Sneddon's Syndrome is a rare, highly threatening, neurovascular disorder
that is often misunderstood and frequently misdiagnosed. The Sneddon's
Foundation of the U.S. was formed in May 2008:
1. To develop a clearinghouse of information on Sneddon's Syndrome
in two formats, one for the medical community and one for the
community of patients, families, and the general public, and to
disseminate both sorts of information through every possible means;
2. To develop a nexus of commmunication about Sneddon's Syndrome
within the patient community, within the medical community and
across the divide between the two; and
3. To encourage and support research on Sneddon's Syndrome in hopes
of clarifying both a cause and a cure for this devastating disease.
~ The Sneddon's Foundation: Healing through the flow of information ~