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Related Links

Albinism-Related Sites

ALBA (Asociación de ayuda a personas con albinismo) is the Spanish association that aims to help and support people with albinism and their relatives. ALBA also promotes a wider knowledge about albinism through conferences and seminars.

Albinism and Development This group exists for parents of children with a diagnosis of ocular or oculocutaneous albinism who also have developmental issues such as language, social and/or behavior. Join the group to share information, give and receive support and to keep in touch with others.

Albinism Fellowship of Australia the Fellowship provides a united voice to encourage productive developments and support within business, government and media.

Albinism Fellowship (UK) provides advice and support for people with an interest in albinism. The site offers a range of appropriate services that:

  • Provides information
  • Raises awareness
  • Challenges misrepresentations
  • Improves self-esteem
  • Gives opportunities to meet other people affected by albinism

Albinism in Popular Culture explores the mythology of albinism. Take an in-depth look at the various ways in which this unique trait has been perceived and presented across cultures and during various eras.

Albinism Trust New Zealand - We are established to share ideas and information which enable people with Albinism to live, learn, work and play. We do this through promotion of general understanding and the encouraging of positive enabling attitudes about Albinism.

Albinismus Info a German site that provides medical and ophthalmological, low-vision and educational information for persons with albinism.

Albinismus Selbsthifegruppe a German web site for people with albinism

The Albino Foundation In Nigeria (TAF) is the largest albinism association in Africa. The Albino Foundation is committed to addressing the plight of albinos and to change negative mind-sets and socio-cultural stereotypes about albinism in Nigeria and the world.

Asante Mariamu is a grassroots campaign dedicated to increasing awareness about the immediate and long-term mortal threats to people living with albinism in East Africa.

BAI China is an online adoption support group for friends and family of Children from China with albinism. BAI China provides information and support for people in the process of adopting a child with albinism from an Asian country and for families who have already adopted an Asian child with albinism

Chicago Connection for Minorities with Albinism CCMA’s goal is to bring together persons who are isolated to inform them about issues related to their ethnicity and the condition of albinism in order to bring about empowerment and a sense of community for all minorities or relative(s) of persons with albinism.

Chicago Connection for Minorities with Albinism CCMA’s goal is to bring together persons who are isolated to inform them about issues related to their ethnicity and the condition of albinism in order to bring about empowerment and a sense of community for all minorities or relative(s) of persons with albinism.

Dermatology in the Cinema This site has been put together by Vail Reese, MD, a dermatologist who is also a film buff. Albinism is only one of the conditions covered.

A Dutch site about albinism includes drawings of how albinism affects the eye.

The Hermansky Pudlak Syndrome Network The Hermansky-Pudlak Syndrome Network Inc. is a volunteer, not-for-profit, self-help support group for persons and families dealing with Hermansky-Pudlak Syndrome.

The International Albinism Center at the University of Minnesota. The IAC is a team of research professionals interested in understanding the basis of albinism in humans. This site features a current paper on human pigmentation and albinism as well as a bibliography of papers on different aspects of albinism. It also has an email link where you can submit questions about albinism to graduate students in genetic counseling. Special thanks goes to Dr. Bill Oetting of the IAC for getting this site together and also to Dr. Richard King and Dr. Gail Summers for their ongoing commitment and support.

Nigerian Albinism Support Group A Nigerian non-profit group whose aim is to enhance the well-being of people with albinism by providing information, increasing awareness and organizing workshops and conferences.

Nineteenth Century Images of Albinism  This site shows a variety of American images that date from the 1870s - 1890s.

Norwegian Association For Albinism (NFFA) A Norwegian site about albinism.

Positive Exposure is a project with a goal to complete a portfolio of empowering, evocative photographs representing persons of various ages and cultures with albinism. Like many others, people with albinism face the fears, myths and stereotypes associated with difference. This project challenges the stigma associated with physical difference using one of the 20th century's most powerful tools to fight discrimination: photography. These pages also include copies of the much-celebrated photo essay in Life magazine “Redefining Beauty”.

http://www.albinismo.it/

http://www.albinit.org/


These are sites that have information related to albinism or visual impairment. If you have a site that you would like to see added, please let us know. After consideration, relevant sites will be added.

Please note — These links are provided for informational purposes only. Listing on this page does NOT constitute an endorsement by NOAH. 

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NOAH
The National Organization for Albinism and Hypopigmentation
PO Box 959, East Hampstead, NH 03826-0959
Phone: 800 473-2310 (US and Canada) Phone: 603 887-2310 Fax: 800-648-2310
http://www.albinism.org

If you have any questions or comments, please e-mail us at webmaster@albinism.org

NOAH is a volunteer organization for persons and families involved with the condition of albinism. It does not diagnose, treat, or provide genetic counseling. It is involved in self-help, while trying to promote research and education.

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