
Sean’s Story
As a little girl, I always dreamed of becoming a mother. At a very young age, I was always the
As a little girl, I always dreamed of becoming a mother. At a very young age, I was always the
He has a big, heartwarming smile. He has a full mop of adorable curly blond hair. He has chunky cheeks
Rylan is a sweet, happy 7 year old boy. His mom, Jenny, describes Rylan as having a bubbly soul with
Gage is an easy going 5 year old boy that loves his monster trucks, fire trucks and the St. Louis
The word polymicrogyria first entered our family’s vocabulary on June 28th, 2010 when our son TJ was 6 months old. We
If you’re reading this blog, you are probably already familiar with Polymicrogyria. You probably already know that there are conditions
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
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
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