November is Complex Regional Pain Syndrome (CRPS) Awareness Month, and I’m one of the unfortunate ones who live with not one, but two, rare diseases that don’t get near enough awareness, attention or funding.
Without these, and without advocating, there is little-to-no-hope for a cure; a cure so many of us living with CRPS and keratoconus so desperately want and need.
CRPS is sometimes dubbed the suicide disease (and I totally get why), and is rated the highest on the pain scale. For many of us, this disease of the sympathetic nervous system has robbed us of a lot of our former lives.
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