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Husband with Seizures

Wed, 02/09/2005 - 17:08

Does anyone else have a spouse with seizures?-My dh has Grand Mals probably 3 or 4 times a year-he will usually have 3 of them  or so in a 36 hour period and then is out of it for just about a week later. He has had them since puberty and was put on all kinds of drugs,phenobarb,dilantin etc. -these just caused more seizures so his dad had him taken off all meds. He mostly gets them form lack of sleep or stress. He has the flu and was up all night and then he had one this morning-they are very upsetting to watch and not be able to do anything. It is also very scary because he wants to get up and go to the bathroom and always falls-sometimes hits his head. Does anyone else experience this?

Mary

Comments

RE: Husband with Seizures

Submitted by Gretchen on Mon, 2005-01-31 - 10:30
Hi MaryI'm the epileptic spouse but I read your post to my husband who isn't signed up here but I can give you his response, coupled with my "editorial comments".For one thing I sz a lot more than your husband which I think does change our two pictures. He's more used to it probably which we both agreed we'd hate to call it an edge for us over you, I would sure hate to say that, but in a way I can see it too. We have this down to a science now.My son, father (deceased) and grand daughter also have epilepsy, so I also raised an epileptic son. There were some times when he had a seizure it scared me witless. If I got that frightened? Also if I had any situation with him I couldn't handle or felt I needed support? I called an ambulance. Maybe more for me than him but that's okay. Do it. You count too. If your husband doesn't need transport they will still be there to help you and him. We've never been charged in 3 communi9ties if I'm not transported. My husband did this frequently right after I was diagnosed. Usually I do need transport to the ER but even if I was recovering by the time they got there? I can get REAL combative from fear. Fear over what? Nothing and everything. The mind is recovering, not reacting in the usual manner - post ictal. I always have to go to the bathroom right after a bad t/c (grand mal) and usually before my legs are working.Another difference we have most likely over the both of you is that I'm smaller and lighter than my spouse. So my husband can help me more than likely easier than you can support your husband BUT when people try to haul me up to my feet or try to help me walk? It hurts me under my arms or my ribs, where ever they're clutching me. I'm not that heavy but a nearly dead weight in an adult is hard on anyone.What I worked out with my son and I do the same thing is we crawl to the bathroom. Crawl to a piece of furniture to pull ourselves up to sit in too. We're both very suggestive. IF someone doesn't start getting very excited and demanding in their voice but coaches us firmly but gently and don't feel threatening and repeatedly tell me to crawl, I do. Pretty much now on my own I'm "trained". It took awhile of falling, sz'ing, trying to get up, falling again. The problem for me as the sz'ing person is? My cognition is so reduced I can't figure out how to get to the bathroom I just know my bladder sphincter is letting loose and I feel desperate to get to the bathroom.I'm also an RN who worked in L&D for years. Often a family member would faint right after a delivery of a baby. If a person fainted often they'd try to bolt right back up on very unsteady legs. If that person such as a man usually, the husband, would be "legless" or nearly so? I'd grasp tightly their belt from behind with both hands to help them stay upright, spread my legs to get a wide solid stance to help them to a chair. That too depended on how big the person was and how combative. Then there are times? People are going to sz, try to get up too soon, and fall again and there isn't anything you can do about it. I did learn eventually and so did my husband. He has had a lot of frustration and is in the continual process of learning, and realizing he does the best he can. That's the very best you can do. You care about him. That's a lot right there. But anyway a very non threatening voice suggesting I crawl will usually direct both my son and I to crawl into the bathroom. A few times with my son I've given him a towel and told him to put it between his legs and just let it go, towels can be washed. He usually will. I weigh about 120 pounds, he weighs 225. I can't safely get him to the bathroom. One of the problems with trying to support someone into the bathroom is all the very hard things a person can whack their head on if they fall. That's why years ago with him, and now with me, we try to do the crawling thing.Good luckGretchen

RE: RE: Husband with Seizures

Submitted by sharaw on Mon, 2005-02-07 - 18:19

I have a husband with pm sz.  How do you deal with the driving issue.  The work issue.   How do you hold onto having a future when you dont know when the next sz is comming.  I am so filled with anxiety  that I am going nuts. 

What is a woman to do when her prince cant provide as he once did or protect.  I can't even begin to tell you how broken hearted I am. 

 

I have a husband with pm sz.  How do you deal with the driving issue.  The work issue.   How do you hold onto having a future when you dont know when the next sz is comming.  I am so filled with anxiety  that I am going nuts. 

What is a woman to do when her prince cant provide as he once did or protect.  I can't even begin to tell you how broken hearted I am. 

 

RE: RE: RE: Husband with Seizures

Submitted by pongosmommy on Mon, 2005-02-07 - 18:58
Hi all,As for your prince? Hold on to him and give him all the love you can. I am sure he is probably feeling just as bad if not worse about the seizures...I am unable to control mine from coming on. I used to see it in my hubby's eyes...the acusation, the anger about my episodes. It was almost as if he was saying "why are you doing this to me?". But after the night that I went "status" I saw a different look in his eyes. I saw the pain he felt for not being able to help/protect me from these seizures.I am the spouse with szs but my Husband and I can understand your situation. I have been on disability since May 04. Now this is not too bad because it is through my work and I am not losing any pay...they pay 100% of my sick pay for now. Our financial trouble started because my Hubby didn't want to leave me in fear of another episode hitting me. I would send him off with the I'll be fine...and Wam, Bam I would be down for the count. Thankfully I have friends that do not let me be alone too often. Now some times I complain...but I would not trade them for anything.After 6 months of being scared to leave me, we found a great solution. My buddy Jimmy stays with me and my hubby no longer worries. He feels better that there is a "man in the house"...just in case. I know he is a bit of a chauvanist. It is just that I am a bit too big for my little girl to try and pick up. And my father lives about 10 miles away, so if anything happens they call my Dad.Now as for the not driving part...that is a sticky situation. If your husband is working still...maybe he can ride with someone. When I was on the late shift at work, I carpooled with a couple ladies. Only problem was that I lived the farthest away, so I ended up driving somewhere anyway. Now if I need go to Los Angeles I catch a ride with my brother (he works there) or I can get a ride with one of the vanpools that go down there. I just chip in for the gas. Maybe your husband can do something like that.If he is not working...there are many programs that help families in need. I personally know that the utilities have programs that can help you with your utilities. Some are through the utility...Some are through churches and others. In California these organizations make a pledge to help with Gas & Electricity Bills.I don't know where you live. But I had a hard time swallowing my pride and asking for help. But as my daughter said "you are only human".Best of luck,Dayna

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