I hope you will be able to go. Yea, I know the sun is very strong in July! I plan on wearing a bandana or something too. SPF 50 will also be a must! email me with your info so that I can put you on my contact list. sgomez33@cox.net 480-332-4860.
Hi Lauren, sorry that I haven't been keeping in touch since you last went to our support group meeting. How have you been? I wanted to let you know about an event we are going to be having on July 19 at Big Surf for National Bald Out Day. Email me with your contact info so that I can send you a flyer with all the details. The entrance fee is being sponsored by a local business, so I hope you will mark that day on your calendar, and bring your family! I hope to be hearing from you soon. Take care, Sarah :)
Hi Lauren.....You have a beautiful family. I have had alopecia totalis for 10 yrs and I have a 5 yr old daughter who I have been praying does not develop it. After seeing your pictures of you daughter, it has made me feel a lot better. THANKS
Oh yeah! I spoke w/ Maddy aboyt a week ago! She's great! So positive and upbeat. She also metioned you, and I told her to give you my number. I guess she did! So I'll wait to hear from you. Take care, Sarah
Lauren
You have such a beautiful family! All your girls are just georgous!! So you have not only dealt w/ it yourself, but your dughter as well. I have been totally bald since I was five and am now 31. My 9 year old son has had some very small spots come out just this year, but they don't really seem to be getting any bigger, and they are growing back in. It's one thing to deal with it for yourself, but to see your child go through it must be way harder. I find myself obsessing over his small spots, and I NEVER did that w/ myself. So you go to MCC too!! I'm doing my pre-req's to get into the nursing program. How far along are you in the program? I want to leave you my email address. Email me w/ your name and number. I am a support group leader for poeple w/ alopecia, and we are just getting started w/ doing a children's group. It would be great to see you guys at our next meeting. my address is: sgomez33@cox.net I hope to hear from you soon! Hey, maybe we'll even run into eachother on campus!
Hi, we are still new to this site, Nicky and I were looking at pictures, and finding new friends. We hope this site will be as helpful to you as it has to us.
Hi Lauren, 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. Cheryl, co-founder
Hi Lauren,
My 2 babies have alopecia. I guess I should not say babies, my son is 9 and has AU and my daughter is 6 and had lost erverything, but has grown it back in the last year, without treatment. They are beautiful!! I just had a son about 6 months ago with my new husband. We are not sure yet if he will also develop the condition as well. Your daughter is beautiful!! Have you tried any treatment for her? I gave up and never tried anything after several attempts w/my son did not work. I love that you are here in AZ!!! We have a support group going on, you should come and join if you can. Take care and talk to you soon!
OMG your daughter is absolutley gorgeous..my baby girl jordyn has AA..but she has had AU and it all grew back..she is on her 2nd round of it...your daughter is young like mine was when she first got it. and truthfully it doesnt bother her...I just love their spirits...
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You have such a beautiful family! All your girls are just georgous!! So you have not only dealt w/ it yourself, but your dughter as well. I have been totally bald since I was five and am now 31. My 9 year old son has had some very small spots come out just this year, but they don't really seem to be getting any bigger, and they are growing back in. It's one thing to deal with it for yourself, but to see your child go through it must be way harder. I find myself obsessing over his small spots, and I NEVER did that w/ myself. So you go to MCC too!! I'm doing my pre-req's to get into the nursing program. How far along are you in the program? I want to leave you my email address. Email me w/ your name and number. I am a support group leader for poeple w/ alopecia, and we are just getting started w/ doing a children's group. It would be great to see you guys at our next meeting. my address is: sgomez33@cox.net I hope to hear from you soon! Hey, maybe we'll even run into eachother on campus!
your daugther with alopeica is very cute, i love picture 17!
hope to hear from you soon
carly
My 2 babies have alopecia. I guess I should not say babies, my son is 9 and has AU and my daughter is 6 and had lost erverything, but has grown it back in the last year, without treatment. They are beautiful!! I just had a son about 6 months ago with my new husband. We are not sure yet if he will also develop the condition as well. Your daughter is beautiful!! Have you tried any treatment for her? I gave up and never tried anything after several attempts w/my son did not work. I love that you are here in AZ!!! We have a support group going on, you should come and join if you can. Take care and talk to you soon!
How are you and your little ones doing today? I just wanted to say hello and welcome!
LeslieAnn
Roger.
Your daughter is so cute.
My mom lives in Gilbert.
Good luck with your Nursing program and of course a big welcome to Alopecia World.
Jeff
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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.