Ten Things Medical Personnel Should Not Say

1. This won’t hurt a bit.

2. I know about your veins better than you do because I have been doing this a long time.

3. Don’t worry that your blood pressure is super high, we know what we are doing.

4. We don’t need to check your urine.

5. Did you know that CT scans deliver a ton of radiation and can cause cancer?  You should stop having them.

6. You don’t look sick.

7. You don’t need help to the bathroom after I gave you at least three sedating drugs, you look fine.

8. Show yourself the door.

9. The doctor doesn’t need to see that.

10. Are you always sick like this?

I have literally had all of these things happen and heard all of these things.

Here We Go ‘Round The Merry Go “Round

I feel as though I am on the spin cycle in the washing machine.  Or maybe I am on a spinning carousel and it will never slow or stop long enough for me to get off of my horse.

My life is simply not cooperating with my intentions to have a semblance of normalcy.

I blogged here a week ago (blog is such an awkward verb… it sounds like a body function).

So, the stent was placed and in general things have gone along better than before.  This is good news.  I have been  waiting to hear from the big wigs in Houston so I can have a green light to move on to the next thing.

Then, day before yesterday, it all started to hurt again.

This resulted in calls to the gastro dr. here and culminated in an ER visit at the hospital where he practices.

IT WAS A CLUSTER FUCK.

They did not treat my pain.  They did not treat the anxiety attack I was having as a result of the whole mess.  It was a waste of time, money and energy.

The ER dr. refused to help me out with comfort care because he ‘doesn’t like dilaudid.’

You know, I thought the phrase was, “do no harm.”  The doctors at Scott and White at Round Rock have not gotten the memo.  Every time I am in that facility, I am treated as a crazy person because I have chronic pain.  Also, they cannot see my pancreatitis so even though my dr. went in and found sludge and a swollen bile duct, they say I don’t have it.

 

That again.

I am just done.  I hurt and I want help NOW.

Here I am, two days later, still sick but still alive. I cannot hold anything down but a few liquids.  But, thank God, my aunt has now clarified things for me.

She explained to me this morning that I create all of this with my mind and that the doctor only put the stent in so I would have something to think about.  Oh, and going to the Houston specialist is just a silly adventure.

That hurt.  I mean, I know she is old and mean and crazy but that was just uncalled for.  This from a woman who broke her hip and refused to do the rehab so now she cannot walk well and we are supposed to operate around that.

Sorry to be bitter.

Ya know… I am going to end this on that sad, minor note.  It was a bad, bad week all ’round.  My whole family was trading a virus back and forth, which turned out to be making things worse.

The End.

Just Enough Time For a Quickie

So, today is the day.  Or, at least it is another of those days.  I am having a second ERCP.  I had one in early January and it was really, really hard but it seemed to work.  The dr. cut a hole in my biliary duct, released a lot of pressure and slime and put in a stent.  As soon as I got over being really sore, it felt good.

Then the stent came out. And, it hurt like hell again.

So, today we do it again, with a longer stent and hope it holds up.  If so, I go to Houston for a more permanent stenting procedure in my pancreas.  It is a bit dangerous but could get me more long term relief.

I was scheduled for tomorrow a.m. but the dr. got me into his schedule for this afternoon because I am miserable.   I appreciate that.

I have not had anything to eat or drink all day and it is now 2:00.  I am thirsty and nauseated and in pain.  I want this over with as soon as possible.

I am a bit scared.  I wish I didn’t have to do this again.

I feel like I am getting ready to stand in the middle of traffic and hope nothing hits me but I don’t see any alternatives.  I have to be brave.  I have to keep smile on to keep my family believing that I am fine.

My son is upset and I can’t let him see me stumble.

Only when that sweet hiss of stuff goes to my mouth and veins will I let down.

The Sun Is Shining and I am Hanging On By My Dewclaws….

Does everyone here know what dewclaws are?

Humans don’t actually have them. They are a part of a dog or cat’s vestigial anatomy.  They were put there in order to keep the animal in balance as they take off and run, from predators or towards prey.   Over the millenia, as we have domesticated canines and felines, the dewclaw has gone from a sort of ‘thumb’ to being vestigial or ‘extra.’

The general idea is that it serves no purpose for modern day domesticated animals.  (It should be mentioned here that many ungulates (deer types) have a type of dewclaw as well).  Often, people who concern themselves with their domesticated pets’ appearance, have a dog’s dewclaw removed.  From what I can tell, the dogs feel fine about how their dewclaws look and feel.  It is just a problem for certain dog owners.  Perhaps the owners are not comfortable with their own vestigial anatomy.  Which, finally, brings me to my point.

