Tilting at Windmills

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There comes a time when I have to lose the quixotic attitude I have concerning my employment. My capricious ways are exhausting. I know without a doubt this new opportunity is something I need to pursue.

I have spent my entire career in the same health system, and in order to continue to grow, it is time for me to branch out. Yeah, I am scared of going to a new place. New doctors, new patients, new EMR. Then, I remember how lovely the block schedule is going to be. 7- 10 days off at a time. Wow! I am going to have more time to devote to writing, and I just bought a new camera. I want to learn photography.

After spending all these years focused so intently on my career, I have decided I need more. I need to be a whole person. I owe it to myself.

Change is scary. I am leaving my support system at work. I always know who to seek out for advice. They have made a nice work family for me, and I am going to miss them terribly.

Nothing great ever happens if you do not take a chance.

I am going to spend the next two weekends seeing friends and Mudder Buddies. There are a lot of June babies in our group, and I can’t wait to celebrate with them. I never dreamed it would take me 35 years to get some courage. Concerts and Barbecues. It is gonna be fantastic. I think we are meeting up to go hiking with some Tough Mudder Dallas peeps.

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My first picture with my new camera. I have no idea what I am doing, and I need to get some editing software and learn to use it. However, I think it is rather symbolic. There are alway blue skies behind the clouds.

Life is an adventure. May as well explore the possibilities.

West of the Moon, East of the Sun

Outside San Angelo, actually- in Christoval. I love it there.

I was driving home from a job interview 400 miles away from my city, and the journey took me through my hometown. As I pulled out of town, I saw a huge moon rising in my rearview mirror, while the sun was setting ahead of me. It was a stunning sight.

I was reminded of a book I read, West of The Moon. It is about a little boy who is dying from cancer, and the mediation he used required him to go to his safe place. It was a meadow that was West of the Moon, and East of the Sun. He had a guide, who if I remember correctly was a cowboy.

There are lots of cowboys in my hometown.

I love when I get lucky enough to see the moon rising while the sun is setting. It makes me feel centered. Almost like there are bookends around our planet.

There are so many things I am so grateful for. I have been given so many opportunities, and many people have helped me become the person I am. I have had amazing teachers, mentors, family, and friends. They have been my guides.

I can only hope I am able to find new guides while I branch out and learn new skills. I plan to take the lessons I have learned with me, and to be a good example of the kind of person they have taught me to be.

I am so excited to see what the future holds for me, and I can’t wait to embark on the next chapter.

*I should probably stop playing with the photo editing app I have on my iPhone, and actually learn how to edit photos. Right now, all I do is randomly select things and see what they do. I am probably making a mess of it all.

New Adventures

I have finally made some decisions. I am leaving my dream job, and taking a locum tenens position. I want to have time to focus on new hobbies and endeavors.

When I take a step back and honestly evaluate my life up to this point, I realize my career and education have been my priority and focus. I have even gone as far as to make my career the center of my identity.

Frankly, this is a scary step for me. What if I don’t succeed? What if I am not good at this new job? What if I am wasting my time writing? So many questions and doubts.

Then, I remember this is my dream! To have time to write, the means to travel some, and to learn new things. If I consider the situation honestly, this is perfect for me!

While I am going to miss working with the people who have been my mentors and friends through this journey, they are not going anywhere. It is perfectly acceptable to meet new people and to find new experiences.

I cannot wait until I am “ready” to branch out. The time is now. I am excited for my new adventures.

You say you want a revolution…

Well, you know… we all want to change the world. (Not sure why this song is running through my head this morning.)

How did I forget I wanted to be a writer? I allowed stress to interfere with my goals! No more of that nonsense. Back to work.

Life is full of exciting opportunities, and it does not really take much more than an open mind to see what is out there.

How does one go about making potentially life changing decisions? Do you follow your heart and emotions? Do you attempt to objectively weigh the pros and cons of each choice? Do you seek the advice of a trusted mentor? Flip a coin? (and then keep flipping until you get the option you want? 2 out of 3 anyone?)

I am somewhat certain it is a combination of all of the above. The most important thing for me is to simply give myself permission to evaluate the choices. The tendency to avoid change is hard to overcome. Am I selling myself short?

