We are a registered
charity that helps those with Lupus; we support our members
and advise others as requried, and strive to increase the public's
awareness of the disease and its impact.
We publish a newsletter every 4 months and have published
leaflets and booklets explaining the condition.
We arrange meetings and medical talks for members, their families
We are self-financing through donations from members and moneys
raised from sponsorship. We receive no government grants but
have in the past received help towards the publication of our
leaflets and booklets.
We are members of the European Lupus Erythematosus Federation
and communicate with the Lupus Foundation of America.
In the Training and Support Service we offer a range of services
that aim to help you and your organisation find workable answers to these
kinds of challenges and many more. Click on the links below or left for