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 and
Submitted by Anonymous on Tue, 2020-03-10 - 09:42
Hi,Thank you for posting and understand your frustrations and concerns. It’s important to remember that you are not alone, and we are here to help support you. We know that living with epilepsy is more than seizures, it also means learning how to handle the way epilepsy affects your life including your physical well-being, social and emotional health. https://www.epilepsy.com/living-epilepsy/healthy-living/emotional-health . One of the most important things to help you live with epilepsy is to find a support network. Learn more about your community support resources available for you and your family in your country, please visit: https://www.epilepsy.org.uk/ https://www.epilepsysociety.org.uk/It’s also important that you’re following up with your healthcare team to explore this further and if you continue to experience any changes in seizure frequency, types, symptoms, side effects, behaviors and moods, to help determine what individual treatment plan is best for you. It’s very important that you’re taking your medications as prescribed by your doctor, it gives you the best chance to achieve the goals of epilepsy therapy: no seizures and no side effects. https://www.epilepsy.com/learn/treating-seizures-and-epilepsy/seizure-and-epilepsy-medicines/importance-taking-medication . However, we understand that managing medications can be challenging for a variety of reasons.You may want to consider documenting every time you miss a dose of medicine or take an extra dose by mistake.You can also have electronic reminders, via text or email, sent to you when it's time for a dose of medicine, so you do not forget and if you do have seizure, write down the side affects you noticed. This will allow you to review and compare with your healthcare team how often you have seizures or side effects when adherence is a problem, versus when you are doing well following your schedule.To learn more about our electronic reminders such as My Seizure Diary & Texting 4 Control, to help you manage your medication visit: https://www.epilepsy.com/learn/managing-your-epilepsy/managing-triggers/medication-adherence Moderate to heavy alcohol use is never recommended for people with epilepsy, as it may worsen seizure control. Some seizure drugs have similar side effects to alcohol and using both at the same time can lead to bothersome and potentially dangerous problems. https://www.epilepsy.com/learn/triggers-seizures/alcohol . Additionally, for some people living with epilepsy things such as, poor quality, or lack of sleep can be a trigger. For additional information regarding triggers, visit: https://www.epilepsy.com/learn/triggers-seizures