things, because he was just saying the same things that we all say (me included) but that he felt anxious by the thought that he had upset me.

How perverted would it sound if I started saying “I’ll feel you later” ! Or my friends said to me, ” Come and touch this!” I know I would probably run in the opposite direction.

So, I will continue to tell my friends that I look forward to seeing them soon and do not want my friends to cringe or feel anxious when they say ” come look at this” or “have you seen this”

So, these are just typical English sayings and part of each and everyone of us.  I can’t talk for every VIP or people with other disabilities, but I doubt they would take offence either.

Burying my head in the sand.

As you have probably worked out by now, receiving the news that you have an eye condition that will only get worse and could result in you loosing all of it in time wasn’t the best news!

 

when I was first diagnosed I researched my condition and looked for the positives…. Or ‘perks’ as I know refer to them.  As silly as it sounds, I had to find some good out of this bad situation.

I received lots of help from my consultant, social worker and good friends.  This was when I discovered just how many VIPs there actually are in Fareham and support groups to help… So I started volunteering, first at an active group called FAAB and was soon followed by volunteering for a local club that ran under the umbrella of the Hampshire based charity Open Sight.

Disability issues and sight loss became my world for a few years, I threw myself into volunteering and in an odd way helping others with their sight issues shelled me.  but I began to feel that I needed to spend more time on myself and my family.  I do still volunteer and enjoy helping out, just a little less than I did.

When I stopped helping others, I realised  just how much my own sight condition did actually upset me, and this was when I fell apart.

This was when I started to really understand my sight loss and me……. To put this post into perspective…… Despite my registration being in 2008, this has only just happened for me!

 

Perspective

imageWhether you have a visual impairment or not, we perceive things very differently.

When you look at the image included with this blog-what do you see? Don’t overthink it or spend more than 2 minutes looking at it before commenting below.

Page Reader Press Enter to Read Page Content Out Loud Press Enter to Pause or Restart Reading Page Content Out Loud Press Enter to Stop Reading Page Content Out Loud Screen Reader Support