Hi, Thanks for the add. Your right it's great to know that your not alone and there are others who live nearby. I see that your going to the support group meeting in the city. I'll see you there! It will be great to meet in person.
Hello, Thanks for stopping by my blog. If you would like a bracelet I think that the best way to do it is if you send me a check and I will then send you the bracelet. How does that sound to you? I will hold the check until you respond to me that you recieved the bracelet.
Ellie
oh...and if your wig supplier wont add hair to your wig, and you are looking for someone else, I know a guy in Mahattan that can give you a nice lace one and he will add hair to it for free ; ) Let me know if you want his name/ number
awe, i've been diagnosed with alopecia for almost 9 months. not long, but yea.
and i've found alot of people on this website who are great to talk to about alopecia stuff.
I think it is fantastic that you got so much out of attending the conference. It sounds like you empowered yourself to take a stand and it is great. Maybe you'll come back in the future and tell the kids how Alopeciapalooza changed your life. It sounds like you will do fine in school this year and in life with the head you seems to have on your shoulders! Keep in touch! Cindy
hey alyssa nice to me you..hows your summer going over there in NY?
so i was reading your profile and i am wondering what u do for eyebrows...im still getting used to having AU and having no eyebrows bugs me more than anything :(.
Hi Alyssa,
I was at the CAP event as well. I don't recall seeing you there. My husband did the secure ID booth. Sam and my husband were were shirts that said I am too sexy for my hair that is why it isn't there. Do you remember seeing them? I also started CAP meeting in Massachusetts. There comes a time when you want to do something you have to just do it yourself and take a stand. Good for you for going out there and meeting others with Alopecia. I hope your mom is supportive to you. Samantha knows she is no different from anyone else just because of her lack of hair. She actually just got her first haircut in two years and will be going to school with out her wig. She is very excited. We live in a great little town. Growing up in NY myself I know how cruel kids can be. It is not easy being a Ny'er sometimes..Have a great year at school! I hope you are finding the support you need. Enjoy your senior year! Sometimes I visit my friend in Bayshore. Maybe we can meet up sometime when I am in town../Sam is a spunky gal with lots of positive energy. She has her own page, Samantha. She'd love to have some wall posts..Cindy
Hi Alyssa, I wanted to welcome you to Alopecia World. I can honestly say that we are a great community here and I hope you enjoy the time you spend with us.
Hi Alysaa, Welcome to AW.. This board rocks! How are you? I am a mom to a 7 yr old with this condition. I grew in Floral Park..We are almost neighboors..Cindy
Any mention of products and services on Alopecia World is for informational purposes only; it does not imply a recommendation or endorsement by Alopecia World. Nor should any statement or representation on this site be construed as professional, medical or expert advice, or as pre-screened or endorsed by Alopecia World. Alopecia World is not responsible or liable for any of the views, opinions or conduct, online or offline, of any user or member of Alopecia World.
Alyssa's Comments
Comment Wall (42 comments)
You need to be a member of Alopecia World to add comments!
Join Alopecia World
Enjoy!
how are you?
Ellie
and i've found alot of people on this website who are great to talk to about alopecia stuff.
so i was reading your profile and i am wondering what u do for eyebrows...im still getting used to having AU and having no eyebrows bugs me more than anything :(.
I was at the CAP event as well. I don't recall seeing you there. My husband did the secure ID booth. Sam and my husband were were shirts that said I am too sexy for my hair that is why it isn't there. Do you remember seeing them? I also started CAP meeting in Massachusetts. There comes a time when you want to do something you have to just do it yourself and take a stand. Good for you for going out there and meeting others with Alopecia. I hope your mom is supportive to you. Samantha knows she is no different from anyone else just because of her lack of hair. She actually just got her first haircut in two years and will be going to school with out her wig. She is very excited. We live in a great little town. Growing up in NY myself I know how cruel kids can be. It is not easy being a Ny'er sometimes..Have a great year at school! I hope you are finding the support you need. Enjoy your senior year! Sometimes I visit my friend in Bayshore. Maybe we can meet up sometime when I am in town../Sam is a spunky gal with lots of positive energy. She has her own page, Samantha. She'd love to have some wall posts..Cindy
How are you?
Tracy and Amanda
thanks for the request, how are you?
Cheryl
co-founder
i'm sixteen.
will you be attending that event too??
Welcome to
Alopecia World
Sign Up
or Sign In
Disclaimer
Any mention of products and services on Alopecia World is for informational purposes only; it does not imply a recommendation or endorsement by Alopecia World. Nor should any statement or representation on this site be construed as professional, medical or expert advice, or as pre-screened or endorsed by Alopecia World. Alopecia World is not responsible or liable for any of the views, opinions or conduct, online or offline, of any user or member of Alopecia World.