Resources for Alopecia
This is a non-profit organization that funds international
research in alopecia areata, provides international support
and education through support groups and contacts, and
annual patient conferences held throughout the U.S.
This a large social networking site for people with
Alopecia with members worldwide.
Thea Chassin founded this non-profit in 2007. This network
was created as the first non-profit support organization
devoting all its resources to the emotional and practical needs
of women with alopecia areata.
The Children’s Alopecia Project is a non-profit organization
directed specifically to children with alopecia. Their goals are
to generate public awareness of the disease, raise money
for research and build self-esteem via support group
participation for children and their parents.