What is most important to her is the hope that she will serve as a source of motivation for other young children who are born with the same issue.
Mia, on her own initiative and with the assistance of her family, founded the Mia Moo Fund with the intention of assisting in the process of ensuring that each and every kid has a grin on their face.
In an interview with Christian Post, Missy Robertson said that “one of the functions of the Mia Moo Fund is to spread awareness of the journey of cleft lip and palate.”
“The other aspect is to provide assistance with medical funds for the families and parents who are currently residing in the United States of America.”
During an episode of his podcast titled “Unashamed,” Jase Robertson provided an update on Mia’s status and discussed how his daughter is doing in terms of her recovery.
“She is doing very well.!” In addition to saying, “Everything seems great, seems to be fine,” he went on to say that she had made a positive turn of events.
