The Albinism Fellowship is a positive and sociable volunteer-run organization that aims to provide information, advice and support for people with Albinism and their families. We also provide information about the condition to professionals working with people with albinism, and other appropriate interested parties. From Jonathan, Debbie and Clio We joined the albinism fellowship when Clio was only 6 months old. We Welcome new boost for mums and dads of young children with albinism While the birth of a new baby is We are aware that some people with Albinism have received shielding letters from their GP’s anAbout the Fellowship
LATEST NEWS
“Why Join The Albinism Fellowship?” &#
Baby Box Launch for International Albinism Awarene
Covid-19 Shielding Letters Statement
About Albinism
Albinism is a comparatively rare genetically inherited group of conditions which results in a reduction or complete lack of pigment (colour) in the skin, hair and eyes
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Albinism charity is run by unpaid volunteers and organize range of Events. We also update latest news to keep our supporters updated. Please scroll below for News and Events sections