Showing posts with label husband. Show all posts
Showing posts with label husband. Show all posts

Saturday, March 10, 2012

Living with Leukemia part 9. The End.


When I started this series of posts on how the Husband’s illness affected us I never thought I’d end up where I am right now. I actually thought I’d be at the opposite of where I am right now. Cause where I am right now is at the dashing of all my hopes and dreams. The other day I mentioned a quote by Dr Seuss from Oh, the places you will go, if only we knew when we embarked on this voyage the places we would go. We would at least have tried to veer off course, perhaps.

The Husband and I, we’ve been off for some time, possibly since a little while before his illness. When I think back to when he was first diagnosed, how we honestly thought it would bring us closer together, how such a serious hurdle to overcome together would help us put aside all our pettiness and it would bridge whatever divide had started to come between us, how silly of us. It did, of course, for a time, it brought us back together, we clung to each other like a drowning man to a life raft. And yet here we are discussing the dreaded S word, the one that precedes the much more final D word, the point of no return.

Tonight I lay in bed next to the Boy and all I could feel was guilty. The endless debate in my head: how can I seriously consider tearing apart his stability, pulling the rug out from under him, how do I break up his home? And yet, how do I not? What am I teaching him, we’re his example of love, of companionship, of partnership, we’re teaching him how to relate to others, is this really what I want for him?

The Husband and I, we’re civil, most of the time, we’re friends, we talk and get along but we also hate each other, we’re mean, and unpleasant, we’re not really good examples. We could go on like this for years, most likely, but why? Why should we, when we still remember what it was like to love each other, to like each other?

I don’t know where this is going, but I do know it can’t stay like this, because if no one is happy then everybody loses.

This is the last living with leukemia post I’ll write, because it’s heartbreaking to me that we managed to avoid the one and only really terrifying ending that could have come from this illness, that of a life without the Husband, ironic then, that now I may still be living my life without the Husband. 


If you're interested in the other Living with Leukemia posts you can find them here:
Part 1 - The Girl
Part 2 - Me
Part 3 - Me again
Part 4 - Broken
Part 5 - Anniversary of T.W.C.O.A.T.
Part 6 - Anger
Part 7 - Loneliness
Part 8 - The Ugly Truth


Monday, February 6, 2012

Sometimes pyjamas just aren't worth the trouble


After bath today:

Husband: ok baby, let’s put your pjs on
Girl: no!

Husband: come on, Girl, pjs
Girl: no!

Husband: Girl, it’s time to put your pjs on
Girl: don’t wanna!

Husband: Ok, sweetie, but it’s cold, let’s just put your pjs on and go read a story.
Girl: story?

Husband: Yes, pjs, then story.
Girl: no, don’t wanna!!

Husband: do I have to get mad at you? Ok, Girl, I’m getting really mad at you! Put your pjs on!
Girl: DON’T WANNA PJS!

Husband: fine, be naked, I don’t care.
….
So, we’re home now.

Saturday, December 17, 2011

Sometimes I just need to randomly write drivel of the top of my head, ok?


I’m sitting here trying to type with the pads of my fingers because despite having worked at or around a Spa for the past six years I can’t ever seem to get a manicure and a wax, for love nor money, when I need one. So I’m hairy-legged (not that that’s anything new) and smudgy because, alas, I’m going to a wedding with the husband tomorrow and though I can disguise my hairiness with some heavy opaque tights or pants I simply do not feel festive without bright red nail polish.

As usual when I travel, I’m at that point in the packing process where it looks like a tornado hit the house and I’m never, ever going to manage to get everything into my allotted suitcases. This point exhausts me, but I’m hanging onto the thought that with or without my bags I will be on the plane next week, for dear life and that’s what’s going to get me through the weekend.

Did I mention it’s supposed to snow at the wedding venue tomorrow? We haven’t seen snow since a short burst of wintertime impetus from the weather in October and now it’s going to snow. How’s that for Murphy’s law? Of course the wedding will be held in a mountain town, because it’s eminently reasonable to plan a destination wedding in the Alps in December. Also, it’s midnight and I have no clue what I’m wearing. At least my nail polish is catchy.

