The HFSA will support individuals and their
families who have been diagnosed with hemifacial spasm, as well as those who
have not yet been diagnosed but who are searching for answers. We will
attempt to provide up-to-date information regarding our common affliction and
support fellow sufferers, and their families, as they seek medical treatment
and options.
The HFSA will also create an online community of those who
have hemifacial spasm, or who have had it in the past and are now cured and
want to provide continued support for others.
The Hemifacial Spasm Association (HFSA) was formed to create a
peaceful, unified place on the Internet for those suffering with hemifacial
spasms that are seeking moral support and truthful, reliable answers to
questions and treatment options.