How diabetes robbed me of my sight

Image shows a close-up shot of a human eye, showing in fine detail the white of the eye, a light brown iris and long, dark eyelashes. The eye is looking up towards a light.

Bairnsdale Regional Health Service Media and Communications Manager Jamie Duncan has had Type II diabetes for almost half his life. A little over a decade ago, it caused him to become blind.

Diabetic retinopathy is one of the five main causes of blindness in Australia today.

While he was able to recover his vision with a series of invasive surgeries and other procedures, many people with diabetic retinopathy do not.

Jamie shares his story for National Diabetes Week, urging others to manage their diabetes properly, seek regular medical check-ups and consult an ophthalmologist before the damage to their eyes is done.

I knew I was in trouble when an optometrist examined my eyes and recoiled in horror at what she saw deep inside them.

Diabetic retinopathy was robbing me of my sight, and I had no idea.

I’d never seen an optometrist before. I noticed that my vision had become a little blurry when I was driving, and I assumed glasses would fix everything – just as they had for other members of my family.

Not quite, as it turned out. I got both a new set of specs and an urgent referral to the Royal Victorian Eye and Ear Hospital.

Diabetic retinopathy damages the tiny blood vessels that supply the retina, the nerve tissue within the eye that’s responsible for vision.

The damaged blood vessels can leak blood and fatty deposits that, over time, obscure the patient’s vision.

I was a 37-year-old husband and father of five.

My diabetic retinopathy was already well advanced despite only recent and subtle changes to my vision. My retinas were a mess.

Initial intervention

A team of ophthalmologists at the Eye and Ear began immediate retinal laser surgery. This involved having thousands of tiny spots burned into my retinas to head off the development of leaks and new, weaker blood vessels that might also bleed.

I had to travel to Melbourne from my home in country Victoria every few weeks and take time off work for treatment.

Despite the ophthalmologists’ best efforts, retinal bleeding began.

At first, it caused small splotches that were an annoyance more than anything, but the damage began to build.

The Eye and Ear team tried eye injections, using a drug that inhibited the development of blood vessels, in conjunction with laser surgery.

Within a few months, I had lost legal driving vision in my left eye but my right eye was more stable.

I consulted Vision Australia, which helped out with some vision aids to keep me reading comfortably at work.

The reality hits home

To minimise the impact of treatment on my working life, I sought private ophthalmology care in my town.

I continued having laser surgery for another year until July 2012, a month before my 40th birthday, when a large bleed in my right eye took my remaining sight.

It was agonising. The bleed happened at the office one afternoon. I realised what was happening, dropped everything and raced home without explanation, knowing that soon my vision would be gone.

My vision had been fading for a long time. I thought I was prepared if the worst happened, but that final blow was devastating.

For the first time, I was frightened about the future and my place in it. I was now legally blind. I couldn’t read, write or drive. Everything was cloaked in a shifting, brown haze – like a liquid version of a greasy fish shop window.

I couldn’t fathom what the next weeks and months would bring. How would I get around? How would I work? How would I perform basic household tasks?

The reality really hit home later that evening when I was cradling my then four-month-old daughter. Her tiny hand reached up to touch a tear rolling down my cheek, and I realised I couldn’t see her face.

My wife shared my fears but also had to cope with my emotions. It was far tougher on her than she deserved. It was the same with my kids, who saw the mess I was in and sensed the tension in the house.

I still carry a lot of guilt about that – mostly because I knew that my failure to properly manage my diabetes was at the heart of this mess.

Adjusting and waiting

The next day, I pulled myself together as best I could. I phoned my ophthalmologist, sent out a distress signal to Vision Australia and caught the bus to work to explain what had happened.

My ophthalmologist recommended an invasive surgical procedure, a vitrectomy, in which the vitreous (a jelly-like substance in front of the retina) is removed along with the retinal blood suspended within it and replaced with gas, a saline solution or an oily liquid.

But surgery was at least six weeks away.

Vision Australia arranged for a new workplace assessment to determine what assistive technology equipment I’d need to keep working.

Within a few days, I had ZoomText software that magnified and read aloud any on-screen text, a CCTV camera and hand-held magnifier for printed text and a high-visibility keyboard.

The support of my ophthalmologist and Vision Australia kept my employer happy and eased my mind immensely.

I spent the next few weeks bumping down corridors and falling flat on my face, but my technology made work easier. Still, the wait was gruelling. There was no guarantee the surgery would succeed.

Enduring surgery

After two months, I had my first vitrectomy on my left eye at a Melbourne hospital. Under this procedure, the patient is initially unconscious but is soon roused for the bulk of the operation, although under heavy sedation.

I was lucid enough to speak to the team during the operation.

Because of the risk of infection, my ophthalmologist operated on one eye rather than both at the same time.

After an overnight stay, I was allowed home with a gas bubble inside my eye to protect the retina as I recovered. It dissipated in a few weeks. Six weeks after surgery, I was back at work.

I had a vitrectomy on my right eye exactly a year later, but some surprise post-operative bleeding a month after the procedure forced a third operation.

A brighter future

It’s now been more than 10 years since my last surgery. My vision remains strong enough to do everything I did before diabetic retinopathy darkened my doorway.

I’m doing my best to maintain my blood pressure and blood sugar, key facets of the progression of the disease.

But I could have avoided it all.

Anyone with diabetes should see their doctor regularly and consult an eye health professional like an optometrist or an ophthalmologist every one to two years.

Look after your health. Don’t let it happen to you.

Are you at risk of diabetes? Do this fast self-assessment here: https://www.health.gov.au/…/the-australian-type-2…/tool

Join the conversation about diabetes here: https://www.diabetesaustralia.com.au/national-diabetes-week/

How prevalent is diabetes in our community? Find out here: https://map.ndss.com.au/#!/

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