
New Hair For Eva
Donation protected
My daughter has had alopecia universalis since she was 3 years old, basically she has no hair on her body!We have had a wig previously through the little princess trust for which we were very grateful, however, the quality was not great and it irritates her head and the unnatural hairline means she can't wear it up at all. Whilst at alopecia camp at the weekend we had the opportunity to try a joli dancer wig which has a superior quality hair and the cap is comfortable and due to the silicone inside there is no slipping meaning she can even do handstands and cartwheels with no risk of it slipping off! It also has a very natural hairline and can be worn up and flicked about and the movement of the hair is soooo natural! The smile on her face was priceless and watching her play with it broke my heart. Unfortunately we can't go to the little princess trust again as they would only allow her the one wig. The price for her to have this hair - so she can feel as girly as all her friends - £2000c
Organizer
Sandy Pawlowski
Organizer