Pain And Drugs
It’s refreshing to read the most recent messages on what’s really going on with us all. Pain !!! Thank you all for your honest sharing. It helps me know that I’m not the only one who has felt dispair. I hate taking medication but I absolutely have to in order to not to experience the dreadful pain involved with PR.
God bless you all and thank you for your stories. It keeps me in reality. I’m sure we all spend most of our day with people who don’t understand this condition, so we put a smile on our faces and pretend that all is ok when it really isn’t.
So we come to our group, read the messages and know that some how we’ll be ok and that we truly do understand.
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I have said it before and I will say it again…if PR turned your skin purple or green everyone, even your doctor, would feel sorry for you and have a little more understanding about how you feel. If you have a cast on your arm no one would expect you to do a FULL DAYS WORK at work and then work at home too.
I always come to work with a smile on my face, smile at everyone at work and laugh all the way home…I fooled them all again…they have no idea how bad off I am the jokes on them! Try to keep a smile on your face, it really does fool everyone and they don’t have a clue what PR is like even your doctor who says “Oh yes I understand your pain” RIGHT! if he really did understand what PR PAIN was like they would give every one with PR a lifetime supply of DARVOCET and a Cortisone Shot to take home just in case. MKalyn