I believe everyone should be treated equal. People with epilepsy should have the right to be themselves and do what they want with an invisible disability. I feel like an outcast sometimes because epilepsy makes me different from everyone else. People think "she had a seizure and acts awkward" and is "missing out". Epilepsy is something that is a part of me, but it is not who I am as a person. Many people I know love video games or movies and due to flashing lights, I could have a seizure. However, not all flashing lights bother my health. Therefore, its a typical stereotype about how flashing lights affect epileptics. Many people tend to have blinders when it comes to flashing lights. One day a group of former friends were going to see a movie we all liked. I asked if I could come and they said no. Their blinders were on, seeing the worries in me rather than enjoying my company. They don't have any epilepsy education and...
It is extremely important to understand how to react when a person has a seizure. My family are the only ones who know exactly how to handle my seizures. When I have had a seizures in public, paramedics, firefighters or any first responders did not know what to do. There are so many signs people miss while I have seizures. If you do not get seizure first aid, then sometimes you might be putting a person at risk to die or make the situation worse. Here is the correct way on how to handle a person who is about to have a seizure. I'm going to explain to you the right from wrong signs on how to approach a seizure. Sign 1 : Look to see if the person is responsive Sign 2 : If the person looks like he/she is going to fall Sign 3 : If the person is hot or crying for no reason Sign 4 :Check for a medical ID bracelet or any way of contacting relatives Sign 5: The person is standing and staring with shaky hands Now that you've learned the signs to be ...
I believe it is important to have a strong education. Whether it is elementary, high school, college, and more. Education can lead us in so many paths. I'm very grateful I get to attend college, because some people with epilepsy are not able to due to certain issues. However, art therapy and our talent in art has helped and I consider that as education. I actually did not need to take seizure aid or go to epilepsy school (if that was real). I got it from my heart, neurologist, research, and being part of the epilepsy community. However, there's no such thing as too much education. I just wish there was an epilepsy school because it can help provide tools incase you encounter someone with epilepsy. Education has actually made me want to start this blog. I've never have gotten this far if it wasn't for my family and the community. I've graduated elementary, high school and even college. I'm going back to school because I like to ...
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