i am 54 years old, single, have alopecia since i was 19 years old, i ,live alone, and find it very difficult wven after all this time to cope with condition,i find it very stressful to try and meet people because of the fear of rejection, and alo with going out on a date is the same way,
Hi Janet,
I know how hard it can be. I have had alopecia for about as long as you have (universalis, too). After I became the spokesperson for the National Alopecia Areata Foundation, a lot of women were needing my help and support, so I wrote a book called, "If Your Hair Falls Out, Keep Dancing!" It might make you feel better. Check it out on my page -- and let me know if there's anything else I can do.
LeslieAnn
Hi Janet, I wanted to take this opportunity to welcome you to Alopecia World. I have been living with Alopecia Areata since 1991 and know full well the struggle it can be. I look forward to getting to know you. Cheryl, Co-founder
Hi, I am new to AA, but have been a Celiac all my life (we are born with it). Anyway I hope you like being here and if theres anything you want to chat about or just need someone to listen I'm right here.
Eileen
I am in the Washington state right now a city called Walla Walla. I can't say what it's like to have AU, but I can only guess. I have AA, going out in public is hard with hats and scarves, people look all the time. Some people go out of their way to try to helpful why? Seems strange to me I have never been treated this way before. I feel your pain and understand. I do hope you will jump in the test the waters here and become friends with many good people.
Hi Janet
I live in Guelph, Ontario now but I have family in Robinsons and St. John's. I may have some family in mt. pearl but I'm not sure cause I haven't found em all yet. Anyways, hope all is going well. Take care!!
LeslieAnn Butler
I know how hard it can be. I have had alopecia for about as long as you have (universalis, too). After I became the spokesperson for the National Alopecia Areata Foundation, a lot of women were needing my help and support, so I wrote a book called, "If Your Hair Falls Out, Keep Dancing!" It might make you feel better. Check it out on my page -- and let me know if there's anything else I can do.
LeslieAnn
Jan 10, 2009
JeffreySF
Welcome to Alopecia World.
Jeff
Jan 10, 2009
Cheryl, Co-founder
Jan 10, 2009
rj, Co-founder
Jan 10, 2009
Eileen Simpson
Eileen
Jan 11, 2009
Carol
Welcome to alopecia world. I have family in Newfoundland! I've had alopecia for 30 years. Message me anytime you like!
Jan 11, 2009
Eileen Simpson
I am in the Washington state right now a city called Walla Walla. I can't say what it's like to have AU, but I can only guess. I have AA, going out in public is hard with hats and scarves, people look all the time. Some people go out of their way to try to helpful why? Seems strange to me I have never been treated this way before. I feel your pain and understand. I do hope you will jump in the test the waters here and become friends with many good people.
Eileen
Jan 11, 2009
Carol
I live in Guelph, Ontario now but I have family in Robinsons and St. John's. I may have some family in mt. pearl but I'm not sure cause I haven't found em all yet. Anyways, hope all is going well. Take care!!
Jan 12, 2009
Cherylnz
Welcome to Alopecia World
Jan 16, 2009