Melani Molina's Comments

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At 11:39am on January 23, 2009, Maygensmom said…
Welcome to Alopeica World. What ever questions you have, please feel free to ask. We are all here for each other.
At 9:38am on January 23, 2009, Penny++Amy's Mom said…
Hi Melani, I am also glad to find a friend. I have 3 children, 2 boys and a girl. But Amy is the only one of the 3 with alopecia. She is my youngest. She lost her hair when sh was 9, she is 14 now. My Dad and brother also have AA. I just never thought of it as something that could happen to a girl. At first things were hard especially at school, but she found her true friends stood up for her. We live in a rural area , so a lot of kids are used to her this way, she tried a wig but it was to distracting for the other girls who could not keep their hands off her hair. I can't lie to you and say its been all peaches and cream there have been some bad days, I think it has made her a stronger person. And i think she is beautiful any way she looks, and I am sure you will find that no matter if your daughter has hair or not you will still find her beautiful. I wish you the best of luck and god bless you and your daughter. Just remember to remind her that she is not her hair.
At 11:15pm on January 22, 2009, Amber Lounder said…
Welcome Melani You will find the answers and information you are looking for here and great support too :0
At 9:36pm on January 22, 2009, Cherylnz said…
Hi Melani
Welcome to Alopecia World
At 4:59pm on January 22, 2009, rj, Co-founder said…
Hi, Melani. Welcome to Alopecia World! This is a great place for great people, so be sure to make your positive presence known. :-) - rj, Co-founder

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