RETINITIS PIGMENTOSA SOCIETYThe Retinitis Pigmentosa Society was set up in 1975 by a young woman
suffering from RP. Since then the Society has given thousands of people the
opportunity to meet fellow-sufferers and resolve common problems. At the same
time it has been working towards a common goal of finding a cure for the
disease. The BPRS is attacking RP on two fronts: - It funds research in many centres, in the UK and abroad.
- The Society also provides help, encouragement and guidance through our
Welfare Committee and its network of Welfare Officers, to members who are
distressed by the condition. There are 36 regional branches.
Retinitis Pigmentosa Society
PO Box 350
Buckingham
MK18 5EL  01280 860363
 01280 860515
 http://www.brps.demon.co.uk/
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