Hey Chris- I am interested in possibly trying a GAPS diet. I've just begun to read about it and why it may help heal those with autoimmune disorders. Is this what you are on? Btw, it seems SO restrictive! I think at first, I would have a lot of trouble adjusting- I had a hard enough time with just gluten.
I really appreciated all the info on how you are doing, what's working for you and what isn't, etc. Maybe we can save each other some strife if we collaborate on healing technique knowledge!
What Chinese herbs have been helpful for you? I just went back for my 2nd Chinese medicine appointment and they did more moxibustion and acupuncture. They also discussed that I had a lot of emotional blockages going on and that we would have to remove them layer by layer. They suggested Craniosacral Therapy for me. Have you done this yet? They have a specialist that does this and they think it would help me greatly...
I've also been reading about meridian tapping and EFT. hmm...
Hey Chris, I am going to try and order some hair from Toplace. Tanya showed us her two new ones, and they look pretty good, so I was wondering what colour did you chose? Thanks for hosting again, I'll bring a wheat free snack of some sort! See you then, Jana
Hey...sorry I saw Tanya's last comment. I live in Vancouver, and have yet to meet anyone with AA. I'm 21 and have had it all my life. I don't wear a wig, but I would love to finally meet another someone(s) with AA. Could you guys keep me in the loop if a meeting or anything like that develops?
Hey Chris! Sorry I've away from the site for too too long, and just saw your comment! I'd love to start an alopecia group, or just have a few friends get together to support one another and share our insights! :)
Hi Chris. Thanks for your note. For some reason it did not come to my email. I will have to look into that. I just saw your post on Canadians with Alopecia. I haven't felt as lonely as you - my mom has alopecia to. She lives downtown Vacouver, I live in Gibsons. Are you familiar with the Sunshine Coast? I have two kids Owen 8 and Gabrielle 6. I have been married for 18 years this Oct. I have had alopecia for 25 years. I started with AA at 13 and then moved on to AT by 21. I had a great hair stylist that actually took me wig shopping on his day off. He was also the one to introduced me to vacuum wigs - changed my life. Look great all the time with out the fuss and muss. How long have you had Alopecia? Hope to chat again soon. I hope I get your comments on my profile page. Otherwise I will keep a look out for you on this group site. Thanks Chris.
I haven't been to any support groups in the Lower Mainland although I understand there is one that meets every three months or so. I was informed about it through Canadians with Alpocia page here on this site. Welcome back to Vancouver!
I'm pretty well adjusted with the whole thing & in some cases it's been a positive experience: as an entertainer, I get a lot of attention (In my field, that's a good thing), so a support group isn't a first priority, but I wouldn't rule it out.
Keep in touch - Jennifer
Thanks a million!! Your are very sweet. I´m very angry for this but I know that feeling is destroying me. I read the first book you mentioned, I will look for the second one. Kary.
Hi Chris ..thanks for your precious time...I´m single without children...living with my parents again. The don´t understand me..I have female baldness pattern...all the front part of my head with little thin hair awful!! I always care what people think...and I´d feel ashamed if they realise I have a wig on. I bought a human hair wig last year but I can´t bear it all the time. Suggestions!! Thanks a lot!
Hi Chris!
Sorry, I don't know of any support groups in the Lower Mainland... When I was going through treatment, my dermatologist tried to find some support groups based around kids, because I was only 11 when diagnosed, but she never found anything, and I still haven't found anything since. I'm not sure if I'd be interested in a support group because I've sort of made peace with the whole thing, and I'm not sure if it would help, or maybe bring back some of the emotions. Right now I'm actually in Quebec for a few months, so I can't do anything until I get back!
Chris...I´m very depressed...I have FBT that bis getting worse...at home nobody understands me... I bought a human hair wig but I can´t bear it. Any piece of advice?
Hi Chris, I read the blog you wrote about your experiences with alopecia and how you think in most cases it can be healed. This has really given me hope and I can relate to a lot of the things you said, so I just wanted to write to you to thank you for your inspirational words.
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Hey Chris- I am interested in possibly trying a GAPS diet. I've just begun to read about it and why it may help heal those with autoimmune disorders. Is this what you are on? Btw, it seems SO restrictive! I think at first, I would have a lot of trouble adjusting- I had a hard enough time with just gluten.
Hi Chris!
I really appreciated all the info on how you are doing, what's working for you and what isn't, etc. Maybe we can save each other some strife if we collaborate on healing technique knowledge!
What Chinese herbs have been helpful for you? I just went back for my 2nd Chinese medicine appointment and they did more moxibustion and acupuncture. They also discussed that I had a lot of emotional blockages going on and that we would have to remove them layer by layer. They suggested Craniosacral Therapy for me. Have you done this yet? They have a specialist that does this and they think it would help me greatly...
I've also been reading about meridian tapping and EFT. hmm...
Hey Chris, I am going to try and order some hair from Toplace. Tanya showed us her two new ones, and they look pretty good, so I was wondering what colour did you chose? Thanks for hosting again, I'll bring a wheat free snack of some sort! See you then, Jana
I just turned on AlopeciaWorld's email notification again (thought it was on!) I can be better reached at laundrylimbo@gmail.com.
I'm looking forward to us all meeting up :)
I don't mind you posting the blog. I'm glad that you like the idea and thank you for the friend invite.
Hugs,
Galena
I haven't been to any support groups in the Lower Mainland although I understand there is one that meets every three months or so. I was informed about it through Canadians with Alpocia page here on this site. Welcome back to Vancouver!
I'm pretty well adjusted with the whole thing & in some cases it's been a positive experience: as an entertainer, I get a lot of attention (In my field, that's a good thing), so a support group isn't a first priority, but I wouldn't rule it out.
Keep in touch - Jennifer
J
Sorry, I don't know of any support groups in the Lower Mainland... When I was going through treatment, my dermatologist tried to find some support groups based around kids, because I was only 11 when diagnosed, but she never found anything, and I still haven't found anything since. I'm not sure if I'd be interested in a support group because I've sort of made peace with the whole thing, and I'm not sure if it would help, or maybe bring back some of the emotions. Right now I'm actually in Quebec for a few months, so I can't do anything until I get back!
Heather
How are you today?
LeslieAnn
Welcome to Alopecia World.
Jeffrey
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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.