Kate Ball's first seizure was at ten months old. Her parents raced her to the emergency room for medical assistance during this dreadfully frightening time. While Kate was being treated, Child Protective Services was also being called to intervene. Instant suspicion. If not for an additional seizure in the presence of the medical staff, her parents would have been fighting for custody of their beautiful newborn baby girl. Kate was eventually diagnosed with epilepsy after many tests and over a long period of time.
Epilepsy, by definition, is very broad and pertains to anyone living with a series of seizures on an on-going basis. With too many causes to count and so many various seizure types to discuss, epilepsy is a stigma that is difficult to overcome.
Epilepsy Foundation of Michigan is an organization that ensures that people with seizures are able to participate in all life experiences. Epilepsy Foundation works to prevent, control and cure epilepsy through services, education, advocacy, and research. Now 30, Kate has graduated from Grand Rapids Community College and volunteers regularly with the American Red Cross. "(Epilepsy Foundation) is the best thing that's ever happened to me," she says with a smile.
Although there are 100,000 people living with the diagnosis in Michigan today, individuals and families struggle with the diverse symptoms and challenges that epilepsy brings them.
"Working with the Epilepsy Foundation made me realize we're not alone," explains Gary Ball, father to Kate. He's also an active volunteer with the organization by participating in support groups, attending monthly conference calls with physicians on various topics, advocating in Lansing to policy makers and increasing awareness in the community here in West Michigan.
"You have a different level of sensibility when you have a child living with a disability," explains Ball.
While there is no current cure for epilepsy, Ball and the Epilepsy Foundation of Michigan are tireless in their efforts to bring greater awareness to the issue.
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Facebook Source: Gary Ball, Epilepsy Foundation of Michigan
Writer: Jennifer Wilson, Do Good Editor
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