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An advocate for those battling epilepsy

by Natalie L. Boehm

May 21st to May 26th 2026

Natalie doing squats in the gym showing active lifestyle whilst living with epilepsy
Fundraising
There are various ways for you to help raise funds towards our mission to suppport epilepsy awareness. We have list some suggestions below and you’re also more than welcome to contact me for more details or advice.
Help Us Raise
Epilepsy Awareness
If you, or a family member or a friend has been affected by epilepsy, please donate however much you can so that we can raise the awareness of epilepsy to the public on a national level.
Become a Volunteer
The charity relies heavily on support from individuals who donate their time voluntarily to work in either of the charity shops or to assist with our fundraising projects and events.
Natalie with friend at social event showing community support for people living with epilepsy

I am Natalie, an advocate for those battling epilepsy.

I was diagnosed at the age of two with epilepsy due to a traumatic brain injury. I spent my childhood being overmedicated on medicine, not having my seizures under control. I dealt with many of the negative side effects which resulted in me becoming suicidal. Once I reached early adulthood, I made up my mind I was going to become seizure free and live a healthy life.

I went to college, despite many telling me that I was not capable of doing so. I graduated with my associates and bachelors degree. While working on my bachelors, I had a seizure while in class. I was taken to the emergency room and the nurse thought I was on drugs despite having a medical bracelet. She assaulted me by shaking me while I was still seizing. It took me two weeks to recover from my seizure and I made up my mind I was done. I was either going to become seizure free or I was going to end things. I made up my mind I was trying one more time to get my epilepsy under control. I found a new neurologist as well as a psychiatrist to help me. I have PTSD as well as epilepsy so getting my seizures under control was not going to happen unless I got my PTSD under control as well.

I began my treatment as well as my therapy. I continued to work, despite not being in the best of health. I worked as a paralegal in real estate and contract law as well as working as a loan officer.

I met my husband Tobias and two years later, we got married. I supported my husband as he finished graduate school. He graduated with his PhD and I wanted more than anything to start my graduate work as well.

My husband and I decided to start a family, so I put my graduate work on hold. I was told by many doctors I would never be a mother. I have two sons, ages seven and four. I got the honor to be able to stay at home with them and got to bond with them. Once they both went back to school, I knew I wanted to do more.

In 2017, I was invited to attend the epilepsy expo down at Disneyland. At first, I was hesitant to. I had been seizure free at this point for 13 years and didn’t want to talk about epilepsy, I just wanted to forget that I had it. I met a gentleman who I had been speaking to for a few years who also had epilepsy that had invited me to the event. When I arrived at the event, it was the first time I felt I was around others who truly understood what I had been through because of epilepsy. I made up my mind there I was going to advocate for those battling epilepsy.

I began my support group Defeating Epilepsy on Facebook to connect to others who are battling epilepsy. The past year since I started the group has been challenging for me emotionally and mentally. A lot of negative experiences I’ve had due to epilepsy have resurfaced and I am doing what I can to heal. I will not allow them to stop me from helping others.

I stay seizure free through medication and exercise. I powerlift, practice Krav Maga, Yoga, and I run at times. It helps to keep me in balance and see that I have a future ahead of me. I am currently working on my master’s degree in business administration with a focus on finance. I hope to use my degree to help those in the epilepsy community.

If there is anything I can suggest to someone battling epilepsy is this: “Don’t give up. You are capable of more than you could ever imagine.”

I hope before I leave this earth that they find a cure for epilepsy and epilepsy will become a thing of the past.

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The Voice For Epilepsy charity logo with purple awareness ribbon
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