About

Welcome! I’m Susan O’Hara—lipedema patient, advocate, author, and founder of Legs Like Mine®, a footwear company for people with hard-to-fit feet. I write books, share tools, and create resources to help others live better with lipedema and lymphedema. On this channel, you’ll find: 💧 Aqua therapy tips 📚 Lipedema education 👟 Footwear solutions 🌿 Self-care and support Whether you're newly diagnosed or have been managing for years, you’re not alone. Subscribe to join a community that understands and supports you. Let’s walk this journey together! 💙

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