Susan Ballis’ daughter has albinism and she is happy to share her story and lend an ear. Reach out to Susan via email at [email protected].
The Vision For Tomorrow Facebook Page has an active community of individuals who ask questions and share experiences. In addition, we continuously post any information which may be of interest to individuals living with albinism.
We hope you choose to reach out and get support from a wonderful community of people living with albinism!