I’m so glad I found your channel! I also remember trying to hide my microtia when I was younger, even when the kids didn’t say anything. After a botched reconstructive surgery I was so down but I’m trying to get more comfortable with it. I still don’t tell people right away but your video helped me so much :)
you are such a rockstar. thank you so much for speaking about your story and making the world easier for other kids who are looking for someone to look up to 💖
I am so glad you made this. Our 20 month old has left microtia atresia and Goldenhar and, although everyone’s experience is unique, your story, your perspective and your memories of childhood experiences has given me some comfort in what we may have in front of us. Thank you so, so much for this. I already follow you on IG and I appreciate you sharing this part of your life- it means so much to parents like me.
I love to see you, I am the mother of a child With microtia, and obviously I am always investigating this, and you appeared in my videos, it feels very good to see someone making his life with this type of conditions, it is good that you are no longer hiding Because now you are the example and inspiration of many people, I live in California and make picnics to bring all families together with people who have Microtia and Atressia, and this year everyone talked about you, they use you as an example for their children! you don't have to hide anything, you are beautiful! and thanks for sharing a little of your life ♡, when you come to California you are welcome to our house!😘
SO PROUD OF YOU FOR TAKING US THROUGH YOUR JOURNEY. I LOVE YOU SO MUCH!
THANK YOU MY LOVE I LOVE YOU SO MUCH MORE
I’m so glad I found your channel! I also remember trying to hide my microtia when I was younger, even when the kids didn’t say anything. After a botched reconstructive surgery I was so down but I’m trying to get more comfortable with it. I still don’t tell people right away but your video helped me so much :)
you are such a rockstar. thank you so much for speaking about your story and making the world easier for other kids who are looking for someone to look up to 💖
JESS! MY BABY
I am so glad you made this. Our 20 month old has left microtia atresia and Goldenhar and, although everyone’s experience is unique, your story, your perspective and your memories of childhood experiences has given me some comfort in what we may have in front of us. Thank you so, so much for this. I already follow you on IG and I appreciate you sharing this part of your life- it means so much to parents like me.
We support Hayley in this household😤
She is gorgeous with or without 👂👂
I love to see you, I am the mother of a child With microtia, and obviously I am always investigating this, and you appeared in my videos, it feels very good to see someone making his life with this type of conditions, it is good that you are no longer hiding Because now you are the example and inspiration of many people, I live in California and make picnics to bring all families together with people who have Microtia and Atressia, and this year everyone talked about you, they use you as an example for their children! you don't have to hide anything, you are beautiful! and thanks for sharing a little of your life ♡, when you come to California you are welcome to our house!😘
Hi Hayley, thanks for the video! Did your condition include any facial palsy?
YOU ARE BEAUTIFUL 😇 & TOTALLY ROCK!🤩Thank you for the inspiration, much love from my family to yours.💖
I have bilateral microtia too ! I am so proud of you :D Does anyone have this too?
Thank you!!
My son is BMA ❤
Aissatu Sila Pereira can he hear ?
I have it only on my right Ear tho
My Baby Brother Has bilateral anotia! which is very similar to bilateral microtia but there is nothing on the outside of his ears
Respectfully asking. How do she hears or listens ???
Quisiera leer los comentarios y saber que dice ella
Pero no se nada de inglés 😭
X2
Wow interesting story
i love u omg
💜❤️💜
My name is William. I was born with Goldenhar Syndrome.
Amazing video