In 2018, thanks to the bravery of Hannah Deacon, the law was changed so children with severe epilepsy could finally access life-changing cannabinoid medicines on the NHS. It was a moment of hope. A promise that things would be different.

But seven years later, that promise has been broken. Families are still being forced to pay thousands every month or watch their children suffer seizures that could be prevented. Some have had to fight in court, fundraise, or go without — just to keep their children alive, to give them some form of quality of life. 

Now, at last, there is a chance to put this right.

The government’s drugs advisory committee is reviewing whether Hannah’s law has had the desired impact. This is the moment to make her legacy count — to prove Parliament can deliver for the 35,000 children still waiting for NHS access.

But MPs won’t act unless they hear us. That’s why we need them in the room at a crucial parliamentary event, where Hannah's family will be speaking and families Hannah supported will speak the truth about what’s happening.

👉 Please email your MP today. Tell them to show up, listen, and fight for our children.

https://medcan-foundation.emailyourmp.uk/

Together, we can make sure no child is left behind.

Thank you for your continued support. 

Medcan Family Foundation. 
www.medcanfoundation.co.uk