For six years straight, the Northeast Regional Epilepsy Group (NEREG), hosted an annual PNES conference for patients, caregivers, and in the last few years, for health professionals too. Our last and sixth conference was held in 2019 and then, as we all know, the world ground to a halt due to the 2020 pandemic. So, […]
For this month’s blog post, we have the pleasure and honor of having invited writer, Katie Berger, author of “View from the Floor: Psychogenic non-epileptic seizures: A patient’s perspective” share her experiences with us. Wonderfully, she has now been seizure-free for two years, but I urge you to read her story because in it you
In a few weeks, a new book on PNES is going to be published and will be called: The Psychogenic Non-Epileptic Seizures (also known as dissociative seizures) Pocketbook. The word “pocketbook” is in its title because it is meant to be just that: a book that a clinician might carry in her/his pocket for
For almost 20 years, I have been a school nurse. During one of my first years as a school nurse, I met a student with what health care providers were then calling pseudoseizures. While many school personnel were very supportive of this student, there were just as many who were NOT. I heard comments
Students living with psychogenic non-epileptic seizures (PNES)-a new study Read More »
I get asked about service dogs for PNES quite a bit and over the last few years, I have had the opportunity to observe my patients’ service dogs and emotional support animals in action. The ones who are really well-trained have left me very impressed at how useful they are in ensuring safety and also
For this month’s blog post, we have invited a young researcher to share her call for research subjects on this site. This research has been approved by an institutional review board and is completely voluntary. If you are interested in reading more about it or in participating if you fit the inclusion criteria, click on
Moral injury in female US combat veterans diagnosed with PNES Read More »
One of the ways in which we can help improve the lives of those living with PNES or dissociative seizures is through scientific research. Fortunately, in the last couple of decades, there has been a proliferation of research studies that have focused on risk, prognostic and outcome factors, diagnostic tools, treatment modalities, among other
This year, the Epilepsy Alliance of America awarded eight fantastic women scholarships to assist them in pursuing their education. The main criteria for this award is that the applicant must have a diagnosis of psychogenic non-epileptic seizures (PNES) and can show that he/she is planning on using these funds to further his/her education. Why was
Please join me in celebrating the 2021 winners of the Lorna Myers PNES scholarship! Read More »
For six years straight, the Northeast Regional Epilepsy Group (NEREG), hosted an annual PNES conference for patients, caregivers, and in the later years, for health professionals too. Our last conference was held on 2019 and then, as we all know, the world ground to a halt due to the 2020 pandemic. Although we did not
There is so much that we need to do to improve the lives of those living with PNES. We definitely need to increase treatment options and to ensure a growing number of clinicians are available to treat this health condition. To achieve this, research on treatment outcome is a necessity, and as such, funding is
