AtresiaMicrotia.org — Tiny Ears, Big Hearts help
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Our Stories

By reading just a couple stories written by parents of patients (or patients) who have atresia or microtia, you will know more about the issues involved and your options than 98 % of the medical community in North America.

The best thing you can do for yourself and/or your child is to arm yourself with education, whether it is to go up against the insurance companies who think any board certified plastic surgeon can do a microtia reconstruction or the medical community who thinks no person with a unilateral hearing loss ever needs to be aided.

All of the material in these blogs is copyrighted, and may not be duplicated in whole or part without the express written consent of the author. We do scan the Internet for our own data frequently, and will vigorously pursue action against those who violate this simple rule – including requesting page removal and site deactivation.

Enter The Blog


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