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Hello and welcome, Terri!
I'm in Portland, too. Right now there is no support group here, but another Portland woman has started the process. Check in with the National Alopecia Areata Foundation in another month or two and something should have happened by then. It's www.naaf.org.
Leslie Ann
Hi Terri! A NAAF rep tole me that a man in Lake Oswego just submitted an application to start a group. As soon as I get an update, I'll let everyone in the Pacific Northwest Alopecian's group know about it. It's so great to be able to find others in the area that are going through the same experiences. I can't wait to meet people face to face!