Something that happened a few weeks ago, twice, because I didn’t use my handy magnifyer. I wouldn’t mind but it’s always in the front of my handbag.
I ended up taking too many Co-codamols for pain thinking they were Paracetamols because I was in a rush to meet my friends at Pontefract, for the VIP meeting there we have every month.
I’d forgotten I had these in my bag and only thought I had Paracetamol.
I ended up realising what I’d done so didn’t drink anything till alot later on. Just because I couldn’t be bothered to use it. It nearly ended up in me not attending at all.
Then, like a complete idiot, I took 2 of the same night-time tablets instead of one of each that I take to help me sleep and for my mental health. So I couldn’t hardly take the correct one aswell, as I’d already taken too many.
Bonkers isn’t it.
I can’t read the back of the pill packets to differentiate what’s what with just my glasses on and these silly moments of not getting my magnifyer out could have caused no end of sickness or problems for me so I’ve learnt my lesson.
PD 1 Cartoon image of a blonde long haired woman. Sat with knees bent with pill packets in different colours and pills, on the floor, by her knees. She holds a bright neon yellow magnifying glass reading the packets and discovering what they are.
PD 2 A photograph of a neon yellow magnifying glass placed on a brown table in close up.
28th of May 2015 was the day I was diagnosed with Macular Dystrophy.
Ten years ago today.
“I’m so sorry” said The Consultant. “There’s nothing we can do”. I didn’t understand. I’d never heard of a macula. Just thought I’m in my 40s, will probably need glasses. There can’t be anything wrong.
She asked if there was anyone with me. There wasn’t. As I’d just thought there wouldn’t be anything wrong.
I was let go. Popped my yellow sheet in the tray at reception, to receive another appointment.
I had a confusing, stunned, walk back alone through the hospital grounds and through the park. I sat for a little bit on a bench. Somehow knowing this was a ‘big’ thing I’d have to face, without knowing what that was exactly. Just enjoying the late spring sunshine and looking at the beautiful trees dotted around.
PD A brown long haired cartoon woman, sits on a green bench in a park setting. In the background there is grass and tall trees. She wears a purple skirt, black leggings, Black vest top with red shoes. Her green eyes are looking towards the camera
At this point and the few months afterwards, they were abit of a dazed blur to be honest. Trying to understand what this diagnosis was, when there was hardly any information or blogs around, was an astounding learning curve.
I learned that even though I had 20/20 vision at that point, it wouldn’t always be this way. This is genetic.
For the first few weeks I was avidly eating Vitamin A enriched foods as I was initially mixing this up with Macular Degeneration (NOT my condition) and then after learning my eyes don’t process Vitamin A properly, and finally realising that this was the problem with my eyes and the driving force of the damage and therefore the progression of this condition, I made sure I just ate a normal daily allowance of these foods.
I was in shock for a long time afterwards with worry for my future.
Eagerly Googling, searching social media, blogs, everyday for ages, trying to find someone with this malady. So they could tell me how long I’ve got to see properly. I realise now that was fruitless. We are all different.
Initially I panicked and tried to find everything about how people with this condition progressed in the future. How long would it take till I would have real problems? Would I go Blind? What would my future look like?
I stopped smoking (Eventually) I settled into what I knew about this condition and came to the conclusion there was nothing I could do and worrying, causing me stress, was probably not going to help matters.
I had a boat load of tests and check ups. All to no avail really. Saw lots of different consultants, at 3 different hospitals. Apart from them finding two medium sized retinal detatchments, that grounded me for a while in the UK. They eventually shrunk over the years and the last time they checked they were an extra small one in my left eye and none, in my right.
It did became seemingly pointless to me to have anymore of the tests after these detatchments had shrunk down. After all there is nothing that can be done about my Macular Dystrophy diagnosis… Yet. Then Covid-19 came, and I never did get to see the results. That really messed it all up.
10 years on I’m so very thankful my progression has been slow. Any adjustments to my sight, I’ve been able to cope. Subconsciously or consciously. My eyes are adapting, I’m learning to take things slower and be more patient with myself.
I was worried this condition was speeding up abit when I stopped driving, as this was before the 5 to 15 year window that the first consultant said I had before being within the Blindness spectrum and therefore having to rethink alot of my life as it was.
