To answer your questions:
No, nothing like this runs in my family.
I don’t know what the original injury was. No idea. The only time I was in the hospital before all this was 20 years ago when I broke a leg skiing. Other than colds, I had been completely healthy before this. Then I got Endometriosis and the nerve problems showed up about halfway through my treatment for that. We thought they were related until the pain started in my leg.
I was really grumpy last night.
I did get these new pain patches from my doc. They are called Lidoderm and they are sticky pads with Lidocaine on them. They are only FDA approved for Shingles so some insurance companies might not allow them for “other” pain. Mine did, and I’m trying them out now.
[QUOTE=Equine Adhesive;6462202]
Farethee- WOW. Thank-you for sharing your story. It is very inspirational, what you have accomplished. You are a light to us all.
GotGait - you’ve really become a pin cushion, haven’t you?! What was your original injury? Do neuro issues run in your family? My heart is with you. You are right, a lot of people do not understand chronic pain. What makes it worse is that those people seem to avoid suffering people. Why? Why can’t people be more conscientious and empathetic? It seems likely they are afraid of something. Which just makes your life that much harder. Count me in as someone who is here to listen and support. Focusing on the positive is important, whining is necessary, and not making progress is devastating. I hope you are making progress, even if it is small. Stories like Farethee’s should give us all inspiration, no?[/QUOTE]