Hi Everyone,
I was diagnosed with FFA six months ago after losing my eyebrows and having my hairline recede by about two inches. I also have other autoimmune symptoms. About four years ago I got silicone gel breast implants and wonder if anyone else with FFA has implants and wonders if they have triggered their autoimmune conditions including FFA. Just trying to figure all this out and trying to figure out the cause
Kathleen.

All my life I was known for my beautiful red curls. My hair was my most unique and prized physical feature. Three years ago when my hair suddenly fell out, I was totally shocked. It turns out that I have an autoimmune condition called Alopecia, where the immune system mistakenly attacks the hair and causes it to fall out. I was devastated. I had never even heard of Alopecia before. I was uncomfortable in my own skin and confused about who I was without my hair. I knew deep down that the loss…

My daughter is only 5 yrs old dealing with this and is in early stages of alopecia. I was secretly hoping it was areata however as of this week her eyebrows n lashes are falling off. I have done all home remedies that has so far allowed her to keep bout 30% of her hair. Still falling off but at a slower rate, i dont know if thats a good or bad thing. My mom had alopecia Universales since she was 15, bak in the 70s wen no one knew about it. She was tortured everyday to a point she moved out…

im 18 and just found a new patch on my crown size of two finger tips. I had alopecia from the age of 11-15 the size of my hand on the top of my head im terrified it will get that big again my scalp is tingling and itching is this A sign of more hair loss to come? please help :)

I have looked under the bed, I have checked my pockets, I have searched high and low and my hair was nowhere to be found. You see, since I was 21 I have been losing my hair and have done everything short of sending out an Amber Alert for it! My name is Scott and this is my story how I fell into Depression when my hair fell out and how I recovered from it.

Like…

In my last blog post, Acceptance, I mentioned that I told my boyfriend that I have alopecia. Well, two weeks ago, we broke up. He was my first boyfriend that I've told about my alopecia. And for that reason, I withheld the part about wearing a hairpiece (he just knows about the loss of hair everywhere else, like eyebrows, eyelashes etc). I would of eventually told him if we continued dating but I'm glad I didn't tell him. Because two days ago, on twitter, he tweeted: "Lmfao if your a girl…

SO A LOT HAS GONE ON SINCE I WAS LAST ON HERE, SO UPDATE WITH ME, WELL ON MAY 19, 2013 AT 9:09 AM I WAS TAKING IN FOR AN EMERGENCY C- AT 27 WEEKS AND 3 DAYS DUE TO BEING IN FULL LABOR, AND THEY TOOK HIM BECAUSE HIS UMBILICAL BEING IN FRONT OF HIS HEAD, AND I WOULD HAVE LOST HIM IF I DELIVERED HIM NATURALLY. OUR SON WAS 2 LBS 5 OZ AND 14 1/2 IN LONGS AND HE IS DOING JUST FINE HE IS A LITTLE FIGHTER. AND HE KEEPS GETTING STRONGER EVERY DAY. AS OF 6-3-2013 HE IS 15 DAYS OLD AND IS GETTING BIG.…

I haven't been on the site for a while, but its good to see so much happening as far as help, support and advice.

I first started losing my hair back in Oct 2011. I was 41 then. I had just been through a marriage break up and having never had hair loss before I have staunchly put it all down to stress. I started with just a small bald patch on my chin. I didn't worry and thought it must be "one of those things" A week or two later my daughter was giving my hair a trim and told me I had…

I must must must stop getting pleasure of out freaking ppl out, although my hair is now short I can still wear my long hair pieces, which I did to show a friend how natural they can look (ironically). Anyway a group of teenage girls, who had sow me the day before (with short hair) were asking if it was a wig/hair piece/extensions ect (genuinlely interested in extension), and a smart mouth teenage boy shouted 'What r u going bald or something??' I shouted back 'Yes, wanted to see' wiped off…

I have had allopecia for 40 years now and have worn just about every type of wig there is. For a long time, I wore human hair wigs that were made for me, but then we moved to Hong Kong for a while and they would not withstand the humidity there- and I couldn't learn to do them myself. So I changed to wigs with mono-caps, but synthetic hair. I liked them a lot better because I could maintain them. But a couple of years ago, I found a wig that really gave me a nice new look and I get…

For that matter, am I brave?

People seem to think I am. But in all honesty I don't know that I'm any different from the next person who just doesn't let things stop them. Especially the things that may seem impossible from the onset.

Maybe it's Faith - Faith in the knowledge that things just have a way of working out in the end.

But, for all my seeming to be strong and comfortable in my skin, I do have a few concerns. One in particular is me trying to wrap my head around…

Hey, its me again!!! Okay so first of all I am going to be going into seventh grade in August. Second I am seeking help on ideas or cute sayings about alopecia to put on some T-shirts me and my mom are making for school. We already have a few like " I'm to sexy for my hair that's why there is isn't any there" (Summer Hopper) and "God is good, God is fair to some he gave brains the rest he gave hair" (Erik Kern)or a totally random one "If you don't know what Alopecia is then you need to go…

Is there anyone in the Toronto area that Alopecia, the reason I'm asking is my little girl as alopecia and she does not know anyone that as alopecia, like her it would be nice for her to have a friend who is just like her, she is a good kid, she loves to dance,sing,etc Thank you.

Back in January I wrote about being diagnosed with shingles on my head. I had a burning red patch on my scalp. It began at night, on my way home from a gig. I didn't feel it at first, but my husband noticed it saying to me "Lili your head is bright red". It burned. That was a Saturday. I went to my primary care physician. He said I had shingles. Gave me an antibiotic and a cream. It did nothing to help. 3 weeks later I saw my dermatologist. Since the condition persisted he thought I had…

“It’s a wig!” I’m all too happy to tell you this upon our first meeting. I really don’t mind informing you of that whatsoever. I’ve always felt a bit like I’m a made-up, false Hollywood façade. You know the kind of fake building facades that you might find on a Hollywood Studio backlot? Wearing a wig and being complimented on my hair makes me feel like this.

But I’ve jumped way ahead. So, let me back up a bit…

To begin, I was diagnosed with Androgenetic Alopecia nearly 13 years…

It's now... after another dermatologist opinion and tired of this stressing hair loss i decided... Tired of waking up everyday and saw them at my pillow, tired of being afraid of touching my hair, washing it and brushing it, tired of being sad about my bald spots i'll save it! In a few minutes i'll become bald! thanks everyone from all the support, best regards, Cátia