We are focusing very specifically on #SayEpilepsy, as we have heard all too often that there are people living with epilepsy who are told that they have a “generalized seizure disorder” rather than being told that they have “epilepsy,” and other individuals who just aren’t comfortable acknowledging to others that they live with epilepsy. Unfortunately, avoiding the word “epilepsy” can make finding the right treatment plan, doctor, specialist, or support system even harder. Additionally, the less people within the epilepsy community (patients, caregivers, advocates, friends, clinicians, and researchers) use the word “epilepsy” the harder it becomes for the non-epilepsy community to understand how prevalent this neurological disorder is. By choosing to #SayEpilepsy, you are showing your support for the epilepsy community, helping educate your friends/family/colleagues, and working to raise awareness about epilepsy.
Check out some of the many #SayEpilepsy videos on our website to hear individuals share why it is important we Say the Word #SayEpilepsy. Help us spread awareness by sharing these videos on social media or sharing your own #SayEpilepsy story (in written or video format) on social media and don’t forget to tag us!
Through research and through saying the word “epilepsy” there is hope.
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