About Us


Who we are?

We are a family, who have a beautiful girl Michaela born with lissencephaly. We will do everything for her to have the best quality of life! she is our angel from above, she is our miracle and we love her more than anything. We want to prove to the world that any child in the world is a miracle regardless of their capabilities and delays. Please help us to raise awareness for Michaela and others with this condition.


What is lissencephaly?


Lissencephaly, which literally means "smooth brain," is a rare, gene-linked brain malformation characterized by the absence of normal convolutions (folds) in the cerebral cortex. In the usual condition of lissencephaly, children usually have a normal sized head at birth.  Lissencephaly is caused by defective neuronal migration during embryonic development,  the process in which nerve cells move from their place of origin to their permanent location within the cerebral cortex gray matter. Symptoms of the disorder may include unusual facial appearance, difficulty swallowing, failure to thrive, muscle spasms, seizures, and severe psychomotor retardation. 


Thank You

We are still under construction and I will add more information and blog when I can. Thank you, Whether you help through monetary donations or spreading our mission through word-of-mouth, thank you. We couldn't accomplish our goals without the help of supporters like you. 

Support Now

Go Fund Me

Your generous gift will help Michaela and other kids in her condition with equipment, therapies that will help us give lissencephaly kids a better quality of life and as we grow to fund our mission to help those in need. Together, we can make a difference.

Click here to donate using  GoFundMe