Right now this page shows what the charity register holds about ANIRIDIA NETWORK. Claiming it lets you tell your own story — what you do, who you help, how to reach you and how to give — so someone who finds you here sees your organisation as you'd want it seen.
Next, we'll email a verification link to your charity's registered address to confirm you represent ANIRIDIA NETWORK. Once you've clicked it, filling in your profile takes about two minutes.
Curious what a claimed profile looks like? See an example.
We support people in the UK affected by aniridia: those who have it plus their family, carers, doctors, educators and others. We want all these people to be hopeful, confident, supported and well informed regarding aniridia.For them we: organise conferences, meetups and befriendi
We support people in the UK affected by aniridia: those who have it plus their family, carers, doctors, educators and others. We want all these people to be hopeful, confident, supported and well informed regarding aniridia.For them we: organise conferences, meetups and befriending, provide access to professionals and distriubute or signpost to useful information.
Areas of focus