Hosted by Susan O’Hara · 🇺🇸 US · EN-US · 42 episodes
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🎧 Legs Like Mine: The PodcastA patient-powered podcast about lipedema — the painful fat disorder that’s underdiagnosed, misunderstood, & often dismissed.Hosted by Susan O’Hara, a lipedema patient, advocate, & author, this podcast explores the real-life challenges of living with lipedema through honest conversations, current research breakdowns, and empowering stories. Each episode combines science & storytelling to raise awareness, build community, and give voice to millions of people living with this chronic and progressive condition.Follow me on IG: @legs_likeminewww.LegsLikeMine.com
Susan O’Hara hosts Legs Like Mine: The Podcast, a health show with 42 episodes published.
There are all kinds of online resources for providers showing them what to look for physically when diagnosing lipedema. But not a ton of information on what it feels like from the perspective of a patient - the pain, te
I'm pretty excited today! In this update, we share a major national development that could reshape the future of care, research, and awareness for lipedema and other lymphatic diseases: the work of the National Commissio
In this episode, I talk about my experience as a patient who shares online and just some of the crazy things people have tried to sell me. But then I also share several valuable and FREE resources providing everything yo
In this episode, we talk about the top ten reasons why we have a lipedema awareness month every June, and outcomes I expect to see. We'll talk about why I don't want to "preach to the choir" with my outreach this year, b
Could the most overlooked conservative treatment for lipedema be... muscle? For years, lipedema conversations have focused on diagnosis, compression, surgery, pain management, lymphatics, and symptom control. All importa
In this episode I discuss a new research study from Spain that just came out, where researchers surveyed more than 1000 lipedema patients and compared the results to the national health survey. The findings confirm the o
There's been a lot of hype, and different people trying to sell patients information, about a possible blood test for lipedema. Guess what? Research IS happening on it, and yes, they have found some biomarkers that will
Today I am discussing the newly-dropped Global Lipedema Consensus Document that was published by members of the Lipedema World Alliance. (link) In this comeback of Legs Like Mine, I break down a major new international m
Take action: Email the CDC at nchsicd10CM@cdc.gov before October 9, 2025 to support the initiative — and ask ten friends or supporters to do the same. Together, our voices can make a lasting impact. Welcome to Legs Lik
Welcome to Legs Like Mine: The Podcast — where we explore lipedema from a patient’s perspective, break down the latest research, and share real-life experiences of living with this often misunderstood condition.In this e
This one is a little bit heavy on the science but what the big takeaway is, is that researchers are looking into our genetics, our bloodwork, and our fat cells, and are learning how to identify lipedema from blood tests,
As the month progresses, I'm enjoying all of the challenge bits more and more, especially the drinking of water and moisturizing. These are things I needed to be doing. In this episode I also talk about the OKC Thunder,
Come sit with me for a while while I tell a tall tale of making call to action videos for national news media and a long lipedema ladies meet up in OKC this weekend. It was good and busy and I'm happy it all happened! #l
Welcome to Legs Like Mine, the podcast, where we talk about all things lipedema from a patient's perspective. I watch for new research and news about lipedema every day and come to share it with you. And today, we have a
Follow along with me to see what I've learned, what challenges I've experienced, and glories gained by going through my own Lipedema Awareness Month challenge. This week is all about reaching out to BIG media and today I
Hi friends! Wondering how my challenge is going and if I've given up yet? LOL. Join me this Monday morning for an update.
In this episode, I am personally inviting you to join me in the Lipedema Awareness Month Challenge — a 30-day journey designed to raise awareness outside the lipedema community. Why? Because 1 in 9 women may have lipedem
In this episode I'm talking about my success yesterday, sharing lipedema stuff on an influencer's page (Jeremiah Daniel Johnson on FB), using AI to write songs using Suno AI, and how I used DALL-E image generation to ill
Today's video goes over my personal Lipedema Awareness Month Challenge consisting of seven things I want to do this month. And on day 4, I missed the mark by 1 out of seven. Which one will it be?Check out the blog on www
🎧 Welcome to Legs Like Mine: The Podcast — where we explore lipedema from a patient’s perspective, break down the latest research, and share real-life experiences of living with this often misunderstood condition. In to
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Legs Like Mine: The Podcast is hosted by Susan O’Hara. The show is categorised under health (fitness) and has published 42 episodes.
Legs Like Mine: The Podcast has published 42 episodes.
Legs Like Mine: The Podcast regularly covers health, fitness. It sits in the health category, with a fitness focus.
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