Wondering if anyone with Alopecia also has any joint issues. I have calcific tendonities both shoulders and arthritic hips feel sort of young for these issues and it has been 10 years or so diagnosed (Alopecia since 4)

This past January will be 4 years since I lost all my hair. I think I have coped pretty well with it, tried to stay strong & up; but, lately, it just seems I am missing my hair, angry at my body. The why's coming back. Why the eye brows & eye lashes, will they or my hair ever come back. Do we all go through this? I know that my wounds ar still fresh, 4 years isnt really that along. I admire so many Alopecian sisters & brothers who have delt with this damn disease with such…

Alopecia World turned four years old on March 8, 2012, and we could not be more pleased with its growth.

There is no doubt that Alopecia World is one of the leading social networking sites for people from around the world who are living with alopecia.

Who made it so?

You - the members of Alopecia World!

You provide the support. You provide the encouragement. You provide the inspiration and information Alopecia World's thousands of members and monthly visitors need…

I hadn't realized so much time had passed since we were first struggling to understand and cope with Shannon's hair loss. It's interesting how people adapt and cope with changes in their lives, to the point you forget it was ever any other way.

Shannon's hair started falling out the summer before her 6th grade year, and was completely gone by Thanksgiving. It was a scary and confusing time - trying to figure out what was wrong, getting to the specialist, arguing with him when he tried…

I'm new to AW, so someone may have shared this already. U. of Texas/MD Anderson Center is building a national alopecia registry to use in genetic analysis. You (and your family) can add your information via their web site at:…

...and that's how it started for me, 8 months ago. That silver-dollar sized patch I found behind my ear has since spread almost to the part on the top of my head and continues to spread on either side. Not to be outdone, the other side has started a collection of competing, smaller patches and TODAY I noticed thinning in one eyebrow?! Just when I adjust to a new normal, normal becomes something else. :-( Been cycling in and out of depression, struggling to keep a positive outlook as my doc…

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…

Moving to Garland, Texas the 1st of next month and was looking for some beautiful bald peeps to have tea with !

One day when I was nine or ten, I got into a fight with my sister. She pulled my hair and I went screaming to my parents. My stepmother checked my head and noticed a bald spot about the size of a quarter. My sister was grounded for pulling out my hair but really it wasn't her fault, it was alopecia areata. The spots would come and go over the years and for a long time was restricted to the back of my head and I was able to hide it. I was 27 when my son was born and when he was 4 months old…

Hey everyone, just thought I'd write a quick blog about my trip to Nigeria( I went for a month, dec to jan) and what I experienced while I was there.I went to Nigeria for 2 of my cousins weddings, they were held in two different cities, I traveled to Lagos( a large city in the southern part of the country) and benin.I did wear my wig when I was there and it got really unconfortable, had to stick it out though. But what I really want to write about is the BIG cultural differences. When I got…

Im going to list my hardest moments and greatest moments from 1 to 5 :'D

Hardest:

5~Going compleatly bald!

4~Got called "baldy"

3~Me and my two bestfriends were sitting in music class , i was leaning on my chair and without realizing my wig got caught on the drum behind me and i put my chair down and it came off ! , i ran to the toilets and cryed all day and wouldnt come out till everyone went home.

2~A boy i liked was riding on his bike , he cicled past me and my…

Having alopecia means im differrent and being different makes me stand out and because i stand out that mean people notice me and if people notice me more people know me and if someone knows me they know alopecia x

Are there any parent of children with alopecia that live in Pensacola, Fl? My daughter, who is just 16 months old was recently diagnosed with this condition and I am activley trying to seek out support. It's very heartbreaking to witness this happening to my little girl, although she has no clue of whats happening to her at this time. I still feel concern for her and her future with this condition.

As most of you know, I have alopecia universalis an autoimmune skin condition which causes the loss of hair on the scalp and in my case my entire body. Although not life-threatening, alopecia is most certainly life-altering and its sudden onset, recurrent episodes, and unpredictable course have a profound psychological impact on the lives of those disrupted by this disease.

The National Alopecia Areata Foundation (NAAF) is the largest, most influential foundation associated with…

Well my Dr. called me and said antibodies were found in my thyroid. I am not exactly sure what this means so I was wondering if any of you had any knowledge about it.

My Dr. is talking with an endocrinologist about the next steps to take before I go in to see him, but I am impatient. I have been googling as best as I can but I like person experience from people with aa.

I want to understand as best as I can if this means my hair might come back.

I am a bit sad as I was just…

Thanks everyone for favoring the blog "Define your total Package". I hope that it was helpful as it has helped me.

So my husband and i are taking my 7 year old daughter to Disney World in april and im not sure what i can wear on my head that wont fall off on rides! Yes i can tape my wig on but its going to be Hot! open for suggestion!! WE are still un sure if we are going to the water parks yet and if we do that what should i wear there??

I was only 8,

Am i normal?,

Is this bad ?,

i asked myself,

Im ugly !,

Digusting !,

a dissapoinment to everyone !,

i told myself,

Everyone will hate me !,

Ill get bullied !,

Left out !,

So i thought,

People stareing,

Judging me as if they know me !,

I (thought) I saw ,

BUT I WAS WRONG SOOOO WRONG !!!!!

im normal and its not bad,

Im not ugly or disgusting or a disapointment to anyone !,

Im pretty sure…

This is a quick little post. I just wanted to share an experience that I had yesterday. Now that today is a new day.

Yesterday when making my way around town, I experienced the stop and gawk that comes with embracing my baldness. In fact while walking into the gym 2 young girls almost tripped and felled down while walking backwards, staring with their jaws open. Most days this type of thing doesnt effect me, but as we all know, we have not so great days. I tapped into my inner…

Something we could all use more of. I love this video. It's not hair loss related, but it is sweet and comforting. It makes me feel a deep love for my fellow humans :) I hope you enjoy it.

https://www.youtube.com/watch?feature=player_embedded&v=hN8CKwdosjE