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The Unprofessional Guide to mandibulofacial dysostosis, Guion-Almeida

A Plain-Language Guide for Patients and Caregivers — What You Need to Know, For Informational Purposes Only

by Alumigogo Books

Chapter 1: What Is mandibulofacial dysostosis, Guion-Almeida, Really?

Important notice: This guide is for general informational and educational purposes only. It does not constitute medical advice, diagnosis, or treatment. Always consult a qualified healthcare professional before making any medical decisions. Never disregard or delay seeking professional medical advice because of something you read in this guide.

Okay. Breathe. You just heard a phrase that sounds like it belongs in a medical journal from 1985: mandibulofacial dysostosis, Guion-Almeida. Maybe you had to look at it on a piece of paper to make sure you were spelling it right. Maybe your doctor said it and you felt your brain go completely blank after the first two words. That is a completely normal response, by the way. It's a scary-sounding name for something you probably know very little about, and you are not alone if you feel like you've just been handed a riddle without a key.

So, let's start with the first thing you need to know: this is not a death sentence, and it is not your fault. These are the two facts you will need to hold onto as we walk through everything else. Mandibulofacial dysostosis (which we will call MFD-GA from now on, because honestly, that name is a mouthful) is a rare genetic condition that affects how your face and sometimes other parts of your body developed. The name comes from Latin and Greek roots. "Mandibulo" refers to your jawbone, the mandible. "Facial" means it affects your face

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