Lots of you will know that tragically we lost Noah this year to a rare Mitochondrial disease called Alpers Huttenlocher Syndrome. Lots of you knew Noah from attending Kate’s Baby Sensory® classes with his lovely mummy Natasha. It has been an incredibly tough year for the Jordan family. Through this very difficult time, this amazing family have set up a wonderful foundation in memory of their little boy and we want to help as much as possible. We are also running a very special event in February to remember Noah and raise funds for the foundation.

The Noah Jordan Foundation funds research to develop treatments and find a cure for rare terminal paediatric mitochondrial diseases. The charity also raises awareness of these rare diseases and supports those affected.

Please, if you can donate even £1 to this wonderful foundation we can help change the lives of so many families who are continuing to battle with this tragedy everyday.

Let’s never forget Noah and let’s raise as much money as we can in his memory.

Thank you.

For more information on how you can support the Noah Jordan Foundation please follow the links below.    

Website: www.tnjf.org.uk    

Instagram: noahsfoundation    

Facebook: TheNoahJordanFoundation    

Email: contact@thenoahjordanfoundation.org.uk