RLS and Plantar faciatis

[ctravel12]

Hi Jocinda do not remember if I welcomed you to the board, if not welcome and if I did well welcome again. I do have rls but not the plantar faciatis so can relate to this post to the rls.

Have a wonderful time in Arkansas and Virginia seeing family and have a safe trip.

When you get back, please keep us posted on what your new dr says.

This is just food for thought, but do not know where in Washington you live, but have you checked out to see if they have any support groups for rls. I am a support group leader where I live and the people are so appreciative and you learn from each other.

[jocinda]

Charlene: thanks for the warm welcome. there is a support group near here. i called a number on a flyer shortly after i discovered the mirapex had been the source of my gambling conpulsion, but my call wasn't returned. since then the flyer is down. i need to locate them again, i may have written the wrong number down. that was not a good week for me. rest well everyone. cindy

[ViewsAskew]

Cindy, if you go to the main RLS.org site, you can find a list of support groups and phone numbers. That's probably the fastest way unless you are in Dallas, Az, or Mo - support group leaders from those places are members here. I know we've got one from somewhere else, too, just can't remember the somewhere!