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SCS & Pain Pumps For spinal cord stimulator (SCS) and pain pump discussions. |
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Here on this thread http://neurotalk.psychcentral.com/thread163083.html, a few of us were talking about people who are not as understanding as we'd like. Dr. Smith brought up the idea of a buisiness-sized card with a list of things not to say to us that you could hand out to them. I thought that it would be fun to compile a list just for it's own sake, and if some of the entries made it onto such a card, great. If not, it would still be gratifying. I'm sure that not all will universally applicable.
I'll start with some of my favorites: Maybe if you just exercised more, you'd feel better. It's all mind over matter, you know. Have you tried compression socks? (I have PN in my feet--just kill me now!) ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() ![]() I know you all have some gems too--show us what you got!
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PPMS Rx 2013, symptoms since 2000 |
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"Thanks for this!" says: | Dr. Smith (01-11-2012), ElizaJane23 (01-12-2012), eva5667faliure (11-21-2013), Mark56 (01-10-2012), Rrae (01-11-2012), seahorse02 (01-19-2012), Sophie_ (01-11-2012) |
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