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Pigmentosa (RP) is an hereditary, progressive eye disease that affects a person's
night and peripheral vision. See these sites for more information.
- Australian Retinitis Pigmentosa
and Retinal Degeneration
- Good resources from down
under! This site includes information and links relating to computer access
and adaptive equipment, international and Australian RP and low vision support
organizations, links to research sites and sites by persons with RP, chat,
mailing lists, and more.
- Focus is a "a grass-roots
group of RP patients calling for new and expanded directions in scientific
research and applied medicine for their condition." Its website provides
information about alternative treatments and current research and studies,
which are provided on "an information only basis and do not intend or
imply that they are the correct or only course of treatments that should be
administered." The site includes extensive information about RP and nutrition,
FAQs, and a newsletter. As always, DRM recommends viewing medical and legal
information on personal websites with caution.
- RP - Retinitis Pigmentosa
- John Wenberg, the author
of this personal homepage, has compiled an extensive guide to RP and RP resources
online. Topics covered include RP links, RP E-Pals, mailing lists, research,
RP Internet chat, the inheritance of retinal degeneration, online articles,
contacts, FAQs, personal experiences, and more. As always, DRM recommends
viewing medical and legal information on personal websites with caution.
- Blindness and Visual Impairments
- Resources in your state
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