It's amazing how much painting you can do while you're laid up
This one is called 'Checkers'
Monday, October 17, 2011
Sunday, October 16, 2011
Sad.......But True
Had to share this picture.
I couldn't believe just how true it is. I've heard them all, these ones and more.
I couldn't believe just how true it is. I've heard them all, these ones and more.
Wednesday, October 12, 2011
Porcelain Mistress
It's weird, but as a Crohnie, and a married one at that, I feel like I'm cheating on my wife with the toilet. It's like, everytime I have to go to the washroom, I'm "sneeking away" to visit my porcelain mistress.
Hey, I've been laid up for the past week from surgery (non Crohns).....your mind wanders.
Hey, I've been laid up for the past week from surgery (non Crohns).....your mind wanders.
Tuesday, October 4, 2011
Get Checked
October is Breast Cancer Awareness Month. I lost my mum to this disease, so I'm asking everyone to go get checked.
Come on....go touch yourself!!!
Come on....go touch yourself!!!
Wednesday, September 21, 2011
Starting to Paint Again
I haven't been in the mood lately to paint.....but got in to it the other night.
So, here's "Waterfall II"
So, here's "Waterfall II"
Thursday, September 15, 2011
Weight gain or not weight gain, that is the question
Well, I think I've decided on the Remicade, but I found out I have to wait til the end of November for my next gastro appt. So, almost 3 months to "stir". Fun. I guess the benefits outweigh the costs. If I get cancer, I get cancer. There's no way to stop it really. I could get cancer whether I take the Remicade or not. I'm more worried about my liver and the fact they have to test it all the time....but....if it'll heal me and take away the pain, or even let me gain some weight! I'll be happy. I need to find out how much this is going to cost, money wise as well.........Let's see where this new journey takes us shall we......
Saturday, September 10, 2011
Decision Time
Talked to my Dr after my colonoscopy, still groggy of course, so I'm glad my wife was there, and she said what I didn't want to hear. She found "significant inflammation" about 10 inches in. Options given..?
1. Surgery
2. Start on a drug called Remicade
3. Start on a drug called Humera
Now, the problem I'm having is, that I need to do one of them. I've already ruled out #3 as it involves injections. Remicade is intravenously, but some of the possible side effects are what I'm worried about (cancer). And surgery doesn't really solve anything, it'll return either way.
Not alot of choices.....
Anyone out there on either Humera or Remicade..??????
Help.
1. Surgery
2. Start on a drug called Remicade
3. Start on a drug called Humera
Now, the problem I'm having is, that I need to do one of them. I've already ruled out #3 as it involves injections. Remicade is intravenously, but some of the possible side effects are what I'm worried about (cancer). And surgery doesn't really solve anything, it'll return either way.
Not alot of choices.....
Anyone out there on either Humera or Remicade..??????
Help.
Wednesday, September 7, 2011
It's a Bird, It's a Plane, It's, It's....
....Angry, Frustrated Man!!!!
I had a specialist appt on Tuesday and she wants me to go in for a colonoscopy....on Friday. That's pretty quick I'm thinking. I'm also thinking, what the hell is wrong. So, here we go. Today is Wednesday and my gut is doing flip flops like it's taking part in the Gastro Olympics or something! Going to the washroom every half hour, eventhough I haven't barely eaten anything. Angry and frustrated..? Yyyyyyep, you could say that. (insert apology here for my family)
But there's nothing like a Friday being knocked out and having a camera shoved up your ass! Unless you're in college, then that's a regular occurance.
I had a specialist appt on Tuesday and she wants me to go in for a colonoscopy....on Friday. That's pretty quick I'm thinking. I'm also thinking, what the hell is wrong. So, here we go. Today is Wednesday and my gut is doing flip flops like it's taking part in the Gastro Olympics or something! Going to the washroom every half hour, eventhough I haven't barely eaten anything. Angry and frustrated..? Yyyyyyep, you could say that. (insert apology here for my family)
But there's nothing like a Friday being knocked out and having a camera shoved up your ass! Unless you're in college, then that's a regular occurance.
Thursday, September 1, 2011
100th Post
So, I noticed that this is my 100th post and I can't believe I've written on here so many times. Even my wife said, "Has it been that many already?". Now comes the task of what to write for such a special occasion. I thought about it for a few days and came up with something that I haven't written about yet. Sooooo, I thought, why not write a "Thank you" card.
Where to start. There are literally hundreds of people I can thank during my bout with Crohn's and I know I'm going to forget some (sorry).
I want to start by thanking the doctor who finally diagnosed me after months and months of seeing doctors. Then all the doctors I've seen since, in hospitals, offices and clinics. My current family doctor, my surgeon, my gastroenterologist, all can never ever be thanked enough.....ever. The fabulous nurses that I've had the pleasure of knowing and even the ones I don't know (operating room nurses). Dieticians, counselors and other hospital patients. Current and past employers and employees who put up with my abscences, especially since I never know when I'm going to be abscent (last minute). Those other Crohn's patients, sufferers, battlers and survivors who I've talked to and helped me and those I've helped in my own little way. My friends who have helped me and my family over the 20+ years, not only with helping out physically and monetarily, but mentally as well. Alot can be said with just words....thank you.
