New Medical Advisors

We have appointed two distinguished medical experts to continue our support for the aniridia community. Mr John Brookes and Professor Mariya Moosajee are now our medical advisors, ready to respond to enquiries from our members and their families.

Both are consultant ophthalmic surgeons, experienced at treating adults and children with aniridia. They work at Moorfields Eye Hospital that many with aniridia in the UK attend. Their clinical experience at one of the world’s leading eye hospitals, ensures our community will get guidance from the forefront of rare eye disease care.

John Brookes

Mr John Brookes

He brings extensive knowledge of eye surgery and the challenges faced by people with aniridia. He first volunteered with us in 2021 providing online patient consultations as part of our hosting of the European Aniridia Conference. His expertise was invaluable to those who spoke with him.

Professor Mariya Moosajee

Dr Mariya Moosajee

She is a doctor whose research and clinical work has significantly advanced the understanding and treatment of inherited rare eye conditions, including aniridia. Being both a clinician and a researcher, she brings knowledge of cutting-edge current and emerging treatments.

She has been a valued partner for several years. She and her team have presented their findings at several events, to much appreciation. Their studies have grown our understanding of the natural history of aniridia and the effect of genetics on symptoms.

Plus she volunteered to provide weekly “Ask the expert” sessions during the COVID-19 lockdown, when patients could not go to hospital appointments. These were very well received.

She also pioneered the Gene Vision website as a resource for patients and professionals – a very valuable resource.

Both advisors are committed to providing thoughtful, evidence-based responses to medical enquiries, helping our members navigate their care with confidence and clarity.

Advice for members

Mr Brookes and Professor Moosajee are here to help you, if you have questions about

  • treatment options
  • managing symptoms
  • understanding what the future may hold.

Aniridia Network members can ask questions to us and a range of other doctors by contacting our Medical advice service. Note that they can give really useful general guidance based on the information you provide. However, you should always seek specific advice from your own doctor, based on an examination you and a review of medical notes.

Continuing our specialist support

Mariya has been working with us for many years. John is a more recent addition. We are delighted that they are continuing the excellent service kindly previously provided by now our retired Medical Adviser Melanie Hingorani. Together they have helped many individuals and families better understand aniridia and make informed decisions about their care.

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About Aniridia Network

A charity support group for people with the genetic visual impairment aniridia and their families in the UK and Ireland. Our vision is that people with/associated with aniridia are hopeful, confident, supported and well informed regarding aniridia. Founded in 2000. First registered as a charity in 2011 and fully in 2018.
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