Alexander's Story - Craniosynostosis

When Alexander was born, two of the bones in his head were fused together. At about six months of age his parents learned that he had craniosynostosis and would need to undergo surgery. Watch as the incredible team at Loma Linda University Children's Hospital guides Alexander and his parents though this difficult yet transforming experience.

[@theothernikisixx2004]

Alexander is my nephew and he's is doing awesome! He's very much a normal kid, knows two languages and is very active! We're super glad everything at Loma Linda worked out! :)

[@pattymunoz2389]

Johnathan Guzman my daughter is havin her surgery on tues in loma linda childrens hospital seein these videos freak me out

[@toyanajackson5839]

God bless..

[@kgbdiaz8626]

I had this surgery on my first birthday , have a scar from ear to ear developed perfectly normal speak sign language to my deaf parents and also speak and hear , I was wondering if you know if he can be involved in contact sports in the future like football or kickboxing

[@user-ot5dg8kp4v]

My God bless him more and more!!

[@simransandhu25]

Hi can somebody give me Alexander' s parent contact number .my son will have this surgery I need help

[@pennyfrancis5492]

My son as well had this surgery. He is great now he is going to be 13 this year, He was 2 months old when he had the surgery. Bless ya'll. It is more hard on the parents then the child it seems. Hugs.

[@lawaunagrimes2555]

He is beautiful God Bless you all

[@jhas839]

I so happy everything went amazing for your boy ! ♡

[@deliamunodawafa1022]

wonderfull.....i was unfortunate i didnt have the opportunity for the surgery to be done on me

[@mrstahirqayyum2764]

How old are you now, my son is14month old we are planning now but thinking may be we are lil late ? What do you think?

[@mercy_g8978]

Same here 13 months..... :-( super scared and just want to know if we are too late

[@zoyazoi2388]

My son doctor prescribed this surgery 😢 I'm scared how doing after surgery. Its successful for every kid 😭

[@TheBigfishhead]

yes I know how it feels xx

[@jhas839]

I cried watching this :,( Doctors are telling me my little girl maybe has that . And it really make me scared :/ i dont want her to get a surgery she already had a major one at the age of 1 :((((

[@glambyabe]

How old was she when she was first diagnosed. Did she have the surgery eventually

[@shellbyaguayo297]

How is she doing now ?

[@Demeemartinez]

Hi, how is she now? We were told the same. We are pending results. Next month we take her to the specialist.

[@ashnkksmom2264]

What a little cutie

[@ivaniaflores6630]

Interesante tengo un bb de un año con craneosinostosis pero no entiendo nada .Todo está en inglés ..Soy de Nicaragua Matagalpa lamentablemente esa Operación aquí no se hace

[@bracehater]

omg i know what he had do cause i had it do 2 time 9mouths and 6 years old my first surgery was 6hours long and my secondo one was 4hours long i was in the icu of a day in a half i was there for 2 almost 3 weeks 8days after my second surgery my eyes and face was swollen i just need oxgen not a breathing tub my head was raped i had to ware a helemnt for 6 to 11 weeks i miss 2-3 mouths for school and had a toutor for 8-9 weeks and i was so lukey that my cousin ryan nie was my toutor. my story