www.alopeciaworld.com
Just last year my daughter, who is in elementary school, lost all of her hair. She's had alopecia areata for a few years but we always managed to cover her bald spots. All of a sudden all of her hair was coming out. It turned into alopecia universalis. At first she wore hats to school, then we got her a wig. Kids immediately made fun of her for not having hair and then for wearing the wig. When school got out for the summer she was so relieved. She had a great low stress summer but just started school again. This is only her second week of school and to date there have been three different incidents of kids making very mean comments about her wig and also about her lack of eyebrows and eyelashes. The school has been very good about helping as far as letting the kids know it's wrong to bully but I'm feeling so hopeless. It kills me to see her going through this and I really don't know what I can do to help her. I'm pretty sure she's going to need counseling but other than that what more can I do to help her get through all of this? I don't want to put her in homeschool and withdraw her from social interaction because I don't want her to be ashamed or feel like there is anything wrong with her. However, at the same time I don't know how much more I can take of watching her be sad because another person put her down. Any suggestions or anyone who's been through this I'd really appreciate some ideas! Thanks
I am so, so sorry to hear that your daughter is going through this. My son, who's 6 and has AU, just started Kindergarten this year. Before school started, we went in and sat down with the principal and his teacher and talked with them about alopecia. We also gave them letters to hand out to all of the teachers and staff in the school, telling them about alopecia and asking for their help in educating their students. In addition, we had a similiar letter e-mailed to every single family in the school. Another option would be to have a school assembly and talk directly to the students, I've heard of many parents doing this, although at this point we're not planning to.
For the letters we wrote, we had gotten a booklet from NAAF with some sample letters. I used those as a starting point for our letters and it was really helpful.
Good luck and I really hope that things improve for your daughter!
I'm with Cindi on this one. Some battles are just not worth fighting. Your child's mental health is more important. I do wonder where the "adults" are in these cases. I am talking about the school staff and the parents of the bullies. As far as Kelsey's story (where her daughter was pushed down the stairs by bullies), those students should have been charged with assault and battery. Seniors in high school are old enough to know better!
I tried my best to push the school to something but surprise surprise by the time I arrived at the school the video tape of the stairwell was blank it must have "malfunctioned". To this day we don't know who did the pushing. But enough of that your child's mental health is of the utmost importance.
I remember handicapped children in my own elementary school who were not bullied.
I remember a teacher telling us in no uncertain terms that anyone giving them problems would be in a lot of trouble.
I remember also that the compromised child's practitioner come into the school to educate
us about them. As a child, I used to like having limits set on me concerning things like this.
I completely agree with the idea of educating the kids at school.
Another thing that came to mind as I was reading this was to get in touch with a fashion consultant who might be able to help with the choice of a head-cover, wig and make-up in a non-abusive way.
I know this has helped me in times past.
Maybe it's just me, but I think a child who has had this fate and is being bullied should get their anger out and they should do it right in front of their abusers.
I also think anyone who has lost their eyelashes and eyebrows needs to learn how to apply make up and needs to know what colors work for them.
I hope things get better for you.
I would put my child in a private school and make the board of education of your town pay for it.
what mineral did you use from IT WORKS
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
You need to be a member of Alopecia World to add comments!
Join Alopecia World