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Welcome to the Ear Community Organization! I'm Melissa, and I'm so happy you found our community!
I founded Ear Community just six months after my youngest daughter, Ally, was born with Microtia and Aural Atresia of her right ear. I remember feeling lost and alone when my family struggled to find the answers we were looking for. So, I started the Ear Community to make things easier for the next family who has a baby born with Microtia and Atresia.
Since 2010, Ear Community has paved the way for thousands of Microtia and Atresia families as the leading parent-driven nonprofit in the world that gives back directly to our community.
Ear Community's mission is to provide our community with the answers we are looking for, to educate about all options, provide new findings through genetic research and to promote advocacy and raise awareness while shining a light on our rare cause. We also bring families together in the same situation at our priceless events so no one ever feels alone with microtia and atresia.
Here, you'll find anything and everything you need:
Read on to learn about the programs we support and how we can help and be a resource for you.
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