Following the success of the recent BBC Documentary My Life Without hair the BBC have contacted BeBold with an interest in producing a full length documentary about adults living with alopecia, a target audience 18-30.

In order to get this commissioned we are currently looking for about three individuals in the above age range who would like to take part.

For this to work we are looking for individuals with a really interesting story to tell. This will be a fantastic chance for…

Is there someone in your life that has loved you and accepted you even though you were bald from Alopecia? If so, nominate that person as a Women Behaving Baldly Hairy Hero! Visit us here to submit your nomination.

I just want to get my feelings out...I see people on this site especially parents asking what to do, and stuff...I don't know if I'd ever give good advice about it because we're all different, different strokes for different folks...

But I just wanted to say my peace...I've been full on bald since I was four years old. I was never normal well...I used to have a full head of curly black hair that I would never let anyone but my dad touch. I don't remember much of my years WITH hair as…

Yesterday at work I had to stay late to help unpack some new mannequins that we had received. So, at the store I work at our mannequins wear wigs.. and I thought since the store was closed it was the perfect opportunity to try one on! Hahahaha, it was just for fun, I would never actually wear a wig. But me and my co-workers sure got a kick out of it. :)

PS: My eyelashes are growing back!…

Hi Guys,

Hope you are all well.

I am really really confused. I have been diagnosed with Lichen Planopilaris which results in scarring alopecia. In the past month I’ve lost a lot of hair from my crown area and have been wearing my hair back….sort of like a comb over for a girl.

Before the alopecia got bad I always wore my hair open, I’m scared people will soon start asking the reason as to why I wear my hair up especially at family occasions or nights out. My parents are…

Many of you have seen regrowth, this is my son's head (close up). He has these small hair on his scalp now, which are much thinner but still black in color. He never had the white peach fuzz that I expected. I am not sure if this is something positive? Please help me decide what to make of it.

1/5/2012

1/9/2012…

My 16 month old has been diagnosed with Alopecia, so I am talking to everyone who knows anything about this problem. Someone mentioned if this could be related to Radon Gas, and If I ever have tested my house for Radon. So I went first thing today morning and got a Radon Test Kit which takes about 2 weeks to get results, and I am growing impatient to figure out if it could be related. Has anyone who suffering from Alopecia looked into Radon gas in their house or work place?

There is so much support out there for Alopecia. I had no idea and I just want to scream it from my house-top. I felt so lost (still do for the most part) but I feel there is hope. Life will go on whether my hair chooses to join in or not. I think I may even be able to go back to church and not fear for the person sitting behind me to look at the back of my balding head. (Of course I will have my "fabulous, perfect hair on).....I think I can do this....maybe :/

Hi Friends,

I'm a little late but maybe we can make this work. Share your line and have some fun!

On the 1st day of Alopecia Areata I recieved my first little bald spot on me.

What happened on the 2nd day?