Remember when I kept saying I wanted to go on adventures? If that is true, why do I find myself avoiding them? It is time to see what is out there for me. I cannot allow myself to be complacent. I have too much to do.

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I highly doubt it is going to be as dramatic as rowing off into a foggy unknown. For one thing, I doubt that a boat is actually a good metaphor for my life. I don’t even hang out on boats all that often. (Or ever! I never hang out on boats! I live in a pretty dry place.)

No, my life is more like a winding road. (I do love road trips!) I am ready for adventure. (Don’t worry, the adventure may leave me close to home.) The adventure could lead me to some travels though. I am not committing to anything just yet. I am going to explore all the options, and then make the best decision for my life.

Oh! One more thing. What’s the worst thing that can happen? I make the wrong choice? Well, that will just have to be a learning experience.

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I love Northern California. Stole this photo from:http://www.destination360.com/north-america/us/california/napa/highway-29

 

Right and Wrong and Shades of Gray

As I get older, I am finding it more difficult to self- righteously judge others for their actions. I am seeing a disturbing pattern of people responding the best way they know how (or perhaps even the only way they know how) and trying to find the middle ground. More importantly, I find myself searching for the flaw in the system that led to the trouble in the first place.

The past few days I have been mulling over responsibility within hierarchical groups. Whether we want to admit it or not, our society remains a hierarchy. There are vulnerable people who look to leaders to guide and protect them. This places the burden of responsibility on our leaders.

Remember the movie Flight? I took my son to see it in the theater, and aside from the opening scene, I am so glad I did. It gave me the opportunity to discuss professionals who are held to higher standard of ethical conduct. We discussed the importance of ethical behavior when you are responsible for other people’s lives. It did not matter that the main character of the movie saved many lives, and that no one else could have pulled off the miracle crash landing the way he did. He violated the rules. Do you forgive someone for violating those rules just because he did a reportedly better job than someone else would have done?

Airline pilots are held to very strict standards and the events that took place in Flight are highly unlikely, however it did serve as a handy metaphor for an ethical dilemma for my son and I to discuss. It gave me the opportunity to try to explain public trust, and how you are held to higher standards of conduct when your impairment could jeopardize public safety.

Teachers, medical professionals, law enforcement, transportation workers, and the armed forces are just a few of the professionals who are held to these higher standards. There is a reason we do background checks on people who want to enter these professions. We are hoping to weed out some of the corruption. We are hoping to decrease the chance for tragedy.

I may be a little naive, but I sincerely believe that most people enter these professions with good intentions. I do not want to change my stance on this. I need to believe in the basic good nature of people, and that these professionals want to help.

Sometimes, being of service is a difficult endeavor, and frequently these professionals are subjected to horrors beyond imagination. There is nothing to shield them. This is when they are most at risk for secondary trauma, burnout, and compassion fatigue. There is a whole theory based on this, and there is a scale to measure Professional Quality of Life.

It is imperative that we support our professional caretakers so that they can continue to care for our society. It is time for someone to walk into the gray zone, and offer support and understanding, so that finally there can be healing.

Furthermore, we have to hold our leaders accountable for their lack of protection for the individuals who work on the front lines. We need to have more strenuous reporting and follow-up for the first responders. We need to facilitate a healthier work place, and promote open communication. Instead of telling people to just do their job, and get over the stress, we need to let them have time to debrief and be honest about how traumatic situations affect them.

Secrets are like poison, and while it is understandable that you cannot tell just anyone, everyone needs a safe place and a reasonable sounding board. Everyone needs somebody sometime.

It’s okay. It’s a dungeon anyway.

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Okay, it’s not this bad…

 

I have not decorated my office. I took my already framed BSN and hung it on the wall (my MSN is still safely ensconced in the cardboard tube it came it), put a sugar skull penny bank on my desk, and filled the desk drawer with pens and other random things from my pockets.

Today, they asked me if a new person (who really does need an office much more than I do) could have my office, and if I would not mind moving somewhere else. Of course I don’t mind! It’s a terrible office. It resembles a sauna in the winter, and a walk-in beer cooler in the summer. The walls are a hideous shade of blah, and there is an ancient wall paper border near the ceiling. Well, part of one. We tried to pull it down, and just ended up making the mess worse. (oops.)

