Community Forum Archive
The Epilepsy Community Forums are closed, and the information is archived. The content in this section may not be current or apply to all situations. In addition, forum questions and responses include information and content that has been generated by epilepsy community members. This content is not moderated. The information on these pages should not be substituted for medical advice from a healthcare provider. Experiences with epilepsy can vary greatly on an individual basis. Please contact your doctor or medical team if you have any questions about your situation. For more information, learn about epilepsy or visit our resources section.
Hi,Thank you for posting.
Submitted by Anonymous on Fri, 2020-02-28 - 09:45
Hi,Thank you for posting. Treatment and how the body may react to certain medications, including supplements or vitamins, varies for each individual. For some individuals living with epilepsy vitamin B6 deficiency may trigger or worsen seizures. This deficiency occurs mainly in newborns and infants and causes seizures that are hard to control. Some doctors may also try vitamin B6 in older children with difficult-to-control seizures, but there is no solid evidence that it will be helpful. https://www.epilepsy.com/learn/triggers-seizures/nutritional-deficiencies. It’s best that you continue to follow the individual treatment plan recommended by your son’s healthcare team. When discussing your concerns with his neurologist, it’s important that you review all medications and vitamins your son is taking to make sure they're not interfering with each other. You all may want to consider keeping a journal or diary. My Seizure Diary:https://www.epilepsy.com/living-epilepsy/epilepsy-foundation-my-seizure-diaryis a great tool for identifying & tracking seizures, setting reminders, managing medications & side effects, recording medical history, moods, behaviors, triggers,and other therapies or personal experiences, that may affect seizures and wellness, which can be shared with his healthcare team.It may also be helpful to connect with other parents who may have similar experiences, to ask questions, find & give support to each other,by visiting: https://www.epilepsy.com/living-epilepsy/parents-and-caregivers/parents-helping-parents Additionally, you may always contact our 24/7 Helpline, where trained information specialists are available to answer your questions, offer help, hope, support, guidance, and access to national and local resources. 1-800-332-1000, or contactus@efa.org. epilepsy.com/helpline Or contact your local Epilepsy Foundation: https://www.epilepsy.com/affiliates , to find support groups, events and programs in your community.