Support the Foundation for Children with Microcephaly

Adam 10 days ago

I have two boys with micro. Jack is three and Luke is 15 months. I love my boys infinitely!

Rachael 18 days ago

My little boy was dagnosed with microcephaly at 3months old

Adam 29 days ago

My Birthday was complete in knowing I have amazing friends with wonderful hearts. I love you all.

Lisa about 1 month ago

Hello everyone Jayden is my great nephew that i have custody of i got him when he was 8 1/2 months old. His mom was and still is heavey with drugs and she knew she had a proble so she gave her three children to family members to take care for her. if we didnt do it then the stat would of took our babys away and we would of never seen them again so I got baby Jayden he is my chuncky chunk. I love this baby as if he was mine..I sit here and i read all your storys of your children and i cry with sadnest and happiness for all of you. Jayden was born with Liss/microcephaly he has sizures and muscel spazams and he also has cataracks in his right eye and then his left eye has a thin layer of skin over it so he cant see very well if any. but ill tell you this he know who iam he knows my voice and every morring he has the biggest smile for me.. Jayden has to be fed through a G-tube and everyday i try with him to at least try to get him to take a passie but he wants nothing to do with it.. he dont want anything in his mouth. he has 6 teeth 3 on top 3 on bottom with 2 more comeing in on the top so he is gonna have a mouth ful real soon. I didnt tell you all how old my baby Jayden is the doctors said he would never live through the frist 48 hours he proved them wrong then they said he will never see his frist birthday he proved them wrong my baby just turned 1 april 29th now they are saying he wont see his 5th birthday we will prove them wrong because Jayden is a strong little boy and he has my blood in him also even though he is my nepew he has some strong blood running through him he is gonna live to be a old man.. with all the prayers we give him..Jayden has alot of love.....

Heidi about 1 month ago

Hi Everyone!! My little boy Zayden has microcephaly, developmental delays, and epilepsy. He eats through a feeding tube and has a meda port. Despite it all he always has a huge smile. He has the most beautiful eyes and cutest mohawk. He is almost 10 months old. My husband and I also have a healthy little girl who will be 3 next month. We are sooo blessed to have these two angels in our lives. This foundation has been the light in my darkest times. The support group that I have from other parents is truly amazing. I understand more of my sons disorder everyday. I am in tears just trying to say thank you. There is not a single word that will measure up to how thankful I am. I love all of you so much. I have not met many of you but you are all a part of my family. Our special babies have connected us in an inspiring way!!

Shy Supporter about 1 month ago

My son Jayden was diagnosed wth Microcephaly a couple of months ago and he also has perisylvian syndrome. He is my world, my little miricle baby as I call him...He is still trying to learn to sit up by himself

Amy about 1 month ago

My son was diagnosed with microcephaly when he was 1 month old. He is now 16 months old. We are working on walking and eating. He is such a joy and blessing to my husband and I. The love we have for him is unexplainable. If anyone has any questions, please feel free to contact me!

Tracey 2 months ago

I support this case because my daughter has been diagnosed with this medical condition. It is just as common as Autism but it doen not have the awareness that Autism does.

Tracey 2 months ago

My daughter was diagnosed with microcephaly at 11 months. She is now 16 months. She is making progress with help from her therapists. She is such joy and love. We have learned to take one day at a time and enjoy each day with her. I never heard of this medical condition until my daugther was diagnosed.

Deborah 2 months ago

This is Stephanie's picture, she has Lissencephaly/Pachygyria. She is 21, thinks like a 3 year old, talks like a 18 month old & walks like a toddler & has seizures. She is "my shaddow for ever!"

Marie 2 months ago

my little boy has this condition, we dont no much about it he his developing fine at the min, he has just turned 2 but his head is just no growin. if any one could give me some advise that would be great.

Tim 3 months ago

My stepson Spencer is nine and was born with Micro...He is sweet boy but his is a stuggle to keep up with daily

Stephanie 3 months ago

Destiny was born with this due to complications at birth. I thought it was rare but there are so many children born with this. It is sad to watch the videos of these children but even with all their problems they are still so beautiful. Life is not fair but maybe we can help even if it's just a little.