Tag Archives: Shit

Only I Would Call It “Poop Week”

In May 2012, about a year after I started blogging, I came out of the closet here on FiftyFourAndAHalf.  Out of the water closet that is.  I fessed up.

I posted this:

My life is shitty.

No, no, no.  I can’t say that, they’ll think I’m suicidal.

My life is in the toilet.

Ditto.

Saturday, May 19th is World IBD Day.  World Irritable Bowel Disease Day.

That’s it!

Recently I learned about this, umm, holiday.  It is a very personal one for me.  Way more personal than I want to admit.  But of course it’s not my fault.   I blame my sister, Judy.

You see, some time in the late sixties Judy pasted a picture on the front of the medicine cabinet above the toilet in our one bathroom.

*

Little did I know at whatever tender age I was that that picture would illustrate my life.  Because in 1972, not long after it went up, I found out that I had ulcerative colitis.  An inflammatory bowel disease.  The bloody flux.  I was in and out of the bathroom and the hospital for much of my teens and early 20s.  What a blast!

Long story short, it ended up that I didn’t have colitis!  But we only found that out when a bunch of men (led by Dr. Herbert Hoover) came at me with knives, removed my large intestine and reorganized my plumbing.  That was when they found out that I really had Crohn’s Disease.

Crohn’s Disease, is, well, worse.  Partly because I can’t for the life of me spell it.  But also because it means I still spend way too much time in the bathroom (although I am very well read).  Oh, and it can affect the entire rest of your body.  Trust me when I say it’s nasty, and that there is no cure.  I would be delighted if that were to change in my lifetime.

*****

Fast forward to now, today, December 7, 2016.  Today ends Crohn’s and Colitis Awareness Week.  There will be a Thunderclap of posts, and tweets, blogs, and Facebook postings to call attention to Crohn’s and Colitis — to Irritable Bowel Disease — diseases that are often “invisible.” Because unless a person goes onto the Internet and proclaims that their life is in the toilet, well, nobody knows.  Unless perhaps if they are in the next stall.

In all seriousness, 1.6 million people in the U.S. alone suffer from Crohn’s or colitis.  These diagnoses are life changing — they cramp not just your gut, but your life.  Your life really does revolve around the toilet.

So I have a favor to ask of you guys.

You’ve all been wonderful, supportive friends, who have laughed with me about my poop problems.  I thank you from the bottom of my heart.  Or maybe just from my bottom.

But here is the favor.

I have been working with the Crohn’s and Colitis Foundation of America to get member of the House of Representatives to join the Congressional Crohn’s and Colitis Caucus.  These Representatives will, hopefully, help direct funding into research towards a cure.  To, in fact, get me (and 1,599,999 others) off the pot.

Please send an email to your Congressman/woman (you can find their information here:  http://www.house.gov/representatives/) and ask them to join the Caucus.  In fact, just cut and paste this into the email/form:

PLEASE JOIN THE CONGRESSIONAL CROHN’S & COLITIS CAUCUS!

Led by Representatives Ander Crenshaw (R-FL-4) and Nita Lowey (D-NY-17), the Congressional Crohn’s & Colitis Caucus is a bipartisan group of Members of Congress dedicated to educating their colleagues and the American public on Crohn’s disease and ulcerative colitis. The Caucus works together to raise awareness, support IBD medical research, and protect patient access to care. The Caucus also works to assert the patient perspective in regulatory decision-making, including the development of a biosimilar regulatory pathway. To join or to learn more information, please contact Matthew Moore in Rep. Crenshaw’s office (matthew.moore@mail.house.gov; 202-225-2501), or Dana Miller in Rep. Lowey’s office (dana.miller@mail.house.gov; 202-225-6506).

Thanks.  You guys are the best.

be-idvisible

 

 

 

 

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Times of Trouble

They always come off the shelf at this time of year.  The Harry Potter books.  I’ve read and re-read all of them until the pages are worn and grimy.  They give me comfort when I am fighting off “The Missing.”

https://www.youtube.com/watch?v=9VoRAZdc85I

“When I find myself in times of trouble …”

“The Missing” — Sounds like a “who-dunnit,” doesn’t it.  But that’s not what I mean.

Go ahead and laugh.  But I honestly mean that the Harry Potter books — kids books — help me fight off the sadness of missing people.

You see, in Harry Potter, the folks Harry loves and has lost get to come back sometimes.  Once in every few books. OK, in the first, the fourth, and the seventh.  What — you need page numbers?

And each time I read how they, those dead people, give Harry courage, I find my own again.

And you know what especially makes a difference?  Throughout the entire series, folks talk normally about people who have passed.  Just as if they were, and still are, an important part of a person’s life.  The characters do, and are expected to, think about people who are no longer around.  Grief, missing them is part of life; an acknowledged part.

