NOAR stands for National Organization for Albinism and Hypopigmentation. It is a non-profit organization that aims to support individuals with albinism and hypopigmentation by promoting awareness, providing education, and advocating for equal rights and opportunities.
Albinism is a genetic condition characterized by the lack or absence of pigmentation in the skin, hair, and eyes, resulting in a lighter complexion and visual impairments. Hypopigmentation, on the other hand, refers to a reduction in the production or distribution of melanin, the pigment responsible for the color of the skin, hair, and eyes.
The National Organization for Albinism and Hypopigmentation works towards creating a supportive community for individuals with these conditions. They strive to raise public awareness about the challenges faced by individuals with albinism and hypopigmentation, while also dispelling misconceptions and stereotypes.
Through their educational programs, NOAR provides resources, information, and support to individuals and families affected by albinism and hypopigmentation. This includes assisting with access to proper medical care, vision aids, and other necessary accommodations to enhance quality of life.
NOAR also actively engages in advocacy efforts to ensure that individuals with albinism and hypopigmentation are afforded equal rights, opportunities, and protections against discrimination. They work towards eliminating barriers faced in education, employment, healthcare, and social inclusion.
In summary, the National Organization for Albinism and Hypopigmentation serves as a vital resource and support network for individuals with albinism and hypopigmentation, striving to create a more inclusive and understanding society.
