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Member
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Join Date: Jul 2010
Posts: 458
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Member
Join Date: Jul 2010
Posts: 458
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I started getting shocks about 4 months after my PN started and a month before I was officially diagnosed. Now, I get them about 30 times an hour, give or take a few. Sometimes they can be mild shocks, while others totally take my breath away and cause me to scream out in agony. It's the worst type of pain I have.
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♥ "Hope is more than a word; it's a state of being. It's a firm belief God will come through. Life brings rain... hope turns every drop into the power to bloom like never before." -Holley Gerth ♥
My name is Sarah and I am 25 years old. I have a lot of chronic health problems. Peripheral neuropathy and POTS (postural orthostatic tachycardia syndrome) keep me bedridden the majority of the time. I also struggle with degenerative disc disease, disc desiccation, spondylolisthesis, arthritis, polycystic ovarian syndrome (PCOS) with insulin resistance, allergies, sound sensitivities, and other health problems.
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