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Yeah, I can totally understand the desire to be seated looking at the risks and balanced with the needs of others. I don't understand his specific need to be close to the driver though.I hear mixed messages from Jae about his epilepsy. It's severe enough that he feels best seated and near the driver in case he has a grand mal seizure, yet it is also inconsequential enough that he does not wear a medic alert.
Yeah, I can totally understand the desire to be seated looking at the risks and balanced with the needs of others. I don't understand his specific need to be close to the driver though.
I hear mixed messages from Jae about his epilepsy. It's severe enough that he feels best seated and near the driver in case he has a grand mal seizure, yet it is also inconsequential enough that he does not wear a medic alert.
Is there info or a contact who can quickly provide the info about what to do if you are having a seizure?Why should I have to give my money to any particular foundation? I have an ID bracelet which I purchased at my local pharmacy.
Is there info or a contact who can quickly provide the info about what to do if you are having a seizure?
People would do well to be more aware that a disease can be disabling, but a disability is not a disease. a medical impairment can be caused by disease, like genetic or viral, or by an accident causing injury, for example. A disability is a state of being disabled by something. The social model of disability says it's the way society is structured and how it responds to impairment, to diverse ways of being in the world, is the disabling factor. And this makes sense in the context of discussion of Jae's epilepsy, and actually, the discussion itself.@Pr. Jae , I am curious as to how you define disability as opposed to disease.
I think some of you are ganging up on jae. Seizures can be triggered by different things in different people. Sometimes high stress is enough to bring one on. Medications control it for the most part but not always and there's just no telling for sure when or why a seizure might occur. the person I know has them around sleep, something related to sleep cycles, but to have one while awake, if that is a risk....let the man have a seat. Having witnessed several grand mal seizures, I can tell you they are scarey and a person is at risk of serious injury or worse if one comes on and they are not seated and lose consciousness, so are people standing closeby if one were to fall onto them. So, if jae feels safer being seated and close to the driver if he is stressed or over-tired or anytime, then so be it. If there is a risk, for jae, of one happening anywhere, then on a moving bus makes sense to be extra cautious. He's being responsible on a bus. He can guage for himself what he needs. On a particular day he may need it more than someone who "looks like they might". As for whoever suggested he use a wheelchair, that was mean. I don't think that's even a common thing to do, and why suggest it to jae. I think just to be mean. It's not an easy condition to live with, and I think some people here could use a bit more compassion. There are reasons to call people out on behaviour on a forum but picking on Jae's epilepsy is brutal no matter what.