Disturbia, fiction, family, friends, and everything else between the lions.
For awhile.
Published on December 28, 2011 By Tova7 In Blogging

 

Today was deportation day.

Not in a crackdown on illegal aliens, but a crackdown of another sort.

Since my heart has shown “no improvement” over the last 4 months, I am officially off chemo.

Done with importing un-desirables who suck up all the resources (and nine times out of ten leave the area worse off than they found it), that little super highway is shut down, obliterated, gone.  A fence is constructed and baby, it’s live fire.  No prisoners.

The actual deportation is 30 minutes long tops, usually done by the surgeon who placed it, an easy in/out procedure, little pain.

Uh-huh.

Medical jargon translation in my world of treatment:  Will take at least an hour and frankly, you better plan on an ER visit or two out of this.  First and third year interns are performing the surgery without supervision, NOT a real surgeon.  And, since it doesn’t really hurt, we probably won’t numb you very well, so you’ll feel pretty much everything.  Don’t be such a baby!

This is how the surgery is supposed to go.  I watched it and was prepared.  Even, might I say, looking forward to it?

Just a few differences. True to jargon, interns performed the surgery.  My port, placed by a real surgeon (who is deployed to the desert), was sutured into the tissue. The two interns yanked on it half a dozen times before discovering, um, we can’t just pull it out?  Have you seen any sewn in like this?  Who put it in?  How did he get that suture in there on the bottom?  And the conversation flowed over my breast.  The only thing missing was a little wine and some cheese.

And the numbing thing? Didn’t happen.  You’d think they purchased the meds right out of their Xbox funds.  Three little shots.  Great for skin, not so much for deeper.

Each yank tore a little tissue inside.  (Gross I know!  Try laying still for it!)

Much cussing ensued.

Third year intern took over at the 60 minute mark because strangely ”the scar tissue was robust" and “fighting” them. What the hell does that mean? Lots of pulling, scraping, cutting, and yes more cussing. 

Though I’ll be honest, that was my biggest contribution.

Well, besides suggesting several times they go get a real doctor. 

Each time they assured me “almost done.”

Uh huh.

Medical jargon translation in my world of treatment:  Listen here guinea pig.  You’re done when we say you’re done.  Suck it up.  And stop saying you can feel it!  We know you can’t!!

At 90 minutes the original incision (from placement) was twice the size, and sutures began.  I couldn’t feel those.

Much.

Fifteen minutes to sew internal/external stitches, a little glue, and I am officially de-ported!

Sore and bruised, but back in the land of the living.

The alien is ejected.  The hole to the superhighway is officially CLOSED.

Deportation Day was, in the end, a success.

Medical jargon translation in my world of treatment:  Barring infection, suture failure, or general wonkiness, you will probably be ok.

For awhile.


Comments (Page 2)
2 Pages1 2 
on May 13, 2012

Thanks for that heads up, BFD.  Great news.  Not on FB here, so let her know her JU friends are thinking of her.

on May 15, 2012

Thanks D!  I'm not dead yet! lol  Having fun with the warm weather...have been re-doing my flowerbeds, etc....one more surgery in Texas in July and then hopefully, that is all...

 

I'm working on an article for JU, one in my head anyway....lots to share

More later!

T

on May 15, 2012

Attagirl!

on May 18, 2012

Sorry I missed this Tova.  Thanks to BFD for making it pop up again.

 

My mother had a lung removed 3 years ago.  And she JUST had her port removed.  She has shown no sign of the cancer since the lung was removed, but doctors are always super careful these days.

I hope the same can be said in your case.  Best to get rid of those foreign objects!

on May 19, 2012

Doc,

Good to see ya.  Was wondering if you were still around.  Glad your mother's lung cancer is in remission!  That's great news.

My med. team wanted me to keep the port FIVE years.  A certain nurse, who I won't name, took GREAT satisfaction in telling me that every time I mentioned a problem with it. 

In this whole ordeal, one of the things I learned hard and fast is this.....too often the medical team forgot this is MY body, my disease, I have to live with the consequences of their treatment.  Therefore THEY don't get to decide how long I keep my port, how much heart damage I must suffer before calling it quits...and a bunch of other "standard" practice type things I wasn't on board with.

I have to live with the consequences, so I should be making the decisions I'm capable (ie, educated enough about...and I can't tell you how much I've read..professional journals, clinical trials, etc....in a very technical term I've read GOBS!) to make.

Of course I've "paid" for taking charge of my care and "bucking" the standard practices by not getting scans (still have never had a PET)...and a myriad other ways they can subtly stick it to me...but oh well.  Such is my life!

I'm active, and the port was uncomfortable....and frankly, I just want to move on with whatever life I have left without worrying about it getting hit, etc.

So out it came.

Couldn't be happier

on May 20, 2012

I identify with your self-education on your own disease.  MC has been battling Parkinson's for years and she,too, has studied it.  Seems that a lot of the time she is better informed than the medics who are charged with her care.  Keep fighting the good fight, sweetheart, you are a beacon and great example.  Thanks for being here.   Heeeheeeheee....green side of the grass....

on May 20, 2012

Thanks BFD...I think I read a green side of the grass reference from you or one of my other FB friends....I stole it, made it my own....

on May 21, 2012

I think the trend, with instant access on the internet, is as you and MC have done.  We have all probably seen the Lou Gehrig story - when the doctors told you as little as they could get away with.  Some probably still try that route, but when you can do your own research, you do not need sugar coatings.  just the facts.  And then with that, you make the decision that is best for you.

As you said, it is your body to live with and your life to live it with.

on May 22, 2012

What country was this in and how come you couldn't get a real doctor or proper anesthesia?

on May 23, 2012

Taltamir,

It is in America, at a military facility.  Military hospitals are essentially mini-socialized medicine scenarios.  Bureaucrats decide more often than not (military and civilian) what treatments I can get, and the ones I can't..regardless of what the medical field may have to say on the topic.  Which is why even though I have Stage 3 cancer, and it traveled outside my tumor into my lymph system....I've never had any PET or other scans (except an MRI).   

In this particular instance, I was at a training hospital.  The residents were stingy with the pain killer because they were inexperienced and because of the rank structure involved, likely intimidated about asking for more.

 

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