Thank you for getting involved and taking action this SUDEP Action Day!
Join us in tackling the many #WHYs and challenges linked to SUDEP.
Whether you have lots or a little time to give, you can play an important part in helping us bring epilepsy and SUDEP out of the shadows to help save lives.
Thank you for your support and all you do to help raise awareness both within your profession and with your patients.
Some ideas for how you can help get involved, & steps you could take as part of your care for people with epilepsy are below:
Top 5 things you can do:
Pushed for time? #Why not:
Discuss SUDEP & risk with your patients
Share #WHY knowing about SUDEP is important
Be aware of patients with epilepsy;
- Not attending appointments or medical reviews
- Not picking up prescriptions
- Experiencing changes to their epilepsy, mood or lifestyle
Promote best practice
Show #WHY it’s important to discuss & understand epilepsy risks
Consider using available endorsed resources as part your clinical practice to help discuss and monitor rising risks & any in your patients’ condition to:
- Promote positive, routine discussion of risk
- empower patients’ self-management
Signpost to Epilepsy Organisations
For information on how people with epilepsy can reduce risks and manage their epilepsy to keep themselves safer.
- Often the leaflets are free & are specific for professionals too!
Support those affected by SUDEP
If you hear of an epilepsy death in your department / organisation, signpost the family & you colleagues involved to specialist epilepsy bereavement services.
- Is there a deaths registry they can complete? Anyone linked to an epilepsy death can share information to help inform future research
Get your colleagues involved in our #WHY campaign
- Share the campaign materials with your colleagues.
- Create an epilepsy information board: include key facts about SUDEP & Epilepsy – signpost to epilepsy organisations.
- Are there training resources to help extend your knowledge? Could you hold a staff training day on the topic? Many epilepsy organisations have resources for this.