Real life, however, outside of books, is not at all like that.  The bereaved are allowed 1 week to 1 year to grieve, depending on the relationship and the circumstances.  Within that time, and especially way beyond it, talking about a lost loved one is awkward. It makes other people uncomfortable.  They don’t know what to say.  What to do.  Where to look.  It’s taboo.

Death in our society pretty much wipes a person off the slate — we say good-bye, are moved to shed tears, and then expected to get beyond it.  We are essentially expected to metaphorically “unfriend” them.

Of course, we all fear our own death, so we don’t want to talk about someone else’s death.  We just can’t deal with someone else who has gone to that wizarding school in the sky.

Reading Harry Potter helps me feel like my missing are close by.  Let’s me feel that there are folks, even if they are fictional, who let me remember and who also remember their own loved ones.  Very much like my bloggin’ buddies, who let me lean on them from time to time.  For which I will be eternally grateful.

It’s coming on the anniversary of my sister Judy’s passing, a time that is always difficult for me.

Judy too was a Potterhead, although she only lived long enough to read the first three books. I’m quite sure that that is one of the things that most annoyed her about dying, actually.  Nobody likes to miss the ending.

So I’m really hoping she’ll hook up with Alan Rickman pretty soon.  Because she’ll show him the ropes, and he’ll fill her in on the rest of the story.  A match made in, well, heaven.

Alan Rickman.

Fanpop.com Image

R.I.P. to so very many people gone way too soon.

Thanks to Deb of The Monster In Your Closet for making me come out of my closet as a Potterhead!

 

 

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Too Much Scoop

There are responsibilities that I take seriously.  And giving all of you the scoop on poop is one of them.

But this week there is just too much.  Too much scoop on poop, even for me.

Still, I can’t hold it all in.  I must let it go.  Besides, as I explained in Trifecta! all good comedy bits come in threes.  So I had to, ummm, unload.

Number One:  The first story is one that will, perhaps, ease your mind about all that  downtime you spend at work in the bathroom.  Because someone has invented a calculator to, well, calculate, how much money you make while on the pot.

Paid to poo

Please don’t anyone tell my boss about this calculator.  This image from the “Paid To Poo Calculator/Plumbworld”.  I did not make that up.

***

Number Two:  This one is toilet-focused as well.  And really as suggested in this article, it could really save all of our asses, worldwide.  I’m not just shitting you!

The article says that a British University (too embarrassed to own up to its research and identify itself) has developed:

A toilet that does not need water, a sewage system or external power but instead uses nanotechnology to treat human waste, produce clean water and keep smells at bay.

You won’t need that Brita Filter for long!

Brita

No need for this!  Wikimedia Image

Seriously, though, a waterless toilet that could be developed and mass produced cheaply, and that would produce potable water, well, that would be truly wonderful for the world.

Science is pretty damn cool sometimes.

***

Number Three:

As a kid, a “Number Three” meant a fart.  Usually an SBD — a “silent but deadly” one.  But this number three? Far less benign.

Now as a person with serious bowel disease, I will confess that I worry that some day I will “go” the way of many famous people.  That I will die literally on the loo.  Those people include Elvis (who did not leave the building),  Judy Garland (who did not make this list), and Catherine the Great of Russia (who may or may not have died on the toilet but her descendants have preferred the version to the one that says she died-while-having-sex-with-a-horse).

Still, if I die by poop, I’d always expected it would come from below the belt.  Not above.  And certainly not far above.

Shit!  Now I have something new to worry about.  Just what I need.  Death via blue ice falling from the sky.

Wanna guess what blue ice is?

Apparently, blue ice is frozen shit falling from the sky.  And pee too.  Raining down from airplanes.  And it is landing on and injuring unsuspecting people.

As the article states:

The Times of India reports that Rajrani Gaud from Madhya Pradesh suffered a severe shoulder injury when she was hit by a football-sized chunk of ice last month.

[…]

The newspaper claims that aviation scientists believe she may well have had the misfortune to become one of an incredibly rare group: people who have been hit by what the airline industry coyly calls “blue ice”.

That’s its euphemism for the frozen human waste that very occasionally forms around the overflow outlets for aeroplane toilets, and then falls to earth. “Blue” because of the chemicals added to the toilets in planes to reduce odour and break down the waste.

Oh shit (from above).  Hurting people.

Judy Garland.  Who was  happy before blue ice hit.

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It’s a Frog’s Life

Recently, a close friend/relative was diagnosed with a chronic disease. He’s pretty miserable.

It’s a hard thing to accept, that diagnosis. To find out that you have something nasty that you don’t want, and it’ll always be with you. Gee Willikers, who the hell do you thank for that?

