How Seizure Sync will help you

Epilepsy is a condition that will affect 1 in 26 people over the course of a lifetime. It’s a very common condition. Despite its prevalence and all of the phenomenal advancements that we have become used to seeing on the frontier of science and technology, it’s still a condition that isn’t curable – it’s only manageable.

There are two big factors when it comes to managing a condition:

  • You have to adhere whatever you doctor prescribes to you (take medications, be healthy, etc)
  • Your doctor has to provide you with the best possible treatment that they can

Sounds pretty easy, right? A lot of the time it isn’t. We are all people living our own very complicated lives and it’s very easy to stray off schedule, or to give less than optimal treatment as a doctor.


Seizure Sync is an epilepsy management app that was created by it’s founders due to their mother’s battle with the condition. This is how it will help you manage your epilepsy.

Adhering to what your doctor prescribed for you

Seizure Sync will help you do this is in two ways. The first is by providing medication reminders for you. We’ll send you reminders every single day at the time that you’re supposed to take your medications so that you never forget again.

The second way it will help you is by making medications much more affordable. Seizure Sync offers massive medication discounts, even if you have insurance. Medications are something that are needed to manage epilepsy, but money can be a huge problem when it comes to taking all the medications that are prescribed to you.

Helping your doctor to give you the best care possible

This is something that often feels to be out of our control. But little do we know, we can actually impact this pretty significantly. The way to do this is by providing the best data we possibly can to our doctors.

Most doctor’s appointments pertaining epilepsy don’t occur too often. They’re spread throughout a number of months. Let’s say you’re seeing your doctor for the first time in 3 months. At this appointment, you have to provide him/her with a recap of those past few months. This includes information about the seizures that you experienced, their effects on you (injuries, possible triggers, etc), your medication adherence and days where you might have missed your medications, side effects that you may have experienced due to medications, etc.

This is hard to do. Most people have difficulty remembering what they did the last week, let alone the last few months. It’s very likely that the information that you provide your doctor with during these visits is inaccurate. And with this inaccurate information, your doctor has to make decisions about your future treatment.

This is how Seizure Sync will help your doctor help you. Through our seizure tracking, medication reminders and history, and journals, you can provide your doctor with the most accurate information possible about your condition. Using this information, they will know better whether to increase or decrease your dosage, change your medications, advise you to change up your lifestyle, etc.


To summarize everything, this is how Seizure Sync will help you.

  • Track and record your seizures
  • Provide you with prescription discounts, even if you have insurance
  • Provide you with medication reminders and keep track of your medication history
  • Allow you to log your days, side effects, triggers, and other important information through the journal





Ending the Stigma

Epilepsy is categorized by an individual having 2 or more unprovoked seizures. About 1 in every 26 people will develop epilepsy at some point in their life (Source). It’s one of the most common neurological conditions affecting the brain today.

Epilepsy is controllable, for most individuals. About 50-60% of people suffering from it will be seizure free after the first seizure medication tried. Adding a second medication will help another 10% become seizure free. 5% will have relative control over their epilepsy, with occasional seizures and side effects. (Source)

Yet it’s still a condition that’s followed around by a daunting stigma. With epilepsy being so prevalent and controllable in today’s world, why is it that epilepsy expert Dr. Sallie Baxendale has said that stigma surrounding the condition can actually be worse than the seizures themselves? (Source)

Living with the stigma of having epilepsy means living with the fear, misunderstanding, and discrimination that surrounds it. Being looked at as dangerous and unreliable. Being cast into the shadows by society, catalyzing depression, anxiety, and stress.

The first step to examining this stigma is by exploring its history and origin. 

Historical Stigma

Living with epilepsy has never been easy. The earliest mention of epilepsy begins with the Babylonians. They saw it as a symptom of demonic possession and thought that the different types of seizures were influenced by the specific demon that had infected the individual. The Romans also shared this belief. They thought that if a person with epilepsy either breathed on or touched another person, that individual would then also become infectected by the demon, unless they spit immediately. The Greeks called epilepsy the Sacred Disease, believing that it was a curse from the Gods for offending the goddess Selene. Throughout the middle ages, epilepsy was believed to have been a curse upon someone by a witch. (Source)

People living in these societies were shunned and isolated. As science progressed and society realized that it was a natural disease, you would expect for the treatment of epileptics to improve. And it did. But to what extent? People were no longer put through terrible treatment methods and were no longer killed for their condition. But they still faced severe discrimination up until the 1900’s.

