News and blogs

Young girl smiling next to a Christmas tree

To the parent of a recently diagnosed child

A parent shares a heartfelt and honest look at life after getting a tough diagnosis for a child. It talks about the initial shock and the journey to finding a new normal. It highlights the importance of building a supportive community, adjusting to new routines, and trusting medical professionals. Discover the emotional ups and downs of getting unsolicited advice and comparisons from others.

Young man outside staring into the distance

Can I work with epilepsy?

Trying to choose a career path and search for a job can be daunting for everyone, but even more so if you have epilepsy. Find out about disclosing your epilepsy, your rights at work and discrimination.

Young woman outside looking down the camera

How to minimise stress at work

Work can be stressful enough without adding an invisible disability into the mix. Here are our top three tips to help you decrease anxiety, feeling overwhelmed and cope with stress in the workplace.

Photograph of the front door of number 10 Downing Street

Peerage for Jane Ramsey

Jane Ramsey, Young Epilepsy Chair of Trustees, is to have a peerage conferred by His Majesty The King.

Epilepsy medication shortages

Difficulty getting your meds?

The UK is experiencing shortages in certain medications, many of which are prescribed for epilepsy. If you are worried about your supply of anti-seizure medications or are having difficulty getting hold of certain prescribed medications speak to your epilepsy team for more advice. Do not stop taking your medication or reduce dosage. Always speak to your doctor before making any changes to your meds.

medication pills

Changes to Advice for Males on Valproate

The Medicines and Healthcare products Regulatory Agency (MHRA) has recently updated their advice for all males taking valproate. Learn more about the new guidance.

Bea

I am Bea

Meet Bea, one of the heroes of our #UnderstandMyEpilepsy Campaign. Bea is 15 and experiences focal seizures. For Bea this has meant that her teachers and students at school don't understand her epilepsy and the challenges that she faces.