Oh, and the carpet? It is maroon, which is oddly appropriate for this space. You get the sense that you have been marooned to the middle of the building, far away from any sign of sunlight. Personally, I would prefer to be marooned on a desert island (well, only if it has a 5 star resort handy with cabana boys to bring me free frozen fruity drinks.)

So, I suppose I am going to say goodbye to my little office sometime in the near future, and I will move to an equally awkward space in the building, at least I did not have to pick the closet. I remember when I started this job, one of the super exciting parts was that I had an office! I felt like a real professional. It took me months to spend more than a couple of minutes in it. It’s lonely and isolated. I really have never been very fond of the room anyway.

However, there is a very small part of me that is a little sad. I no longer have my very own office. Maybe my new space will not have that terrible phone that I do not know how to use. That would be a big improvement.

I do reserve the right to whine about this turn of events, and make the new guy feel guilty at least once a week. Perhaps he will make a gesture of good will, and buy some flowers to brighten up my new corner of the world. (That may be a hint, a certain nurse practitioner who shall remained unnamed, would really like for someone to buy her some freaking flowers.) After all, I am giving away my dungeon.

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borrowed from this page.

 

Medical Advice From Dummies

Okay, I am not calling any specific person a dummy. (Well, I might be doing that, however that is totally not the point.)

I am noticing an alarming increase in the number of internet experts in the world, and in our conspiracy theory soaked culture, we are at the mercy of every armchair diagnostician who cares to impart their great wisdom and prescription for health.

Okay folks, give me a break. I am so tired of reading people’s swill. All of these self-appointed experts who have “done my research,” are actually perpetuating a cycle of misinformed self-righteousness. The exact thing that they accuse the medical establishment of doing.

This article was sitting quite proudly on my Facebook newsfeed, and caused me to waste two hours reading the comments and trying to figure out what on earth all these people were applauding. She was quoting old sources, and most were not from peer-reviewed journals. (I cannot believe I am linking this to my blog- THIS IS NOT ACCURATE- PLEASE, DO NOT USE THIS AS MEDICAL ADVICE- OR EDUCATION!)

As healthcare providers, we seek to provide safe, effective, and accessible healthcare. Evidence Based Medicine means that your doctor is adding to their knowledge base with continuing education, in order to take the best care of you and your family. They collect information about you (the patient) and use those findings to seek answers.They also understand the difference between correlation and causation.

Social media is a dangerous place for sick people. I see things that make me cringe every day. Just look at your newsfeed and read the comments. I feel certain that you have seen this scenario. Someone posts that they have been diagnosed with cancer. Immediately, there are a plethora of well-meaning supporters.

  • You can fight this!
  • Stay strong.
  • My cousin’s aunt had a friend’s husband’s cousin had that EXACT cancer, she beat it by eating the placenta of a virgin. Or some other equally absurd “cure.”
  • Take this vitamin,I do. I did not get cancer.
  • Go to Mexico and get peach pits- they are proven to cure cancer. The FDA wants to hide the cure, so they can sell you chemotherapy.
  • Ignore that doctor, you can beat this if you try hard enough. No one dies from cancer.
  • Read this website- prayer cures everything!
  • Your flu vaccine gave you cancer.
  • Eat organic vegetables. No meat- vegetarians don’t get cancer.
  • Avoid gluten, it gives you cancer.

The offensive thing about all this well- intentioned advice is that apparently, there have been a lot of patients out there who had crappy doctors. They were not treating as a whole person, and their doctor LIED to them! Hid cures! They have been getting money under the table for years! They want you to be sick! Then, they have something to treat! Give me a break. Do people seriously continue seeing doctors who they think that little of?

Most people use anecdotal evidence as their go to for sharing what they understand about a disease. Imagine sitting in a doctor’s office and being told you have cancer. Are you still comprehending everything that comes out of the physicians’ mouth? When you try to tell people about the diagnosis, can you remember everything he said? Probably not. So, what do you do? You go home and google. (I go home and google too. It does not make you a bad person.)

Here is an interesting piece about anecdotal medicine that I think nicely sums up the fallacies of these experiences. Every situation is unique, and it is dangerous to assume that one person’s story of a cure is applicable to you, or even accurate. I hear people say all the time that such and such or so and so saved them. Great! I am so happy you found something that worked for you. That does not mean that it will work for everyone. 

