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.

HOW CAN SEIZURE SYNC HELP THESE TWO FACTORS

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.

SUMMARY

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

DOWNLOAD:

iPhone: https://itunes.apple.com/us/app/seizure-sync-medication-epilepsy/id1084926036?mt=8

Android: https://play.google.com/store/apps/details?id=com.neutun.web&hl=en

 

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?

Education.

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.