my-epilepsy

staying sane with day to day life…having epilepsy

Well, that was a non-event

Went to the neurologist yesterday. I was so sure he would take me off this drug but instead he has increased the dose. Blah. I think he was impressed when I told him it didn’t give me any bad side effects. (This is rare). So dose increased and we’ll see how it goes for two months. And then? We’ll wait and see.

Hasn’t started well anyway, this new dosage because I’ve already had a seizure this afternoon. One that I will laugh at soon but not yet, not tonight. In fact surprisingly I am so tired I can’t even begin to describe it. Going to bed. Even while Offspring is on and that’s saying something. Goodnight x

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Had to happen

Twice this time. Last night I sat on the couch and apparently rubbed my chin like I was in deep thought. And then this morning I seizured mid-toothbrushing getting ready to leave to take Lilly to child care. Can’t remember anything else Stephen has said, except that they seem to be in two stages and longer these days. The normal “rigid” phase, where I grip things, then I think he said the second stage is I am quite floppy and need to be sat down. And am unaware of my surroundings (sounds better than unconscious) and confused for longer.

I’m going to see my neurologist on Tuesday so I’m quite pleased about that, I think I keep saying that but I am v curious as to what the next step is going to be. I know one option will be to turn my VNS up a notch; I’m quite happy with that.

Stay tuned, let’s see what happens…

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Almost a seizure diary really…

Yesterday was my “due date” for a seizure, as they seemed to be happening every Thursday. But yesterday passed and woohoo!!!! no seizure.

But early this morning – boooooooo – seizure. Just the same old complex partial, however this time I was mean to my little girl. Well, I didn’t hurt her and I didn’t yell at her, but apparently I pushed her out of the way when I woke from my post-seizure doze. I feel so horrible, and this is just the icing on the cake now when it comes to asking my doctor to take me off these drugs, as they are of absolutely no benefit whatsoever.

I’ve decided that I have ‘drug resistant epilepsy‘ after reading this article –  CAN YOU PREDICT WHO ARE LIKELY TO HAVE DRUG RESISTANT EPILEPSY?. And I can learn to accept that, and not keep hoping that one day a new drug will come out that will work for me. Such is life, it’s who I am and there are a lot of worse things that I could be suffering from.

I’m going back down to my morning hang-out shortly, my local pub. Sounds terrible I know as it is not even 10am. But it’s not to drink alcohol, I promise! It’s to have my morning coffee with my good buddy the publican Brandon. This morning is his shout, and he’ll be back from the shops/cafe shortly. Thrilling news I know, but he is a wonderful person and is a real help on my seizure days. As I have said previously, I am not very comfortable being alone on days when there is a good chance I will have a seizure (although recently there hasn’t been more than one a week). And Brandon is a great person to be around, he is funny and also very helpful with advice on various issues. So as dodgy as it sounds, on the way home from dropping Lilly off at child care, I call in at the pub for at least an hour or so. WITH TAKE AWAY COFFEES!!!!

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Completely unrelated post

I’ve realised, quite some time ago, but still don’t remember, that asking a three year old the question “are you sure?” is pointless because they do not understand it. For example:

Mummy: “do you want to go to the toilet?

Lilly: “no

Mummy: “are you sure?

Lilly: “no” – therefore if she understood that she’s contemplating and she’s now wondering if perhaps she does need to go. HA!

But I still say it! Every time! Can’t seem to help it! Must be the epilepsy 😉 (Gotta use that word in some context don’t I?)

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Mexican seizure – incautación

Only one seizure this round (touch wood as usual). Yesterday I met up with various friends and spent the time in between walking back and forth up and down King Street to meet them. Good exercise though, particularly helpful for all the Canberra food I ate (even though most of the meetings were again to eat 🙂 But finally I was walking up King St to go meet Lilly at child care. And I was alone. But the reason I know I had a seizure was that the first post-seizure memory I had was that I was sitting at one of the benches outside Guzman y Gomez, the yummy Mexican take-away that’s been there for a few years. And it was 4:30 – when I was supposed to pick Ms Lillian up. So I realised what had happened. I got up and left, rather embarrassed and hoping I hadn’t ordered something and was running away.

