cally
  • Female
  • Vacaville, CA
  • United States
Share on Facebook
Share Twitter

Cally's Friends

  • Alina07
  • Bobbie
  • Deana
  • samantha
  • Jennifer Pliler
  • x3Awesome'TTx3
  • jennifer
 

cally's Page

Gifts Received

Gift

cally has not received any gifts yet

Give cally a Gift

Latest Activity

cally replied to Alina07's discussion Scared and confused !
"Hi, I really feel for you. I was diagnosed with aa in 04. The first time it was very textbook . One very large round patch with no hair. It happened in what seemed like over night. This time around it has been confusing . I got two small patches in…"
Jan 5
Bobbie left a comment for cally
"Hey Cally of course @ first I hated it but now I can't go out without it. It covers the top very well my problem now is I'm losing my hairline at my temples so I will b moving on 2 a full wig which I am very nervous about :( I've…"
Nov 11, 2011
Deana left a comment for cally
"Isn't that weird and ironic that we do hair for a living? I have never seen  or heard of anyone having this before. I know I learned about it in cosmetology school but it didn't register with me until it happened to me. My mother had…"
Nov 8, 2011
Cheryl, Co-founder left a comment for cally
"Hi Cally, 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 and we look forward to your input. Be sure to check out "10 tips for getting the most out…"
Nov 8, 2011
cally joined JayB's group
Thumbnail

California World

Discussion forum for the land of sunshine andavocados..See More
Nov 7, 2011
Deana left a comment for cally
"Thank you for your friend request!"
Nov 7, 2011
cally joined Alopecia World's group
Thumbnail

Alopecia Areata

Join today to meet, support and share information and resources with others who are also living with patchy hair loss.
Nov 7, 2011
cally joined Megan's group
Thumbnail

Christians With Alopecia

Come chat about how your alopecia has affected your faith,how your faith has affected your alopecia,or just for plain old chatter.Open to questions,debates etc.But please always respect others beliefs.
Nov 4, 2011
cally is now a member of Alopecia World
Nov 3, 2011

Profile Information

Relationship Status:
Married
About Me:
I was diagnosed with alopecia areata in 2004. Im married with three little ones , Im just here to find support :)
Do you have alopecia?
Alopecia areata
Are you age 18 or older?
Yes - I am 18 or older
Your Website (Leave blank if you don't have one):
http://www.etsy.com/shop/SugarMarieVintage

Comment Wall (5 comments)

You need to be a member of Alopecia World to add comments!

Join Alopecia World

At 8:18pm on November 15, 2011, LeslieAnn Butler said…

Hello and welcome, Cally!
How are you today?
Leslie Ann

At 11:52am on November 11, 2011, Bobbie said…

Hey Cally of course @ first I hated it but now I can't go out without it. It covers the top very well my problem now is I'm losing my hairline at my temples so I will b moving on 2 a full wig which I am very nervous about :( I've tried 2 toppers 1 was the Jon Renau mono long which I started with & now I use the Noriko Milan which has lots of hair! Hope u have a great weekend! :)

At 12:38am on November 8, 2011, Deana said…
Isn't that weird and ironic that we do hair for a living? I have never seen  or heard of anyone having this before. I know I learned about it in cosmetology school but it didn't register with me until it happened to me. My mother had a bad perm and a lot of stress which made her hair thin and patchy but nothing like this kind of alopecia. Her thinning hair and crying every day over it is what made me go into the field in hopes of helping in some way. Who knew the future would AU my way? I am still trying to find my niche in helping people. I wish I knew more about the wig industry!
At 12:34am on November 8, 2011, Cheryl, Co-founder said…
Hi Cally, 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 and we look forward to your input. Be sure to check out "10 tips for getting the most out of Alopecia World” which include a few tips to get you started!
Cheryl, co-founder
At 9:37am on November 7, 2011, Deana said…
Thank you for your friend request!
 
 
 
YOUR AD HERE

Latest Activity

LN_DARK posted a discussion
34 minutes ago
dcwalsh replied to dcwalsh's discussion Need wig but still have some hair...help?
43 minutes ago
dcwalsh replied to dcwalsh's discussion Need wig but still have some hair...help?
45 minutes ago
Lola updated their profile
1 hour ago

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.

© 2012   Created by Alopecia World.

Badges  |  Report an Issue  |  Terms of Service