<p>💙 It's May 12th, International ME/CFS Awareness Day 💙</p><p>My ME/CFS onset was in Jan 1990<br> <br>🚨 Many recent ME/CFS cases have been triggered by COVID 🚨</p><p>In this thread I plan to post about 3 main things:</p><p>1. My ME/CFS story (briefly)</p><p>2. Helpful resources for patients and clinicians</p><p>3. Advocacy options for patients & allies (friends/family) - mostly US based</p><p>1/n</p><p>@mecfs @longcovid </p><p><a href="/tags/mecfs/" rel="tag">#MEcfs</a> <a href="/tags/longcovid/" rel="tag">#LongCovid</a> <a href="/tags/postcovid/" rel="tag">#PostCovid</a> <a href="/tags/disability/" rel="tag">#Disability</a> <a href="/tags/disabilitysos/" rel="tag">#DisabilitySOS</a> <a href="/tags/covidisnotover/" rel="tag">#CovidIsNotOver</a> <a href="/tags/millionsmissing/" rel="tag">#MillionsMissing</a> <a href="/tags/meawareness/" rel="tag">#MEAwareness</a> <a href="/tags/worldmeday/" rel="tag">#WorldMEDay</a></p>
