This charity is very close to our heart as our loving daughter Simran was diagnosed with Rett Syndrome at the age of 18 months and now is 10yrs. Were wanting to raise as much as we can so it helps families like us to find a cure for this syndrome. So please donate today for Rett Syndrome Awareness Month of October. Read below as it tells you about the condition.

Rett syndrome is a rare neurological disorder affecting mainly females and very few males. It is present from conception and usually remains undetected until major regression occurs at around one year of age, when children may lose acquired skills and become withdrawn. Genetic but largely not in herited, Rett syndrome is usually caused by a fault on a gene called MECP2 which is found on the X chromosome. People with Rett syndrome have profound and multiple physical and communication disabilities and are totally reliant on others for support throughout their lives.