Imo the medical profession worsens our CRPS, because their lack of knowledge about it contributes to our stress. It certainly has escalated mine. I am sick of documenting my symptoms so that I have proof of my misery, so Zi can get care.

It has created a cycle of negative attention, that I purposely avoided in the beginning, but now I have no other choice. Looking at the photos, etc, just makes me enraged. My only comforts are being on my couch with my legs elevated or in a warm tub with epsom salts, baking soda,sea salt, but lately the latter both soothes and aggravates.

I would love to get back into a heated pool, but fighting with WC is too much.