My name is Evie.
I am 7 years old.
I have cerebral palsy and epilepsy.
I suffered birth trauma.
I also have global developmental delay.
I am also gastric tube fed.
I have a new diagnosis of Lennox Gastaut Syndrome.
I have a few different types of seizures daily.
There is no warning that any of my seizures are going to happen.
I am non verbal.
I take a mixture of epilepsy medication daily.
I also take daily meds for my Cerebral palsy and other problems.
This is my mums favourite picture of me as I haven’t got too much to smile about at the moment.
Mum says I’m her beautiful princess 🙂
Epilepsy Sucks UK has helped me please say thanks and vote for them to help others!