MUD Volunteers Needed!

We are gearing up for MUD Volleyball for Epilepsy Tournament on July 12th and we need your help!

We need volunteers on the day of the event, as well as for set up on July 11 and clean up on July 13th.

Volunteers Needed. Help With Mud Volleyball. July 11.


Various tasks and shifts are available on the day of the event.

If you are willing to volunteer, please call us at 937-233-2500 or email events@ohioepilepsy.org.

Epilepsy Foundation of Western Ohio

Wiley's Comedy NiteClub Fundraiser

Wiley's Comedy Club. April 25th and 26th.We are selling tickets to Wiley's Comedy Club to support epilepsy programs and services.

Comedian, Tim O'Rourke, will be featured. Tim is a stand up comedian and is best known as Tim the Bartender on the Drew Carey show and is a writer for Sponge Bob Square Pants.

April 25th and 26th (Friday and Saturday)
Show times: 8 pm and 10:30 pm
Tickets are $12 each
Reservations required
For more information, call 937-233-2500.

WALK for Epilepsy and Encephalitis

WALK for Epilepsy & Encephalitis

Saturday, May 3
Delco Park
Kettering, Ohio

Registration 9:30 am ~ Walk starts 10:30 am

Picnic immediately following - please bring a potluck dish for 10

Grilled hotdogs and drinks will be provided

To find out more about the Walk visit www.firstgiving.com/efwo

From there you can register for the Walk, make a general donation, or simply create your own team page with your story and photo and send it out to all your contacts.

It's simple to do, and an easy way to help raise money for a good cause and to educate about epilepsy and encephalitis.

If you can't come to the Walk itself, become a Virtual walker and help to raise money and awareness by sending your fundraising page to everyone you know!

Be sure to read about Xander Tipton - the 2008 honoree

We hope to see you at the Walk on May 3rd!

Top Story: Epilepsy Right to Know (HB 99 and SB 114)

The Epilepsy Foundation of Western Ohio is currently involved in advocating for the HB 99 and SB 114 known as the Epilepsy Right to Know Bill. The bill is needed to stop the practice of dangerous drug switching without notification to the patient and physician.

Drug switching occurs when pharmacists take patients off medication that is working for them and switch them to another variation of the medication, either brand to generic, brand to brand, generic to brand, or generic to generic. The small variations in these drugs can cause toxic effects and seizures in people with epilepsy who have been seizure free for years.

The Epilepsy Right to Know Bill simply requires a pharmacist to ask for written permission to make a medication change.

We need your help to lobby for this important piece of legislation. If you are a person with epilepsy, caregiver, donor or just a concerned citizen, please take action now! You can visit www.legislature.state.oh.usto find the legislators in your area and call or write to them and ask for their support.

If you do not have access to the internet, please call the Epilepsy Foundation at 937-233-2500 and we will help you find the legislators in your area. Thank you for your support!

Jeanne A. Carpenter Epilepsy Legal Defense Fund

The Jeanne A. Carpenter Epilepsy Legal Defense Fund has been createdby theNationalOfficeto help people with epilepsy fight discrimination. The fund helps protect the civil rights of people with epilepsy and helps refer discrimination cases to competent attorneys. Consumers can request attorney referral online and access legal fact sheets and other resources to assist with their self-advocacy efforts.

Please visit the website at www.epilepsylegal.orgfor more information.

Is it epilepsy?

Epilepsy is a condition in which a person has two or more seizures without a clear cause. Some people refer to themselves as having a seizure disorder, though technically this is epilepsy.

A seizure happens when a brief, strong surge of electrical activity affects either part or all of the brain.

For 70 percent of people with seizures and epilepsy, the cause of their condition is unknown.

» Read the full story.


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The Epilepsy Foundation of Western Ohio serves residents of the following eleven counties in Western Ohio: Auglaize, Champaign, Clark, Darke, Greene, Logan, Mercer, Miami, Montgomery, Preble, and Shelby.

Mission

The Epilepsy Foundation will ensure that people with seizures are able to participate in all life experiences; and will prevent, control and cure epilepsy through research, education, advocacy and services.

Vision

We are committed to helping create an environment where there is no stigma or fear associated with seizure disorders; where persons affected by epilepsy have the knowledge, self esteem and support to participate in normal life experiences; and where the barriers that they face have been removed.

History

The Epilepsy Foundation of Western Ohio is an independently incorporated affiliate of the national office of the Epilepsy Foundation and an Outcome and System Partner with the United Way of the Greater Dayton Area.

It was founded as a non-profit corporation in 1974. Its creation was the culmination of efforts started by one individual, Mrs. Joan Schreck, joined by others with epilepsy, parents, and concerned citizens.

Please feel free to contact us!

Email
us or call us at (937) 233-2500 or (800) 360-3296.


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Not Another Moment Lost to Seizures

 

visit our donation page at firstgiving.com/efwo

Find out how you can support our mission. Visit firstgiving.com/efwo.


Find out about our planned giving program

Help support critical epilepsy programs and services. Learn more about our planned giving program