Until 1956, people with epilepsy in many states of the USA were eugenically sterilized, not allowing them to reproduce. The same law was enacted in Sweden and lasted until 1975 (Source). It wasn’t until 1970 that people with epilepsy were allowed to marry in the UK, and it wasn’t until 1980 that all states in the USA allowed people with epilepsy to marry (Source). Until 1990, when the American’s with Disabilities Acts covered epileptics, many employers refused to hire individuals with the condition (Source).

Today’s Stigma

There’s been a strong history of discrimination against epilepsy patients in past, and although it has been improved, how much have times really changed?

In 2012, an article was published with the following title: “Epileptic man stabbed his noisy neighbour to death with a fish knife in row over eviction”.  What did the man’s epilepsy have to do with the stabbing? Nothing.

A study conducted in Dalhousie University in Canada on epilepsy stigmatization in social media found that out of 10,662 tweets containing the word “seizure”, tweeted out in a single week in 2011, 41% of them were derogatory in nature.

According to this survey, conducted in 2016, 26% of workers in Great Britain would not be comfortable working with someone that has epilepsy.

Reddit user Araneth commented the following in a Reddit thread:

I am apparently incapable of doing the same work other staff can do in my workplace.

Just started a new job. I require 3 weeks shadowing, dispite having done care for 6 years.

I am not allowed to work 1:1 or 2:2 out in the community, dispite being allowed to drive a car.

I am to phone and check in with the seniors when I am on shift, dispite wearing an alert button I am to use if I feel I’m going to have a seizure.

I require more meetings with management to see how I am coping, dispite having worked 40 hour weeks or longer throughout my diagnosis (4 years)

There are discussions taking place to see if it is safe for me to work 1:1 in the building itself, down to can I even assist someone to take their pants down to use the toilet.

I am a condition. I am not a person.

Although the treatment of people with epilepsy has greatly improved both medically and psychosocially, it’s apparent that there is still a dangerous stigma following them around, impacting their everyday life.

Ending the Stigma

People with epilepsy are not outliers of society who can’t function properly. They’re people, just like anyone else. They have families, responsibilities, jobs, and friends. They too worry about what to wear in the morning and whether they’ll have time to catch the game after work. They understand their conditions, and if any, they understand their limitations. They know what they can and can’t do. As mentioned earlier, 70% of people with epilepsy have full control over their seizures.

The question then becomes, why is this stigma still around, when science has taken our understanding so far?


Diane Patternak, a social worker at the Comprehensive Epilepsy Center at Hofstra Medical School, has said, “This is the most important way to change the stigma associated with epilepsy. Schools, organizations, medical professionals, police, and the general public need to be better educated on epilepsy.”

Although our understanding of the disease has increased many fold in the past 50 years, the ones benefitting from this knowledge are scientists, doctors, patients, and family/friends of said patient. In other words, unless epilepsy directly affects you, you likely don’t know too much about it.

The survey mentioned earlier goes on to show the lack of education the general public has when it comes to epilepsy. 63% of workers stated that they would have no idea what to do if someone were to have a seizure in front of them. 76% of people questioned had not been offered any training at all, when it came to seizures at work. 1 in 5 people were unaware that epilepsy can be fatal, and only 17% of people claimed that they would definitely know what to do if someone were having a seizure.

This stigma could very likely be perpetuated by fear of the unknown. Most people simply don’t understand what epilepsy is and how it affects an individual. People fear what they don’t understand.

Having epilepsy isn’t something that makes you weird, a bad employee, or undateable. It’s part of what makes you human.

Educate, educate, educate. If you have epilepsy, let people know you have it, but don’t leave it at that. Explain it to them. Make sure they know that it’s just part of who you are, and not what you are. It doesn’t define you. You’re a person with epilepsy. Not an epileptic. Stigmas often start due to a lack of education. People fear the unknown. Make the unknown, known.

Dr. Baxendale has also said that people who try to hide their epilepsy often experience increased anxiety and depression. When the same people started to feel comfortable with sharing their epilepsy, those negative feels decreased.

