Lundbeck LTAI Event Series
Join us at one of our Lundbeck sponsored Let's Talk About It events to kick off November Epilepsy Awareness Month
Click on the flyer to purchase tickets for your location's event!
Gainesville LTAI Dinner - October 22, 2015
Jacksonville LTAI Dinner - October 27, 2015
Broward LTAI Breakfast - November 21, 2015
Miami LTAI Masquerade Cocktail Party - October 29, 2015
Epilepsy Exchange Webinar
Epilepsy and CBD Webinar Recording - July 7, 2015
Dr. Ian Miller, Director of the Epilepsy Program at Nicklaus Children’s Hospital
This webinar is the first of our newly launched "Epilepsy Exchange Webinar Series" that was held on Tuesday, July 7, 2015, on the topic of CBD (cannabidiol) and epilepsy. It featured Dr. Ian Miller, Director of the Epilepsy Program at Nicklaus Children’s Hospital – Miami Children’s Brain Institute who discussed alternative solutions and methods for epilepsy treatment, the science of cannabidiol, and the current state of the law in Florida as it relates to this topic.
The Epilepsy Exchange Webinar was created to help members of the public learn more about the services the Foundation provides and highlight topics important to those living with seizures. Stayed tuned for the next webinar coming soon!
Epilepsy Exchange Blog
The First Time
By: Jonathan Anderson
You never forget the first time.
My wife and I stood helplessly as a debilitating seizure took over our young daughter's defenseless body. In that moment, our greatest fears as parents unfolding before our eyes.
In just under a year, we watched our daughter's seizures become increasingly severe and frequent, eventually taking her body over every hour on the hour, 24 hours a day.
And with that, our journey, our mission, our quest began. We frantically looked for answers and scoured for any information we could find - credible our not.
Like every parent, our first instinct was to protect our child. When an illness as incapacitating as epilepsy strikes, we were powerless while waiting for answers from medical professionals. But, in these moments of crisis, the Epilepsy Foundation of Florida was a source of support and information to us, and many of the 375,000 Floridians suffering from, and families like ours impacted by this disease looking for answers and advice.
Legislators will gather this week in Tallahassee for a special session to pass a budget. On behalf of every parent who's been forced to stand by helplessly as their child suffers, I pray they will preserve the funding that allows the Foundation to continue providing services and resources families across our state so desperately need.
What Does Epilepsy Look Like?
By: Jonathan Anderson
What is epilepsy? Epilepsy is a neurological condition characterized by recurring seizures that result from temporary electrical disturbance in the brain.
But what does epilepsy look like?
Although the disease can strike anyone at any time, it is most prevalent in the very young and very old; two groups that comprise large segments of Florida’s population
Today, 12 percent of Americans with epilepsy live in Florida and indicators are that this number may increase, not only as baby boomers age but also because Florida is home to the second largest veteran population in the nation.
That is what epilepsy looks like.
With troops returning home from Iraq and Afghanistan, it’s estimated that 20 percent experienced traumatic brain injury, the leading cause of epilepsy.
The Epilepsy Foundation of Florida has offices across the state working to support individuals and families living with epilepsy. Our local offices provide educational presentations, individualized case management, medical services, support groups, camp for kids and so much more. For more information, contact us at 1-877-553-7453.