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. Teens with Albinism (Age 10 – 15) 1pm – 2pm This one-hour session will give... Read More Newly Diagnosed Parent Group 3pm – 4pm This session is open to parents whose child... Read More Parents of Albinism (Going to School) 5pm – 6pm For many parents, children going to... Read More We are aware that some people with Albinism have received shielding letters from their GP’s an A blog by Gareth Brydon on his experience of attending Albinism Conference in Oct 2019 We have started a waiting list in case we can take late bookings please email info@albinism.org.uk tAbout the Fellowship
Upcoming Events
TEENS ( AGE 10-15) WITH ALBINISM ZOOM GET TOGETHER
Newly Diagnosed Parent Zoom get together
Parents School Zoom Discussion
LATEST NEWS
Covid-19 Shielding Letters Statement
A Blog on Albinism Conference 2019
Conference Bookings now CLOSED…
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 a
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 a