Disclaimer: The information provided on this website is to inform and help new parents cope with the sudden, unexpected change in their life. The
information contained on this site is not intended to replace information you have received from doctors or other health professionals. Though there are
many facts on this website, there are also many opinions. We are not doctors, we are parents with children diagnosed with Microcephaly.
information contained on this site is not intended to replace information you have received from doctors or other health professionals. Though there are
many facts on this website, there are also many opinions. We are not doctors, we are parents with children diagnosed with Microcephaly.
| Meet Our Children... |
| Cam |
| Carter |
| Christopher |
| Ethan |
| Jameson |
| Jayla |
| Kaylie |
| Kaylee |
| Luke |
| Maya |
| Sydney |
| Shiloh |
| Catie |
| Charlotte |
| Jaidyn |
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Andrea
| Xavier |
| Emma Leigh |
| Afnan |
| Tish |
| Keera |
Samantha
Zac
Lexi & Rocky
| Sean |
| Aizza |
| Kyler |
Autrey
| Christina Marie |
| Andres |
| Elia |
| Paige |
| Send us a picture of your child diagnosed with microcephaly, lissencephaly or polymicrogyria! Pictures@childrenwithmicro.org |
| Look at her now! |