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    Showing posts with label cancer. Show all posts
    Showing posts with label cancer. Show all posts

    Tuesday, May 26, 2009

    Before I Forget

    This was also a bittersweet Memorial Day. Normally I spend the afternoon at the cemetery for the Veterans tribute, and then meet up for lunch at Julie's house. I wasn't there last year, and it didn't really faze me.

    This year I would have had a better reason to visit. Here are some shots of the headstone that I totally jacked from my sisters blog. Thanks, Jill.

    The headstone is granite, and it was carved in Belgium. My mom would be pissed that it's so big. Not her style at all. But that temple engraving is so gorgeous, she would forget all about the size issue.


    I love how it says "Pokey". She would get such a laugh over that. I wish I could hear her laugh just one more time. And her smile was always so sincere. She deserves the beauty of this headstone, and so much more.

    I miss you, mom. I love you.


    Photobucket

    Friday, November 21, 2008

    Things I Hate

    I hate that I only have today and tomorrow left to get ready for next Saturday's craft show.

    I hate that I have piles of laundry on the dryer that need to be put away.

    I hate having kids on anitbiotics, and repeatedly forgetting to give it to them.

    I hate waking up cold and headachy.

    I hate that I have to leave Sugar Daddy alone for Thanksgiving.

    I hate that my dog has a uterine infection and I hate that it will cost a fortune to treat her.

    I hate it when my Voice Mail light is blinking, and then there isn't even a message.

    I hate lying awake stewing about life.

    I hate cancer.

    I hate being in a bad mood first thing in the morning.

    I hate that I still have 3 more days until I get to see my family.

    Photobucket

    Thursday, November 06, 2008

    A Special Month

    I am so disappointed with myself. I had a post all written out, and thought I had scheduled it to publish today. And yet, I cannot find it anywhere. Apparently I need to rehash the pain that is cancer. November is Pancreatic Cancer Awareness month. Don't you love having a month dedicated to every cause? I think December should be Cash Depletion Awareness month. January should be Sanity Losing Awareness month. But lets just focus on this here month. November. There is a certain symbolism involved here.

    My mom loved the Holidays. She would set up the Christmas tree at the office on the day after Halloween. She would cut out the Christmas show schedule from the newspaper and tape it to the fridge. Her embellished sweaters and watches and bracelets and pins and socks would be out in full force. And November was her jumping off point for all of this craziness. It is no small irony that the very cancer that took her life has it's scheduled awareness month at the very time of year she lived for.

    I hate that I need to be aware of cancer in general. I especially hate that I have to be aware of pancreatic cancer specifically. I hate all that the awareness means. It means so many people are losing the battle. It means so many families are torn apart. But specifically for me, it means I have to remember all the feelings that come along with losing my mother. Every June I will remember that day of the diagnosis. Every July I will remember the dying and the funeral. Every August I will remember that drive across the plains to my home, knowing on return it would never be the same. September and October will bring thoughts of her birthday and conference weekend. And now November will bring the awareness. Only to usher in December and the Holidays. This seems to be some sort of sick monthly countdown. I wonder if every month will be special?

    Wednesday, November 05, 2008

    Again I Say

    You might remember a little while ago I posted about a booger being stuck to my mouse. And it wasn't mine. I swear.

    Well, it has happened again. Only this time it wasn't on my mouse. It was suck on the closet doors in my entry way. Nice.

    I guess this is what happens when 2 kids have runny/stuffy noses, and the other one just has a special affinity for picking hers. And 1 of the 2 kids has croup, and the other one of the 2 kids has an ear infection. How lucky are we? Just in time to pass it all through the family for our trip to Utah. Yippee.

    And today, after hearing of a friends passing from cancer, I miss my mom. I hate knowing what they are in store for over the next few months. It makes my heart hurt.

    Wednesday, October 08, 2008

    Spiritual Aardvark Theory

    I was listening to Kathy and Judy yesterday. They have a wonderful talk radio show that totally cracks me up. I'm not normally a talk radio person, because let's face it, I'm not that into politics, and I don't pretend to be smart enough to know what the heck they're talking about anyway. But K and J, their show reminds me of something like an audio blog. You know, just kind of random things, not much of a filter, etc. etc. Yesterday they had on a girl (woman?) that had just copyrighted a new "scientific theory". Now this is good. Apparently one day, she and her friend were watching TV, and a commercial came on that had a scene with a girl in an aardvark costume that was participating in a school play. She commented to her friend about how random an aardvark was, and how you never see them. Well, the next day, for some odd reason, the word aardvark came up 3 different times, with no help from her! So this got her thinking. Doesn't this happen a lot? You see something, or hear something, and sure enough, it's everywhere. It's like your brain is suddenly more aware of that specific subject, so you notice it more.

