any help in Oklahoma?

I just joined this site, so please bare with me. And have Lupus
Is there anyone out there in Tulsa Oklahoma? Support groups? Friends, Do you know any Good Dr.'s.
I have only lived here for a couple of months.
thank you

[luppygirl]

Sorry I live in Canada so i know i will really be of no help. I would definitely check with the arthritis society if they have one there because my lupus support group meetings are held at the arthritis society. They are most likely in the yellow pages. Ask your dr's or even there nurses or receptionist if they know of anything I am sure they would be happy to help you and they also get a chance to talk to alot of patients so i am sure at least one patient has talked about or have even asked them so they might have  information that could help you.  Also we have the Canadian Lupus Society here so in the state they have to have an American lupus foundation or something check on the internet for that and i am sure they would have a way to contact them and then you can ask them what they have to offer in your neck of the woods.I hope i was some help being from another country and all.  Good luck and let me know what happens

[luppygirl]

Just thought I would check to see if anything I suggested helped at all.  I need feedback because if I know i helped you someone else will come up with same question but just different place.  Also if it was not help I don't want to waste peoples time suggesting things that are useless.