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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,
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Alopecia universalis
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Tired of walking this road alone

Posted on November 17, 2011 at 10:00pm 9 Comments

i am reaching outto anyone out there with alopecia[ESPECIALLY ALOPECIA UNIVERALIS,iam 57 years old and have this terrible condition for 38 years now, is thereanyone out there who would like to get in touch with by way of email, i do feel so al alone, god bless you all.

Comment Wall (12 comments)

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At 9:11pm on January 24, 2017, Grandmajoy said…
Yes I would love to talk with you. I was diagnosed with AU in April 2015. I have several autoimmune diseases which I did not realize until the AU.

I wish we had a support group in Las Cruces where I live. It's a small town with very few specialists.
At 2:55pm on January 22, 2014, skit said…

Hi I know what you mean Hair loss for over 35 years myself.Totalalis then universalis.I grew eyebrows&lashes only this last 3 years!

Howver I am more at peace with hair loss now than ever before thanks to local support group and going to AA meetings.

At 8:19pm on January 16, 2009, Lori Black said…
I posted to your query on AU group too! Welcome to Alopecia World! I am new to this site too, I wosh there would have been such a thing 20 yrs ago, the encouragement and sense of being among friends has been wonderful after all the years of feeling like the "Lone Ranger" .
Lord Bless you!!
At 3:37pm on January 16, 2009, Cherylnz said…
Hi Janet

Welcome to Alopecia World
At 8:08am on January 12, 2009, Carol said…
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!!
At 10:10pm on January 11, 2009, Eileen Simpson said…

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.

At 9:43am on January 11, 2009, Carol said…
Hi Janet
Welcome to alopecia world. I have family in Newfoundland! I've had alopecia for 30 years. Message me anytime you like!
At 12:52am on January 11, 2009, Eileen Simpson said…
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.
At 8:50pm on January 10, 2009, rj, Co-founder said…
Hi, Janet. Welcome to Alopecia World! This is a great place for great people, so be sure to make your positive presence known. :-) - rj, Co-founder
At 7:48pm on January 10, 2009, Cheryl, Co-founder said…
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


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