My usual content talks about the story of my own journey fighting the rarely diagnosed disease called Lipedema.
But Lipedema isn't just one story - it's the stories of thousands of people around the world. It's the stories of teenagers, of young women and of ladies of all ages. It's more than their symptoms: it's the story of their struggles and their successes.
For Lipedema Awareness Month, I asked these beautiful Lipoedema sufferers one question; "What would you want the world to know about Lipedema?"
And I complied their very emotional and authentic answers talking about "This is is what it's really like to have Lipedema".
These are some of those stories. 💖
If this message means something to you, please share.
If you'd like to know more, please follow me and all those women on Instagram;
@lipedeme4770
@jen_lipedema_surgery_
@unlippy_jo
@lipedema_and_me
@ana_banana_health
@lesslipoedema
@danakieferwaier
@sandrabouhanna
@aprilsluder
@my_lippy_pear
@el.lipedema.de.sally
@liplip.co
@nucha_lipedema_portugal