Faces of PMG

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Do you have photos you would like to share with us? If so, please use this form to upload your photos:

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Users who upload photos via this form are hereby granting PMG Awareness Organization, Inc., and all persons or entities acting on behalf of the PMG Awareness Organization, permission to use the photos submitted for purposes of raising awareness of Polymicrogyria. This may include, but is not limited to, educational, advertising, promotional, electronic media purposes and the like. Users who submit photos via this form are also aware and understand that uploading images to the pmgawareness.org website is done purely at their own risk. It is possible once their digital images are entrusted to our servers that the images could be downloaded/copied by site visitors and used without their permission elsewhere.
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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.