National Microcephaly Day is TOMORROW Friday, September 30th!

Don't forget to wear yellow and help raise awareness for our special stars! Visit for more information!

Early Bird Pricing Is Back - 3 Days Only - Register for "We Are Not Alone"

To All of Our Special Stars & Their Family's, The Foundation for Children with Microcephaly has recently celebrated their 3rd birthday having official 501(c)(3) nonprofit status. We want to include our families in our celebration by offering Early Bird…Read More

"We Are Not Alone" - the 3rd Annual Microcephaly Convention - Registration Is Open!

"We Are Not Alone" - the 3rd Annual Microcephaly Convention's information and registration form is now AVAILABLE! First off, we want to thank everyone for their continued patience. The Foundation for Children with Microcephaly worked hard to make sure that…Read More

Loving our Children with Microcephaly is in America's Giving Challenge—Let's win $50,000!

Hi Everyone, Our cause just entered in America's Giving Challenge, which gives us a chance to win $50,000! Please donate today: To win, between now and November 7th we have to get the…Read More

National Microcephaly Day is Wednesday, September 30th

Join us to help raise awareness of Microcephaly this Wednesday, by wearing the color yellow! Tell everyone you know what microcephaly is and how under-recognized it is! Microcephaly is not rare - it affects 2 - 2 1/2% of the entire population! Don't forget to…Read More

Equestrian Riding Helmets for children with microcephaly

Does anyone know where I can order an XXS riding helmet for my daughter to wear while riding in hippotherapy sessions? Her head size is about 14.5 inches in diameter. The smallest helmets I can find are 20.5". Please help.
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