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) Emergency Seizure Medication Assistance &
Discount Drug Cards 2) Education About Seizures For Schools, Communities &
Work Force 3) Monthly Newsletter 4) Website With Resources & Epilepsy
Facebook 5) Annual Epilepsy Camp & Health Fairs To Educate 6) Support
Groups Throughout Oklahoma
You May Also Donate By Check, Please Make Payable To:
Association of Oklahoma 11212 N. May Ave. Suite 108 Oklahoma City, OK.
Like Us on Facebook
Welcome to the Home of the
Epilepsy Foundation of Oklahoma
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.
“Knowledge is power, or so it is said.
Often times when receiving a diagnosis of disability it does not
feel very empowering.”
OUR MISSION STATEMENT Our mission of the Epilepsy Association of Oklahoma is to:
A – S – A – P
A - Raise Awareness
S - Service To Community
A - Advance / Fundraising
P - Participate
Emergency Seizure Medication Assistance & Discount Drug Cards
Education About Seizures For Schools, Communities & Work Force
Office Staff & Monthly Newsletter
Website With Resources & Epilepsy Facebook
Annual Epilepsy Camp & Health Fairs To Educate
Support Groups Throughout Oklahoma
EPILEPSY – PREVENT, CONTROL & CURE EPILEPSY THROUGH SERVICES...
LET THE EPILEPSY ASSOCIATION/FOUNDATION OF OKLAHOMA HELP YOU!
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
CAN PROJECT IN OKLAHOMA
CAN PROJECT IN OKLAHOMA YES You CAN Be Apart Of This Project
Community Action Network Mission:
The core principle of the Community Action Network for Epilepsy is to establish volunteer groups across the country. The groups will support individuals living with epilepsy by enabling and advancing the mission of the Epilepsy Foundation. The Foundation’s mission is to lead the fight to overcome the challenges of living with epilepsy and to accelerate therapies to stop seizures, find cures, and save lives. Involvement where you live and work creates partnerships that raise awareness about epilepsy and the programs the Foundation provides. You have the opportunity to support those with epilepsy by bringing programs and services directly into your communities. Whether it’s creating awareness, informing people about services, discovering new fundraising opportunities, or participating in innovation and public policy advocacy, these powerful Community Action Networks build lasting relationships in your neighborhood.
Jonathan’s Story: Promise to Livy
"Jonathan Scheinman leads the national Community Action Network program"
If You Would Like To Be Apart Of EPILEPSY AWARENESS In Oklahoma, Please Contact the Epilepsy Foundation Of Oklahoma Office To Learn More:
Epilepsy Association of Oklahoma Merges With The Epilesy Foundation of America
*** AMAZING INFORMATION ***
PRESIDENT OF THE EPILEPSY FOUNDATION OF AMERICA
PHIL GATTONE & JENNIAFER WALTERS EXECUTIVE DIRECTOR OF
EPILEPSY ASSOCIATION OF OKLAHOMA
SIGNING OFFICIAL DOCUMENTS ON THE MERGE BETWEEN THE
TWO ORGANIZATIONS AND SOON TO BE NAMED
“EPILEPSY FOUNDATION OF OKLAHOMA”
CELEBRATION WITH THE STAFF AT THE EPILEPSY
FOUNDATION OF AMERICA AFTER THE SIGNING
*** HURRAY ***
PROUD SPONSORS OF THE EPILEPSY ASSOCIATION/FOUNDATION OF OKLAHOMA
THANK YOU FOR YOUR SUPPORT!
CALLING ARTISTS WITH EPILEPSY
CALLING ARTISTS WITH EPILEPSY
2016 Hidden Truths, The Mind Unraveled
Juried Art Show Competition
To help us continue enhancing epilepsy.com, we are asking our users for a better understanding of what you know about the impact of epilepsy and seizures. Your answers to this survey will help us build a better website to help you manage your seizures.
Like most girls her age, Brynlee likes to play dress-up, play with dolls and play with her brothers and sisters. When Brynlee was 2 years old she began having seizures and was later diagnosed with epilepsy. Since that time she has been on 6 different anti-seizure medications and gone through numerous tests and hospitalizations and we still do not have effective seizure control. She has multiple types of seizures at night and during the day. We have decided to get Brynlee a service dog. The dog will alert us to seizures at night and help her if she has a seizure at school or away from home. The training of a service dog is time consuming and very expensive. Because of this we will be accepting sponsors and holding various fundraising events over the next few months. Thank you for your prayers, support and encouragement!
PR2 SYSTEMS FUNDRAISING FOR THE EPILEPSY FOUNDATION OF OKLAHOMA
pr2TM Systems is a nutritional supplement company, dedicated to the health and performance of athletes who compete at any level of intensity, as well as individuals interested in maximizing their health and nutrition. pr2TMproducts consist of great tasting, whole protein and vitamin supplements, and were developed by a former Olympic, collegiate and professional athletic trainer.
Daniel L. Dodson, Ph.D., A.T.,C. has developed pr2 products based on his research and experience with athletes and their specific recovery needs. pr2TM products are designed to promote efficient recovery from exercise and daily activities by strengthening the immune system and supporting the health of muscles and joints. Whether by capsule form or powder in a ready-to-mix drink formula, pr2TM provides a superior blend of nutrients, including top-quality whey protein isolate as sole source of whole protein, an exceptional blend of amino acids and an outstanding vitamin profile, including Vitamin E, D, B6, B12, folic acid and biotin. pr2TM Systems has always been committed to the highest standard of quality products.
OKEpilepsy -45% off your purchase (no donation for this one, it is for the epilepsy families that would like to try the product)
Epilepsy -15% off your purchase (10% of Gross Purchase will be donated to the Epilepsy Association/Foundation of Oklahoma) PR2 Members
Joe Dorman: has his discount code set up too, YES That Joe Dorman!
Joe -15% off your purchase (10% of Gross Purchase will be donated to the Epilepsy Association/Foundation of Oklahoma)
Any Questions Please Contact:
Daniel Dodson PhD, ATC
PR2 Systems, LLC
COMMUNITY HEALTH CHARITIES
UNITED DONORS IN THE WORKPLACE WITH OUR NATION’S TRUSTED HEALTH
BUILD CULTURES OF COMMUNITY INVOLVEMENT
FIND COMMUNITY HEALTH CHARITIES, SUPPORT THE CHARITIES YOU KNOW – LIKE –
“EPILEPSY ASSOCIATION OF OKLAHOMA”
CFC – COMBINED FEDERAL CAMPAIGN #27949
CFC IS THROUGH OUT THE COUNTRY
CHC – PUBLIC SECTOR CAMPAIGN #8007
Thank you Freddy's, they have opened the EAO fundraiser for all day. If you go to this location and mention I am here for the Epilepsy Association Fundraiser, they will donate 15% of your purchase to us and you dont need a flyer.
Epilepsy research received $129 million in federal funding in 2013.
That's $59 per person with epilepsy. There are more with EPILEPSY than
all the people with Multiple Sclerosis + Muscular Dystrophy +
Parkinson’s disease put together, but EPILEPSY only receives 31% of what
they receive in federal research funding. Our intent is certainly not to
take research funding from any other disease, because they all need more
support! We just want EPILEPSY to get a fairer share. We journey to D.C.
each year to join our Epilepsy Foundation in advocating for more $ for
research. Like and Share to show you want EPILEPSY to get a more equal
share. #EndEpilepsy — with Ryan Thomas.
VNS MONTHLY CONFERENCE CALL
EPILEPSY ASSOCIAION OF OKLAHOMA
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 help give a voice to
people living with epilepsy. To get more people talking about