Erin, 8, who was bullied for having hair loss condition has her life changed with donation

Erin Blackwell, eight, from Basildon, is living with alopecia areata - also known as spotted baldness.

The condition has caused Erin to be very self-consciousness and wary about how people see her.

Mum Nadine Blackwell, 33, said: “We noticed Erin’s hair started to thin in December 2016 after looking at some photos. It wasn’t obvious to the naked eye but the flash light in the photos made it obvious.

“At first Erin could just cover the small patches with her hair. But as they got bigger she became more self-conscious and she was worried about people staring.

“We took Erin to the GP for some blood tests but it didn’t show any underlying causes. The GP told us it was very likely she has alopecia areata and then we were referred to a paediatrician.

“I found out about the Little Princess Trust, I contacted them and they donated a wig to Erin within a week. She had it fitted at a salon and she was very delighted.

“The colour is the same as Erin’s dark brown hair and she has become confident again.

“She was called nasty names by a kid at school who said she hated Erin and wished her hair would never grow back again. Thankfully she has left Erin alone now.

“Luckily the school and other kids are supportive of her and they’re respectful.”

While Mrs Blackwell is relieved her daughter can still enjoy school but there are more woes lying ahead.

She said: “Erin will grow out of her wig soon and I’ve been told real hair wigs could cost £500 so we need to save up for that. For any girls living with alopecia areata, don’t let your hair define who you are because you are still beautiful.”

The Little Princess Trust provides real hair wigs free of charge to children and young adults up to the age of 24 that have sadly lost their own hair due to cancer treatment and other illnesses. Often young girls cut off their long locks and donate them to the trust.

Visit www.littleprincesses.org.uk/