Pacific Northwest Alopecians

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Pacific Northwest Alopecians

For Alopecians who live in or love ones in the Pacific Northwest.

Members: 67
Latest Activity: Apr 24

Discussion Forum

Local wig/scarf/hat shops

Started by Cat. Last reply by lina Aug 27, 2013. 10 Replies

treatment for alopecia

Started by Yvette. Last reply by JeffreySF Jul 14, 2010. 8 Replies

Fun things to do in Pacific NW

Started by Danna. Last reply by Georgie Sep 25, 2008. 4 Replies

Comment Wall

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Comment by lea on September 13, 2017 at 1:38pm

Hello all, this is a good group in Seattle and upcoming event...

21314832_2067243813301051_5093081426557200209_n.jpg

https://www.eventbrite.com/e/asg-panel-discussion-tickets-375602747...

Sep

30

ASG - Panel Discussion

Date and Time

Sat, September 30, 2017

3:30 PM – 5:30 PM PDT

Add to Calendar

Location

Douglass-Truth Library

2300 East Yesler Way

Seattle, WA 98122

http://www.alopeciasupport.org/

Comment by ayshia2000 on July 10, 2017 at 1:10pm

Hi, I am a grandmother of a beautiful 7 yr. old little girl who was recently diagnosed with alopecia. My daughter and I would like to meet up and learn more. We need a lot of support and I would  love for her to meet others who understand.  Are there any meet ups in the Tacoma area?

Thank you kindly

Comment by pdxnurse503 on October 10, 2016 at 12:49pm

Hi Tanya,

Thank you for taking the time to respond to my post. Yes, I am interested in meeting ppl with the same condition. This has been a difficult journey and I don't feel anyone understands.

Comment by Tanya on October 10, 2016 at 12:24am

Hi pdxnurse503

We have a support group on Vancouver, Canada, though we have members coming from Bellingham area often! I can connect you with some of the people there if you'd like!

Tanya

Comment by pdxnurse503 on October 10, 2016 at 12:00am

Hello,

Does anyone come on here? I am looking to meet other ppl with alopecia . I feel so alone. I am in the Portland area

Comment by Tanya on April 26, 2013 at 3:16am

Dear All, I'd like to quickly talk about two things!

1. The Vancouver group has a meetup tonight! Come if you are nearby. Just email me at alopecia.vancouverpa[at]gmail.com for details. (Here's our group http://www.alopeciaworld.com/group/vancouveralopeciasupportgroup)

2. This is from end of last month: On my birthday I "came out" to my friends, telling everyone my alopecia story in this video. It was well received and got 300 shares on Facebook (around 17,000 views)! Here it is on youtube :) http://www.youtube.com/watch?v=S0BGIqMCD1Q

xo
Tanya

Comment by Tanya on February 1, 2013 at 1:15am

Hey everyone!

I'm the founder of the Vancouver Group on AW. We are an active and awesome group that meets every month or six weeks, at one of the members' homes. We have a meetup tomorrow @ 7:30pm. Since I just discovered this group, I want to invite you all! :) We currently have 1 US member who crosses the border to meet with us every month! Totally worth it, haha.

Message me for more info (address, phone numbers etc)

cheers ;)

Comment by Phyllis Wallace on April 22, 2011 at 10:31am
Me too! I can't wait to meet others who are on this same crazy journey.
Comment by Jeannie Terrel on April 21, 2011 at 8:43pm
I'm excited I just talked to my husband and he is going to come with me to the meeting as well.
Comment by Phyllis Wallace on April 11, 2011 at 10:28am
Oops! Sorry about that. The e-mail address should be: or.alopecia@gmail.com
 

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