This means that we need to ensure that people are comfortable to talk about epilepsy. But for people to become comfortable talking about it, they have to know that they won’t be judged, and it won’t impact their relationship with the person that they are talking to.

This isn’t a short, nor easy process. Change take generations. But what we can do is keep pushing positive change.

With the combined effort of us as individuals to educate the general public, the days of people not seeking treatment, or hiding a diagnosis, due to the way that epilepsy stigma could harm their job prospects, or relationships with friends, family, and loved ones, will soon be behind us.


Epilepsy and the Keto Diet

Disclaimer: Please consult with your doctor before starting the keto diet, or considering dropping or reducing your daily medication intake.

For most, epilepsy is something that is completely manageable with the introduction of medication. But not everyone wants to take medication every single day.

It’s tough to carry around an array of pills with you at all times. There are side effects to certain medications, such as drowsiness, reduced concentration, personality changes, and reduced IQ . Taking medication is stigmatized. A large number of people don’t want to be seen taking medication all the time. It can make you feel like a patient.¹

An avenue explored by a select number of people with epilepsy that has worked very well is following a diet. More specifically, the keto diet. The Keto diet is popular among people exploring alternatives to medication with epilepsy, and has been shown to reduce, and even eliminate day-to-day medication in some cases.

What is Keto?

The goal of a keto diet is to put the body into ketosis. Ketosis is a state where the body primarily consumes ketones (fat) for energy versus using glucose (sugar). A ketone is a substance produced in the body, by fat, when blood glucose (blood sugar) levels are low.

This means the body is relying on fats for energy versus relying on sugar (carbs). When blood glucose levels in a person are low, insulin levels drop. When insulin levels drop the body realizes that it has to turn to a form of energy that isn’t sugar. The body turns to ketones, thus entering ketosis. Ketones are produced in the liver from fat. When your body enters ketosis, it uses fat almost exclusively as it’s energy source.²

The reasons why most people switch to a Keto diet are simple – it often results in an increase in energy, both physical and mental, reduces hunger and results in weightloss.

But there’s also a lesser known effect of a Keto diet. Since the 1920’s, it has actually been shown to help control epilepsy in patients with fewer, and often no drugs.

What does science say?

What does science have to say about Keto and epilepsy? A ketogenic diet has been shown to bring upon positive effects in both children and adults.

study published in 2007 examined the effects of the keto diet on children as well as the effects of discontinuing the diet after its effects took place. It found the following:

  • 12% of the 557 children in the study discontinued the diet after a median of 2.1 years, due to freedom from seizures
  • 92% of those children were also medication free
  • 20% of those children had a recurrence of seizures a median of 2.4 years after the diet was stopped
  • 58% of those children became seizure free a second time
  • Only 4% of those children continued to have daily seizures, despite medication and dietary treatments

A study published in 2014 found that a keto diet can also be very helpful for adults. It found:

  • A 50% reduction in seizures in 32% of patients that were on the keto diet
  • 9% of people on the keto diet had a >90% decrease in the frequency of their seizures
  • The anticonvulsant effects took place weekly, within days to weeks
  • The most common side effect was weight loss, which may be a positive side effect for many people

What does all of this mean? In many people that followed a keto diet in these studies, a positive difference was observed. The effect that it had differed per person. Some people reduced mediations. Some people eliminated it. Some people saw a reduction in seizures. Some people stopped having seizures. But it’s important to note that only 14 cases of Keto diet treatments in adults have been published, so evidence is still insufficient to make any concrete claims.

However, for some, anecdotal evidence may be more convincing than scientific studies.

What are people’s experiences?

When Michel Lundell was diagnosed with epilepsy, the dosages and frequency of medications scared him. Instead, he looked for other possible alternatives and came across keto. 4 months after starting the diet, he said the following:

“I’ve now gone four months without medication and no seizures.My diet is a 80/15/5 (fat/protein/carbs) ratio diet, and it works very well for me.”

To read his full story, click here.

The editor-in-chief of Swedish newspaper Corren, Christer Kustvik, said the following:

“I hope you can stand some rampant joy, dear readers, because this column will be written in a state of euphoria. The past week has been one of the absolute best in my life.

