Collaboration between healthcare professionals, researchers, and patient associations from diverse nations is a core belief for all of us in LWA, so we are delighted to see the range of patient associations and supporters endorsing this Lipedema Manifesto.
We couldn’t be prouder to be part of this and support the calls for:
• increased funding for #lipedema research
• involvement of people living with lipedema in determining research priorities
• educational programs for healthcare professionals
• improved access to specialised care for those living with lipedema
Please share this Lipedema Manifesto with your contacts and help extend its reach. If you would like to sign up to the manifesto, please contact us through the LWA website https://lipedemaworldalliance.com/ and we will pass your message on.