Added: 5 months ago
From: jennyw67
Views: 10,932
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  • Wow! Your daughter deserves all the admiration in the world! She is beautiful:)

  • KE HERMOSAAAAAAAA

  • three words... strong and beautiful.

  • A beautiful little girl. I could not imagine what you all have gone through...I have a lil 2 year old and I give you guys props fgor being strong.

  • great video, thank you for sharing you and your daughters experiences!

  • Thanks so much for sharing Melissa's story! What an incredible change in her face structure - especially from the side, but wow!! I know a lovely little girl, who also has Crouzon Syndrome... I think, perhaps, based on her appearance now, compared to Melissa's before the RED, that hers may be more severe.... but it does make me wonder if her parents have considered - or if it is even possible for her - to have the same sort of surgery done!

  • Thank you for sharing your story. Melissa was and is a very beautiful little girl.

  • what a sweetheart. She's very brave for what she went through.

  • CONGRATULATIONS, fell in love with Melissa's have a child with craniosynostosis, His name is Renan. SEND THIS NEWS *-* BEAUTIFUL GIRL CONGRATULATIONS! GOD BLESS + E + YOU. JULIANA.

  • I AM FROM BRAZIL, my son has craniosynostosis. I THINK IF ONE DAY MY SON WILL DO THIS SURGERY AND IF HE .. We should bear But you gave me a lot of courage and strength too, MELISSA A QUIZ THAT DO THIS SURGERY? SHE HAD MANY PAIN? ASK SORRY, BUT NOT ME NOT TAKE A BAD (ALSO AS I SAID SO STEP WITH MY SON)

  • Please send news of her, and make another video for us? THANK YOU .. GOD BLESS MUCH OF YOUR LIFE FAMILY, AND MOST OF MELISSA! (I know nothing of English, nor is spelled right, PUT ON GOOGLE TRANSLATOR) haha:) KISSES .. JULIANA

  • im from saudi arabia and i feel hapy for her ^_^

  • c'est incroyable, merci la chirurgie

  • Thanks for sharing with us. What a amazing result bur what a big operation it was. I have respect for your girl but also for you as parents. Please give your beautiful girl a big hug from us!!

  • oh f***. I've just had a Lefort 1 (while being 24) and it was horrible... Melissa had to endure an even tougher surgery at such an early age. At least she won't have to face it, later... and she won't suffer from a "different" face, which would be tormenting as a teen ager...

  • amazing, big big change beautiful and no more apnea. Ten thumbs up!

  • Amazing!!! She is absolutely gorgeous...before and after! My son was born with Apert Syndrome. He had the Lefort done when he was 5. Bless you for sharing!

  • she is most beautiful. I hope all the best. you as parents and family are so strong. I heard about this syndrome today for first time. thanks for uploading this vid, now I know the 2 years old girl of my friends will also make it through. the medicine will also improve with the time. good luck dear.

  • Cried watching this, thinking of my darling neice who just got her RED halo today, the suffering, but the joy in the end. Thank you for sharing your journey with us Melissa--you are a beautiful young lady! Many Blessings!

  • OMG what a change, my congratulations to the doctors that made that surgery possible, and congratulations to you both for having such a beautiful child and very very brave one too. Melissa you look beautiful, I'm sure you already have heard that :)

    The best of life for you, after all that you more than deserve it.

  • Wow!! Please tell Melissa that she looks beautiful, but more importantly, she's BRAVE!!

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