Now that I have expressed some of my opinions about internet medicine… What about the asshats who try to influence you and your medical decisions?

stolen from:http://www.shellshock.ws/wp-content/uploads/2014/01/conspiracy.jpg

 

I have ADHD. I was not diagnosed as a child, and have a complicated educational background as a direct result of no treatment. Now, I am a Nurse Practitioner with an excellent college track record. My son, who is so very much like me, was diagnosed earlier. We knew what to look for. We are not on the same treatment. What worked for me, did not work as well for him.There is no miracle solution, and we have had to utilize tools including medication and dietary changes along with behavior modification.

There are asshats (this dude is a huge asshat, he also dismisses celiac sprue as fake, and I feel certain he is an expert) who judges me for my choices regarding my family’s medical care. They did their research! ADHD is Bullshit! ADHD is invented by pharmaceutical companies because they don’t want to cure cancer or AIDS. My only problem is that I am lazy. Don’t worry, I am sure they will loan me their tinfoil hat. It’s exasperating. If only I were a better mother, I would have sought their advice prior to seeking a professional. Obviously, I failed to google the disorder.

The stigmatization of seeking medical care has become rampant in our holistic- organic- supplement inhaling- DIY- self made man society. (I do believe there is a role for complementary medicine, however it should not replace sound medical advice.)

Frankly, it is none of your damned business. It is a private matter, and it should be left to the patient and their medical team to evaluate. There are a multitude of factors that must be considered, and a proper risk- benefit analysis should be performed. In other words, are the potential benefits worth the potential risk? This should include any treatment options vs. not treating.

As a reasonable, responsible, and rational person you have an obligation to be an informed consumer. This is contingent your ability to discern the validity of your sources. If you honestly believe that your healthcare team is corrupt and seeking to harm you, then you have an obligation to seek care elsewhere. If you feel that your provider is inept, you need a new healthcare provider. It is not rocket science.

Do not use the guy down the street who once knew someone who had a friend who ___ (fill in the blank.) Find a professional.

Here are some tips (mostly for the guy down the street) for offering medical advice:

  1. Just Don’t. (They need to choose a medical professional and seek their advice.)
  2. Tell long stories about how you know exactly what they need to do.
  3. Offer the website for the new miracle cure.
  4. Invite them to your prayer circle because you have provided many cures.
  5. Judge their lifestyle choices and condemn their morality.
  6. Gossip about others personal medical condition, and create an action plan for intervention. They really do need your help, they just don’t know it yet.
  7. Actually, just go back to #1 unless you are an expert (actually, a real life medical professional whose opinion was sought)

Come on people, stop being ridiculous. Stop sharing misinformation. Above all, stop assuming you are an expert because you read something on Wikipedia, Web-MD, some blog, or Fox News. Give me a break.

The hardest extubation

Sometimes people go to a hospital, and we cannot save them.

That is one of the worst parts of my job. The toughest thing is when it is one of your people. This story is one that I have hesitated to write, but I think it is time. My biggest fear is that I will be unable to fully convey what this woman meant to me.

In May, 2011 I am graduating from graduate school. (Well, we were walking then, we still had a summer session of clinical work to do.) I have a great weekend. Angela comes from California, My friend Aneta, who I had not seen in years comes from New Mexico, and we all have a great time. Angela and I stay up all night after my party Saturday night talking. So, the next day after I take her to the airport I am in dire need of sleep.

I did not realize that I had never turned my phone ringer back on. When I woke up later that day, I have missed several missed calls and voicemail from my friend Stacy. She sounds confused and lethargic (encephalopathy sucks.) Then, the last two messages are the worst. Steve (her husband) and Christopher (her son that is a year younger than my son,) have left messages asking me where I am, and that there is something wrong with her. I call their house and get the answering machine. I figure that she is either okay, or that they have taken her to the hospital. I have to be at the hospital early on Monday for clinical time, so I jokingly tell myself, “Worst case scenario, she will be in my unit in the morning.”

The next morning, I walk into the unit, look at the patient assignment sheet, and there is the worst thing I can imagine. Stacy’s name. I am instantly pissed. What is this all about? I look at the monitors, she is stable, so I wait to go talk to her. I am confused and hurt. I do not understand what is going on.

