On the National Alopecia Areata Foundation – Maureen McGettigan

published 5 years ago by dermcast.tv

This video is about the National Alopecia Areata Foundation with Maureen McGettigan and was recorded at the 2013 Summer SDPA Conference in St. Louis.

Studios needs to know that I'm here with marina get again. And she's here with the national alopecia areata foundation welcoming well thank impact eager. It's really wonderful to learn more about your organization could you tell us perhaps and some background on nafta thank you so it's the national alopecia areata foundation. And we've been in existence for over 30 years currently based in northern California. And Sandra fell California and the whole mission is for support awareness and research. So for anyone who's been diagnosed with alopecia areata and even their family members and friends where the actual international resource for those to learn about what the disease is to gain support for local support groups to learn about new treatments and just to get the help because when you're diagnosed you feel like you're the only one that has alopecia areata and this is a great read ...

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