@laurenelizabethash: In honor of #pcos awareness month (now #PMOS) I spoke to Andrea about my experiences navigating this truly infuriating disorder. Stream to the full @pregnantish interview anywhere you listen to podcasts! #pcosawareness #pmosawareness #pregnantish

Moonie :

Thank you for talking about this. I myself have adenomyosis and PMOS

Cazzerami :

I’m a PMOS gal too, I’ve been gaslit for 30 plus years. I’ve done my own research as I’d be dead before I got help! Thanks for speaking up [Red heart]

itsMicMic :

Where can I find the full podcast? And any tips for pcos?

Ashley 🇨🇦 :

Amazing :) I was just diagnosed with pcos and adenmyosis at 37. I’m sure I’ve had it for a long time, but glad to have found a doctor who is listening to me. Also she diagnosed me with pots. The doctor before, male, said I’m a female with anxiety. Try some antidepressants. I’m excited to listen about your journey :)

Mary 🇨🇦 :

Thank you for advocating for all women!! Every day I learn about new ways women have been medically gaslight and it makes me WILD with rage!

Yeet_Lite :

Yes! Drs have never had this and they claim to know it all! Endo stage 4 here. I do have a great male specialist.

Allie :

I just got diagnosed a few weeks ago and I’m so lost on everything… I’ve always suspected something was wrong but wasn’t sure what and it’s so eye opening on things.

Ari♡ :

heavy on the online resources/community. without it i dont think id ever advocated enough for myself to get the PCOS/PMOS diagnosis. i still feel like my doctors don’t understand it enough to fully treat it though🫩

E🐚 :

Early I love ur music

AJ :

Girl you’re amazing honestly! I loved you in super store and love you even more with your music 👏🏻 you’re just so down to earth

R 🧟‍♂️ :

Well done for speaking up!! Go diva go love uuu

L A Bevan :

What has helped you managed and improve your PMOS?

Beccee :

Love you Lauren

Hannah Leigh :

I have a neuromuscular disease and they do the same with that. They don’t listen. It’s horrible

brandyml78 :

With the change in name of this we are finally just scratching the surface.

tarouge1 :

I was diagnosed with this 20ish years ago. no one knew what to do except throw off- label needs at it (which did nothing). it wrecked a lot of things but I've now got control & am working towards a healthy body.

🐉Chloe (Lauren's Version)🐉 :

im so beyond proud of you, truly i am. you really inspire me to actually speak up and be myself

charlie :

im so so proud of you!! so many people feel like they can’t talk about this and you’ve made a huge difference!

Kyrlo :

Dinnaaaaaa. I love youuu❤️❤️❤️

Ri :

Preach it cyster!

Aleshiamichelle :

I have been going to doctor after doctor for ten years with symptoms and was constantly ignored because I never had cysts. Literally Today after all these years I was finally diagnosed with pmos and I’m so glad I finally found a doctor that cared and listened.

ֆǟǟʟɨ (Lauren's version)🦄☮️ :

NEW SONG YESSSSASS😫

Kelsey 2View Photo&Design :

I listened to this entire episode. So many mixed feelings of validation and continued hopelessness of finding someone who is good/cares to help. It's exhausting to pay basically out of pocket for "specialists" to say I'm fat, go exercise, and send me on my way

🍃 :

HEYYY

Ollie💫🪽 :