I’ve had distinct periods of my eyesight getting worse. The times I’ve thought it would ‘mend’ itself because I must be tired or stressed, wasn’t to be.
I’ve noticed big jumps in the difference if I’ve not done something for a while. This usually involved something like painting the fence a year on. Painting the house with reading glasses on to which both still was a patchy mess.
I stopped driving in 2019. 4 and a half years on from being diagnosed. That was sooner than I expected.
It was hard because I had driven for 29 and a half years at this point. I was used to, for nearly 3 decades, bobbing about when I wanted to. Nipping here and there.
I was a nervous bus passenger at first. Same with taxis. Didn’t think they would turn up or they would take me to the wrong places.
Now, I love the bus and trains especially. Looking out of the window is still a novelty to me, even after all this time. I couldn’t do that driving. Relaxed and now confident with other forms of transport, I go on my merry way and have had adventures I wouldn’t have had and the coach holidays seeing all parts of the UK I may never have seen.
Last year I had a period of falling over and hurting myself.
I definitely need a cane for night time. That’s without a doubt. A battle in my head I have to get over with. I’ll talk about it one day. I cannot at the moment.
It is time to do some cane training. I’ve known this for a while.
All in all I’m not anywhere near I’d thought I’d be at the start.
I’m lucky. I know that. For alot of things are so different than 10 years ago.
I’m better than ever. A much healthier and happier person than I was.
I appreciate so much. The little things. I do stop and look around if I’m on a walk or even just out shopping. I try to see everything I can, albeit in a blurred world.
Sometimes it’s abit like being a swan gliding along on the surface. In reality, nobody can see how hard underneath I’m concentrating on moving along, scanning, trying to make objects out, blumming kerbs and uneven surfaces. Steps are an absolute pain.
One thing’s for sure in my uncertain world. Is that I’m very grateful for how I’m still managing this in my own little way. 10 years ago, I don’t think I could have wished for more than to be as I am now.
If you’d like to read a more indepth diagnosis post. Below is a link to my first ever post. This was about what happened at my appointment with the eye clinic and what happened there 10 years ago today.
One thing that I never thought about until I went to a gig since my eyesight started really progressing a few years ago, was any problems whilst I was there.
I went to see Duran Duran (Standard. My faves since 1982) with my two friends so I thought I’d be fine.
One thing that I always like to do is go to the merch stand and get myself a tour t-shirt. I’ve seen them alot and have quite a collection.
I was stood there at somepoint when it was still light and realised that I couldn’t come and go when I pleased anymore anywhere around the hall when I wanted to. I knew I couldn’t just stroll away later and leisurely spend time looking around by myself when darkness fell.
I suppose what I’m saying is, if you are planning going to see any bands, be aware, especially if this is all relatively new and you’re experiencing a period of further sightloss and therefore adjustment. Being aware of certain things before you go, will make your enjoyment as good as before.
I was surprised really as I hadn’t given anything any thought.
When it’s light before the gig has started (This was an open air event) go for your merch. It’s easier to get back to where you are (and your friends also if you prefer taking someone) and also it isn’t as frightening watching the floor, the people and less stressful all round. Because I liked to do things by myself this is what I decided to do. I didn’t want to put my friends out even though they wouldn’t have minded.
Same goes with the drinks. Whilst you’re passing get a drink or drinks if going in rounds first. By extra for later if you wish. Then when it’s dark or the lights are off you don’t have to move.
One thing I’ve stopped doing is drinking enough that I always need to find the toilets. It’s better to stop at somepoint than struggle finding them and your way through people and whatever you cannot see on the floor or ending up in the wrong place .
I don’t want to be dragging friends out of a gig to the loo to help me at the moment. That will change though as I’ll need help later on.
Once I’d fathomed this out in my head, I really enjoyed myself. I grabbed on to my friends leaving after it had finished and everything was all good.
Obviously depending on what level sightloss you have depends on what plan you have. With a little forethought we can still enjoy things we used to do.
I’m still very lucky at the moment. Although the days of me wandering off now on my own in situations like that have gone.
PICTURE DESCRIPTION Simon Le Bon stands on stage and 3 cartoon women, One with Black hair, One with brown hair and one with silver hair, stand with there backs towards the image with arms up.
One Vision Blog 