I have made this page to fundraise for my daughter, Sophie who has a rare type of epilepsy called Lennox Gastaut Syndrome. She is almost 3 and started having seizures when she was just 7weeks old.
Sophie is developmentally delayed but is slowly progressing. She can now touch and feel toys as well as pushing herself up to sit which is a huge step forward for her.
Her seizures have not been brought under control and we only have one more medication to try.
We are raising money for Sensory Equipment that will help Sophie develop and other things that we are having trouble buying due to equipment being so expensive.
Any help you can give, big or small is greatly appreciated.