By the way, I have found a lot of people that have AGA on a website called www.heralopecia.com. You might find some good information on there. I'm not sure if that's what I have yet, my doctor told me that they think I have AA, but the biopsy results are not in yet. I'm now loosing hair on the hair line so I'm not sure what I have! frustrating!!
Melissa
Hi Lisa!! I would love to share stories! I will post up my experience on the site and then if you like you can send me yours too, (you can e-mail me or write on the site, either way). Your right, it does help you to talk to someone who really gets it!! Thanks!
Melissa
Hi Lisa,
I do not have AGA, but I do have a form of AA. If you would like to talk to someone going through this too, please e-mail me at mjharris27@hotmail.com. I'm can sooooo relate to what you are saying in your blogs! I hate to fix my hair now as before I used to love it. I would like to share stories with you if you would like to. Take care and hang in there.
Melissa
Thank you for your our words. It's comforting to know that I'm not alone with this thoughts. I just find it to be so many people that have this disease and they have hardly made any progress in their research, non at all. Sometimes that's the worst thing of it all, that it doesn't matter how hard I try, I still can't change the outcome of this. Are you loosing all your hair or just spots?
Hi Lisa, If you want to add photo to your page you can just click on the photo tab along the top of the page. Then click "add photo" it will be added to your page. After you have added them you can go to your page and to the photo section and click on edit. There you can chose whether you want them to be a slideshow or thumbnail. Let me know how it goes or if you have any other questions.
I know, it's really hard. I've had au for about 20 years so no more worries about what hair is staying and which are leaving! You might want to check out my book -- look at my page. A lot of women say it really helped them deal with this stuff.
Hugs in the meantime!
Those of you who have written me have made me feel very welcome here. I wanted to say thank you. I keep browsing blogs and members and I am just so happy to have found this place! I invite any and all of you to share with me. I am not alone and that feels sooooo good.
Hi Lisa, 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. Cheryl, co-founder
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Melissa
Melissa
I do not have AGA, but I do have a form of AA. If you would like to talk to someone going through this too, please e-mail me at mjharris27@hotmail.com. I'm can sooooo relate to what you are saying in your blogs! I hate to fix my hair now as before I used to love it. I would like to share stories with you if you would like to. Take care and hang in there.
Melissa
Hugs in the meantime!
I'm so glad you found this site. It is truly a wonderful resource!
I just wanted to say hello and find out how you are doing today.
LeslieAnn
Thanks for the sweet blog comment.
XOXO
CAR
Happy to see you here! It's a great community.
Heart,
CAR
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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.