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#1
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#2
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| Wow, I'm so sorry -- having a seizure in water is very frightening. Thank goodness you were with friends. I hope you get the medication stuff figured out. And I guess be extra careful in the heat... Best, Nakamova |
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#3
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Awwwwwww, man, Crystal, that just sucks a hill o' beans. I'm sorry. Hopefully you get things figured out soon. Stay cool! Maybe you can just dangle your feet over the edge of the pool? Or sit on the steps? |
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#4
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| I am becoming afraid again of the pool- even though I know how to swim and have enjoyed it a lot. I think that I will probably just sit on the edge and not go in. When I do go in, I cannot use my hearing aids and so it makes communication difficult. So I think for right now, no swimming until I get my seizure under better control. It was just scary to me, just scary to know it happened. Be safe everyone.. Crystal |
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#5
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| I really miss taking my kids swimming, before I had my first seizure, I used to take my daughter twice a week, but my 2 boys have never been. As I am a single parent with epilepsy, with a daughter with epilepsy, I think the lifeguards would have a coronary at the thought of us 2 and 2 young boys! It's the one thing I REALLY miss, even more than driving. |
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#6
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| Maybe you could invite some friends to be with you and your boys? I was so thankful that I had my twin and best friend Rachel who has Epilepsy, and my other friend there with me. I am still freaked out about it because I remembered earlier today that I went under and felt my body stay still and water become level with the top of my head and hair. Then I don't remember anything else. Just scared me that I was under and could have inhaled some water- freaks me out to think about it. BUT I am thankful for my twin and my friends that helped me. I plan on going swimming again but not right now LOL. Everyone take care, be safe. |
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#7
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| About two weeks ago I decided I wanted go swimming in my apartment complex.I had my husband Dennis with me.I found out later I'd had a seizure in the pool.I never go swimming unless someone is with me but know one should swim alone anyway. Belinda
__________________ (A)abort (B)fail (C)retry (D)throw computer against wall southern and proud of it. I've had a VNS since 2000 |
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#8
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| Right- I agree. I am blind and hard of hearing and without my hearing aids I'm deaf. So I prefer someone to be with me becuase of three reasons- or becuase of my disabilities. But I still like to have fun but I'm more nervous all over again. Epilepsy is what kept me from swimming for almost 10 years. I was talking with Rachel, my friend who also has Epilepsy, last night about the incodent. She reassured me that everyone kept me safe and didn't let anything happen to me... and I said "I just remember the water being level with my head and my hair just sort of floating around, I dont remember anything else." It almost made me cry. Just a loss of control, being semi-conscious, and being put in such a dangerous situation just really got to me. Thank you everyone for you replies. -Crystal |
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#9
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| I don't really have many friends left now, none of them knew what to say to me at the end of last yr (post in riva's memorial) and they just started avoiding me, and the one friend who still talks to me has never seen me have a seizure and has been honest with me that she wouldn't know what to do if I did, so there isn't really anyone who can go with us. I am very glad that you seem to have a group of very supportive friends and family around you. Give them a clap! |
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#10
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| I am lucky to have friends and family that are supportive. My Mom doesn't seem to understand a lot about seizures themselves but its understandable since we don't live at home anymore. She helped us a lot when we were little and teenagers with Absence seizures and complex partials. Now they are a little longer and sometimes cause more trouble than before. Anyways- I would educate your friend, if you feel its a good idea, about your epilepsy and how to help you during a seizure- they may be more receptive of the idea of helping you than you might think. But you never know- you would obviously know your friends better than anyone else lol. I've noticed that my friends or my friends' friends tend to be pretty receptive about how to deal with someone with deafblindness as well as seizures- but education is a big part, knowing how to communitate information also helps.. emphasise the basics. Wish you the best.. -Crystal |
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