Still, having had a chronic disease for forty years, I’ve learned a thing or two that I can pass along.

I’ve learned that basically, it’s a frog’s life.  Yup.  A while ago I figured out that living life with a chronic disease simply means you’re a frog.

You don't look like a frog! Google Image

You don’t look like a frog!

You see, most of the time, life is normal. You hang out in the pond with your family and friends. You eat bugs which is gross, of course.  But still, life is good most of the time.

Contrary to popular belief, flies are delicious!

This pond has an all you can eat buffet!

But naturally, life isn’t quite that easy. It isn’t quite that easy if you don’t have health problems. But if you do, well, you have to pay attention to what happens to you.  The Devil is in the details.  Actually, the devil is in the damn symptoms you probably think aren’t worth bothering with.

You have to watch out for pot. Pots. You have to watch out for pots.

Huh?

Oh surely you’ve heard about frogs and pots!

No?  Let me rekindle that image.

Rumor has it* that sometimes someone (an asshole no doubt) puts a poor, unsuspecting frog into a pot of boiling water. The frog (being smarter than the average bear) immediately jumps out. Of course s/he does! It’s painful! If s/he doesn’t, well, we won’t need to worry about that frog’s gender much longer.

Shit!  THAT HURTS!

Shit! THAT HURTS!

Sometimes with a chronic illness, you get really sick. It’s dramatic, debilitating. It sucks.  And generally, the reaction is to JUMP!

Jump!  To the phone to call the doctor. Jump!  To call the nurse. Jump!  To call my husband. Jump!  To scream to heaven for my mother (because, in spite of the fact that she is in another realm, when something hurts, I want Mooooooooooooooom!). Jump!  To call my sympathetic friends.

Hell, I’ll call whoever will come and help me. Because the water in that pot is too damn hot; I must react. Whatever it takes. I then follow the advice I’m given, and feel better. Much better.

Sadly, it’s not always easy being green.  Or having a chronic disease.

You see, sometimes, the frog ends up in a pot of cool, refreshing water. And then, dammit, that same  asshole turns on the heat.  The results ain’t pretty.

Shit

Shit

Twice in the past few years, I’ve found myself hanging out in that stupid damn pot after someone turned on the gas (sometimes literally). In retrospect, it seems idiotic of me.. Me! The expert patient, with 40 years of practice!  It seems so obvious. But day to day, really, it is not at all clear that the water I’m in has heated up so much that, well, getting out just doesn’t seem worth the effort.

Because, you see, when you have a chronic illness, there are little things that creep up, little pains that are really nothing. Nothing at all.  Certainly nothing to complain about.  Nothing to worry about. Nothing to mention to that person on the other side of the bed.

symptom-creep

Just as surely, it’s nothing worth calling the doctor about. Nothing even worth remembering during those routine visits. Nope, it’s all good.

But then suddenly, unexpectedly, you realize that that little ache, that pain that started off so mild, that has stayed with you and built up.  Day by day. Suddenly it becomes unbearable.

So, I thought of what advice I should give to my poor depressed friend.

Pay attention to your symptoms. If you have an acute problem, jump out of the pot. Call your doctor.  Duh!

Pay attention to your symptoms. If something little seems hardly worth mentioning – JUMP ANYWAY!!! JUMP OUT OF THE DAMN POT!

More specifically, call your doctor. Let him or her know what is happening. SQUEAK! I know that’s what mice do, but I’m sure frogs squeak too,when they have to, too. It may be nothing, in fact, it probably is. But mention it anyway.  And if it is something, there may be help closer to hand than you think.

The two times I stayed in the pot?

The first time I didn’t want to go on a medicine my doctor thought would help me; I read too much.  The day after my first dose of that medication I was nearly pain free.  Gradually, I had been barely able to walk, sit or stand. I have a good doctor but I didn’t want to follow her advice.

The second time, I was somewhat less stupid.  I was away, and developed a painful skin condition, that started up slowly.  It was no big deal.  NBD at all.  Until, after a couple of weeks, it was.  When I talked to my doctor, she made a simple recommendation.  I followed it and the pain went away.

I’ve lived with Crohn’s for 40+ years. And you know what I’ve learned? Find a good doctor, and listen to him or her.  Then just float along as best you can.

Because except for eating bugs, a frog’s life is pretty damn good.

* When I was looking this up on my bible, Wikipedia, I learned that this whole “frog in the pot” thing may not be precisely true. It may not be that a frog will just hang out until it dies while the water heats up. Fuck you Wikipedia. Way to ruin a good metaphor. Go eat bugs, Wikipedia.

All images are from Google.  I leap in your general direction, Google images!

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