Are there any teachers out here with EDS and/or dysautonomia (POTS)? I feel like I’m the only one... I’d love the community and ability to speak to others in my profession. #EhlersDanlosSyndrome #Dysautonomia #LivingWithPOTS #Teacher #SpecialEducators #SpecialEducationTeachers #EDSAwareness #HypermobileTypeEDS #Chronicallyillteacher
I had my infusion on Thursday afternoon for #RheumatoidArthritis and then my #Methotrexate shot Friday morning but I had to go to work Friday because it’s the day before Spring Break and I didn’t have a Dr’s note to miss so I had to go or lose a day of pay..luckily my students know all about my cool masks...unfortunately no one else had seen my masks and we had an assembly so I was quite the talk of the other students and faculty...my students think I am pretty, funny, and cool with my masks... #ChronicIllness #Chronicallyillteacher #CRPS #Lupus #UndifferentiatedConnectiveTissueDisease
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