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 - WebsiteAlpha-Gals Basics Free Resource Guide - Free DownloadAlpha-Gal 101 Resource Guide - WeblinkAlpha-Gal Foundation - WebsiteIn the Tall Grass Two Alpha-Gals - PodcastThe Alpha-Gal Allergen Inclusion Act - WeblinkSocial MediaInstagramFacebookLinkedInTikTokX (formerly known as Twitter)YouTubeYou can find FAACT's Roundtable Podcast on Apple Podcast, Pandora, Spotify, Podbay, iHeart Radio or wherever you listen to your podcasts.Follow us on Facebook, X (formerly known as Twitter), Instagram, Threads, LinkedIn, Pinterest, TikTok, and YouTube.Thanks for listening! FAACT invites you to discover more exciting food allergy resources at FoodAllergyAwareness.org!

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