The Husband turned forty today. I’ve been planning a recap post of his party last Saturday all week and have yet to get around it, it’s like this wedding, the last minute Christmas shopping, and our imminent trip have completely taken over my few remaining brain cells.  But I needed to acknowledge his birthday today because forty is kind of a big deal. Although, I always thought fifty was the real big deal, what with it being half a century and all, but he disagrees. Apparently, forty is the biggest deal of all, in fact he mentioned he had to start thinking about my fortieth party now, four years ahead of time. Really honey, forty’s not that big a deal.

I have a completely unhealthy co-dependent relationship with Nutella. In fact, I feel an irrepressible urge to go have some right now, kind of like I’m a werewolf and Nutella’s the moon.
And I think Nutella’s a good note on which to end this completely useless post. This is how my brain works. I’m sorry.

Wednesday, November 16, 2011

There, but for the grace of God


A few days ago I ran into a lady I know, and I found out that she recently lost her husband. Her husband had cancer, from asbestos. They diagnosed him last December, he passed in August. She’s doing what any of us would be doing in her place, she’s going to work, going about her daily activities, doing what needs to be done, she’s holding up, she’s… surviving…

But she’s devastated, she looks terrible, she’s aged, and her eyes are sad. Her eyes are vast pits of sadness, I could barely stand to look into them, such was the loneliness, the hopelessness, the unadulterated, boundless, inexplicable, all-encompassing despair.

Seeing her didn’t so much as take my breath away as it quite simply sucked it so violently out of my ribcage I wondered if I would ever breath again. I had no words, no comfort to give, nothing to offer that could possibly make her feel better, because, let’s be honest nothing will make her feel better for a really, really long time.

And all throughout this brief encounter, as I let her talk because talking about it seemed what she needed in that moment, as I looked at her, tried to show her support, tried to express something, anything that would show her I cared, a teeny voice whispered in my ear… “there, but for the grace of God, go I”.




Linking up today with Shell at Things I Can't Say

Wednesday, October 19, 2011

Living with Leukemia part 8: The Ugly Truth

The thing about cancer is that it completely changes your life, whether you’re the one to have it or someone close to you. What’s surprising is the extent to which it changes you, I can honestly say that I’m a completely different person now than I was two years ago, and I have no idea whether I will ever go back to being the person that I was then. Probably not. Another surprising thing is that, at least in my case, most of the changes aren’t positive, I truly wish I hadn’t become this way.

I used to be pretty judgmental, motherhood took care of some of that attitude, and then cancer took care of the rest, so you won’t find me judging as readily anymore. At the beginning of this whole cancer debacle I was talking to my therapist and telling her I was upset with myself cause I felt like I wasn’t doing enough, and that it bothered me how often people would come up to me and say I was so strong, and I was dealing with this so well and what with a new baby and all, and my answer was always, well, what the hell else am I supposed to do? And my therapist said that I’d be surprised at how many people leave when they find themselves in my situation. 

Obviously, my initial reaction was disbelief, I mean, really leaving a loved one who’s just been diagnosed with leukemia? Who does that? What sort of horrible human being abandons another in a time of need? And then you start hearing things, because you start paying attention, and you realized that you’re surrounded by “people who leave”, the husband who runs off never to be heard from again when his wife is diagnosed with breast cancer, the girlfriend who breaks off the engagement… there are so many, more than one can even imagine. I was appalled, who does such a horrible thing, I’d think, why would you react like that, how can you leave?

They say you shouldn’t judge until you’ve walked a mile in another man’s shoes, right? Well, now I’ve walked that mile, and I’m not so quick to judge. Cancer changes things, a lot. It’s a long, sad and sorry process with no guarantee of anything at the end. There are days, there are many days, when I wish I could be one of those people who leave. Have I shocked you?

Cancer changes things. I love my husband, I always will, he’s the father of my children, but we’re barely husband and wife anymore. We live our lives beside each other, but not together anymore, and we have no energy and no hope to look to the future anymore. So, yeah, the truth is sometimes I wish I could leave because I’ve realized that leaving would be so much easier. 
A few weeks ago, at my Mom’s wedding, one of my cousins who I hadn’t seen in years, said to me that I was the column of the family, always taking care of things, always doing what I’m supposed to. How sad is that? But, uncomfortably true. I need to take care of things, make them work, make them right. I’m not a person who leaves, but god do I wish I was.

