Supporting Others With Epilepsy as a Peer Mentor
The power of peer support
This has been greatly beneficial to me as a peer mentor as it forces me to reflect on my history and think about my future so that I can portray a message of hope – but truthfulness – to my peers. It helps me give them advice on what I wouldn't recommend and what I would.
Sharing my own epilepsy experiences is rewarding
I find myself to be a good peer mentor in the sense that I can turn any experience into a lesson to be learnt and I have many experiences given that I've been epileptic for over half my life now. I'm also quite an open book, and I have yet to find an epilepsy-related experience that I'm not willing to turn into a lesson for both my peer and myself to learn from.
We can be hard on ourselves
A lot of us struggle with internalized ableism even if it's in such a small fraction that we don't initially notice it ourselves. Because of this, we carry around a backpack full of negative feelings and connotations, such shame or regret, for some quick examples.What we carry with us depends mainly on our experiences with epilepsy in the formative period of learning what it is and how to cope mentally and physically with it.
How to become an epilepsy peer mentor
If you think you have the strength to look inside of yourself and use that to help both yourself and others who need somebody to lead them away from negative experiences, please consider becoming a peer mentor. You can be online and help people across the world, although this comes with the niche of having to understand people in different countries and that they can have very different experiences to you.You can also be a local face-to-face mentor if that's the path best-suited to you. You can do either by finding your closest epilepsy support organization or by posting your offer on community service and notice boards so people can reach out to you independently.It is a lot of work, though, and you must know when to step back and take a day for yourself and unload. You are carrying your own epilepsy journey on your back first and foremost, of course.
Source: epilepsydisease.com. Renee Williams