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717d
hey! diagnosed with eds in 2016...managing but would love to hear others stories!
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Ehlers-Danlos Syndrome (EDS)
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Hello! Another zebra here since 2016, and since have learned I have many of the debilitating comorbidities. I hate it, it’s all exhausting but I’m working hard at trying to rise above the symptoms to live my best life. It will not rule me. I’ve just learned to listen to my body and rest when I need rest. Anything you do or suggest that really help? Where are you from? Nice to meet you spoonie!
☝ This content is generated by our users and it is not a substitute for professional medical advice. Please consult with your physician before making any medical decision
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Bupropion
night sweats
paranoid
Valium
sertraline
palpitations
Anxiety (Including GAD)
Depression
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