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The Albinism Fellowship was there to help us through the first few months of Yasmin’s diagnosis. They are a continued support for our family. It’s an organisation where you can discuss anything you need, they are a fantastic group for sounding ideas out, also it’s a place where Yasmin can meet fellow children and adults who understand what it’s like to have Albinism. It’s so important to have that contact.

They are a not for profit organisation and rely on membership, donations and fund raisers to keep a telephone helpline, website and events running.

I do really want to give something back to this group as their help has been invaluable to us.If you could find the time to donate it’s going to a really good curse.

Thank you xx