Infusion #47, almost 5 and a half years now and still going strong.
Remicade has reduced my symptoms drastically, but hasn't eliminated them totally and I'm OK with that.
The days sometimes are tough and tiring, but at least I haven't ended up in hospital for them and I can deal with my Crohnie problems from the comfort of my own home instead of the hospital environment.
Don't get me wrong, it's good to know that the hospital is there if I need it, I'm just glad I don't need it. I still need to make a decision regarding an ostomy or not. It's a hard decision but I think I'm leaning to the "not right now" side of things. It's taken me almost 30 years to get use to doing things a certain way and dealing with my Crohn's, I don't know if I want to learn it all over again.
Right now, I don't "need" the surgery, but when I do, or if I do, I'll deal with it then.
Friday, October 27, 2017
Sunday, October 22, 2017
The Faces of Crohn's
So, have you ever wondered what Crohn's looks like? And I don't mean the graphic photos of intestines etc, I mean the people. I personally have become an expert on "looking well" instead of looking sick.
The face of Crohn's/IBD can be your mother, father, brother, sister, child, grandparent, friend, foe, teacher, co worker, boss, neighbor, celebrity, sports star, Olympic athlete, etc.
As an invisible illness, you just never know who's suffering and a daily basis.
You want to know what someone with IBD looks like?
It's me.
The face of Crohn's/IBD can be your mother, father, brother, sister, child, grandparent, friend, foe, teacher, co worker, boss, neighbor, celebrity, sports star, Olympic athlete, etc.
As an invisible illness, you just never know who's suffering and a daily basis.
You want to know what someone with IBD looks like?
It's me.
Sunday, October 15, 2017
Friday, October 13, 2017
Crohns Disease Essentials and Emergency Kits
Again, from IBD News Today, a fantastic column by Mary Horsley
I would encourage everyone to follow her blog It Could Be Worse
IBD News Today
I would encourage everyone to follow her blog It Could Be Worse
IBD News Today
Protein Deficiency Research
I came across this study done in the Netherlands regarding the SHIP1 protein.
We're getting closer and closer....
IBD News Today
We're getting closer and closer....
IBD News Today
Wednesday, October 11, 2017
Crohnie Quote of the Day
Healing is not controlling damage within;
It's not allowing damage to your life.
It's not allowing damage to your life.
Thursday, October 5, 2017
You Might Be A Crohnie
If you can "extreme-multi-task" (do everything while sitting on a toilet)
... you might be a Crohnie
... you might be a Crohnie
Tuesday, September 26, 2017
You're Gonna Put That Gel Where...??!!
Further to my visit to the surgeon, last week I had my MRI appointment. I've had MRI's before, so this was old hat to me, nothing new, nothing exciting......or so I thought.
I arrived early, as I always do, and sat in the waiting room with all the other medical imaging "hopefuls", anxiously waiting for your name to be called. You know that feeling...when the technician comes out and everyone sits up hoping to hear your name cuz you don't want to wait anymore, either because you just want to get out of there, or simply because you don't want to wait to catch something that's floating around in the air. Because hospitals are so clean... not.
My name was called and was handed a packet of paperwork and told to follow the blue line to MRI...another waiting room, good lord. Not so much of a wait this time, but then had to get changed into the fancy blue "smock" and comfy yellow pants and sit some more in the waiting room.
I got called into the large MRI room which actually is dwarfed by the huge MRI machine and told to lay down while they put on IV into my arm.
Then the lovely news I wasn't told about....
We're going to put in some rectal gel for contrast. Ummmm, excuse me? I actually had to get clarification on this because after 30 years of testing, I have never had rectal gel shoved up my ass. I had to explain to the technician that because of my anal stenosis, that might be a problem. There is no way you're getting a finger up there. Even when I have colonoscopies, they use the pediatric scope and I'm OUT for that! He would have to contact the doctor on call to see what can be done. The doctor showed up and was going through drawers pulling out all kinds of things all the while telling me what he's gonna do....ummmm, nope. He was getting all technical and explaining how he has this flexi tube with a balloon on the end and then inject the gel, blah, blah, blah....ummmmm...nope. I then explained to the doctor how I basically only have the rectum left which is attached to my small intestine and if he injects that into me without me doing any colon prep (which I wasn't required to do), he's going to have a mess all over his nice MRI table. It's funny how quickly he said....
ummmmmm, nope, no gel for you.
I arrived early, as I always do, and sat in the waiting room with all the other medical imaging "hopefuls", anxiously waiting for your name to be called. You know that feeling...when the technician comes out and everyone sits up hoping to hear your name cuz you don't want to wait anymore, either because you just want to get out of there, or simply because you don't want to wait to catch something that's floating around in the air. Because hospitals are so clean... not.
My name was called and was handed a packet of paperwork and told to follow the blue line to MRI...another waiting room, good lord. Not so much of a wait this time, but then had to get changed into the fancy blue "smock" and comfy yellow pants and sit some more in the waiting room.
I got called into the large MRI room which actually is dwarfed by the huge MRI machine and told to lay down while they put on IV into my arm.
Then the lovely news I wasn't told about....
We're going to put in some rectal gel for contrast. Ummmm, excuse me? I actually had to get clarification on this because after 30 years of testing, I have never had rectal gel shoved up my ass. I had to explain to the technician that because of my anal stenosis, that might be a problem. There is no way you're getting a finger up there. Even when I have colonoscopies, they use the pediatric scope and I'm OUT for that! He would have to contact the doctor on call to see what can be done. The doctor showed up and was going through drawers pulling out all kinds of things all the while telling me what he's gonna do....ummmm, nope. He was getting all technical and explaining how he has this flexi tube with a balloon on the end and then inject the gel, blah, blah, blah....ummmmm...nope. I then explained to the doctor how I basically only have the rectum left which is attached to my small intestine and if he injects that into me without me doing any colon prep (which I wasn't required to do), he's going to have a mess all over his nice MRI table. It's funny how quickly he said....
ummmmmm, nope, no gel for you.
2017 WEGO Health Activist Awards
I am happy, humbled and surprised to announce that I am a top 5 finalist for a WEGO health activist award for this blog in the category of Best in Show: Blog.
Thanks to everyone that nominated and endorsed me.
Even if I don't win when the award is announced in October, it really does feel great just to be nominated.
Thanks to the judges and to everyone.
Thanks to everyone that nominated and endorsed me.
Even if I don't win when the award is announced in October, it really does feel great just to be nominated.
Thanks to the judges and to everyone.
Tuesday, September 12, 2017
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