As I wrote on Facebook:

‘Yiiiihaaaa! For the first time in 20 years, I am OFF ALL MEDICATIONS!! Two decades of epilepsy problems are suddenly under control thanks to changing my diet (fewer carbohydrates /sugar). Absolutely amazing, I feel like I’m flying!’

That’s how it is. Fewer carbohydrates/sugar has given me a new life. A healthy life. Suddenly I feel strong. Energetic. Light. To get well when you’re sick is like a dream. A feeling difficult to understand for healthy people, I think.”

Full Story

And my personal favourite quote, from Reddit user “hardnormaldaddy”:

“This is HUGE for me. I feel like i am experiencing life for the first time. I feel like I am meeting the REAL ME for the FIRST TIME! I can’t NOT cry while i type this. I am now 2 weeks in, and i have not had one seizure. I don’t even think about it. How rad is that?

Keto gave me my life back. After all the doctors, and the tests and the drugs that have been wasting my time for the past 22 years. I FEEL LIKE I CAN DO ANYTHING!!

Not to mention I’m looking sexier by the day.”

Full Post 

Given the research articles and anecdotes above, it is still very important to remember that ketogenic diets do not work for everyone, and you should consult your doctor before considering eliminating medication from your routine.

Following a Keto Diet

A keto diet is based on the following:

  • Keep carbs below 20g a day
  • Keep protein to 1g per kg of bodyweight a day. So if you weigh 100kg, then you should ingest no more than 100g of protein in a day.
  • Eat enough fat. Fat should account for >70% of your calories for the day.

On paper, this looks simple. In practice, this can be hard. Carbs are a big part of most diets. To put 20g of carbs a day into perspective, a small banana (less than 6” in length) has 19g of carbs in it. That already throws you right at your threshold for the day. You’ll need to avoid sugary, starchy foods like bread, pasta, rice, and potatoes.

This might have a lot of you thinking: “Hey, that’s not very much food – couldn’t this be considered starvation?”.

The difference between between ketosis and starvation is the intake of fats. Your body needs fat to produce ketones, which in turn it uses for energy. Not eating enough fats is detrimental not only to the diet, but also to your health. If you don’t eat enough fats while following this diet, your brain won’t have anything to rely on for energy, and that would be starvation.

A common mistake that many people make while following this diet is eating too much protein. This is because when eaten in excess, proteins are converted to sugar in the body, increasing insulin levels, thus removing body out of the state of ketosis.

The following pictures are from They are great visualizations of foods that you can and can’t eat while on a keto diet. For a more detailed look into what a day-to-day keto diet can look like, check out this.


How long does it take to be in ketosis?

It takes about two days for your body to enter ketosis. This is because the body can only store two days worth of glucose, so after two days of a keto diet, the body realizes that it’s glucose supplies are low and turns to ketones for energy instead, resulting in ketosis. ³

A popular way to check to see if you’re in ketosis is by using urine testing strips. These strips have a chemical on them that changes colour when it comes in contact with ketones. While in ketosis, ketones will be present in your urine. So by putting these strips into contact with your urine, you will be able to tell whether you are where you want to be or not. The container in which these strips are purchased will have a colour grading on them, so you will know what colour the strip should be changing to.

These strips can either be purchased online, or can be purchased at a pharmacy, usually behind the counter.


In summary, the keto diet can be a great diet to explore if you are looking for ways to potentially reduce your reliance on mediation for epilepsy management. In many people, they have reduced, and sometimes eliminated, day-to-day medication use. However, the scientific studies still are inconclusive, and keto does not work for everyone. Most evidence is currently based on anecdotal claims.

Please consult with your doctor before considering dropping or reducing your daily medication intake.





How one mom is beating epilepsy after 26 years

This article is completely written by Amy Sayers, sharing her experience with epilepsy. This is the first part of a multi part series sharing hope and experiences of those individuals and families overcoming epilepsy. Amy Sayers is a user from Sturgis, Michigan.

