Age-Related Macular Degeneration (AMD): A Guide for Ontario Patients
Age-related macular degeneration is the leading cause of central vision loss in Canadians over 50. Early detection through routine eye exams can prevent progression to severe vision loss.
Updated · Dr. Ema Hazra
Age-related macular degeneration (AMD) affects approximately 2.5 million Canadians and is the leading cause of vision loss in those over 50. It does not cause complete blindness — peripheral vision is preserved — but it eliminates the central vision used for reading, driving, and recognizing faces.
The macula
The macula is a small, specialized area at the centre of the retina, approximately 5mm in diameter. It contains the highest concentration of cone photoreceptors and is responsible for fine detail, colour vision, and all tasks requiring central vision. AMD damages this region progressively.
Dry AMD
Dry AMD is characterized by the accumulation of drusen — yellowish protein and lipid deposits under the retina — and the gradual atrophy of retinal pigment epithelium (RPE) cells. It progresses through three stages:
- Early AMD — small drusen, no vision symptoms
- Intermediate AMD — larger drusen, possible mild vision changes
- Advanced dry AMD (geographic atrophy) — large areas of RPE and photoreceptor death; central vision loss
Dry AMD progresses slowly over years. It accounts for about 90% of AMD cases but causes the majority of advanced vision loss only in its geographic atrophy stage.
Wet AMD
Wet AMD occurs when abnormal new blood vessels (choroidal neovascularization) grow under the retina. These vessels are fragile and leak fluid or blood, damaging photoreceptors rapidly. Wet AMD can cause severe central vision loss within weeks if untreated.
Warning signs that require same-day evaluation:
- Sudden distortion of straight lines
- New central blur or dark spot
- Rapid change in vision
Use the Amsler grid — a grid of horizontal and vertical lines with a central dot — to monitor for distortion at home. Your optometrist can provide one.
Risk factors
- Age — risk increases significantly after 55
- Smoking — the single most modifiable risk factor; smokers have 2–4x the risk
- Family history — strong genetic component
- Cardiovascular disease, high blood pressure, obesity
- Lighter iris colour (blue or green eyes)
- Prolonged UV exposure without protection
AREDS2 supplementation
For intermediate AMD or advanced AMD in one eye, the AREDS2 formula (Age-Related Eye Disease Study 2) has been shown to reduce progression risk by approximately 25%:
- Vitamin C 500mg
- Vitamin E 400 IU
- Lutein 10mg
- Zeaxanthin 2mg
- Zinc 80mg
- Copper 2mg
These supplements are available over the counter and are not covered by OHIP, but are widely available at Ontario pharmacies. They are not recommended for early AMD or as a general preventive measure in those without AMD.
Anti-VEGF treatment for wet AMD
Anti-VEGF injections (aflibercept/Eylea, ranibizumab/Lucentis, faricimab/Vabysmo) are administered directly into the eye by a retinal specialist. They block the growth factor responsible for abnormal vessel growth and leakage. Most patients require injections every 4–16 weeks, often indefinitely. These treatments are covered by the Ontario Drug Benefit (ODB) program for eligible patients.
Monitoring at home
Anyone diagnosed with AMD should monitor daily with an Amsler grid and report any new distortion immediately. Do not wait for your next scheduled appointment — wet AMD requires urgent treatment.
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Book an appointment →Frequently Asked Questions
- What is age-related macular degeneration?
- Age-related macular degeneration (AMD) is a disease that damages the macula — the central portion of the retina responsible for sharp, detailed vision. It causes progressive loss of central vision used for reading, driving, and recognizing faces, while peripheral vision is preserved. AMD is the leading cause of severe vision loss in Canadians over 50.
- What is the difference between dry AMD and wet AMD?
- Dry AMD is the more common form (accounting for about 85-90% of cases) and progresses slowly over years through the accumulation of drusen (protein deposits) under the retina. Wet AMD is less common but more severe — abnormal blood vessels grow under the retina and leak fluid or blood, causing rapid central vision loss. Dry AMD can convert to wet AMD.
- What are the warning signs of AMD?
- Early AMD has no symptoms. As it progresses, warning signs include blurred or distorted central vision, straight lines appearing wavy or bent (metamorphopsia), a blurry or dark spot in the centre of vision, and difficulty reading or recognizing faces. Any of these symptoms require prompt evaluation — wet AMD can progress rapidly.
- Can AMD be treated?
- Dry AMD in early and intermediate stages has no proven treatment, but AREDS2 vitamin supplementation (vitamins C, E, lutein, zeaxanthin, zinc, copper) is recommended for intermediate AMD to reduce progression risk by about 25%. Wet AMD is treated with anti-VEGF injections (Eylea, Lucentis, Vabysmo) administered into the eye by an ophthalmologist, which are highly effective at stabilizing or improving vision.
- Is AMD hereditary?
- Yes. Family history is a significant risk factor. If a first-degree relative has AMD, your risk is 3–4 times higher. Genetic testing is available but not routinely recommended in clinical practice. The most actionable steps remain regular monitoring and lifestyle modifications.
Author
Dr. Ema Hazra, OD — Pending clinical review
Optometrist, Spadina Optometry
A Toronto native, Dr. Ema Hazra earned her Doctor of Optometry from the University of Waterloo in 2018 and returned to Spadina Optometry — where she had previously interned — bringing experience from an ocular disease externship at Eye Associates of Pinellas in Florida alongside leading ophthalmologists specializing in glaucoma, macular degeneration, and retinal disease. Her clinical interests include myopia control, specialty contact lenses, dry eye disease, and refractive surgery, and she is passionate about providing comprehensive care for patients of all ages, especially children.