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Sjogren’s Syndrome and LEMS
I recently was tested for Sjogren’s because of symptoms of dry eyes, mouth sores, paresthesia in hands and feet, which I thought were LEMS related. I tested negative for this syndrome as a differential diagnosis when I was first dx with LEMS in 2021. My ANA and SSA are now positive so apparently I have acquired it since then. My doctor says they often co occur. Can anyone tell me about their experiences with this condition, does a rheumatologist manage the condition, and what therapies do you use? Are LEMS therapies effective?
Thanks so much for any insights
Deborah Carpenter
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