Faces of PMG

The PMG Awareness website has been incredibly helpful for us. At the time of our daughters diagnosis,  we were overwhelmed and devastated. Yet discovering this site not only helped us to educate ourselves further about Polymicrogyria, but it also opened up a whole new community of support and helpful resources. We are so grateful for this incredible hub of information, delivered in an educational and compassionate way that families all over the world can relate to.

Natalie - Miracle Mama & Chiaras Journey

Melbourne Australia

I found the Facebook PMG Support group through another group for parents with children with development delays.  I have found that it's members are very helpful in answering questions to the best of their ability or experience and in general just being there for support, when I am having a bad day and need somewhere to vent, or people who really understand and live with PMG everyday.  I have learnt through this group that every PMG child is different and that no one can really tell me what is to be expected for my son's future.  So I plan to enjoy all that my son is going to teach me about being a parent to a special child. My Hero!

-Claire Carter

Nova Scotia, Canada