• Skip to primary navigation
  • Skip to main content
  • Skip to footer
Keep Me Updated
PMG Logo

PMG Awareness Organization Inc.

Unlocking the mysteries of PMG (Polymicrogyria)

Make a Donation
MENUMENU
  • About Us
        • Our Mission

        • Who We Are
        • Mission Statement – Our Core Values
        • Our People

        • Founders
        • Board of Directors
        • Medical & Scientific Advisory Board
        • Our Allies

        • Sponsors
        • Partners
  • Learn More
        • What is PMG?

        • What is Polymicrogyria?
        • Newly Diagnosed?
        • CMV & PMG
        • PMG Education

        • Resources
        • Patient Brochure
  • Events
  • Connect
        • How You Can Help

        • Interested in Volunteering?
        • What Can You Do To Help?
        • Our Programs

        • Birthday Program
        • Our Community

        • Contact a Family
        • Faces of PMG
        • Family Stories
        • Community News
  • Contact Us

Unlocking the Mysteries of Polymicrogyria

Who We Are
About Polymicrogyria

Community News

2023 Team PMG Awareness Racing Schedule

Team PMG Awareness Racing is off to another fun-packed season. These races are open to all PMG families, we would

Read More »

It’s Coming…the 2024 PMGA Family Convention!

We are beginning to finalize plans for the 2024 PMGA Family Convention! Stay tuned for details to come VERY soon.

Read More »

Virtual Walk 2022: Raising Awareness and Breaking Records!

The PMG Awareness Organization’s Virtual 5k “Steps to Bring Us Together” is in the books and what a record-breaking year we

Read More »

Our Partners & Sponsors

hudson-logo
tru-speed-logo
billy-footwear-logo
wep-logo
fluid-logo
maglock-logo
mothers-logo
g1-logo

Merchandise

Team PMG Awareness 2021 Racing Shirt

Shop Now

Faces of PMG 2021 Calendar

Shop Now

Team PMG Awareness Car Decals

Shop Now

PMG Awareness Mini Traveling Bears

Shop Now

Footer

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/
0
PMG Awareness Organization Inc.

Connect on Social Media

  • Facebook
  • Instagram
  • Pinterest
  • Twitter
PMG Awareness Organization, Inc. Nonprofit Overview and Reviews on GreatNonprofits

Copyright © 2023 - PMGAwareness.org | Terms & Conditions | Privacy Policy