I got an email a few weeks ago from a girl who reads this blog, I have yet to find the words to answer her. She finds herself in a situation similar to mine, which in a way was comforting to me because it made me feel much less lonely; now I’m not going to get all up in her business here because it’s not my place, but her email got me thinking (among many, many things) this: her boyfriend has leukemia with a very similar path to my husband’s but the thing is, they hadn’t been together very long when this all started for them, they’d only recently moved in together… and lately all I want to say to her with all the strength in my body is get out, get out while you still can. I can’t even imagine facing this whole, long, terrible ordeal without the strength of years together to help you through. I’m barely making it and I’ve been with the husband for twelve years, we have two kids, we stood up in front of church and state and swore to stay together in sickness and in health. And most of the time I feel like I’m a strong wind away from it all falling apart. 
But the truth is, I don’t think she’s one of the people who leave either.

I realize there’s no limitation period for leaving, one can up and go at any time, but there are people who can and people who can’t. Sometimes I try and look to the future and it depresses me to no end, because this illness is one step forward two steps back the whole way. Last year I used to think in terms of when the husband gets better, when we’ll get back to normal, when we’ll be able to do this or that, this year, after the second transplant, I cautiously thought if we get back to normal, but now, now I have no hope. Nothing specific has happened, his blood work is good, but he still feels pretty consistently like shit. And let me tell you, a person who feels like shit all the time tends to be an asshole most of the time. Through no fault of his, let’s be clear, but still it’s a normal and consistent reaction.

And now before you judge me, think, seriously think about living with someone who feels ill most of the time, who can’t eat because most foods and smells disgust him and you’re the one cooking, who acts normally one minute and then yells at you the next because he’s trying to act normal but snaps because he’s just uncomfortable all the time, but you’re the one getting snapped at, who always shuts you down when you suggest something because his initial reaction to everything is negative. Of course I understand that he’s like this because he feels like crap ALL THE TIME. I get it. And I also realize that I can’t really know how he feels, because, well, I’m not in his shoes, and I don’t want to be, I thank God every day that I’m not. I get that it’s not his fault. I get that he’s struggling more than I am. I get it. My brain understands all of it, I swear, but my heart is tired and sad and lonely. Cancer changes things more than I thought possible, and now I’ve found myself waking up in a panic at night wondering if things will ever go back, if they will ever get better. And that’s why I wish I was one of the people who leave. Because if you leave you may well feel guilty and ashamed but you’re living your life, you’re working towards something, you’ve got a future to build and at this point I honestly can’t say which is the better trade off.

The point is moot, of course, cause I can’t leave. I don’t know if it’s genetic wiring, if it’s an overwhelming sense of duty, if it’s love, but for now leaving is not an option for me, but let’s not judge too harshly the people who can and do leave. Having cancer is terrible, it’s undeniably worst for the person who has it than for anyone else around them, but being the person taking care of things, picking up the slack, being the sounding board, the shoulder to cry on and the punching bag isn’t exactly a walk in the park either. Being the person next to someone who is fighting cancer is sad, and frustrating, and exasperating, and tiring, and it’s very, very lonely. Cancer changes everything, and that, my friends, is the ugly truth.




I'm linking up today with Shell at Things I Can't Say.

Wednesday, July 20, 2011

Virtual Coffee {17}

Hello dear friends and welcome to coffee. I’ve missed our coffee date lately and am very happy to be back. Last week we went to France for a little vacation, I shared some pictures yesterday and I figure that today they’re the best accompaniment to a nice cup of coffee so sit back and take a little virtual vacation with me along with our virtual coffee.

We met a really nice statue in Menton, it didn’t freak us out at all.

















We have a fixation with the merry-go-round apparently:



And we made funny faces:

We lounged around:



We went to the park:


We found out that Daddy's face is squishy:


And then we slept:


When we woke up, we went swimming:




Then we went to town and took lots of pictures:


We anxiously waited for fireworks to celebrate July 14th Bastille Day in France:




And here they are:







And then the next morning we played peekaboo:


And did a little dance:


And chilled on the stairs:


Thanks for coming for coffee, more pics tomorrow if you’re interested!


And don't forget to visit Amy, her pictures are definitely better than mine!

p.s. Just checking again: I’ve been told by a friend that she can’t comment with Disqus, and as I’ve noticed a certain decrease in the number of comments I was just wondering if Disqus is, in fact, causing problems. If you would like to comment but can’t seem to for some reason could you drop me an email at {moomser at gmail dot com} to let me know, please.
THANKS!