Humans have vestigial anatomy too. In fact, we have many of them.  Darwin pointed out that we have structures that clearly point out that we have evolved away from the use of one piece of anatomy in favor of another.  A good example would be our earlobes.  They don’t really do anything.  Earlier on, when were more chimpanzee like, they were perhaps more useful.  Now, they just hang there, so we decorate them.  They are vestigial.

Unless you don’t buy that argument.

Don’t worry.  I am not going to go all deconstructionist a la Derrida  on you here.

I just want to make a point.  I know I have one here somewhere:

I am operating on those vestigial, seemingly useless parts of myself just now.  These are things that I used to not even notice about myself or the world about me: the sun is shining, I’m not broke, my kids are healthy, clean sheets on the bed, gluten free pancakes, good books, my dogs, my cat, my husband (sorry dear), and all the other parts of me that have become vestigial because I am used to them.  These things, you may argue, are outside of me. Yes, in a way, but it depends on how you see it.  They are normal, everyday pieces of my world that I have taken for granted.

Today and every day for the last ten or more, I am living in a great deal of pain.  It hurts to breathe.  I feel like there is knife in my side.

I got my pain meds amped up and that still isn’t enough.  Probably eating today was a huge error on my part.  But, it seemed a good idea at the time:)

So, I have to hang on my vestigial fingernails, to whatever I can.

I have to last through four more complete days.  Then I can get some help.

I will do this any way I can.

And I think I am going to need my dewclaws.

 

 

Acceptance

As per my last post, things are still not running smoothly in Katie-land.  But, I don’t imagine that they ever will.  This is the life of a person with chronic illness.  It goes up, down and sideways.  The up periods feel pretty short and fairly few between.  The down parts feel very, awfully, and uncontrollably down.

I would say that sideways is the most common state of being for me.

Right now, I am sliding sideways and headed down.  I have to have two more nasty bits of surgery on my biliary system.  It does not drain correctly at all.  It just sits there, stewing in its own juices.  So, they need to open it up and stick in some new stents and actually make a slice in my pancreas this time.

There are risks and it will definitely be very, very painful.

I’m scared.  I have heard all of the warnings from my doctor.  They are dire and frightening.  I could develop a life threatening infection.

All I know is, I can’t really live the way I am now.  Constant, slamming pain and the inability to eat much of anything, is not really a life.

I titled this entry ‘Acceptance’ because that is where I have landed today.  I have been headed there for a week, screaming and kicking.  But today I saw my therapist and we talked about all the irrational stuff going on in my head and we agreed I was entitled to be irrational about it all because it sucks.

You don’t choose to step in front of an oncoming train because you know, in the end, it will make you feel better.

That is what this feels like.

Also, she and I agreed I could make tons of nit picky lists of stuff that I felt were necessary to keep the house, pets, children and world in general running while I am out of commission. I am doing just that.  I started with a list of how to’s for my 14 year old son.  He is complicated; as is any 14 year old boy.

We also talked about pain, chronic pain and the sort of post procedure blues or blackness that I always seem to fall prey to at some point after a surgery or hospital stay.  I end up in a place so awful it feels like I will never come back out.

But now, I think if I can accept that the horrible, black, nothingness and pain is coming for me and that I will live through it, maybe it won’t be so frightening.

Maybe I can share with my husband ahead of time what that feels like and he will know that all I need is a hug.

So, acceptance.

In a way, it feels spiritual.  I don’t mean that I accept all of this because G–d planned it for me: NO WAY.  I want to be clear here.  I don’t believe in a G–d that plans for his creatures to suffer as a way to learn.  I just mean, for the first time in a long, long, time, I think maybe the Divine has my back going into this.

Whatever happens is okay.  I don’t have to fight it.

As Jews we are known as the people of the book and  the people of the covenant.  I know that people suffer and die all the time.  My struggles are minuscule on a grand scale.  But, they are mine, and I am Known and loved by Adonai;  the One who chooses to be in a giving, covenantal relationship with His creation.

It doesn’t get any better than that.

 

I Need To ‘Fess Up

Things are not peachy keen in Katie land.  I have been loath to post here because I don’t want to be the harbinger of pain and sadness.  It’s interesting; I don’t mind writing my essays all gloom and doom and then filing them away, but putting things ‘out here’ in the public forum, seems different.  Maybe that is a clue why I have yet to send any essays out to publishers.  Hmmmmm.

So, it looks like my ERCP surgery with a cut to the Sphincter of Oddi, was a step in the right direction.  I got relief from it.  However, when the stent was removed, the pain started coming back.  According to the doctor, this really shouldn’t be happening.

Yeah, well, according to doctors, I really shouldn’t be happening.  I am a zebra and I have a set of stripes no one has ever seen before.  So, what next?

My gastro dr. is really quite good.  I really appreciate him.  He gets the Zebra thing. He is really frustrated for me that the pain is back.  But, he says at least that gives us an idea about what is going on.  So far, no tests have come back with a single hint of how to proceed.

