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When
the group was formed,
dystonia patients were affiliated with the Finnish Parkinson’s
Society, which had already all the services required. In 1998 a separate
Dystonia Society was founded with at present 547 members. There are a
large number of regional support
groups in different parts of the country and patients, who have no
access to any group, keep contact by telephone. A newsletter is
published four times a year and, annually
in September, ‘Dystonia Days’ are organised for
members.
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