    I have taken this theory one step further (farther? I can never remember, please correct me, Eliza). When we were dealing with the sickness and subsequent death of my mom, we were all acutely aware of so many miracles happening around us every day. From the smallest things, like the hospital cafeteria having the best cookies ever, to the big things, like all being in the right place at the right time to be there when she needed us most. Whatever the miracles, we saw them. Sadly, I've started to be blinded to them again. I knew it would happen, life takes over, and days turn into weeks, and before you know it, months have passed. We were all living in a cocoon of small miracles for those 6 weeks, and lived and breathed to see a miracle every day. Now, it's just a matter of making it through the day.

    So I've decided to reinstate the Spiritual Aardvark Theory in my life. I need to start looking for those miracles every day. I need to see it in my kids, in life around me, and most of all, in myself. I need to have the courage to make it over this hump and to embrace the miracles that I am entitled to. That we're all entitled to. I need my eyes opened to the gifts that are all around me. I need to see that life has a meaning beyond the hurt and pain I feel now. Any ideas are welcome, but mostly, just a big thanks to all of you for reading this. I know, it gets all blah blah blah, but it helps my brain.

    Sunday, October 05, 2008

    Untitled

    Wow. Today is quite the day. It's a Sunday, which is not a usual blogging day for me. But today, today I have to write. There are just too many words in my head, and let's face it, it gets crowded in there with the voices.

    Today is my mom's birthday. She'd be 60. I miss her. A lot.

    Today is also Conference Sunday. She loved Conference Sunday. She would cook turkey dinner, and we would meet up at her house to eat between sessions. It was the best.

    17 years ago today, she and my dad were returning home with my brother from his mission to Japan. And guess what? She made sure Jill knew how to cook the turkey dinner so it would be ready for us when they arrived home.

    1 year ago today we were enjoying our last "girls trip" to Seattle. We had the best time. The underground tour, the locks cruise, and Ruth's Chris. We practically had to wrestle my mom to the ground to get that bill away from her. But we did it, and it was the least we could do to show our appreciation. I would wrestle her to the ground in a second now, if i could.

    I'm not sure if it's a good thing or a bad thing that all of these events circle around this date. I find it strange that this has always been a special weekend for our family, even back 17 years. I know it will be comforting to hear our Prophet speak each year, around her birthday, and know that the words he and his disciples say will bring comfort to me. The last few days have been very emotional because of the anticipation of this weekend. I've had my share of anxiety attacks, pity party, and crying during dinner. But now, now I know that I have the knowledge and keys to see her again. And that makes this weekend even more special.

    And I will be making a turkey dinner in her honor. Yams and all. And I will do it every conference Sunday, just like she did.

    Happy birthday, Mom. I love you. I miss you.

    Thursday, September 11, 2008

    For Today

    Today's post can be seen over at the Cancer Sucks blog. It's just so much easier to add a link than it is to copy and paste. So click on over, and enjoy.

    Friday, September 05, 2008

    Funky Funk

    Here I sit, adorned in my super sexy sweats, and my "CANCER SUCKS" T-shirt.
    I indulged today in a little retail therapy in an attempt to make myself feel better. I raided Sephora, and scored some seriously crazy mad samples. I made home made pizza, bought an entire bushel of tomatoes, a gazillion other items of produce and cute imported German canning jars, and still I feel the funk setting in.

    I think most of it has to do with the fact that I'm currently watching Stand Up For Cancer on EVERY.SINGLE.CHANNEL.

    S∆4C

    And really, it kind of pisses me off.

    Don't get me wrong, I'm all about having a cause. Hell, I still wear my CS T-shirt to the bus stop every morning. I even wore a yellow wristband for a while. But when suddenly you realize the empowerment is all for naught, it seems so, well, naught. Donate your money, people. Please do. But then don't come crying to me when your mom dies anyway.

    Okay, I didn't mean that last part. You can still cry. But doesn't it seem so shallow? Do any of those "celebrities" even know what a real battle is? Have they had their liver shut down? Have they turned ugly shades of yellow? Have they been so weak they can't even lift their heads? I doubt it. So don't give me this literal song and dance and ask for help when not one of them gave a crap about us when our mom was dying.