But it got me thinking, I wonder if I had had some sort of aura, which made me sit down and have the seizure. I have read that you often don’t remember these, so maybe I did have one – I knew I was going to have a seizure so I decided to sit down in case I did something dangerous like run across the road. Trouble is, I’ll never know. But it’s a nice thought.:)

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Winter Winter Winter

Yes there’s been a big gap between posts. We went down South to see Stephen’s family in Canberra. It was cold!!!!! I should not complain about the temperature, I will always remember what an ex-colleague (you know who you are) told me the winter temperatures were where she comes from (-25) so why on earth am I complaining about +6?????

So what did we do there? Mostly we ate. Ate. Oh, and we ate as well. The most fantastic food you could imagine. I just love the food at both Stephen’s parent’s and Stephen’s sister’s houses. I wish I enjoyed cooking, and I can’t even use epilepsy as an excuse for not cooking. It’s just pure laziness. I’ve never liked cooking. I don’t mind following a recipe now and then, but I have to follow it word for word and I just find it tiring. I wish I wasn’t like that. Oh well. Lucky that cooking skills runs in Stephen’s family and my husband himself is a fantastic cook.

Tomorrow I am due to have a seizure or two or three if this routine keeps up. I think I am going to stop taking these drugs. I’m seeing my neuro in 3 weeks and I’ll tell him if anything they’ve worsened my seizures. Plus Stephen has said that I have become very “vague“. I hadn’t noticed that but I guess it’s something that only gets noticed by others. He said he is worried about me a lot because my replies to conversations have been slow and sometimes I’m just not there, almost like I’ve been in a seizure.

I realised when he said that, that he’s never known me as someone without epilepsy. He’s only seen me as someone on different drugs, and how they have affected me. Some have side effects that affect Stephen just as much as they affect me (and now Lilly too). It must be pretty hard – reverse the roles and I think I would have trouble being married to someone with epilepsy. So once again, thanks Stephen, for putting up with the various Donna versions you have to live with. Wonder what he’d think of me if I took none? I asked him that, and he said, he probably wouldn’t like me 🙂

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Guess these drugs don’t work…

It was three seizures only a week ago, with the last one on Thursday morning. I got to a week but then today I’ve had one definite and one probably seizure.

The probably came first. Stephen took the day off and after eating lots of great yum cha in the city, we went home both very very tired (you know how exhausting it is, eating and shopping) and went straight to bed. Stephen tells me I sat up mid sleep and “started rambling, eyes wide open”. But can’t be sure that is a seizure really. People do that often when dreaming, mid-sleep. Don’t they? Shrug. Just can’t be 100% sure.

But then I had a real one in the car when we picked up Lilly from child care. Stephen said I just turned off, apart from muttering a bit and giving drunk-style directions home. Then I looked at him and got freaked out – he said possibly because I am so used to sitting in taxis with strangers. And then I asked where my daughter was (maybe because if I am in a taxi I am in the back seat next to her??). Poor Stephen, he isn’t treated very nicely during my seizures. But he says he is just relieved that I always ask Lilly’s whereabouts.

So if I’m going to do three in a row I’d like to get number three done in the next 12 hours because tomorrow mid morning we’re going to Canberra and then the South Coast until next Wednesday. I don’t want to have holiday seizures. So bring on the next one while I’m sitting here on the couch 🙂

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My epi-buddy

Hi there, today I spent a good part of the day with someone who has greatly influenced my light-hearted nature in regards to the epilepsy. I met her at the Prince of Wales hospital in 2007 when we were both being tested to see if we could get the nasty bits of our brains that cause our epilepsy removed. We both failed. But became friends.