We meet at the opposite end of the unit for rounds. We methodically go through the unit until we are at Stacy’s room. I stand back out of the group. I am not sure of what my place is here. Am I her friend? Am I a nurse? Am I a student? What the hell is my role?

Finally after rounds, I go in to talk to her. I ask her what on earth is going on. She says she did not take anything. She had been complaining of vague stomach pain for several weeks. Nothing too serious. Steve has brought her medicine, and there is the proper amount in the bottles. This was not an overdose or suicide attempt. Now, she is in liver failure. I feel guilty that I did not know that immediately. I just assumed the admitting diagnosis was accurate.

Unfortunately, there is not a lot to do for this. We consult specialists, and they come and offer their best advice. I am not aware of how sick she is. I tell the nurses to please call me if anything changes. I tell them that she is one of my best friends, and that she is like family to me. I go home, do some homework, and fall into bed exhausted. I leave my phone right next to bed, with the ringer on high.

The next morning, I walk into the unit and she is on a ventilator. Things have gotten so much worse. She was having seizures, and was not able to protect her airway. I am furious that no one called me. I cannot say anything for fear that I will make people mad. After all, I still work with these people. I spend a lot of time biting my tongue. Stacy’s friends and family are crowded into the waiting room. I am struggling to maintain a professional demeanor.

These people have known me since I was a (for lack of a better word,) troubled teenage punk. Now, I am updating them on the condition of our friend, My “Momma Stace.” I am confused and desperately hurting. At one point, I go into the break room and have a minor meltdown. This is one of the most stressful events of my life. I am terrified.

I go home and I am sick. I have rarely felt so helpless. That night I do not sleep. Finally, I give up and get dressed in jeans and a baseball cap. I go to the hospital. Every one is gathered outside her room. She is desperately unstable, she is no longer breathing over the ventilator. Her blood pressure is being supported with high doses of vasopressors (and still falling.) It is my worst nightmare. Once again, no one called me. I only got there by chance.

I am frantically trying to ascertain what is happening, and I am trying to wrap my brain around the situation. I knew this was a possibility. Fulminant liver failure is serious. There is not much you can do once the liver is that sick. She had every major organ system failing. We are losing her.

Now, Stacy had been my confidant many times. We had an understanding. She said she would never want to be in the situation that she was in. She would never want to be kept on machines if she was not going to survive. Her death is imminent. Her husband and her family are at her bedside. I have to be honest with them. I have to tell them that she is dying. It is hard enough to admit it to myself. I know she would want the tube out of throat before she dies.

Her husband asks me what happens now. I tell him that we can wait for her heart to stop, and start CPR, and do the horrendous code blue that has no chance of saving her. We can leave her on the ventilator, but make her a DNR- which means we will not do CPR. The last option, the one that I know Stacy prefers, is to stop the machines, and let her go naturally. This option is the scariest one to choose. It feels so final. It means that you are accepting the inevitability of losing your loved one.

After he and I talk in the quiet waiting room, I go back into the unit to stand guard. I feel responsible. I feel like if I loved her, I would do something to save her. There is absolutely nothing to do. We are doing everything, and she is still dying.

Steve tells me his decision. We have to call the physician, and get orders to change her code status, and remove the machines that she is hooked up to. I am reeling at this point. I want to run away and go home. I never want to step foot in this building again. I am seriously considering switching careers. When it is time to remove the tube, I go to head of the bed. Just like I have done so many times as a nurse. She is wearing sunglasses that we bought in the gift shop to hide the scleral edema  that comes with this kind of devastating illness. I do not take them off.

She is no longer here. She has no brain function. She has no reflexes. Her pupils are fixed and dilated. I am still so careful when I pull on the tape that secures her ET tube in her airway. I do not want to pull her hair, or rip her swollen skin. Once the tape is loose, I lean over and whisper in her ear. I am telling her goodbye, I love you, and I am so sorry I could not save you. Once the tubes are out, and I see that she is not going to breathe, I walk outside the door, and Jamie immediately hugs me and I start sobbing.

