SEIZURES
Hi, how does anyone cope with FND seizures?
My friend was dx with FND and has multiple seizures a day. Hospital and doctors say they can do nothing as it’s all anxiety related and CBT would be the only treatment Avenue to explore. She has no life now, is terrified, struggling and has an autistic young dependant who is under 10 (albeit he is in boarding school during the week). Any advice to cope or eradicate/reduce the seizures?
Ask to see an FND specialist and speak to the epilepsy society helpline and check out their website as they have information on thereabout non epileptic seizures which maybe very helpful to her.
Hi Sonja, when I was first diagnosed with, it was the same for me and interestingly, I have an autistic son under 10 also! They were back to back and also i had tics and needed physio plus pain management.
It eventually resolved itself and they do seem to come in ‘flares’ i really hope it gets better for her also.
The more stressed you are, the worse it is which is frustrating because it’s a circle!
Now I only have one now and again and manage well using medication, cbt, no longer need physio but do just try to exercise myself.
If your friend needs any advice I’m happy to give my details.
Best of luck,
Zoe
Thank you so very much x
I get these seizures. I’ve learned that bright and flashing lights as well as sudden noises trigger them. I wear a baseball cap, sunglasses, and ear pods when going out.
Learning the early warning feeling can help.
I also started taking CBD at night to help with sleep. Rest is important.
I am taking a 12 week long course on FND. it’s all online and it’s super helpful for reducing symptoms. Find out more at FNDcourage. Find community that understands FND. If the doctors are dismissive, find someone else
My daughter has had some success with medical cannabis for the seizures. CBT did nothing to help her. If it's an option where you are, I'd recommend it.
Recovering from FND
Fnd flare ups
FND and chronic pain
FND 😢
