Gracias!!
xxx

Hi Yokasta
Thanks for adding me as your friend. Your rely to Jenna's mom was great. I agree with your father. You are Beauitful with or without hair.
We must change society attiude about what made a women beautiful.
Continue to do God work.

Thanks for the welcome note! Cheers :) Katie

Hello! Thanks for becoming a friend! Memphis ey? Well your not real far from me.....long walk though lol
Your hairloss looks similar to mine!
You have a beautiful family!

Hello, you have really nice pictures=) It´s really fun that I have found this webside.

Hi - on a different note, really love your music. Wonderful selection.

Vahishta

Just popping in to say hello, and that you have a beautiful family. Hope to chat with you soon.

Thank you, you have such a beautiful family!

Hi, thanks for the welcome. Glad to be here!

YoKasta, I just had to come by your space on Alopecia World and personally thank you for your invaluable contributions to our new community. Keep doin' whatcha do! Wishing you great joy and good success, richard jones (iAMrj).

Hi YoKasta!!!

Thank you..... super to see so many wonderful people on this site!!

filakia (greek kisses)

Hi YoKasta,
Thanx for the comment, and, yes my head is tattooed. I love it!!! It was my therapy after the hairloss, so it did hurt, but it was a different type of hurt!!! I sat 22 times for a total of 36 hours. And, in answer to your question, if my hair grows back, I will be happy and will probably keep it in the winter for warmth, but shave it in the summer. :-)

Hi YoKasta, good to meet you and everyone else here. How long has this site been up?

thanks for the weLcome. it's good to be here. i'm excited to meet new peopLe&buiLd support systems.

Thanks. It's so nice to find a place where I'm not the only one with alopecia. It's a nice feelibng.

Thanks for the add Yokasta x Im very pleased to be here x

What is that? My case was documented through state and mental helath people. They would not change the words "what physical illness does she have that prevented her from working???" I was not mentally ill but my family doctor and daughter had me behind my back sent to a mental hospital. I was there over night and they said this is physicil not mental. But the doctors there told Goodwill they had to change the term to mental so they could fill out the papers and clear all this up. My family doctor refused to be involved and there was nothing physical proven eiher. All my tests showed normal. So Goodwill gave me 30 days to get this paper filled out or I was voluntarily quit and the state doctors and etc were telling them they couldn't if they didn't change the term. Goodwill drug me along for 6 months. Then sent a paper saying I was voluntarily quit. And when I tried to hire back in they said I was a no rehire. I found out about a year and a half later that I was not a no rehire and there is no real reason in my file as to why I quit. Every reason they claimed there is proof behind it that wasn't it. So they have taken the no rehire off but I know how they click and they won't rehire me...will always claim someone was more experienced or something. I have seen them throw away aps because they didn't want someone there because of color and etc. Then turn around and hire a family member or friend when it says very plain in the policy that two family members or someone dating can't work at the same place. So I guess I was just dumped on for illness and nothing much I can do. I would love to help someone put them in their place though. Along with the public here. They complain all time and nothing is ever done. they also had documentation from the mental health doctors that something medical was why I had to wear the hat. They refused it because they were mental. Finally got a doctor statement for the hat and then they said I was out to many days...I was trying to work and they wouldn't let me because of the hat. Just one big circle and wasting my time and dumped me out with V. Quit.

I saw your post for Dotty. Yes her head is tatooed. She hates wigs. She is a wonderful person and been such an inspiration to me. I met her on Wig Support and also the Alopecia Areata community. She is a wonderful person. And a heart bigger than the earth itself.

Thanks for the welcome...I THINK ITS REALLY COOL THAT YOU INFORMED PEOPLE OF THE MD ANDERSON RESEARCH..MY DAUGHTER IS PART OF THE PROGRAM..WE SIGNED UP AND DONATED BLOOD THROUGH COLUMBIA PRES. NY.maybe if more people join there is a greater chance of finding a cure or finding a better understanding of alopecia.
stay strong.