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In 2016, I was officially diagnosed with Chronic Fatigue Syndrome and PoTS. Being able to put a name to my years of illness was great, but it didn't make me feel any better. What did make me feel better was connecting with thousands of others who are going through exactly what I am, and being able to laugh. For these two reasons, I wanted to share the laughter (and everything else spoonie related) with my new community of chronically incredible friends. Hope you enjoy!
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