Instagram story viewer> @miiadio> Post
Mia Dio(miiadio)'s profile avatar

Mia Dio

@miiadio

2 years ago
Download
1183
Posted On: April 9th 2025, 10:26 pm
You are a walking love spell ✨ #selfconfidence #prettyprivilege #love #advice
Comments (1183)
turtle.4818646 5 months ago

turtle.4818646

❤️

mcroz379463 a year ago

mcroz379463

❤️love babe❤️

rick90640 a year ago

rick90640

I think I love you

2235.josh a year ago

2235.josh

Yes🔥 Beautiful ❤️ Thank you so much 🔥❤️

fazilf90 a year ago

fazilf90

Thankyou soo much 💖🤍

lg498978 a year ago

lg498978

Amen

williamhale153 a year ago

williamhale153

❤️❤️❤️🔥🔥🔥🔥🔥

clohessyd a year ago

clohessyd

It hurts sometimes

clohessyd a year ago

clohessyd

I feel like you know me

elischrimsher a year ago

elischrimsher

Well, then I cast my love spell on you. And our eyes shall meet And we shall get dessert. 😍😍

mikehrebin a year ago

mikehrebin

Good advice I am exactly what you were talking about . But still be alone till I find her hasn't happened so far but ya never give up

tasnimaea a year ago

tasnimaea

💗💗

ghostsamuraiwolfsbane a year ago

ghostsamuraiwolfsbane

Thank you for telling me 😢😢 I used to not believe it ❤️❤️people usually don't read my eyes it's like what are they afraid of

westcoastsanchez a year ago

westcoastsanchez

❤️

westcoastsanchez a year ago

westcoastsanchez

Thank you Babe

Load More

More posts

For years, I knew something was wrong with my body. I went from doctor to doctor, trying to explain the pain and symptoms that were taking over my life, only to be told that nothing was wrong. Eventually, I was diagnosed with endometriosis and PCOS. Endometriosis meant surgery. I underwent excision surgery in 2023 to remove the disease tissue growing inside my body after years of pain and unanswered questions. It was a major moment in my life, both physically and emotionally. I finally had an explanation for what I had been experiencing, but surgery wasn’t the end of my health journey. Despite treatment, lifestyle changes, and continuing to search for answers, my symptoms persisted. The pain began affecting my entire body. Eventually, I was diagnosed with lupus, a serious autoimmune disease that can affect multiple organs and become life-threatening. Research has found associations between endometriosis and certain autoimmune diseases, including lupus, although we still have much to learn about why these conditions overlap. Living through this has made me think deeply about women’s health, the effects of chronic illness on the body, and how much we still don’t understand. Too many women are taught to normalize debilitating pain instead of being given answers, support, and appropriate care. I know how isolating it feels to fight for answers while trying to keep your life moving. I also know how fortunate I am to have a supportive family and access to medical care. Not everyone has those resources, and that is one of the reasons this matters so much to me. I used to think I’d wait until I had my health figured out before sharing my story. But I don’t want to wait for a perfect ending to start a conversation that needs to be happening now. I’m incredibly grateful to be getting involved with the Endometriosis Foundation and to contribute to the work being done around endometriosis awareness and women’s reproductive health. I’m excited to share more soon. For now, I wanted to start by sharing an overview of my story, because no woman should have to fight this hard to be heard. 💛
Indonesia needs help.
and just like that, we’re halfway there 🥹🤍👼🏼
yk that ride home was SILENT 😭
Somewhere between The Black Swan and The Nutcracker.🦢 @mbbfw_official #mbbfw #bucharest #fashionweek
Yay or nay
back to up