Helping Oklahomans with Epilepsy

Since 1978
Epilepsy is Not a MENTAL illness
Epilepsy is Not a CURSE
Epilepsy is Not CONTAGIOUS
Epilepsy is a Disorder, Not a DISEASE!

What's New

 
 

Go To The Events Page For Details

Events

  • July 4th, 2013
    • 12:00am: Independence Day
  • July 8th, 2013
    • 7:00pm: Epilepsy Support Group Meeting
  • July 10th, 2013
    • 12:00am: Epilepsy Camp at Camp Cavett
  • July 11th, 2013
    • 12:00am: Epilepsy Camp at Camp Cavett
  • July 12th, 2013
    • 12:00am: Epilepsy Camp at Camp Cavett
  • July 13th, 2013
    • 12:00am: Epilepsy Camp at Camp Cavett
    July 13th, 2013
    • 6:00am: Triathlon
  • July 14th, 2013
    • 12:00am: Epilepsy Camp at Camp Cavett
  • August 13th, 2013
    • 10:00pm: Training for Epilepsy
  • August 17th, 2013
    • 9:00am: Strong & Healthy Oklahoma FREE EVENT

   

 

Donate Now

 
 

Your Donations Are Appreciated

We now take credit card donations through PayPal and GiveSmartOKC.

Checks that you send should be made out to:
The Epilepsy Association of Oklahoma.
Donations are fully tax deductible and will be used to fund our programs:

1) Speaker’s bureau.
2) Medication assistance.
3) Support groups.
4) Annual Epilepsy Youth Camp
5) The Newsletter.
6) Association meetings.



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Welcome to the Home of the Epilepsy Association of Oklahoma

 
 
Mrs. Jenniafer Walters - President  A tongue has NO bone but it can BREAK a heart.
So, watch what you say...to someone


Since 1978, the Epilepsy Association of Oklahoma has been incorporated as a nonprofit health agency with the mission of helping Oklahomans who have epilepsy and their families.
 


OUR MISSION STATEMENT
Our mission of the Epilepsy Association of Oklahoma is to:
  • Continue our speaker’s bureau.
  • Education about seizures for schools and communities
  • Emergency seizure medication assistance
  • Support groups in as many cities/towns in Oklahoma as possible
  • Annual Epilepsy Youth Camp; Health Fair booths
  • Quarterly newsletter and state-wide Association meetings.

I call epilepsy a “stealth” disease, but it’s difficult to imagine how so few people can know about a disease that affects so many. For example, few people know:

* Epilepsy affects over 3 million Americans of all ages – more than Multiple Sclerosis, Cerebral Palsy, Muscular Dystrophy, and Parkinson’s Disease combined.
* In America, Epilepsy is as common as Breast Cancer, and takes as many lives.
*Almost 500 new cases of Epilepsy are diagnosed every day in the United States.
* Epilepsy affects 50,000,000 people worldwide.
* One in 100 people will develop Epilepsy.
* One in 10 people will suffer a seizure in their lifetime.
* This year another 200,000 people in the U.S. will be diagnosed with Epilepsy.
* Each year over 125,000 to 150,000 are newly diagnosed with Epilepsy.
* 30% of those diagnosed are children.
* Epilepsy can develop at any age and can be a result of genetics, stroke, head injury, and many other factors.
* For many soldiers suffering traumatic brain injury on the battlefield, Epilepsy will be a long-term consequence.
* In two-thirds of patients diagnosed with Epilepsy, the cause is unknown.
* In over 30% of patients, seizures cannot be controlled with treatment.
* Uncontrolled seizures may lead to brain damage and death.
* Up to 50,000 Americans die each year from seizures and related causes.
* The mortality rate among people with Epilepsy is two to three times higher than the general population.
* Risk of sudden death among those with Epilepsy is twenty-four times greater.
* Epilepsy results in an estimated annual cost of $15.5 billion in medical costs and lost or reduced earnings and production.
* Historically, epilepsy research has been under-funded. Each year NIH spends $30 billion of medical research, but just ½ of 1% is spent on epilepsy.
* The Federal government spends much less on Epilepsy research compared to other diseases, many which affect fewer people.
* St Valentine is the patron saint of people with epilepsy!


 
ScanMed QR Coming Soon
ScanMedQR With the recent tornadoes, it's become even more painfully obvious that we must be prepared! Even for those without chronic illness, you never know when the unexpected can happen; why not have your vital, life-saving electronic health record with you.

ScanMed QR allows you to carry your electronic health record with you with a wallet card, a tag for your purse, backpack, etc., a tag that can be tied into shoelaces and/or a silicone sports band. By scanning your unique Quick Response (QR) code displayed on these items, your medical history, medications and dosages, emergency contact names and numbers and much more is available to First Responders in seconds. When your information changes, go online, make the revisions and save; that's it! Carry the card, wear the band or both.

Silicone sports band will have the Epilepsy Association logo on it. Purchase instructions will be posted shortly to order your new ScanMedQR bracelet when they become available.

If you have any questions, don't hesitate to call the Epilepsy Association of Oklahoma office 405-271-3232.

Thank you for supporting epilepsy and the Epilepsy Association of Oklahoma.

God Bless!

Jenniafer Walters - President
Epilepsy Association of Oklahoma
 
Hidden Truths  Calling All Artists With Epilepsy!
Open to Artists with Epilepsy - No Entry Fee 
 
Andee Cooper and Son Andee Cooper is one of my hero’s...she went out of her way to raise over $11,000 for The Epilepsy Association of Oklahoma. Her life was touched by epilepsy through her little guy here. Thank you for this Andee. Read more under Appreciation tab.
 
Crosspoint Camp 2013 Sign Up today for Crosspoint Camp 2013.
Click on the image on the left and download the flyer for sign up information and details.
 
Talk About It  This is an AMAZING site for people with EPILEPSY. If you have been recently diagnosed or been living with EPILEPSY for a while, PLEASE visit this site. You're NOT alone.

Talk About It.org created by Greg Grunberg (star of LOVE BITES, HEROES, ALIAS and FELICITY) unites Hollywood celebrities and top health care experts to end the misperceptions and misunderstanding about epilepsy and seizure disorders. Greg Grunberg, whose eldest son has epilepsy, has dedicated his time, energy and passion to working toward ending the stigma around epilepsy and bringing public focus on the need to find a cure and to to help give a voice to people living with epilepsy. To get more people talking about epilepsy!