www.alopeciaworld.com
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
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!
Started by Tanya. Last reply by Sher Nov 6, 2015. 20 Replies 0 Likes
Started by Tanya. Last reply by Tanya Aug 15, 2015. 6 Replies 0 Likes
Started by Tanya. Last reply by lookswow Oct 18, 2014. 3 Replies 0 Likes
Comment
A weekend activity would be fun. And it would be cool to have our kids with us at some point; great for them to experience a gathering as well!
I'll miss seeing you. Perhaps we can do a weekend thing that will work for everybody. It's so tough to get a day that works for everybody. Hopefully we can catch up again soon.
Enjoy the warm vacation Deeann!! Won't see you on the 2nd, but am enjoying our exchanges in this group. : )
It is very...cold outside. I'm supposed to be heading somewhere warm tomorrow, but not sure how the weather will effect the flight. See you when I return. I'll be sure to watch the EFT video, but it sounds like most of you know more than me about the power of positive thinking, and can definitely show me a thing or two. See you soon.
Thanks for sharing the Louise Hay link Cat. I just watched all 10 of them. Powerful stuff. I can think of so many friends who will benefit from watching this :)
Hey, Deeann
I have also heard about EFT and tried it. It felt really good when I tapped on my forehead..:) If you can find the video that would be great:) I'm interested to hear more.
It's sooooo bloody cold outside..
Hey, Chris and Silkhead
I'm just amazed on how changing the way your think affects your body. In addition to the affirmations, I have also been meditating daily and i don't know if its coincidence or placebo affect but a patch of psoriasis which I had for over 25 years is going away..its almost looks like a normal elbow:) lol
Chris, I'm so gland the hypnosis is working for you:)
Devan, thanks for the making a copy of the Louise Hay CD. I look forward to meeting you.
I
Welcome, Pins77! I'm glad you found us, and would like to invite you to come to our meet up on Feb 2 if you are available. I'll send you a message with the details.
cheers,
Tanya
Hi all, ive just joined up to this site. Im from England but am currently on holiday in Vancouver for the next 3 weeks. Just thought it would be a good opportunity to meet up with some other people with alopecia while seeing some of the sights of Vancouver, so if anyone would like to meet up for a coffee at some point that would be great :)
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
You need to be a member of Vancouver Alopecia Areata Support Group to add comments!