Living with

My child has just been diagnosed with Aniridia, what should I do?

The first, best thing to do is to get informed. The strongest advocate for a child reads information about aniridia on credible websites and using well-researched resources. Peer support is a must: many websites and support groups online can connect parents of children with aniridia in order to share their experiences and insights.

SOURCE: Emory University - Department of Human Genetics in collaboration with ThinkGenetic • • DATE UPDATED: 2019-06-14


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