"Are you on Facebook Mike! AlopeciaCanada is both a group and a page. Find us and join if you like. There may well be a member near Nelson!"
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Jana's Groups
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Welcome, Jana
Profile Information
- Relationship Status:
- Single
- About Me:
- I have had alopecia for more years than not, and would like to share the person I have become with those that are experiencing a similar truth. I know I will receive something in return. : )
- Do you have alopecia?
- Alopecia universalis
- Are you age 18 or older?
- Yes - I am 18 or older
Jana's Photos
Comment Wall (10 comments)
- At 7:46pm on January 31, 2015,
janetparsons said…
hi I am a 60 year old lady living in newfoundland, I have au for 40 years now, tell me aboutyourself.
- At 10:33pm on April 9, 2014,
Mike said…
- Hi Jana I am Mike Mayas Dad. I joined to find more people in the Vancouver area to find more people kids or parents that r going through the same thing we r. Maya has had Alopecia for about two yrs now. Where or when is the next meeting? Thx Mike
- At 4:35pm on February 6, 2013,
Debbi Fuller said…
Hi Jana, Thanks for reaching out! You look COOL in your shades.
- At 1:22pm on July 26, 2012,
LilyBell*Murphy'sLawLuvsMe said…
You asked some very good questions on the ohter website concerning the new patent. I have to wonder if this is why he would not disclose how he 'cured' himself - because he wanted to patent it so he could make money. Sure the 'intention' is to give the profits to his group but with no board of directors - he is his group. Profits can be manipulated and frankly I think it stinks that he has held off telling what he did saying it needed 'more research' when all along this is what he had in mind. If I ever thought I would give that group a chance I surely will not now. I hope you will continue to ask the tough questions.
- At 5:06pm on February 12, 2012,
Hello! Thank you for the add : ) Hope you are doing well!
- At 8:01am on February 11, 2012,
Jennifer Krahn said…
Hello. I don't know what I did wrong with the facebook link for CANAAF...I assumed copy and paste would work (arghhhhhh)http://www.facebook.com/index.php?lh=f0c30a2e691baed46e8ed098f3c5787c#!/groups/138725316179572/ (second try) You can look them up from their webpage perhaps??
As for getting a support group up and running it seems like crickets in my city. I have met a few people with alopecia but most don't want to meet as a group. I was thinking of heading to a couple local wig shops to post informative posters about a meeting but my major issue is that for me a support group is a conflict of interest as I am now a Rep for Freedom Wigs and I don't want to come off as trying to sell a product. What I have been trying to do is see if my clients would like me to hook them up to begin support groups in their area (with their permission of course)or I refer them to CANAAF. I would LOVE to start a group and really get it to fly...there are so many amazing people with alopecia to meet!
- At 4:04pm on February 8, 2012,
Thank you for the request. Love the pictures you have! Your tatoo is fantastic!
- At 11:54am on February 6, 2012,
Sandra Fournier said…
Thanks of the friend add!
Cheers - Sandra
- At 5:13pm on September 27, 2011,
JBean said…
- Hi! Im from Vancouver too...although I have yet to go to a meeting. I want to, just need to find the time! Hopefully we'll run into each other some time. Good to hear from you!
- At 5:42pm on September 21, 2011,
LeslieAnn Butler said…
- Hello and welcome!
How are you today? I have AU, too.
Leslie Ann
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