PMR patients in the group?

[Guest guest]

I have been having some new symptoms which I was attributing to the

fibro/ra/lupus overlap stuff, that being just terrible muscle aches.

One of my friends at church, her husband has been dx'ed with

polymyalgia rheumatica. I am having the exact same symptoms he has.

He's a nurse with like 30 odd years practicing and I respect his

opinion. Of course I intend to run this by the rheumie, but as I also

respect what yall say, does anyone in the family here have PMR? If so

what has been your experience, symptomology, etc, if you feel like

sharing this. I believe in being as informed as possible.

Hope yall are staying cool, Dallas is insanely hot. I was in beautiful

East Texas over the weekend at a great B & B, and 104 just did not feel

as hot out there. Like General Sherman said, If I owned hell and

texas, in the summer months i would rent out Texas and live in hell.

Slight overstatement. But not much.

Blessings and hugs to all.

Love

Jane