I usually take my notes digitally so consider handwritten notes as an indicator for me not getting a topic. 📚🌻
xxx Lux

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YOU ARE THE REASON
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@notladygodiva
I usually take my notes digitally so consider handwritten notes as an indicator for me not getting a topic. 📚🌻
xxx Lux
dnf.n The way life goes ☠️ Los Angeles, California
Coming full circle
In the midst of this coronavirus pandemic, as our positive cases continue to climb (and our unresulted tests do too), I had a patient today come in for something unrelated.
He’s an older gentleman, in his 80s. He had some abnormal lab tests last week - a double-digit bilirubin, and a quadruple-digit alk phos - for which his cardiologist stopped his amiodarone. He saw his PCP today who saw the labs, looked at his newly yellow skin, heard his complaints of fatigue and poor appetite (but no pain), and had him directly admitted to the hospital - to me.
For those med students reading, he sounds like a textbook case - pancreatic cancer.
For me, he sounds like my mom. She was admitted to the hospital for back & abdominal pain and weight loss. Her GI doctor called me, a state away in my last year of med school, and told me to come to the hospital. I get there, 3 trains and a taxi ride later, and see the hospitalist has left her number. I call from my phone, and with the poor reception in the hospital, all I can make out is “pancreatic malignancy.” My mom is sitting on the bed, a foot away, and I don’t know if she knows this yet. So I ask, “Is that what you think this is?” and hear a definitive “yes.”
I hang up the phone, and turn to my mom, and ask her, just like I was taught in med school, “What have you been told about what’s going on?”
She tells me, “They think it’s something with my pancreas, it might just be inflammation.”
I tell her, “Mom, they think it’s cancer.”
She cries. I cry. Neither of us stops crying for quite a while. Her first question for the oncologist is, “Will I make it to her match day and graduation?”
They tell her yes.
They were 50% right.
Between all the chemo, the nausea and vomiting and diarrhea, the begging her to eat, the intolerable side effects, the second line chemo, the failure of the second line chemo, and finally, finally the decision to do home hospice - and all the horrors we dealt with therein - I still think the most awful part was having to tell my own mother that she had cancer, because none of the doctors who saw her were willing to do so.
And now, almost two years later, I look at the man in front of me. He knows he’s doing poorly - he described the last two weeks as “a steep decline, like a ski slope.”
I ask him, “What have you been told about what’s going on?”
He tells me, “My doctor thinks it’s something with my liver or my pancreas. Some kind of rubin?” - I smile, say, “Bilirubin” - “Yeah, that’s it! Anyhow something with that so he wanted more tests. I don’t know if it’s my liver, or if it’s cancer, or what.”
A small part of the knot in my chest unwinds. I explain, the best I can, about how there’s something blocking the flow of bilirubin, which is why it backed up. “It could be a stone from your gallbladder, but usually you’d have pain then; that’s why we’re worried it might be cancer, maybe in the pancreas, blocking the bilirubin and causing these symptoms. That’s why we want to get this CT scan, to see what’s going on, and it can show us if there’s a cancer.”
He nods - he has an excellent primary care doctor, and he wasn’t blindsided by the news. He starts to ask a question, then stops himself, and says, “I’ll wait til we have more answers. Thank you.”
He’s here alone. We have a 0 visitor policy because of the Covid19 pandemic. I’m wearing a mask, hiding half my face, because I’m worried I’m asymptomatic but infected and don’t want to spread it to any of my patients.
But at least I told him the truth. I didn’t keep him in the dark, or dance around the diagnosis.
I’ll see him in the morning. We’ll have some answers then. And he’ll have more questions, and I’ll give him all the answers I can. I can’t do anything else.
080419/
What a mess.
We intubated a 35 year old here.
I can’t wait to be off this rotation. Except we’re looking at cancelling electives for COVID coverage so there’s that.
It’s surreal because I feel like I’m getting thanked in every direction for being like this ‘brave’ person on the front lines but I’m terrified. I get chest pains rolling up into the hospital garage everyday. This used to be my favorite hospital and now I’m so sad to even be a doctor. I just want to hide away with my family and be safe.
I know what you mean.
I don’t feel brave. I appreciate the support and praise but I just feel like a mouse holding a needle as a sword, going up against a dragon. And I know that we aren’t even in the thick of it yet. Part of me feels like I haven’t earned that praise, yet. Because the worst is yet to come. And because I’m just a normal woman doing her job. Her job just happens to be looking after sick people and sometimes saving lives - but I’m human, all the same.
This is the job I chose. And I knew that if a pandemic happened, I’d be on the front line- it was something I’d thought about.
