Advocacy Hub
Lipedema has been ignored by medicine for eighty years. That is not an accident. It is the result of a system that has consistently under-researched, under-funded, and under-prioritised conditions that affect women. It will not change on its own. Elora's advocacy hub gives you the tools to do that, whether you have five minutes to write a letter or the energy to lead a campaign.
Lipedema policy varies significantly by country. This tracker shows where your country stands and how you can push for change.
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Ready-to-use letters for contacting your GP, insurer, or elected representative about Lipedema. Adapt them to your situation.
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Lipedema care changes when people push for it. These are the campaigns Elora is supporting, and how you can join them.
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Elora ambassadors share their stories, support newly diagnosed women, and advocate for change in their own communities.
Read →Healthcare systems, diagnosis pathways, and advocacy networks differ from country to country. These guides break down what you need to know where you live.
