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Ep. 217: Exploring Alpha-Gal Syndrome
Manage episode 447453224 series 3392202
Treść dostarczona przez FAACT's Roundtable Podcast. Cała zawartość podcastów, w tym odcinki, grafika i opisy podcastów, jest przesyłana i udostępniana bezpośrednio przez FAACT's Roundtable Podcast lub jego partnera na platformie podcastów. Jeśli uważasz, że ktoś wykorzystuje Twoje dzieło chronione prawem autorskim bez Twojej zgody, możesz postępować zgodnie z procedurą opisaną tutaj https://pl.player.fm/legal.
The US Centers for Disease Control and Prevention states, “Alpha-Gal syndrome (AGS) is a serious, potentially life-threatening allergic condition that can occur after a tick bite.” But how do you get AGS and tackle this condition? We’re exploring living with AGS with two change makers and AGS powerhouses, Candice Matthis and Debbie Nichols. They are the founders of Two Alpha-Gals and the new Alpha-Gal Foundation, which is committed to offering solutions. We’ll learn more about this growing community of support. This podcast is part 1 of a two-part series exploring life with Alpha-Gal Syndrome.
Resources to keep you in the know:
- Two Alpha-Gals - Website
- Alpha-Gals Basics Free Resource Guide - Free Download
- Alpha-Gal 101 Resource Guide - Weblink
- Alpha-Gal Foundation - Website
- In the Tall Grass Two Alpha-Gals - Podcast
- The Alpha-Gal Allergen Inclusion Act - Weblink
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