There are currently 18 members of IMP, from 3 different continents. All are active national patient organisations representing patients and their families affected by mitochondrial disease. Together they form the voice for approximately 8,000 patients worldwide.
IMP offers support and information to people living in countries without a national mito organisation. Please contact us by This email address is being protected from spambots. You need JavaScript enabled to view it. or on Facebook.
