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In August, we #dazzle4rare to represent HE/SREAT and Seronegative AE. Visit our website for resources hesaonline.info Find Dazzle4Rare at Dazzle4Rare.net. #wearerarefamily #dazzle4rare #hesaonline #seronegativeAE #AEstrong #raredisease #autoimmune #AEaware
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In August, we #dazzle4rare to represent HE/SREAT and Seronegative AE. Visit our website for resources hesaonline.info Find Dazzle4Rare at Dazzle4Rare.net. #wearerarefamily #dazzle4rare #hesaonline #seronegativeAE #AEstrong #raredisease #autoimmune #AEaware
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In August, we #dazzle4rare to represent HE/SREAT and Seronegative AE. Visit our website for resources hesaonline.info Find Dazzle4Rare at Dazzle4Rare.net. #wearerarefamily #dazzle4rare #hesaonline #seronegativeAE #AEstrong #raredisease #autoimmune #AEaware
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In August, we #dazzle4rare to represent HE/SREAT and Seronegative AE. This week, we stampede Social Media. Raise Your Voices. #wearerarefamily #hesaonline #seronegativeAE #AEstrong #raredisease #autoimmune #AEaware #encephalitis #patientadvocacy #mysteryillness
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This week's #IAESBlog by @jmstebbs An important topic & apt read during #Autoimmune #encephalitis #AwarenessMonth She writes- I try to be positive but, there is a dark side of me. IT is a side I have refused to show. I have yet to write about IT #AEaware autoimmune-encephalitis.org/…

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“We would like to invite all AE patients to participate in a study which surveys for symptoms following encephalitis.” #autoimmuneencephalitis #heawareness #hashimotosencephalopathy #patientexperience #medicalresearch #AEAware #autoimmune #dazzle4rare aealliance.org/understanding…

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Throughout the year AARDA has been fortunate enough to be receive the donations from hundreds of our supporters starting Facebook birthday fundraisers for us. We are incredibly grateful for every donation and every supporter we have. facebook.com/donate/46342980…
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Replying to @ZipSprout
Thank you for talking about AE here on Twitter! #AEAware #rareaware #HEAwareness
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