Tag: ehlersdanlos
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Living with POTS, etc.
I wish I could love summer. I grieve the things I can no longer do because they are now a recipe for disaster for my body. I miss being able to hike and enjoy the great outdoors. Although heat and exercise has always been a trigger for my EDS and POTS, it has never been…
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Life with Chronic Pain
I am in pain every single day. Some days are worse than others, some days I only notice it if I decide to stand up for more than a few minutes. But every day to some degree I’m in constant pain. I’ve had doctors say they don’t believe me, tell me I’m just looking for…
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