thanks all,
sorry I didnt get back sooner...this didnt ever show up when I go to new posts....wierd...so all of a sudden tonight in my cogfog mind said..wait I thought I started a thread about pain...and had to find it..as it wasnt under new posts...hmmmm

I might have to go in before sept. apt... I will be very upfront to my pcp about the pain, and the numbness that was happening last week...(couldnt feel my legs below me feeling but also the tingling stuff)

and make sure she knows how much it affects my life....as I keep having to cut back on stuff at home to rest enough to try to get back to work....long struggle...

thanks all for the prayers..and support...this place rocks...

someone gave a neuro dr name to my hubby...someone at his work with MS...that he has talked to a lot about my sxs....and they were surprised nothing so far is figured out.....

I might get referral to see him...neuro number 4 it would be..hehe

the rheumy idea would be good...although back when my pcp said..the fibro idea wasnt right...and that she really thinks neurological...but hey maybe I should see a rheumy too....as someone here said....

Pjames...yes my life is busy....work full time days, hubby works nights....we have five children....so life is busy...just wish I could enjoy the home time better...and not always be trying to get better enough to not struggle at work....that part gets to me...

hugsss and thanks all, sarah