Hi
I am in need of some advice.
I have a 4 year old child who has had AA since she was 9 months old. She has now just lost all her hair for the second time in the period and has just the white downy hair, which I think is quite common and not regrowth of any sort.
When she lost her hair for the first time at 12 months old, it was not a problem as she was a baby and nobody really noticed. Now she is 4.5 she is aware of her hair loss, last summer she had a full head of beautiful curly hair, and she knows she is 'different'.
To me she is beautiful with or without hair. However, I want to ensure that I do what is best for her, now. She is at school. I have explained her situation to the teachers so they are aware. She is not overly bothered at this stage about being bald, but her awareness is increasing with some of the things that she says. For instance "Mummy I want hair like yours" , "I want long hair", "I want to put clips in my hair like my friends".
I recently discovered Freedom wigs and have been in touch with them direct and know the process quite well. I have spoken to her father also about the wigs, but his mother, my daughters grandmother, is now trying to dictate what I should do, and trying to make me feel guilty about considering the wig option. I find some of the comments rather ignorant, even though she considers herself educated.
Please see a snippet from the latest email from Granny dearest below:
4.The wig must be put on precisely each day to achieve a perfect fit. She would not be able to manage herself and would always need adult support. It is easy to damage the silicone base, negating the vacuum effect.
5. To keep the scalp and wig hygenic a daily and weekly complicated maintenance is required. The vacuum fit does not allow the scalp to breathe. Go to and open Freedom Hair; human hair wigs; female hair loss & alopecia areate. Tap on Product Information/Haircare/FAQ. This is essential reading
7. The mothers, of the daughters with alopecia were greatly stressed at their daughters loss of hair, one due to the culmination of a distressing illness, the other through non growth from birth. With Freedom Wigs their daughter's hair loss is now treated as a secret. Freedom Wigs were introduced at the start of a new school allowing a pretence that the hair was natural.
Wigs should be treated in a light hearted way, a "form of dressing up". Or like any head covering - with perhaps two or three to choose from - one could be funky. A pretty waterproof cap could be used for swimming.
I am in favour of the open non-secretive approach. It makes me profoundly unhappy that the hair loss must be made an embarrassment to be shrouded in secrecy.
As for going down the route of a Freedom Wig - I think it would be unsuitable for Madeleine. Bearing in mind the logistics of acquiring, its high maintenance and particularly frequent shaving her little head - no, no, no.
My daughters hairloss is not a secret, and will never be treated as a secret. I want to do what is right for her and hope to keep her confidence intact. If she wants a wig and hair, should I not look to get his for her if it makes her feel more comfortable?
Does anyone have experience of these wigs? I have also heard about the Petite Gripper wig.
I would love to hear about people experiences, and comments to the email above.
Thanks.