The first question usually asked when diagnosed with Sjogren’s is “What do I have?”, or “can you spell that?”, or in the case of Lupe, “Am I going to die?”
Today on Sjogren’s Strong we are going to talk to those newly diagnosed and share a few simple things you can do to help yourself understand what is going on and help with symptoms.
Links
Support the Sjogren’s Foundation by supporting “Team Sjogren’s Strong” for the 2021 Walk for Sjogren’s – https://bit.ly/2021TeamSjogrensStrong
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Childhood SJogren’s Virtual 1-Day Conference – https://f.hubspotusercontent30.net/hubfs/147789/PediatricConference.pdf
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