Ep. 217: Exploring Alpha-Gal Syndrome FAACT's Roundtable podcast

4d ago 37:02

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FAACT's Roundtable Podcast द्वारा प्रदान की गई सामग्री. एपिसोड, ग्राफिक्स और पॉडकास्ट विवरण सहित सभी पॉडकास्ट सामग्री FAACT's Roundtable Podcast या उनके पॉडकास्ट प्लेटफ़ॉर्म पार्टनर द्वारा सीधे अपलोड और प्रदान की जाती है। यदि आपको लगता है कि कोई आपकी अनुमति के बिना आपके कॉपीराइट किए गए कार्य का उपयोग कर रहा है, तो आप यहां बताई गई प्रक्रिया का पालन कर सकते हैं https://hi.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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Thanks for listening! FAACT invites you to discover more exciting food allergy resources at FoodAllergyAwareness.org!

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