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#1
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#2
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Welcome Kharissa Nice to have the Captains other half join in. I've had seizures all my life, mostly partials except for about 15 tonic/clonic (grand mal) seizures. Since I've had them for so long they don't really scare me. I have had a lot of friends that have felt over-protective and even though their intentions were well appreciated the friendships often disappear partly because even though I can't do things like drive I don't like being treated as less than "normal" and partly because it eventually becomes a burden to always worry about someone being OK and friends are supposed to be fun. Sorry I can't give anything more than my own experience. There's lots of people here who are relatives & partners of those with epilepsy that I"m sure will be able to give more and better advice than I can, just give them some time to leave a message. In the meantime check out the nooks & crannies and make yourself comfy here.
__________________ "It's no longer a question of staying healthy. It's a question of finding a sickness you like." -Jackie Mason |
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#3
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| Hi Kharissa, welcome! It can be hard to see someone you love diagnosed with epilepsy. Right after diagnosis it's not unusual for both the person with the seizures and his or her caregiver to be very anxious and scared about the seizures and how they will affect their lives. This is very normal! Once you get a handle on things, the anxiety will moderate. I've had epilepsy for over 10 years; at this point I'm not troubled by anxiety over seizures. And I've had over 20 grand mals. This may be hard to grasp but: They look worse than they are. Yes, there's the potential for injury, yes they are traumatic in many ways. But they rank low on the list of scary, damaging events for me. A health issue CAN put a strain on a relationship, and sometimes it can help to get outside counseling, for you or your husband or both together. If you feel like things are getting worse, (or even you don't), consider asking for referral to a therapist. Best, Nakamova Best |
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#4
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#5
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| CaptKevsWife, Welcome to the forum! It's really normal to worry about seizures, especially at first. There are a lot of unkowns. As your husband's seizures become more under control you'll worry less. Or if they aren't you'll find coping strategies. I agree with the above posts. Counseling is really helpful. CaptKev is going through a lot emotionally right now, and you have your own set of emotions to deal with. I understand how difficult it is to have a spouse who has a life-altering disorder. Please get the extra help sooner rather than later. It's important to get things as steady as possible. It'll help being in here, too. You can lean on us for support - that's what we're for. Hang in there. It DOES get better. |
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#6
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| Thanks Y'all! Y'all are so sweet! I'm trying not to be a babysitter, and I agree... once his seizures are more undercontrol, I really think I can cope with it easier... Right now It's just hard for me to accept he even has epilepsy... |
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#7
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