STEPS TOWARD ZERO is a movement that’s designed to educate, inspire, and activate the epilepsy community to reimagine their goals with the help of their doctors—and that starts with stronger conversations.
Know you’re not alone in your pursuit of zero seizures. There's a whole community that has come together to support your goals.
1 in 26 people in the United States will develop epilepsy at some point in their lifetime, and more than half of people with epilepsy will continue to have seizures despite being currently treated. Everyone's walk with epilepsy is different and speaking to your doctor about treatment options is one important step in the journey.
The Seize the Truth About Epilepsy Perceptions (STEP) Survey was created to understand the current state of epilepsy in the United States. The responses came from 400 adults with epilepsy, 201 caregivers, and 258 doctors.
HERE IS SOME OF WHAT WAS FOUND:
“It’s up to us...to encourage our patients to be open and honest with us about any seizure they may have...this open conversation will allow a partnership between the [doctor] and the patient to give the patient the best quality of care.”
- Danielle Becker, MD, MS
Neurologist
more likely to have problems finding or keeping a job
more likely to have problems related to education
more likely to feel
like they don’t fit in
more likely to have problems finding or keeping a job
more likely to have problems related to education
more likely to feel like they don’t fit in
Based on data that compared patients who had ≥1 seizure in the past 5 years with those who experienced no seizures in the past 5 years.
“It’s always important to try to keep an open conversation with the patient about the frequency of seizures so that the [doctor] and the patient can work together as a team to really reach [the] goal of no seizures.”
- Michael Privitera, MD
Neurologist
Understand what type of epilepsy you have and how it affects you
Track your seizures
Have more meaningful conversations with your doctor
With the right S.T.E.P.S., you can have stronger conversations with your doctor and work together to reach your seizure treatment goals.
LEARN MORE“Ask questions and be open, because as much as your doctors know, they can’t read your mind.”
- Kenzie O'Connell
STZ Champion
Professional Golfer
To watch more S.T.E.P.S. videos, and to learn how to use the discussion guide, STEP toward our Video Library.
S.T.E.P.S. video libraryTreatment routines will change from person to person, so remember to have honest conversations with your doctor if your treatment plan is not helping you meet your goals. If you’re still experiencing seizures, click the link below to learn about another option.
DISCOVER A TREATMENT OPTIONOur Charity Miles initiative turns your physical activity into a donation to the Epilepsy Foundation. We can’t think of a better way to start putting your steps in motion. Can you?
LEARN MORE ABOUT HOW TO GET INVOLVEDUsing the camera on your mobile device, scan this QR code to download the Charity Miles app.
"WE ALL GO THROUGH HARD TIMES WITH EPILEPSY, BUT IT’S HOW WE FIND OUR WAY THROUGH THAT MATTERS."
– Alan Faneca @afan66“Your epilepsy is personal to you, but it feels good to know there’s a whole community rallying behind you, wanting the same thing.”
– Kenzie O'Connell @kenzie.oconnell"THE PERSONAL BATTLE WITH EPILEPSY IS NOT EASY, SO TAKING STEPS TOWARD ZERO IS A GREAT DISPLAY OF BRAVERY."
– Jared Muscat @jaredamuscat"EPILEPSY DOES NOT DEFINE YOU, BUT YOUR STRENGTH AND COURAGE TO BATTLE THIS DISORDER DO."
– Dr CHRISTIN GODALE @christingodale"SPEAKING UP ABOUT YOUR EPILEPSY CAN TAKE YOU ONE STEP CLOSER TO ZERO SEIZURES."
– JENNIFER REYES @jreyepilepsydiaries"WHEN IT COMES TO EPILEPSY, THERE IS COMFORT IN ENCOURAGING YOUR LOVED ONES TO HAVE HONEST CONVERSATIONS."
– BRETT HUNDLEY @BrettHundley7Champions are real patients with epilepsy who are compensated for their participation.
Champions are real patients with epilepsy who are compensated for their participation.
At SK life science, we are driven by the needs of healthcare providers, patients, caregivers and the CNS community—nothing else.
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