Search:   
Home    Search    Invite    Help Signup    Login
View monicamom4's Friends
Report this Person
Statistics
Profile Views:92 views
Friends:5 friends
Last Update:5 months ago
Signup Date:Apr. 7, 2008
Calendar

Recent Activity
5 months ago
monicamom4 and Sweetipie are now friends.
5 months ago
monicamom4 and Dottie are now friends.
5 months ago
monicamom4 and Ann are now friends.
5 months ago
monicamom4 and mominny are now friends.
5 months ago
monicamom4 and womenshairlossproject are now friends.
5 months ago
monicamom4 updated their profile.
Personal Information
Name: Monica
Birthday: Sep. 15, 1953 (54 years old)
Marital Status: Single
Do You Have Children?: Yes
Contact Information
City: Argenta
State/Province: Il
Country: USA
Hair Loss History
Years of Hair Loss?: 3
Treatment Regimen: steroid gel, seeing a dermotologist
Past Treatments: hair shampoo treatments
Time Spent Thinking About Your Hair Loss: 75% of The Day
Do You Count The Hairs You Lose Daily?: I used to not any more
Stage of Hair Loss: Bald and Beautiful!
Type of Hair Loss: Alopecia Areata
What Caused The Onset Of Your Hair Loss?: Thyroid
How has your hair loss changed you?: I don't like to look at myself so I wear a wig when out in the public and a scarf other times. I keep hoping some day that a miracle will happen and I will have hair again.
Friends (5)  [ view all friends ]

womenshairlossproject

Ann

Sweetipie

Dottie

mominny
Comments (3)  [ view all comments ]
Ann - 7:54 PM on Apr. 14, 2008  reply | message
Hi - I wear a wig all the time in public, a cashmere stocking style hat when home and to bed. My hubby is fine with my hair loss, though I think would be embarrassed as much as I would be to try to go public without a wig. While riding in the car on a trip over the weekend, I forgot my stocking hat and had to take off my wig for a little airing and felt very uncomfortable when we passed another car. Isn't that silly? Wow, my vanity can really take over sometimes.

My hair loss was so quick but my wig is wonderful. I hate more the eyebrows getting bald spots and thinning of my lashes... this part will be very hard for me.

Take care!
Dottie - 11:03 AM on Apr. 11, 2008  reply | message
Hey Monica,
Welcome to the Network. I don't have Alopecia Areata, but there are many members here who do. If you haven't already checked them out, I recommend getting to know kathyloulu, cate, and Jeanen for support and emotional uplifting. They are truly amazing and strong women! Their stories and attitudes always inspire me.
Blessings,
Dottie
womenshairlossproject - 1:58 PM on Apr. 7, 2008  reply | message
Hi Monica, Welcome To The Network!