He told me there is another, more drastic and dangerous procedure that could possibly help.  In that procedure, a cut is made in the pancreas itself and a stent is put in the pancreatic duct.  Often, this is a permanent stent.  For some reason, this is a two part surgery.

When we spoke in his office on Tuesday, he told me he would make an appointment for me in Houston with Dr. Eichmann, who is a renowned specialist in this procedure.  He did point out that he does the procedure as well but wanted another opinion.

On Wednesday he called me and told me he had spoken extensively with Dr. Eichmann and his staff and they recommended he do the first part of the surgery here and then send me for the actual stenting to Houston.

It all sounds pretty overwhelming.

The risk of runaway, horrid pancreatitis, is very, very high.

I feel flat.  I don’t know what to do anymore.  I just want to ignore it.  If I don’t eat much, and I only eat bland food, it isn’t too bad.

Maybe I can hold off for a bit.

I am really, really depressed by all of this.  It is taking a huge toll on my family and my marriage.  I feel like saying, “fuck this… I surrender… kill me now.”

I know I should be grateful.  After all, it isn’t cancer, right?  I don’t know.  All I know is that the little bastards with their little bastard knives are back in my right side and they are sharpening the knives and trying to cut holes in me.  Bastards. Go away.

 

 

UP, Up and Away!!!

I thought it might be a good idea if I blogged on a good day:)

The surgery blues have fled and I think I am better as a result of the procedure. That is all good! I do have to go back in for stent removal but I am filing that away until it happens.

Weight watchers and I are beginning yet again today.  I do not find that depressing at all.  It is a constant battle against the bulge for me, but whatever. All I can do is stick to the plan and eat healthy and hope for the best.

Now that I can eat normal (gluten free) food again, it is a hell of a lot easier to count the points!

I am hoping to get some work from the editing signs my boys pasted all over the UT campus yesterday.

So, basically I am boring.  When I am feeling good I think of so many things, so many places I want to go.  But then I remember Saturday.

Saturday I went all day and had a great dog walk, etc.  Sunday I awoke to inflamed joints and fatigue.

I made the choice to get up and out.

I make that choice every single day that I can.  I just can’t get ahead of myself.

I want to join a choir and attend temple services regularly.  For some reason those are big, big things at this point.  I guess it is because I have kiddos to take care of.  I miss my daughter (at University) and am surprised that my 14 year old son takes up all the time I spent on them together!

But, that is his nature.  I have to nurture his nature…

Oh well, today there is sun and I have washed the gray out of my hair.

 

Itty bitty, dippy, whippy, baby steps….

Being a baby must be annoying.  I sure don’t like this whole baby step concept.  I am up and about a bit after a three day melt down of some kind.  I don’t know if it was surgery related or I have a bug.

I was so excited to wake up this morning not feeling like total poo poo that I made soup.  Yep, my husband had already done the hard part, the chicken and the broth, and I just completed it for tortilla soup.

And now I am exhausted.

Geez.

I will get my son from school today; that is the main goal.  He gets pretty upset about his mom being so sick and I know he gets scared.  I need to be there at the end of his school day. My daughter is at a University 90 miles away so she gets to skip all of this..

We commute to a Charter School that is about 20 minutes away and picking him up is our usual ritual; my husband takes him in the morning.   It may seem small but it is actually a time for us to connect.

Raising children is complicated.

Chronic illness is complicated.

Marriage is complicated.

Ok, so everything is complicated!  What do you do about it?

You march on to the beat of your own drum.

My drum is not always in step with the rest of the band.  I mean, sometimes the little drummer girl in my head just turns off and I can’t do squat.

Little bitch.

OH well, I am wandering.

I am:

Thankful for sunshine.

Thankful for my husband.

Thankful for my kids.

Thankful for my pets…

There. That should get the little drummer girl going…(play bitch, play!)

Sorry for the profanity…

 

 

Post Surgical Blues….bah, dah, dah, dum..

Every time I go through something truly awful and beyond my limits of pain and agony management, I get the blues.  I have realized it is a part of the process.  I have been telling myself I need to incorporate it into my expectations; you know, embrace it.

Not working!

I think the very idea of having the blues is that you feel out of control.  At least that is how I experience it.

For me, it went like this: I had the surgery I had been dreading and when I awoke I was told that I was being admitted to the hospital for observation because the procedure took twice as long as normal.  The nurse attending to me in recovery looked bored and irritated, or maybe that was just me…

Anyway, every time I tried to ask a question, she pointed out the doctor had already spoken with me but I had not been coherent.  Well, that’s useful. Why in the hell do the doctors do that?

I was in agonizing pain and she kept telling me she had given me all the medicine she could and I would just have to wait until I got up to my room.