Then there is my family. They have put up with the most crap over the years. First....sorry, then..thank you.
My dad, whom has always been there, no matter what and whatever the distance. My mum, who always tried to keep my spirits up even when I was 120lbs and people thought I had AIDS. She's gone now, but I know she's still got my back. My England family, who helped me out when I became very ill while visiting and were right.....I probably should have stayed longer and had the surgery there instead of flying 8 hours in tremendous pain. My extended family, step and inlaws, who were brought in on this "journey" without being asked. My brothers and sister who have understanded, cared and helped along the way. My two kids, who still don't understand fully what's up with Dad, but try very hard not to "get Daddy" in the stomach area, and I know it must be frustrating for them sometimes trying to understand why Daddy can't play with them or go to some places with them. But maybe one day soon they will get it.
And finally, to the one person who puts up with me daily and sometimes I don't know why....my lovely wife. She has stayed with me, even when we were dating, knowing about what I had. She didn't run away, like others had in the past. She has been there through thick and thin, through hospital visits, surgeries, and the like. Through my stubborness and stupidity over the disease. She has been my rock, my everything. She completes me. I don't know what I would do or where I would be without her.....I love you.
Thank you to you all....I can never repay you.
Where to start. There are literally hundreds of people I can thank during my bout with Crohn's and I know I'm going to forget some (sorry).
I want to start by thanking the doctor who finally diagnosed me after months and months of seeing doctors. Then all the doctors I've seen since, in hospitals, offices and clinics. My current family doctor, my surgeon, my gastroenterologist, all can never ever be thanked enough.....ever. The fabulous nurses that I've had the pleasure of knowing and even the ones I don't know (operating room nurses). Dieticians, counselors and other hospital patients. Current and past employers and employees who put up with my abscences, especially since I never know when I'm going to be abscent (last minute). Those other Crohn's patients, sufferers, battlers and survivors who I've talked to and helped me and those I've helped in my own little way. My friends who have helped me and my family over the 20+ years, not only with helping out physically and monetarily, but mentally as well. Alot can be said with just words....thank you.
Then there is my family. They have put up with the most crap over the years. First....sorry, then..thank you.
My dad, whom has always been there, no matter what and whatever the distance. My mum, who always tried to keep my spirits up even when I was 120lbs and people thought I had AIDS. She's gone now, but I know she's still got my back. My England family, who helped me out when I became very ill while visiting and were right.....I probably should have stayed longer and had the surgery there instead of flying 8 hours in tremendous pain. My extended family, step and inlaws, who were brought in on this "journey" without being asked. My brothers and sister who have understanded, cared and helped along the way. My two kids, who still don't understand fully what's up with Dad, but try very hard not to "get Daddy" in the stomach area, and I know it must be frustrating for them sometimes trying to understand why Daddy can't play with them or go to some places with them. But maybe one day soon they will get it.
And finally, to the one person who puts up with me daily and sometimes I don't know why....my lovely wife. She has stayed with me, even when we were dating, knowing about what I had. She didn't run away, like others had in the past. She has been there through thick and thin, through hospital visits, surgeries, and the like. Through my stubborness and stupidity over the disease. She has been my rock, my everything. She completes me. I don't know what I would do or where I would be without her.....I love you.
Thank you to you all....I can never repay you.
Thursday, August 25, 2011
Attack of the Oreo Cookie
Quietly I waited. Waiting for just the right moment to make my move. After months of waiting in this crowded, dark, dry little space, I will be free. Free to torment another. Shhhhhh....I hear someone coming. Could this be the time? Could this be my moment of glory? We're moving!! They are taking us down off the shelf and opening the bag, my tomb. Come on....pick me dammit! It's MY time. It's MY turn. You know you want to....you know you shouldn't....but you're going to anyway. They are reaching in...I can feel the pressure on my hard cookie exterior....they have me!!!! They bring me out and suddenly there is light...bright blinding light! Then darkness as I am eaten alive!! Then, CRUNCH! They bit into my hard flesh in one bite, the ANIMAL!! But....it's payback time. I can see on my travels along their digestive tract, they are diseased. Muuahhh ahhh hahhhhhhh!!! I've got you now!! They appear to be....hmmm...yes, yes, I can see it now......they are....a Crohnie!!! Muahhhhh ahhh hahhhhh!!! Maybe my hard outer chocolate coating might not harm you, but my creamy sugary center will!!! Eat ME will you!!!! I am going to stay with you at least a few hours and cause you so much pain and discomfort, you will never want to eat an Oreo again! Muahhh ahh hahhhh!!! I sacrificed myself for my fellow package mates. I am a martyr. I AM OREO!!
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