julie
  • 60, Female
  • charlotte nc
  • United States
Share on Facebook MySpace
  • Blog Posts
  • Discussions
  • Events
  • Groups (1)
  • Photos
  • Photo Albums
  • Videos

Julie's Friends

  • Julie Koch
  • Donna DeHoog
  • Kimberly Rolon
  • kimberly dean
  • Heather L
  • Indira
  • Tracy Cheek
  • tiffany wermund
  • J
  • holly
  • Nini
  • Sol
  • Melinda Thiele
  • Kristin
  • stephanie robertson
 

julie's Page

Profile Information

Relationship Status:
Choose one
About Me:
just me
Do you have alopecia?
Other type of alopecia
Are you age 18 or older?
Yes - I am 18 or older

Comment Wall (23 comments)

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

Join Alopecia World

At 3:59am on March 30, 2011, BTB (John) said…
Hi Jules not been here for ages nice to see old friends here. xoxo
At 11:05am on January 21, 2011, becky gave julie a gift
At 3:14pm on November 13, 2010, Kimberly Rolon said…
Hey Julie, How are you doing? I dont know if you remember me but we did email last year. Im still in Germany. Hope all is well with you.
God bless,
Kim
At 9:10pm on October 31, 2010, Julie Koch said…
Thank you for the nice comments about my pictures. Those pictures are several years old. I don't look like that anymore. I appreciate the friend accept!
At 11:34pm on October 27, 2010, Pat said…
Yes your page is still active and I received your test message. How are you?
At 8:27am on September 29, 2010, BTB (John) gave julie a gift
At 4:53pm on October 24, 2009, Kim Culberson said…
Hi Julie, My email is kimculberson@xplornet.com , you can email me anytime....
At 10:40am on October 19, 2009, a. z. said…
my picture is recent. I've had alopecia since I was 2. I go to hair club.
At 1:08pm on September 20, 2009, Susan VanOrder said…
Julie,
I have read some of the other posts that you have written and received. First of all, I see that you are from Charlotte, NC. I lived there for 1 1/2 years and it is a very beautiful city with a lot of opportunity and great people. After looking at your picture that you have posted, I see that you are also beautiful. Don't sell yourself short just because you don't have great hair.
I do suggest that seek some counseling. Most people benefit from just talking to someone about what is bothering them.
Also, There are products on the market for female pattern baldness. They are called integration hairpieces. They are light and comfortable because they are just a netting structure that adds hair just where you need it. I would suggest you use the internet to search for a distributor or look up hair replacement in your area and they will likely have these products. This would be the most comfortable alternative.
Nothing is worth dying for.... I survived a brain aneurysm and that was 20 years after my alopecia areota started.
Find the positives in your life instead of focusing on things you feel are negative.
Everyone has negative things happen to them everyday, but you have to stand up and take control of yourself. Unfortunately, no one else can find happiness for you, you have to make your own.
Thank you for writing. I am pursuing a career in counseling and I wish you the best. Write again whenever you feel the need.
At 2:11am on September 18, 2009, Lee said…
Hi Julie,
I never really got over it. It still hurts till this day. But I just make it work into muy life somehow. I dont know much about female pattern baldness. I kinda agree with Susan below...you gotta just get on with ur life, because you cant let something that you cant control...control you. Have you looked into getting a topper? That may help your self esteem. Also a therapist may help. take care...cheer up its just hair ; )
 
 
 

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.

© 2024   Created by Alopecia World.   Powered by

Badges  |  Report an Issue  |  Terms of Service