It does not take long for her heart to stop. She never takes a single breath and she was already hypoxic due to the ARDS that prevented us from oxygenating her. Once she is gone, someone hugs me and tells me that she is in a better place. I am incensed. No, she is not. THIS is the place she wants to be. She wants to be here for her son. She wants to be here for her husband. She wants to be here for me. However, I say nothing. I go downstairs and sit on the curb. I am crushed. I do not know what to do.

One of my favorite cardiologists pulls up, and he knows that it must be bad. He knows her condition was grave,  because I had asked him questions earlier that day. He gives me a hug, and I am undone all over again. I tell him that I hate people, and that they are assholes. He just agrees with me, and offers that perhaps they are just trying to provide the only comfort they can.

After a while, I go back upstairs. Her family is gone. I walk into her room and shut the door. I sit beside her bed, and don’t move. I do not know how long I sit there. I am not leaving. I know what happens next. We prepare the body to go to the morgue. I hate that part. I will spare you the details.

I do not want any of this to happen to Stacy. So, I sit there. Finally, Tracy walks in and convinces me that it is time to go. She promises to take care of her. I finally go home. I take several days off that week, and stay home until after her funeral. Several of us spoke. I agonized over what to say, and if I had it to over again, I would do it better. My mother helped me arrange for flowers, and I had a ribbon placed on it that said, “My Friend.” She was MY friend. I was bereft and inconsolable. My life had a huge gaping hole. I did not think I would ever feel joy again.

I have struggled with this situation for years. I have read about liver failure and I have experienced regret and sadness. I have grieved for my dear friend a lot. Whenever I have a patient with this condition, I feel sick to my stomach, and I am bombarded by the grief all over again.

You see, Stacy was a very important person in my life. She had been a high school english teacher, and she was helping me get through some of the books that I had missed by not finishing high school. She would discuss them with me, and she helped me process what it was that made the book “important.” She and I had been close for many years. She and Debbie were two of the small number of friends that I had to come to my baby shower. She was very much a mentor, and a confidant. She had seen me grow from an obstinate, rebellious teenager into a responsible (mostly) professional.

She was one of my closest friends. We talked almost every single day. She was the one person I wanted to talk to about my grief and she was gone. I was also hurt that my coworkers had not called me when she started to do worse. They had promised me that they would, and I felt betrayed. It took me a long time to forgive them. Her friends and family assumed that I had been called.

I finally realized that the nurses were busy trying to take care of her. I had no justifiable reason to be angry. So, I forgave them.

To this day, I still tremble a little when I am removing the tape that is securing someone’s life support. My heart races, and I have to take a deep breath and banish the thoughts of that night. I have to focus on the task at hand, and not allow it to be about my grief. That is my responsibility, and it is the best way I can honor her memory.

Writing is the other way I pay homage to Stacy. I imagine that she would have been one of my biggest supporters, and likely would have been willing to offer grammar advice and maybe even some editing. She invested a lot of time and effort in my growth with language. She listened to me prattle on and on about whatever paper I was writing. She wanted me to succeed.

It took a while, but I think it is getting better. I am no longer a student, and I work in the same unit I worked in when she was my patient. Stacy would not have wanted me to give up on my dream of this position. She would have wanted me to be every thing I ever dreamed of and more. I owe it to our friendship to be the best person I can.

I have managed to find joy. I am very happy in my life. There are so many things that I still get excited about. I love a great many people, and I have a group of wonderful friends. I have a family that loves and supports me unconditionally. I have a job that I love. I am learning to write, and I am obsessed with it. I love the process. I want to do more. I want to live my life to the fullest. I cannot allow myself to become bitter and unhappy just because I am sad that my friend died. That would be selfish.

This is one of the reasons that my profession is so difficult. We eventually run into a situation that is personal. One that we cannot escape. We know the course that these situations often take, and we are facing a helplessness that is brutally painful. It can cause you to question your worth. It can make you doubt your abilities. It takes effort, time, and patience to work through all those feelings.

If you are lucky, you find peace on the other side of grief, even if it is after the hardest extubation.

The Danger of Caring

Medical Professionals are an interesting breed of folk. We are not immune from tragedy striking in our personal lives, and some of us are subjected to a constant bombardment of reminders when we go to work.

