About The Mia Moo Fund

Mia Moo Fund - Mia & Jase Mia Moo Fund - Mia Before Surgery Mia Robertson

 

About The Mia Moo Fund

The Mia Moo Fund ia a fund of the Worldwide Foundation which is the 501(c)3 charitable organization. Your donations to the fund are tax deductible. The Mia Moo Fund is dedicated to raising awareness and funds towards research, treatments and causes of cleft lip & palate. We invite everyone countrywide to participate with us as we strive to support one another, lend a helping hand and bring a smile to each and every child.

The organization began in 2014 after Mia Robertson, daughter of Jase and Missy Robertson, completed surgery for her cleft palate. As Mia entered surgery, thousands of supportive fans tweeted, blogged and talked about how strong and beautiful she was. It was both empowering and inspiring. It has since become our mission to bring this type of support and love to each and every child that suffers from cleft lip and palate. These children face difficulties that are hard to comprehend, but with your support, the impossible can be achieved.

With your support, we can help these children view life from a new perspective, gain the confidence they deserve and reach their full potential as they grow and become extraordinary examples to their friends, family, classmates, neighbors and more.

 

How Can I Help?

You can help us, and more importantly, these children, by doing a few, simple things. First, you can donate money that will be put towards the research of new treatments. Each and every penny is helpful as we strive to bring awareness to our community. Second, you can share this page, along with our Facebook page, to help raise awareness and let your friends and family know that we are here, ready and willing to help out.

With our resources, families and children with cleft lip & cleft palate can learn more about treatments, causes and more. We offer around the clock support and friendship to anyone and everyone in need. Third, you can support the Mia Moo Fund. Donating to the Mia Moo Fund does not mean you must donate hours of your time and resources. It simply means that you are willing to be a friend to a child in need. By donating, you show your support and love for children in the US who are born with cleft lip and cleft palate. These children, along with their families, will be forever grateful for your kindness as you both work together to create a better environment throughout the US.

 

We Care...

The Mia Moo Fund cares. We care about seeing each beautiful child grow to become a strong, dedicated member of our society. We care about helping others, and allowing others to reach their full potential. We care about the voices throughout the country, reaching out and crying for your support. We care about finding resources and new technologies that will help decrease the chances of children being born with cleft lip / cleft palate, and eliminating it altogether. We care about the individuals who want to help, but don't know how, and strive to make it easy and worthwhile for you to join us in our cause. At the Mia Moo Fund, we care about you.

The Mia Moo Fund is an organization that is dedicated to raising awareness and funds towards the management, treatments and surgical procedures of cleft lip & cleft palate.

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