Throughout the world lipoedema is not rare but it is only rarely diagnosed. As part of our work with the Lipedema World Alliance (LWA) Lipoedema UK have been instrumental in creating a worldwide patient manifesto. This initiative is now supported by twenty-one international lipoedema patient groups and organisations.
Please download and share our manifesto and if you would like to become a supporting patient group or organisation please contact: info@lipedemaworldalliance.com
