Im having a hard time i know it seems like I always say that but this time I really do. I cannot find a lot of information on pelvic neuropathy. Im spending time with my family this week and all they can think to call me is a druggie because I have had a very odd cycle. it comes and goes not a normal 7 day one. But I have been having to rely on my pain medication so much lately about every 4-6-8 hours or so depending on how much I did. And the neuropathy seems to be getting worse. It is now going all the way down to my toes and my feet turn in and I fall. My hubby wants me to get the nerves cut and be done with all this but im not sure if that is how it works. Im even really worried tonight I broke out in hives but I havent touched, ate or had any new medications besides a nerve block injection in my spine, that was on November 10th and i mean i did swell up after that but tonight i have the hives really really bad. If anyone can help thank you. Im just im going through a deep depression its like when all you want is a hug or someone to tell you it will be ok, this isnt you fault they call you an addict, blame you for forgetting even though you take lyrica and other nerve and pain meds. then they do not think this is a real disease. I have a close family friend who has Lupus and to my family that is more real than neuropathy. I swear if it only showed on the outside they wouldnt say the things they do.
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