I love what I do. I get to hang out with the most eclectic crazy group of people almost every day, which allows me to cope with the sadness that comes along with my job. We develop coping skills over time, and eventually we learn how to watch other people suffering with an objective eye. We would not be able to return day after day if we could not keep everything in perspective.

For many of us, laughter is indeed the best medicine. We are full of inappropriate humor, and while it may seem insensitive to some, it is actually just our way of processing the horrors of ICU, and remaining sane. We develop little rituals and we have a plethora of superstitions. (You never say the Q word, observe how slow the unit is, or mention that frequent flyers name.) We trade war stories, and we collect memories that we can use for a quick laugh.

When our loved ones are patients in our hospital, or worse in our unit, the nice little boundaries get blurred. The personal and professional worlds collide, putting us at risk in every area of our lives. It is imperative to remember that we are only human, and it is okay to feel powerless, and to acknowledge our fears. We do not have to be the professional when we are indeed- the family.

I have had this experience a few times throughout my career, and I will remain forever grateful for my coworkers who allowed me the space to be a family member instead of a nurse or nurse practitioner. It helps.

Good Riddance.

Ok, thanks for that Buzzfeed. You gave me yet another totally inappropriate idea for a blog post. (Mom, you probably will not like this one.) But, I have some plans for my funeral. No, I do not anticipate it is going to happen anytime soon; but, one can never be too prepared. Not that it really matters: I am not even going to actually be there. I want my friends and family to have a good time though.

Okay, let’s get the messy stuff out of the way first. Do not bury me. Seems like a waste of space. I would like to be cremated. AFTER you donate anything at all usable to whatever tissue, eye, or organ bank wants me. This is important to me. Organ donation is not always possible for everyone who dies… but, in the situations where it is- I feel it is the only way to go. If I am not a viable candidate that is okay.

Oh, wait. I forgot- this is supposed to be funny. Let’s skip anymore organ talk. Just know I am a registered donor. Now, what to do with my ashes? You can scatter a few of them here and there. Maybe save a small box of them to throw into the air at birthday parties or something? (Is that weird? I want to still BE there!) But, I really want to be turned into something. Maybe a diamond. Can they make them pink? Let me go look. Be right back.

Skip ahead about 6 weeks. I got distracted while I was researching the whole diamond thing. Turns out they are blue. It has to do with Carbon or something.

Okay, now for the fun part. It’s really a shame I am not going to be there. I am imagining a huge party full of my friends and family (hoping they are all ancient because we lived so long.)

Hey. You know what? Planning my funeral does not sound as interesting as I thought it was six weeks ago. (Who does that?) Apparently, I do.

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Stock photo of stars. http://fc00.deviantart.net/fs70/f/2012/194/5/b/stars_stock_by_euderion-d572x76.jpg

Seriously though, I work in a hard profession. We see a lot of death. This may be part of my preoccupation with it. It’s kinda funny, I have scrapbook upstairs in my office from when I was a kid. There is an unusual number of death notices and obituaries in it. So, maybe I have always been preoccupied with death.

One of my biggest concerns is that something will happen to me, and I will have left something important unsaid. I do not want anyone to wonder how much I loved them, or what an impact they had on my life.

I don’t believe in an afterlife. So, that means that I have to make every day count. I do not want to be filled with regret in my life moments of life. I want to know that I lived.

There is a part of me that wants to know that I made a meaningful difference on the world while I was here. I know, that sounds rather self-important. I do not mean for it to. I just want to help people. It is not fame or money that I seek… (although- some money would be nice.) I just want to look back on my life and to know that I did the best I could with what I had, and that I used my particular skills and gifts for good. So, maybe I want to be a superhero. I wonder what my superpower would be.

To sum it up. When I die, please do not do all that embarrassing funeral stuff. Go to a bar- ask for a whiskey on ice. Top shelf- not that cheap crap. Listen to Green Day’s Good Riddance- and sing along with all your heart, because I promise you- when I was with you, I had the time of my life. Take care of my family and friends. Please, please, please- make inappropriate jokes and make everyone laugh uncomfortably.

I promise, I will do everything I can to live a long and productive life. I will live without regret. I will seek adventure every day. I will love with all my heart.

*** now, for those of you who think this is all macabre and sick- understand- I believe people only fear death because they have not fully lived. I intend to live life fully.