Being offered dugs to treat your daughters epilepsy when your daughters epilepsy is described as drug resistant has from the early days made me wonder... But six years down the line as we have accepted with heavy hearts that the drugs don't work for Ava it is with all I can describe as an increasing sense of panic that we are being offered more pharma medication. Eleven forms of medication later you would imaging that individuals who have spent half there lives in college and on courses to further their qualifications in their choose fields would be able to figure out that these drugs won't work not for us or not for the majority of patients who have an epilepsy as complex and severe as Ava's. We have an alternative we have an option and we are not allowed to access it. Between medical professionals and and laws that are not allowing genuine cases to access medical cannabis entangled together our child continues and continues to have seizure after seizure. We need help for our daughter and change will have to be made or she won't survive without serious damage to her brain and body or else god help us she won't survive at all please help email Simon Harris sign Ava's petition or in any way you can tell the people of this country we need change to save childrens lives before it is too late xxx thanks everyone v