
TruSpeed AutoSports and PMG
I first had the pleasure of meeting the TruSpeed AutoSports team in the summer of 2015 at a race in
I first had the pleasure of meeting the TruSpeed AutoSports team in the summer of 2015 at a race in
Taylor James (TJ) was born on July 25, 2011. He is our third son and is a wonderful gift. We
With our extended family, this year we decided to change from a game for gift giving in which everyone would
As I sit here on the couch, I hear the voice of Sean’s ABA therapist and the sounds of Sean’s
I am Quinn’s mom…that means I am a teacher, a physical therapist, an occupational therapist, a speech therapist, a service
On May 11, 2011…the world became a more beautiful place. Willow Vae Schreiber was born at 9:59pm, at 7lbs 7oz,
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