Annual Report 2023-2024

Read details of what our officials, members and supporters did as well our finances between 1 April 2023 and 31 March 2024 in the Aniridia Network Annual Report for 2023/24.

Aniridia Network Annual Report 2023/2024 title slide

Key points

  • Successful in-person conference
  • Multiple meetups around the country
  • Befriending, education and medical advice services useful and used
  • UK-wide leaflet distribution campaign
  • Converting child members to adult members challenging
  • Very little activity by fundraisers
  • Very few active volunteers
  • Long time Medical Adviser retired
  • Expenditure greater than income for first time

Thanks to the the amazing input by everyone who helped with all these activities.

However, we continue to really struggle to do some basic things well and rely too much on a few very active volunteers. We badly need more people to help us achieve our goals. Please volunteer and fundraise if you can.

The report will be received at the charity’s Annual General Meeting 2024

Katie, James and Andy, the trustees of Aniridia Network
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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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