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Epilepsy and Genetics

How Can Genetic Counseling Help?

 

If your neurologist suspects that your epilepsy is genetic they can refer you to a genetic counselor for genetic testing. By undergoing genetic testing, we can figure out what genetic changes may be contributing to an individuals’ epilepsy. 

Primary indications we see at Clover Genetics include neurological and neuromuscular conditions, movement disorders, and neurodegenerative conditions. During a genetic counseling session, the genetic counselor will:

  • Take a detailed health history of you and your family

  • Determine if genetic testing is an option for you

  • Communicate complex health and genetics information to you

  • Help you make an informed choice about your health care options

  • Provide emotional support while respecting your values, beliefs, and feelings

With this information, you can prevent/delay disease progression or the onset of symptoms (1). Specific treatment, medicine, and diets can be used to target the specific genetic change that is causing your epilepsy, also known as precision medicine. There are also research studies on novel epilepsy treatments that you may be eligible for depending on your genetic testing results. You may speak to your doctor about enrolling in a clinical trial for epilepsy (4).


Additional Patient Resources:

  • Epilepsy Foundation: A charitable organization that helps connect epilepsy patients to treatment, support and resources.

  • My Epilepsy Story: A non-profit organization for collaborating, advocating, researching, and educating about women and girls diagnosed with epilepsy.

  • Seizure Tracker: An app that helps patients easily create, document, and share customized reports of their seizure activity.

  • The North American Antiepileptic Drug Registry: A hospital-based registry for determining the safety of seizure medications during pregnancy.

  • Disability Benefits for People with Epilepsy: A non-profit organization that helps people with epilepsy navigate Social Security disability benefits.

  • My Seizures Know More: A 6-question tool that empowers and provides patients with personalized questions for them to discuss with their medical team.

  • Child Neurology Foundation: An organization that provides knowledge, education, and one-on-one assistance to children and families living with a neurologic disorder.

  • 24/7 Epilepsy Helpline: A helpline that provides assistance, encouragement, support, direction, and access to local and national resources for people with epilepsy.

  • SUDEP Aware: An organization that increases awareness and education on sudden unexpected death in epilepsy.

Learn more about Epilepsy and Genetics