    I'm done.

    Monday, July 28, 2008

    Speech, Speech

    This is the speech I was asked to give at my mom's funeral yesterday. When she asked all of us kids to speak, I was a little shocked, seeing as it's me and all, and I tend to say exactly what she doesn't want me to say. But I figured she must really want me there, and how could I deny her her dying wish? Some of the references are to inside jokes, so you may not understand. The hump refers to my buffalo hump on my back, it always sweats. The sweaty eyeballs are because I don't cry, my eyes sweat. So here it is. Enjoy.

    This summer our family took a vacation. Not the kind of vacation that involved sun, or sand, or even a tropical Wal-Mart. It was a completely different kind of vacation. This vacation consisted of finding the meanings of colors. Let's call it cancer summer camp. None of us wanted to go there. We were afraid of what we might find. But once we got there, we had the time of our lives.

    The first color we discovered was Yellow. Also referred to as flavescent, sallow, or xanthous. But we'll just stick with yellow for ease and proper pronunciation. Normally associated with flowers or the sun or a baby blanket, our yellow became a frightening signal that life was about to change. We knew that things would be different from then on, but we had no idea how. After a weekend of joking about sharing bottled water and spoons, and contracting the dreaded yellow, things suddenly felt different, and we knew it was time for answers.

    The next color we explored was black. The telephone that taunted us late into the night was black. Finally it rang, and all I could see were black ants circling on the floor as I heard words coming from the receiver. I felt the blackness of unconsciousness encroach, but it was staved off by sheer determination to get answers. Blackness of night, as we sat rocking in the swing outside, crying, groaning, and even laughing. Blackness of sleep, welcome yet disturbing all together.

    Blue. Mom's favorite color. Dad has blue eyes, I know she always loved them. The hospital had blue carpeting in the hallway, and we brought her her favorite blue robe. The now infamous "Cancer Sucks" pin, written in blue was pinned on, and never left. The scrubs on the doctors and nurses were blue, and they whirred in and out as the days passed by. The sunny blue sky outside the hospital room window seemed to be ever present, somehow keeping us all in a better mood.

    As we saw how all these colors became representative of an emotion or condition, we each began to take on our own roles. We suddenly became aware of the years, yes years, some of which may have involved me making out with one of our male nurses 15 years or so ago, of preparation that have taken place to bring us to this very moment in our lives.

    Meg became our personal assistant. She was ever willing to run errands, make phone calls, and chat with visitors. She knew when something needed to be picked up, washed, or dropped off. And it was always done in high style.

    Jill is the proxy mom. She cleaned up the house for Frieda, ushered muddy kids back outside to wash off, provided towels and swimsuits effortlessly, and kept the groceries stocked. She even shops like mom, up and down each aisle, picking the perfect bag of ranch rolls and Reese's Peanut Butter Cups.

    Troy became the favorite. I only say became, because after all these years of us knowing it, Mom finally admitted it. And we completely agree. Troy is the rock. He says the right thing. He knows when it's time for a time out, and he makes things happen. But he is the most tender hearted, and finds inspiration among daily life. He held mom's hand, kissed her cheek, and gently guided her where she needed to be. A true gentleman.

    I, of course, became the meek one. Humble, and quiet, I kept the air of reverence abounding. Even though no one but Mom could ever understand my problem with heat, I think we crossed over that hump. I'm fairly sure it was I that got us kicked out of the hospital. Twice. I'm also fairly sure it was I that invented sweaty eyeballs. One thing I know for certain, is no matter how flabbergasted mom pretended to be at my latest "too much information" comment, she knew she was thinking it, and I was the only one that dared say it. I hope she is thankful for that.

    As our roles became more established, our summer camp continued. More colors were to be found and mapped.

    Purple. Bright, vibrant, elegant. The color of choice for my wedding day, and many others in the early 90's. Not exactly the first color you think about when you hear the word cancer. But from now on, purple will represent the fight against pancreatic cancer that mom fought so well.

    Gray. Those last few days were shrouded in a mist of gray. Unanswered questions, words left unsaid, and looks of pity filled our minds with confusion. Was it time? Was she ready? There was so much gray area that we all had an opinion. Dad knew. And he fought hard for what he knew. It was time to make that call, and she was ready for whatever lay ahead.

