Lottie is only 23 months, she was born with a microdeletion of chromosome 13, congenital distal arthrogryposis, oro-motor feeding difficulties, she has developed delayed, seizure disorder and dystonia. This has effected lottie by having low muscle tone. Lottie can now sit independently around 15 minutes and she is working so hard.

Lottie is needing more therapy than the NHS can fund – the family and friends are raising money for Lottie to go to the movement centre at Robert Jones & Ages Hunt Hospital in Oswestry.She will receive target training to help her crawl, stand and walk with therapy and equipment.We are helping to raise more funds for more treatment.