But we aren’t immune to fear - we aorry abput our loved ones and our colleagues and our patients and sometimes ourselves. I have already mourned those who will die. I have mourned all the times with loved ones that I will miss over the next few months. I mourn the fact that I can’t be with them.
this!! I’m starting work earlier than usual because of the crisis and I’m more worried about not getting my family sick than anything else. I don’t want to be “thanked” for being on the frontlines. This is my job. What I want is for the government to do their damn jobs and make sure we have equipment, and for people to stay home instead of frolicking at religious events. ugh.
please stay safe, all of you! thinking of all my colleagues, online or not <3
Art by Josh Newton
Perfect Sunday combination- Anatomy , heavy rain outside , warm tea & piano in the background ❤️ 🎹
quick, tell me the weirdest compliment you’ve ever gotten. my doctor told me i have impeccable eardrums
my dentist once told me (in an appreciative tone) that i have huge neanderthal-like canine teeth
oh i AM losing my mind over this
I have frequently had doctors complain to me that I have tiny ear canals and like
I don’t know what I’m supposed to do with that information besides apologize for providing a subpar patient experience?
When I had surgery, the anesthesiologist had me open up my mouth so they could “see what they were working with” when they intubated me and they were like “oh nice, lots of room! [assistant] come look!” And the assistant came to look down my throat and was like “nice” 😂
My wife, when we were first dating, told me I reminded her of a walrus, you know, a really pretty one.
a dancer once told me i had beautiful achilles tendons. (they are v long, i think. i have always been able to squat with my feet flat on the floor with no practice, which is unusual for americans.)
my doctor told me that my blood pressure is excellent, like yes i’m young and healthy but i have blood pressure out of a medical textbook, and i told my mom that and my mom said oh yes, you have genetically perfect blood pressure. you inherited it from my side of the family.
A mortician told me my skintone is so pale I’d be a pain in the ass to embalm
A yoga instructor complimented me on having “stretchy hips” - I’m not overall flexible I just apparently accidentally trained myself to be a master of all hip opening yoga poses by sitting in the weirdest ways possible at home.
My sonographer exclaimed that I have “the cutest little uterus” while giving me an ultrasound.
I once went to a doctor for hip pain, she proceeded to lay me down and stretch my legs all kinds of ways, going “wow you’re so flexible, I guess you’re fine”. I’m hypermobile.
I have excellent veins. “Very juicy,” said the nice totally-not-a-vampire nurse taking my blood for a hormonal panel.
a hairdresser once got legitimately aggrieved with me because my hair follicles are densely packed (as though if she frowned hard enough I’d relent and space them out properly?)
Obstetrician said I had ‘an extremely functional pancreas, even under challenge’ which I guess was a pleasant surprise.
A resident looked at my fingers and said in total awe “wow I have never seen such a thing” and then he proceeded to caress them (in a very nonsensual/nonsexual way)
I have hypermobile joints and I’m literally unable to keep my fingers not hyperflexed.
Basically the UK for the next three weeks.
My university program is still open for business. We get to do our practical assessments and take part in clinical work and everything else is online. I’m doing well with the whole thing.
I’ve got my dissertation lined up and will be able to do all the work from home since I designed the study that way. Not for the sake of viruses but since we had plans to move.
Today is all about vertigo, otology and neurology.
a shoutout to all the medical students at the moment. speaking from personal experience it’s hard to spend all your time studying infections and medical complications as well as having the entire world and media at the moment focused on coronavirus
you’re doing well and will put all your knowledge to use one day, thank you
also you shouldn’t feel like your entire life is medicine at the moment, take some time to not think about it and the current events
I matched to Internal Medicine!
A VERY delayed post, but important nonetheless!
I dropped down to my #4. I said I’d be happy at my 1-4, and I am! It’s a great program that supports its residents, has the fellowship I want (I think, can’t totally tell because the website is trash but I’m pretty sure), and most importantly, allows my SO to keep his job and stay close to his family!
I am disappointed that 3 other places passed me up (I expected my #1 to). I did read that my #2 is one of the hospitals that isn’t allowing staff to wear their own PPE/masks, so that makes me kind of happy. My #3 was closer to my home, though, and I would have loved to finally be close to my family. It is in a not so great city, though, and probably on the same tier as the one I matched to, if not a bit higher. I am also dealing with feelings of jealousy from those who matched to their #1 and others who matched to better places than me - most I’m excited for, but I can’t help but feel this way. Trying to figure out a way to process this.
Regardless, I am excited to be going to a program where I think I’ll thrive and have a happy SO. It’s very much a non-malignant program, which is perfect for me. It’s also a short drive from my med school, so I don’t have to move cross-country. I’m glad I have a job, and that all of my own personal trials and tribulations have paid off. I’m also trying to keep in mind that my struggles are different from others, and I had a relatively less privileged standpoint from most in med school (parents w/o a college education, first gen US).
I’m trying to be proud and excited, but I’d be lying if I said it was overcast with feelings of being “less-than” and “not-enough.”
I am so happy for you!!! Getting your #4 is still such an achievement! :D
Unknown nurses, Sweden.
60 days to my final exams 🤠