Life was good. Even though I had a history of seizures. It was especially good because those seizures had kept themselves at bay for over 26 years. Good job brain! But — we all know how life has a way of twisting and turning. The path before us isn’t always well lit and every once in a while, we fall. More accurately — we trip and our face introduces itself to the bedroom floor, we sprain our wrist, bite our tongue and claw the palms of our hands. We can’t figure out how to get up, or which way to go because epilepsy jumped up like a big old root on my path and tripped up my life, and the lives of my family.

So — that’s how things were playing out for me. First seizure at 16, one more at 18, and then26 years seizure-free. Life was good. Epilepsy wasn’t even on my radar anymore. I had for some reason, beaten the big “E.” Enter stage left, walking from the bathroom into the bedroom on Christmas Eve, my first reoccurring seizure.

That was about ten years ago, and then, four years ago I was having head pain and experiencing an aura in my 5th grade classroom. My husband came and got me and took me directly to the emergency room. There I was given a great deal of medication to stop both the pain and the seizures. They decided to keep me overnight for observation…and we are so thankful they did. Sometime in the middle of the night, my husband tells me that I turned to him and said, “I need help.” The next thing I remember was waking up in ICU with many monitors on me. Apparently the medications they had given me taxed my respiratory system and put me in to asystole. My heart stopped for 9 seconds. I am thankful I don’t remember this experience. I didn’t understand why I couldn’t leave the hospital the next day. I oversaw the east sideline at Notre Dame Stadium and it was the day of the spring game and I had to be there! It was then that the doctor, trying to talk sense in to me, had the nurse bring in the EKG readout that showed the 9 seconds of flat line. This was very sobering to me — and my world tilted a little bit.

Then, in April of 2015, almost a year ago, (we are gearing up for a big celebration,) I went down in the school parking lot with more seizures.(Hey colleagues, check THIS out — a humbling experience, to say the least.) They could not get them to stop. I was transferred to a hospital that was an hour away as it had a neuro ICU unit and I could be monitored both with an EEG and video monitoring. Over the next two days I experienced over 40 seizures. The worst part of this was coming out of those seizures and seeing my grown girls and their husbands see me in such a state. The pain on their faces was the greatest pain that I have felt in my life — far greater than any physical pain from having a seizure…and this is where the Neutun seizure app comes in to my story.

When I first began experiencing my seizures again, it turned our world upside down. I am a technology integration coach and serve all the schools in our district. Not driving was something that had to be worked around…luckily I have an amazing husband and work with some of the best people ever. One of the other hurdles that I had to get over was an over-protective husband. There were times I felt smothered by his attention. If I had a myoclonic jerk — his eagle eye would detect it and ask me “Are you okay???” If I had a head pain out of the blue and shut my eyes and held my head — he was at my side at an instant (and sometimes still is.) Every day before I leave home, it’s “Do you have your phone? Do you have your medicine?” And I suppose now with my amazing Neutun app on my watch — “Do you have your watch on?” One doctor appointment early on I mentioned to the doctor that it truly was irritating to me that David was offering too much attention and that I was feeling quite smothered by it…and this is what he said to me:

“Amy, you have to remember that a seizure is not only a serious event for you, but it is also a serious event for those that will witness you having one — especially your loved ones. Think about what they are seeing. You don’t see yourself, but they see you in a state that is very distressing.”

This really flipped a switch in me. I had never thought about what my epilepsy was putting my family through. David doesn’t like me to drive out of town by myself. I go to many conferences with my colleagues that are either out of town or out of state, and this leaves him feeling very helpless should I have an event.

The Neutun app has really made a difference in our lives.

It gives both David and I an assurance and peace of mind that when we are not together, that he will be notified at a moment’s notice if I am having a seizure.

You see, this app is just not for me, it is for my family. I may be the one wearing the watch, but it is for those listed in my contacts just as much as it is for me.

I am so thankful for the team of people behind the Neutun app. These people has been extraordinary to work with — and you can sense their commitment to making lives better for those of us that wake everyday unsure of what the day will bring when it comes to our epilepsy. I may not know what my epilepsy holds for me in the future, but thanks to this app, I know my care in the case of an event will be prompt and my family will be able to access me as quickly as possible. If I never have another seizure, I will continue to wear my watch with this amazing app. Thank-you, Neutun team, for realizing this important need within the epilepsy community. You are making a difference in our ability to feel safer as we live out our lives…and you are helping our families feel safer, too.