Firstly congratulations on your little one! At the AFA we appreciate and understand how overwhelming it is to be told your child has Albinism. You will most likely have a list of questions you need answered and concerns for your childs’ day to day life.
Adapting as a family to albinism is a process and, at times, can seem isolating and uncertain. The AFA’s committee are dedicated to ensuring that you are not going through this journey alone and are able to reassure you that you your child will be ok. We are also able to recommended service providers and specialists in your area.
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