My first born child was diagnosed with Alopecia when he was two years old after patches started developing at 9 months old. Killian is a happy, confident child when it comes to his Alopecia and currently has a top knot showing off his patches. 

I am organising a Family Fun Day on Saturday 17th September 2022, as September is Alopecia Awareness Month. The fun day will be held at Odsal Stadium in the AJJB law venue. 

I will be Braving the Shave on this day and if my hair is long enough i will  be donating this to The Little Princess Trust.

If you would like to support us on the day, please email: laurenlee87@yahoo.co.uk 

Any donations would be greatly appreciated 🙂 

Alopecia UK is a small registered charity working hard to improve the lives of those affected by alopecia. The charity has aims of Support, Awareness and Research. A diagnosis of alopecia can make you feel like your world has been turned upside down. It can impact on relationships, work and social life. Many can find it difficult to go out in public to begin with, or even look in a mirror. Alopecia UK is here to help people at this difficult time.