About The Little Princess Trust

The Little Princess Trust was launched in 2006 by the parents of Hannah Tarplee, along with help from friends and from Hannah’s school, Hereford Cathedral Junior School.

Hannah was the original Little Princess.  Sadly she was diagnosed with having a Wilms tumour and after a brave battle, died in 2005.

At that time, finding high quality wigs for children was very difficult and only after a long search was a suitable company eventually found which made a wig for Hannah.  She very much enjoyed wearing her wig, particularly on special occasions.

After Hannah passed away, so many kind people offered help, financial and practical.  Hannah’s parents, Wendy and Simon decided that the most fitting way to use this help was to launch a charity dedicated to providing specialist real hair children’s wigs.  

Since its inception, the charity has now helped thousands of children.  The Little Princess Trust works with suppliers throughout the UK and Ireland, all of whom supply real hair wigs.

Information for those with alopecia

If you have alopecia and aged under 24, the Little Princess Trust will provide you with one real hair wig free of charge. Please note that those with alopecia will only be able to access one wig from the Little Princess Trust.

Website: http://www.littleprincesses.org.uk/

Phone Number: 01432 352359

Email:[email protected]