She’s recently had a baby, so obviously isn’t at work at the moment, so yet another person I can catch up with. I went to her flat in Kogarah and she and her mum were both there taking care of her cute little two month old. Her mum is helping her out so much and I think this is wonderful. Because Rania (she said today “use my name use my name!“) has many more seizures than I do. She might have long breaks between them (say, a couple of months) but then she’ll be smacked in the face with five in one day. And she has ones similar to me- no aura (warning) and then complex partial. And then she’ll continue to have a couple a day for several more days.

But the wonderful thing about Rania is that she is so light-hearted about them. When we first met she was having a very different type- more of an absence seizure where should be conscious the whole time and they would only last 30 seconds maximum. I saw here have one once – she just said “shit I’m going to have a seizure“, stood there for a few seconds then she was fine. But she had them every single day, several times a day. And they would just make her feel weird. But she would just laugh them off. She worked in customer service and knew that often she would stand there in front of a customer and say “shit shit shit shit shit“. And not be able to anything about it. And to be able to laugh at yourself about that is amazing, and brilliant. So I tried so hard, and hopefully succeeded, in becoming more like her, and just thinking, if she can laugh at that, I can laugh at anything.

She now has moved into the type of seizure that I have, for reasons no-one can explain. She still sometimes has the absence types, which she calls “half-seizures” now. For example when I met her today she said she’d had two and a half this morning.

We’ve had lots of funny talks about various seizures, like ones where we’ve both caught public transport way too far, we’ve danced naked after showers (please note, not together, that would be way too much of a coincidence) and other silly behaviours that just happen when you have complex partial seizures.

I’m not religious but if I was I’d say God bless her mum Josie who is there for her whenever she needs her. She is an amazing woman who is doing so much for her daughter and grandson (Rania’s husband works in a job that requires him up at 3:30am but the good side of that is he gets home at 2pm).

ANYway, it was a lovely afternoon (and great food too!!) and reminded me of how easy it really easy to not take yourself seriously.

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Will it be a week or a fortnight?

So tomorrow will be a week since day one of my cluster of seizures last week. So if I make it to tomorrow, is that a week, or do I wait until when the group was over, i.e Thursday, so therefore Friday will be when I’ve passed a week? 

All a bit confusing. Just enjoy each day that I’m not having a seizure. And hopefully it will be two weeks, not one week. Rain rain rain again. At least that means I won’t have to train outside in the morning, I can do it in the comfort of my lounge room. 

Fascinating post I know, apologies! Not much more I can write – had a very quiet day today, booked all the accommodation for our little trip down South next week. Looking forward to that! And Canberra even though it’ll be freezing!! And did housework, so I felt like a real housewife today. Also made me realise I couldn’t do this for a living. Not that it was ever on my list, but scratch out ‘housewife’ from my future careers. 

Time for bed. Sleep tight everyone!

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Uncomfortable conversations

Hey ho, it’s the weekend. My seizures stopped at three, so I’m hoping that the next ones (I mean I’ve got to be realistic, can’t keeping hoping that was the last one) won’t be for another fortnight.

I had an interesting conversation yesterday that relates to a previous post (I think it was ‘My new look’ when I was moaning about being called ‘epileptic’). It was with two acquaintances when I called in to a local cafe to get a take away coffee. To cut a long story short, we were discussing, well, actually they were telling me about a performance at a local pub (no names given!). The older of the two women kept saying how this one act kept jumping around the stage like spastics, which I think, just overall and no relation to epilepsy, is an offensive thing to say. Then they likened to it to how one of them “was going so spastic he looked like he was going to have a fit“.

Now that’s when I get personally offended. I just sat that there really, at a loss at what to say. I couldn’t think of anything, I think I was just kind of dumbstruck. Then I decided that before I left the table I’d make sure I’d weave into the conversation that I had epilepsy. And I did, but you know what I think it was pointless. They hardly responded. I mean, no I wasn’t expecting them to break into tears or jump up and hug me with sorrow, but my intention was so that they may not make comments similar to ones they had several minutes previously. But I think I failed. But I decided to just get over it. People are always going to talk like that, and there is nothing I can do about it.

C’est la vie!!

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