Hi Lee, and all....

I'm sorry to not have answered so many sent letters- thanks to all of
you for the wonderful support!....
My life was loaded when I first signed in with all of you, a baby sisters
wedding to help take care of, a major task in it's self!.... <sigh>
It was held last Sat. and I'm thankful it's over with, but I wouldn't of
missed it for the world- it also laid me out flat on my back with a major
flare for three days, whoa! what an experience!!!....
I'm still in the in and out of it stages, but with a 13 yr old nephew around
to help out for the week, it's been a God send to me!....
Went to my rumo doc Tues. crying the blues and unable to move, at least he
saw the physical pain I was in and didn't go poking around on me.... <sigh>
He has refereed me to a chronic pain expert in our area which I will see on
the 15th.- my rumo doc say's that I'm a mess and he's not sure what to do
next with me- little does he know I'm not certain what to do with myself at
times!!! <soft smile>

Lee- you asked what meds. we were all on for the FMS, well mine is FMS\MPS
complex- not sure if these will help you out or not....
I take neurontin 300mg. caps three of them three times a day, it's for the
numbness in the feet, legs, hands and face- also to help the fibrofog....
celebrex 200mg. twice a day, it's for the inflammation and pain.... The last
has been my lifesaver roxicodone 10mg. two tabs. three times a day as needed
for the pain....
The doc's worry is this tho, I've been on the last one for over three months
and it's a narcodic.... <sigh> Sometimes you can't win for losing, but thank
God I'm still here to at least talk about it all.....

Question for all of you now- other than your online support group do you
attended any other groups in your areas???.... I'm finding it difficult at
best to find one in my area and I'm fairly a metro area, Denver.... Any
suggestions???

Soft caring hugs to you all.... {{{{{}}}}}}
Always, Cheryl in Colorado....