As the title suggests, this blog is going to be about an eye disease called Stargardt's disease.
But before I go on to talk about the disease and my experience with it so far, I'll tell you a little bit about me.
My name is Harriet Doran, I'm 18 years old, and I'm currently living in the UK, Hampshire. Within the last 3 days, I was diagnosed with this condition at Moorfields Eye Hospital in London. I'm not going to call Stargardt's a disease, because it isn't something you catch from someone else. You're born with it, and it slowly decreases the clarity of your central vision over time.
I'm not an expert on this topic, and this blog wasn't designed to give the ins and outs of the genetics of the disease or anything else "technical" related to the disease. However, I will provide links to help you understand the general and known effects of the disease and anything else related to my blogs. But seeing as this is my first blog, I shall tell you all about the outline of the disease, and things that are worth knowing the most.
Typically, the disease is noticeable before the age of 20, but it is most commonly diagnosed between the ages of (I believe) 9 and 13. This condition cannot be corrected with glasses or laser correction services, as the condition does not affect the refraction of light into your eye. There is a tiny, tiny area at the back of your eye called the macula which is responsible for central vision. It also helps you to distinguish different colours and helps you to pick out fine detail. When the macula is damaged when the cells don't work properly, the centre of an affected person's vision become blurry, filled with black or blurry patches. The disease, in most cases, can render a person "legally blind" in a short time. However, since the disease varies considerably from person to person, it is hard to tell when and if the person will become blind or not. But in my case, Prof. Moore has predicted me to lose my vision completely within 1 to 15 years.
A person is considered to be legally blind when they can only read as far as the top letter on a visual acuity chart. Currently, I can read 4 lines down, meaning that I am not allowed to drive. Here is a picture showing one of these charts, and notice where I can read, where I'm predicted to go and where I should be able to read in order to drive. NOTE: I can read all of these letters on this picture, but these visual acuity charts are placed 14-20 feet away from a patient when being tested. Not to size.
When I was told that I would only be able to read the top letter if I were to become legally blind... I was stunned. How would I be able to live in a world where I could only be able to read letters that size? How would I get around, read and do normal things like my food shopping and cooking? What makes everything even more terrifying is my age. I'm only 18. Seeing people driving around, passing their driving tests and not having a care in the world. That is a dream and experience I may never have. And if I'm lucky enough to receive any treatment that could regain my already lost vision, I'm going to be 40 odd! By then it won't be worth learning how to drive would it?
If I am to become legally blind in 15 years, I'm going to be 33. That's just over a third of my life gone. If I get married, I won't be able to see my wedding dress properly, or where I get married properly. If I have a baby, I won't be able to see their face, same goes for my boyfriend. I'm lucky enough for now to be able to see his and my friend's faces... but I doubt for much longer.
For the time being I can only fully focus on one feature on a face. I mostly look at the eyes, but if I can't hear someone I look at their mouth to get a better idea of what they're saying to me. All of the other features on the face look like they have skin pulled over the main features of their face.. like they're wearing a morph suit. This is what I can sort of see, the mouth, moustache and edge of the suit would be more defined when I see it... but I had to enlarge the photo slightly.
That is how I see someone if I look at their mouth. That's what I have to live with every day, and it isn't going to get any better. In fact, it will only get worse.
Another issue with this condition is that it takes a long time for me to adjust to darker rooms when coming out of a light area into a darker one. This is extremely frustrating for me when I'm at work as I can't see people's faces when I'm adjusting to the light changes. If I can't see them, how can I serve them their food quickly? I'm lucky enough to have considerate colleagues who help me in any way they can, and help me when they see that I'm struggling to find a customer, a button the till or even a spirit hanging on display.
Finally, the most annoying thing for the moment, especially when I can't distinguish like colours, such as a light blue and pale pink/purple is when I'm in college. Learning from overhead projectors and PowerPoint presentations proves to be a challenge every college day. Especially when the light coming into the classroom from outside also brightens the board. It makes it that little bit harder to read what I'm meant to be noting down. However, I copy from classmates into our notebooks or ask the teacher to wait before changing slides so I have more time to question if I'm reading what I think I can see correctly, or to buy me more time to read the board carefully. This may not seem hard to ask for.. but being the only person in the class with impaired vision, and learning about it so late is quite a scary, and frankly, embarrassing thing to ask for. Yes, I'm a typical teenage girl who can be self conscious about the normal things... am I pretty? Am I overweight? But I've got an added thing... Will people understand what I'm going through? Do they think I'm "acting it up" to get attention? But I have to make the most of my vision whilst I still have it. I know I shouldn't be worried about what other people think of me, but it's hard to do. But I've only just started this long journey, so I have plenty of time to adjust to people who may not be considerate enough to acknowledge that I, in effect,, do have a disability.
Again, I will have to cope with the condition that I am living with, and I know that I'm strong enough to ignore people who just don't "get" what I have to live with.Thank you to everyone who has spared the time to read this blog! Hopefully everyone can understand the enormity of being diagnosed with this condition, and I thank those of you who have helped and hopefully in future will help those with visual impairment or any other impairment.
In future blogs I'll talk about how I noticed the decrease in my clarity of vision and what testing I've gone through and my journey through hospitals to get the diagnosis I now have.
Thanks for reading!
Links that may be of use:
Overview of Stargardt's Disease:
Visual Acuity tests:
Moorfields Eye Hospital NHS