New Posts-

Get in the Game…to promote Epilepsy Advocacy

June 21 , 2010 | Posted by Alysse | In: Being a Parent with Epilepsy, Epilepsy Advocates, Epilepsy Community, Epilepsy Legislation, Epilepsy Websites, Kids and Epilepsy, New Posts, SUDEP Awareness

Epilepsy and SUDEP has become their mission with the Danny Did Foundation. And, they are doing a fantastic job. Their spirit and their drive to raise awareness and try to teach more people about Epilepsy and SUDEP in particular has truly inspired thousands of us!

2 Comments
Tags: epilepsy advocacy, epilepsy funding, parenting, SUDEP

Let Story of Accused Doctor be a Lesson for all of us with Epilepsy

June 20 , 2010 | Posted by Alysse | In: Being a Parent with Epilepsy, Epilepsy Advocates, Epilepsy Community, Epilepsy Medications, Epilepsy Treatments, Epileptologists, Kids and Epilepsy, Living with Epilepsy, Neurologists, New Epilepsy Diagnosis, New Posts

An Oakwood Hospital (Michigan) pediatric neurologist has allegedly been diagnosing children, hundreds of them, with Epilepsy…FOR CASH. And these kids do not have Epilepsy.

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Tags: anti-seizure drugs, choosing a doctor, Detroit hospitals, diagnosing disease, epilepsy

More Epilepsy Advocacy…

June 14 , 2010 | Posted by Alysse | In: Being a Parent with Epilepsy, Epilepsy Advocates, Epilepsy Community, Kids and Epilepsy, Living with Epilepsy, New Posts, Seizures, Talking About Epilepsy

Living with Epilepsy is featured in an upcoming episode of Health Corner on Lifetime.

Strolling for a Cure!

June 13 , 2010 | Posted by Alysse | In: Epilepsy Advocates, Epilepsy Community, Epilepsy Treatments, Family, Living with Epilepsy, New Posts, Seizures

The Epilepsy Foundation of Michigan held their annual Detroit Summer Stroll for Epilepsy on Saturday, June 12, 2010 at the Detroit Zoo…what a day to reflect on those living with Epilepsy!

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Tags: A cure for Epilepsy, epilepsy, Epilepsy and families, Living with Epilepsy

How to Not Let the ‘Stuff’ in Life get you Down…or Cause you Seizures

June 7 , 2010 | Posted by Alysse | In: Epilepsy Treatments, Life Changes and Epilepsy, Living with Epilepsy, New Posts, Seizures, Stress and Epilepsy, Talking About Epilepsy

As someone with Epilepsy, I must teach myself how to avoid stress and how to take better care of ME. We all should. No one can force us to do this, but we have control.