I have 3 beautiful children. My youngest has alopecia totalis. She is the most beautiful, little girl with the best sense of humor. I'm basically here to learn, to vent, to support, to love, to be the mom that my little girl needs. She is only 5 years old and has so much future ahead of her. I want to make sure she lives it to the fullest.
Thanks for the compliments on my work! In my book there is a painting of a mom with a little one, as the header for my chapter on kids.
Let me know how you like the book, okay?
Big hug to you both!
Hi Annabel, I've talked to a lot of women who have daughters with AA. I know you want her to be happy and keep her from any pain! These little girls always grow up to be more sensitive and kinder than average.
There's a chapter in my new book about this...if you're interested, go to my page.
LeslieAnn
LeslieAnn
Hi Annabel..Im sure your daughter will be just fine..I am new here,but Ive heard other parents say they went to there childs school,and basicily informed all the people there,especially the teacher,that your child has AA,and corse do it in a very nice way of course..That should take a little sting of chldrens haarsh words..Again,Welcome..Bob
Annabel, 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
Hello, My name is Maria and my daughter name is Savanna she has AU since the age of 3 and is now 6yrs old, It has been a rough journey at times but we are learning to adjust, this is a wonderful site I have learned alot of other things and have talked to alot of nice and wonderful people...If you have any questions or would just like to talk feel free to comment back... Maria
Hello- What a beautiful family you have. I have a daughter too with alopecia universalis, she is 20 and has had alopecia since 3rd grade. Her hair has come and gone but now she is totally without hair and it is rough. I am happy for this website so we as parents can talk to other and help/support one another.
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.
Comment Wall (7 comments)
You need to be a member of Alopecia World to add comments!
Join Alopecia World
Let me know how you like the book, okay?
Big hug to you both!
There's a chapter in my new book about this...if you're interested, go to my page.
LeslieAnn
LeslieAnn
Roger.