    That gray area was the hardest day of my life. Inspiration was not hard to find that day, but still it became easy to dismiss. It was no accident that we were all in the same place at the same time that afternoon. It was no accident that as we lay at her bedside getting in those last precious moments, the kids entertained themselves effortlessly, leaving us with more precious time than we ever expected.

    White. Pure, peaceful, graceful, cleansing, final. The heaven on earth we knew it would be. Mom fought a good fight. She fought hard, but knew when it was time to surrender. I think Troy said it best when he said some people are just too good for this earth. Mom is definitely one of those people. She was too good to too many. She worked hard, and prepared us well, and we are so proud of the life she lived. "Birth and death, near and far, it all depends on where you are." Carol Lynn Pearson.

    As we depart this summer camp, we are grateful for the weeks we spent with each other. We were so scared of what we may find, but as it turned out, it was one of the best experiences of my life.

    Saturday, July 26, 2008

    News You Can Use

    Please click here and grab a tissue.

    Thursday, June 26, 2008

    What can I say?

    I feel like a small comment to the wonderful comments I've received wouldn't be adequate enough to thank all of you that have sent well wishes my way. I am sincerely grateful for every word that has been written on behalf of my mom. You will never know what a difference it makes to my day seeing how many of you that have never even met my mom are so concerned about her. Thank you again, from the entirety of my heart.

    And for the record, I hope to be back to my irreverent self soon. Or, as my dad put it, my vile realist self.

    Tuesday, June 17, 2008

    No Words

    Hello, blog friends. I'm back for a short stint as a blogger again. Only this time I reappear a different woman. Remember all that mumbo jumbo about a creative renewal, blah blah blah? Yeah, do I have a story for you. I guess you could say I got what I asked for, and much, much more. Lucky me. And for the record, this computer has no spell check, so I apologize in advance.

    Where do I begin? Should I get right to it or string you along with the memories that litter my brain of what went on that particular night? String you along, you say? Okay, whatever floats your boat.

    Here's what I saw. Father's Day night. Around midnight, in fact. A very full, bright moon. Ants circling the kitchen floor. For some reason my eyes and brain were fixated on those ants. I couldn't tear them away. They just circled and circled, and had not a care in the world. If only I could have felt what those ants felt at that moment, instead of what was about to drop onto my soul. I heard words coming from the other end of the phone. I understood the words, but I didn't, all at the same time. I heard myself saying things like "how big?" and "where is it?" and "how much time?", but the answers didn't register. Honestly, that voice could have told me I'd won the lottery, and it wouldn't have mattered. My life was different. In a flood of nausea and pounding ears, I heard myself scream for my sister. I felt my feet on the floor, but nothing else. I felt my head in my hands, and the cold tile on my soles, and I heard the dog door swing as one of the poodles jumped exitedly through it. But still, I was numb. The details are easy to remember. They are burnt into my memory as fresh as the birth of my children. But it's the words, the reality, the knowing, that are all just feelings. I know I felt a strange sense of calm, and then a subsequent urgency to call my brother and sister to come and be with us, even though it was the middle of the night. We sat outside, smelling the damp summer grass, and hearing the swing squeak as we lightly rocked and reflected on our situation. There were many tears, and surprising bursts of laughter, dotted with bouts of anger and frustration. There was prayer, and more tears, and then finally exhaustion.

    This doesn't happen to me. We are not those people. I am not the one whose children will be raised without a grandparent.

    But it seems I just may be. And it sucks. I'm pissed. And yet, I'm well aware of a strange chain of small miracles that have been happening over the last year or so to prepare me just for this situation.

    I don't understand why She has been chosen to travel this road. I cannot fathom that in the preexistence she would have chosen to leave her family at such a young age. And yet I can. I can't understand that she is fine with it. And for some reason I feel fine with it as long as I'm around her. How is it that she is the one with Pancreatic Cancer with Liver metastises, and she is the one buoying us all up? I know how, it's because She's just that way. She always has been.
    She is the caregiver, not the care receiver. And even in her yellow state, she still wants to make sure we know where the money for groceries is, and that she needs a draw for so-and-so at the office. She's just that way.

    I'm still numb. I'm still pissed. And I'm still in awe of Her strength and beauty. If anyone can make yellow skin fashionable, it's her. She is wonderful.

    I love you , mom.


    For an update on what's going on with the cancer situation, please check our new blog, Cancer Sucks, and feel free to comment.