I got to my room and the pain felt like labor: no joke.  They were giving me fentanyl which does absolutely nothing for me. I lost control: I screamed.

I finally got shot up with dilaudid (the bad drug) that works on me.

My doctor came in and talked to me again so I had a vague idea of what was going on.  My anatomy was strange, (no joke) so it took him forever to get in there and now I have a stent and it will need to come back out, etc.

Shortly thereafter, a hospitalist,  (a new noun created especially for  our fucked up healthcare system) came in to see me.  He was not the doctor on my case,  just the floor doctor.  He proceeded to tell me he disagreed with my specialist about my use of dilaudid for pain and to lecture me on being an addict.  I stuck up for myself and told him to call my pain management doctor if he had questions.  The guy was unbelievably rude and condescending.

After he left, they took me to x-ray and I cried.  The two x- ray techs had heard and seen the whole thing and seemed freaked out by what had happened. They congratulated me for defending myself.

I was exhausted from all of this but frightened that the floor doctor might try to come back in or over ride my surgeon’s orders.  So  I called in the charge nurse and told her what happened.  She promised I would not have to see that doctor and that my surgeon’s orders stood.

A note here: I should not have had to do all of this.  I was in no shape to go to battle and in no shape to be judged by some nitwit of a doctor.

I continued to feel really badly, pain and nausea and dizzy, etc. into the next day.  My doctor came by and said my liver enzymes were up but my pancreatic stuff looked good, which was our main concern.

He said the hospitalist would check back in with me later about releasing me.  I said that I did not want to be seen by that person, Dr. M.  I was assured that he had been spoken to and not to worry.

But I did worry.  I felt violated.  I had to be on my guard.  I did not feel well enough to go home, I know myself, and yet, I felt like I had to do battle about that too.

At some point in all of this I just crashed emotionally.  I was alone, my husband had left and I just fell apart.  I started crying uncontrollably.  I didn’t want anyone to notice because the second they think you are “crazy” in a hospital they treat you like a total freak.  I have experienced that in an ER.

So, who should come back in my room but Dr. M.?  He was clearly on a mission to redeem himself.  I told him I wanted to go ahead and stay the night since it was already 6:00 pm and I could not comfortably hold down solid food.  He agreed and was all smiles and light.

After he left, I sort of slumped into the bed and wished I could disappear.  The only bright spot was that he mentioned that one of his colleagues would be on duty the next day.  That was a relief.

So, was this incident totally because I was treated like an addict because I needed pain meds after surgery?

I don’t think so.

Yesterday was my first day at home.  It was rough, very rough.  In other, more enlightened countries, I would have still been in the hospital.  But that just isn’t how we work here.  I was expected to go home after one night and I stretched it to two.  Clearly, I am some sort of wimp.

So, at some point during the pain and utter misery yesterday, I started to cry again.  I felt like despair, in the form of some horrible black cloud, had descended and landed on my shoulder.  I feared it would not leave.

It is the same fear that I live with every day; that I will hurt and struggle every day of my life, and no one will understand.

But today is a bit better.  I am up and bathed and I did my igg infusion.

The black cloud is still parked right over my shoulder.

I still feel shamed and frightened and alone.  I don’t know how else to feel.  My husband is worn out from carrying my weight this week; I can tell.  I have to get moving.

And yet, what if it rains again?

No amount of Prozac or reading or writing or therapy can make the cloud go completely away.  No drug or movie or book can stop the darkness when it creeps in.

I just have to hang on and pray that somehow, I will make it back out into the light.  I have learned the prayer for healing in Jewish liturgy: Mi sheiberach…

I sing it to myself, “Lord please heal me and let me be one in your spirit.”

Amen.

 

 

 

Here we go ’round the billary tree….

In two days, less than 48 hours, I am going to have a procedure that I have been putting off for over a year.  I am having an ERCP done.

ERCP is where the gastro doc goes in and (this is in the absence of a gall bladder) pokes a hole in your Sphincter of Oddi muscle which is between the liver and pancreas on the biliary tree.

I am looking forward to this because there are little bastards living in my biliary tree.

They have knives and they poke them into me in different ways dependent on their moods.  Sometimes they just hang out in there and apply pressure to the whole area, sort of like a toothache.

Then, sometimes they let up on me entirely and I think they have left the building.

But, NO!  They are just planning an all out attack.  I eat and they all run to my poor forest of bile and start hacking away with knives, screws and whatever else they can find.

One of them, will actually put an arrow in me an pull it in and out, in and out.

I hate the little bastards.  I am hoping the ERCP is the right thing to do.  I have been warned that I could have the opposite result and end up in fiery pain and worse than I was before.

Nice…

No choice now; those bastards have to go…

Watch out you little jerks…you are about to get exterminated!