Vancouver Alopecia Areata Support Group

Information

Vancouver Alopecia Areata Support Group

Hello Vancouverites! Connecting is one of the best ways to feel happier and become more informed! Come as you are, whether you are shy or outgoing. This is a genuine and fun group where all of us - new to alopecia or experienced, hair-wearer or au natural, seeking treatment or not - all come together and be supportive, informative, and positive for one another. After 4+ years of running this group, I can say for sure that you'll feel better after a meetup! :)

Come to our monthly meetups, or, start by joining this group and be in the loop of upcoming meetups! Sometimes I include alopecia news / remedy / stories too.

If your kid / teen has alopecia, please contact us and we'll put you in touch with other parents! It'll be, I believe, quite awesome for your child :)

Location: Vancouver
Members: 90
Latest Activity: Jan 12, 2020

Upcoming Meetups

This group gets together monthly at one of the members' homes - a cozy, positive, and fun environment, for those with alopecia. We are here to support one another, and every meetup has been amazingly mood-lifting.

Join us here and we'll send next meeting details to you in a group email!

You can always get a hold of us via AW messaging or at alopecia.vancouver[at]gmail.com

We are affiliated with CANAAF (Canadian Alopecia Areata Foundation).

Next meet up: We meet about once a month. Please email Tanya at the emil address above!

Comment Wall

Comment

You need to be a member of Vancouver Alopecia Areata Support Group to add comments!

Comment by cati on December 1, 2011 at 10:29pm

lol...I have other spots I could try it on.

Comment by Deeann on November 30, 2011 at 10:21pm

Seriously. I sent it over a week ago. I wonder where it is? By the time it gets there, you won't have a rash anymore (which is good).

Comment by cati on November 30, 2011 at 7:23pm

Hey, Deeann

No, I haven't received it yet but I definitely what to try it:)

Comment by Deeann on November 29, 2011 at 12:54am

Cat: Did you get the stuff I sent? Glad to hear it's going away even if you didn't use it.

Comment by cati on November 28, 2011 at 8:34pm

wow.. Yes, I don't believe in coincidences either.. It was meant to be:)

"There is no such thing as chance; and what seems to us mere accident springs form the deepest source of destiny"

By the way my red spot(Psoriasis) on my arm the one that looks like someone sucked on it too long..lol is fading away:) My legs look like there on there way too.

Comment by Tanya on November 28, 2011 at 1:23am

@SilkHead - I met an AU lady (Connie) at random last week - also the first time in my life!

Comment by Chris Jeffer on November 28, 2011 at 12:15am

SilkHead - I don't believe in coincidences......very cool that you guys hooked up!

Comment by Deeann on November 27, 2011 at 11:19pm

Very cool. I think things fall into place when we get the ball rolling. I look forward to meeting you in January.

Comment by SilkHead on November 27, 2011 at 9:16pm

I went away for the weekend to visit some friends on the island. I was in a coffee shop in Qualicum Beach and a woman approached me. It turned out she has Alopecia Universalis and was meeting another woman with alopecia for the first time in the hopes of starting a support group on the island. It was such a crazy chance meeting. I exchanged numbers and email with the women. I'm still excited about this and I wanted to share it on here. I have only met one other person with Alopecia, and I thought this was just so meant to be. I'm excited to join this support group, January just seems too far away.

Comment by JLo on November 25, 2011 at 12:58am

Hello, Elenore I'm not sure if I met you at the NAAF conference this summer...we'll have to figure that out when we meet up next. I have pvr'd the show and will give a full report when I've seen it!

 

Members (90)

 
 
 

Disclaimer

Any mention of products and services on Alopecia World is for informational purposes only; it does not imply a recommendation or endorsement by Alopecia World. Nor should any statement or representation on this site be construed as professional, medical or expert advice, or as pre-screened or endorsed by Alopecia World. Alopecia World is not responsible or liable for any of the views, opinions or conduct, online or offline, of any user or member of Alopecia World.

© 2024   Created by Alopecia World.   Powered by

Badges  |  Report an Issue  |  Terms of Service