Team PMG Awareness- The Utah Endurance Recap
On Saturday, August 1st, 2020, Team PMG Awareness participated in one of Utah’s premiere motorsports events, the NASA’s Annual
PMG Awareness Organization Inc.
Unlocking the mysteries of PMG (Polymicrogyria)
Utah Motorsports Campus
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Testimonials
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
PMG Awareness Organization Inc.
2016-12-21T19:37:31-06:00
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
https://pmgawareness.org/testimonials/testimonial-1/
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
PMG Awareness Organization Inc.
2018-09-24T14:22:59-06:00
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
https://pmgawareness.org/testimonials/testimonial-2/
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PMG Awareness Organization Inc.
