Over 17 million women live with #Lipedema yet it’s rarely covered by national news. @GMA @TODAYshow @people @nytimes @washingtonpost please share our stories & raise awareness during #LipedemaAwarenessMonth. We deserve to be seen & heard. #WomensHealth
youtu.be/GFR3Q20uLhM?si…
New research shows lipedema isn’t just about pain; it’s about shame, stigma & the fight to be seen.
Listen to the latest episode of Legs Like Mine: The Podcast:
👉youtu.be/vBOFSeg-KU4
#LipedemaAwareness #LipedemaResearch #ChronicIllness #LipedemaPodcast #PatientPerspective
🚨 New episode! #Lipedema doesn’t just affect our bodies — it impacts intimacy, relationships, & self-worth. 💔
We’re talking sex, shame, & what healthcare gets wrong.
🎧 Watch now: youtu.be/sEPL_MgbttE
#LipedemaAwareness #SexualHealth #BodyImage #ChronicIllness #Sex #brave
Had a great Sunday swim and then completed a nice little arm workout without needing mods. Sharing what I found to do from
The web.
We’d love to have you join the American Lipedema association for advocacy!
Good job!
How’s recovery going? I’ve had three so far.
That’s typical Lipedema. Many of us have fabulous bloodwork.
I’m 52, & living with #lipedema — & I just kicked off a 30-day challenge for #LipedemaAwarenessMonth 💪🏽✨
No filters. No excuses. Just real movement, mindset, & visibility.
Watch Day 1: youtu.be/8fg9sjcaa2w
#LipedemaStrong #LegsLikeMine #RealBodyJourney #75hard #lipoedema
🎙️ New episode of Legs Like Mine: The Podcast
Over 50% of doctors in a new study had never heard of #lipedema. It’s a global problem & I’m sharing what needs to change.
🎧 Hear it here: youtu.be/uSVJD9iqlm0?si…
#Lipoedema #LegsLikeMine #ChronicIllness #PatientAdvocacy #lipedema
Lipedema patients are forced to cobble together their own care—alone. I share my story of surgery, travel, recovery & why this system must change.
🎧 Listen: youtu.be/CKaDrKz11tg
We deserve full-spectrum lipedema care.
#Lipedema #LegsLikeMine #HealthCareAccess
I fly ✈️, I road trip 🚗, I travel internationally 🌍—with lipedema & lymphedema. In Legs Like Mine: The Podcast, I’m sharing my real travel routine: compression, hydration, seat hacks & more. 🎧 Listen now! youtu.be/7LKKelaS-gI
#lipedema #travel #lymphedema #lymphedemalife
The Earth isn’t perfectly smooth—and neither are we. Nature doesn’t apologize for curves, and neither should we.
This Earth Day, show your body the same love you show the planet.
Rest. Move. Breathe. You’re doing amazing.
#Lipedema #EarthDay #lipoedema www.legslikemine.com
Do have trouble finding cute shoes that fit due to swollen feet, lymphedema, Lipedema or foot deformities? Look no further! Legs Like Mine footwear is here! LegsLikeMine.com/products
#lipedema #lipoedema #swollenfeet #shoes #widecalf
To my UK lipoedema ladies, I am travelling through and would love for you to pop on by and say hello!
Hubby and I will be at the London Marriott County Hall for a meet and greet Thursday 13 March 2025 from 4-7 PM. We'd love to see you!
#lipoedema #lipedema #meetandgreet #legslikemine
At the doctor & the red shoes always bring up an opportunity to talk about #lipedema & why I started a footwear company.
Ps our order of shoes are at the port of LA right now!!!!
LegsLikeMine.com
#shoes #footwear #lipedema #lipoedema #lipedemaawareness #swollenfeet
Joining blue sky. Hello friends!
Here is our newest slingback loafer made especially for ladies with swollen feet, based off of the measurements and feedback from many women with Lipedema.
For more info visit us at LegsLikeMine.com
#lipedema #lipoedema #lipedemaawareness #shoes