Episode Transcript
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Hi, this is Dr.
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Soma.
Just a disclaimer, this podcast is for informational purposes only and isn't intended as medical advice.
Always consult with your doctor before making any changes to your diet, exercise, or health regimen.
Let's go to the show.
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Being treated as a human feeling, listened to, and heard and seen.
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To me, that's better medicine than anything that we can do in terms of prescriptions and things.
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It's really about how can we preserve the humanity so that people.
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Whatever the course of illness is they're feeling like human beings and not just Yeah.
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A science experiment.
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There's a lot of help out there and with serious illness, people feel so isolated and alone.
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that breaks my heart.
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I would rather.
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Connect people so that you feel like we're all in this together.
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Anne Front is a licensed Marriage and Family Therapist and Advanced Palliative Hospice Social Worker specializing in grief, serious illness, and caregiver support.
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Drawing from her personal experience as a cancer survivor and spouse of a cancer thriver, she offers compassionate, holistic care through her private practice in Studio City, California and via Zoom.
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Anne is also a published author, educator, and the voice behind TikTok’s “The Palliative Therapist,” where she shares insights on navigating life’s most challenging transitions.
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I wanted to officially welcome you to my podcast today.
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we're talking about palliative care.
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It's a topic that, frequently comes up in terms of my own patients.
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And unfortunately there's a lot of confusion on the part of not only patients, but sometimes the doctor about, what palliative care is, how it works, how it differs from hospice So I think this will be a great podcast, to educate people in general, tell us about yourselves and how you basically got into focusing on palliative care.
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Okay, so I'm a psychotherapist and I've been in the field for over 30 years and I've always taken approach with my career that just say yes because you never know where it's gonna go.
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And so it's led me on this circuitous path to getting here.
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I was working in a behavioral health inpatient program and I got really bored.
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It was just like if I told somebody one more time, you matter.
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Life is worth living.
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I was like, I'm gonna kill myself.
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So I switched to working in the medical side and I was doing a lot of case management.
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And I was transferred to the ICU and I had a patient that was in his nineties.
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The adopted son was having a really hard time making decisions about shifting to comfort focused care.
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And I was really working with him on the importance of making decisions is, do we really want chemo and radiation and escalation of care where his heart.
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Was at high risk of stopping.
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So son could not make a decision.
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He ended up, the patient ended up coding and there's these big guys, doing CPR on him and you're hearing the ribs crack, it just felt like an assault to this guy that could have had a really peaceful death.
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And it just broke my heart.
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And I think just still hearing that.
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And seeing that image fuels me that this is really important work and that we have a better better options to die.
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We, a lot of people don't wanna think about dying, but we don't really have a choice.
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And as our the sort of the sandwich generation as we're seeing our parents or the older folks in our lives.
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Having, we're having to make decisions for them or they're making decisions about how to die.
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and I think our generation that, what is the option? What's the bigger picture here and how can we remap the way we want our, our end years to be.
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I agree with you.
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This is always a tough topic for me.
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One of my favorite patients just passed away a week ago.
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I believe she was 95.
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And my most favorite patient is currently still alive, and she's 103 at this point.
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But.
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When it comes to end of life and advanced directives, it is a topic that I always talk about with patients whether they're 25 or they're 95.
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Because it's really important to know what your wishes are.
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What you would like us to do or not do, and that may include everything.
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But what I often find, Anne, is that even when I go through all of that, sometimes it amounts to not having any Effect at all because something, dramatic happens and I'm like, I thought we decided that, we wouldn't be doing all these things.
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So do you find that with your patients? Yes.
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It's really hard because as you're in a medical crisis, it's like.
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I don't know a lot about biology, but it's like we have this natural want to be alive.
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Maybe it's a, survival instinct.
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And so when somebody says you're having a harder time breathing, or you're needing more medical support, what do you wanna do? I think the natural inclination is, I don't wanna die.
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I don't wanna give up.
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I don't.
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I still wanna be here.
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And so all of the planning for the future just gets thrown out the window.
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I think, this is where we could talk about how palliative care can be really helpful 'cause you're building that relationship over time, particularly in the outpatient setting.
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But also I think when you're in those critical situations, like as the.
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Primary physician setting, all those things up.
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But in the moment when the person's dying, you're having specialists say, do you want this or do you want that? And the kidney doctor says, your kidneys look great.
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You're gonna be living a long life.
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And the heart guy is saying, this isn't looking so good, but we could try A, B and C.
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People tend to grab onto the positive news, not really looking at the whole body.
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And that's where I think palliative care can be important, but also just the language.
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I mean it's a lot of it's the patient and the family and just unpacking that stuff.
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That why are we clinging into life when, you know the person is so sick.
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But for the providers, the healthcare, it's really making sure our language is clear.
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Or do you want everything you know, or what do you want? It's everything could mean transferring from the hospital to home with hospice, where you're getting care and support and your family can be there.
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Or it could mean, going up to the ICU and getting on machines and things, and people don't always play out.
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The scene.
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I have a patient right now that I see in the nursing home and it just, every time I see him, it breaks my heart because he wanted, everything when he was in a critical state.
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He ended up having a stroke and now he's on a permanent tracheostomy.
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It's like this is what life looks like.
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Parent family may have come every day or every week and now the visits get slower.
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And I don't know, that's not quality of life to me.
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But when we say, do you wanna do everything, it's assumed yes, because I'm gonna get back to being the person I was yesterday and that's most of the time not the case.
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Unfortunately, you're right.
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Maybe you can educate my listeners because I think I see this a lot in terms of patients where when you bring up the words palliative care versus hospice care they don't necessarily understand the difference.
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And often when you use whichever words interchangeably, they often think it, you are basically saying that.
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Everything will come to a stop that nothing will be done for them.
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So can you educate us about what palliative care is and how it differs from hospice care? Yeah.
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When I was working in the ICU, we had the difficult discussions in a conference room.
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And so I had a patient that was like, I'm not going in there.
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I'm not going in there.
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And it was this idea that if we talk about.
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Goals and what's important to you that this means we're giving up and this means you're dying.
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Whether or not the doctor's saying you have that prognosis, you guys are keeping stuff from me, and that's what's really happening.
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So it is important to have a definition of what palliative care is, beyond what end of life care is.
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And if you think of palliative care as overarching we're working from initial diagnosis.
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Straight through to end of life.
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And hospice is a small part of palliative care, but palliative care is that whole spectrum.
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So a lot of my patients are coming in newly diagnosed with a serious illness.
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We say that you have to have a life limiting or life altering diagnosis.
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So for example, cancer.
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Is a life limiting disease, but with all of the interventions, you can live with cancer for 20, 30, 40 years, or you may not even die of cancer, but just to qualify it, it is a very serious disease that has a trajectory.
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So a lot of my patients are newly diagnosed.
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Sometimes going through chemo or radiation and having symptom burden, whether it's the physical part of the chemotherapy or, nausea, a lot of pain or if there's the psychological part, it's just very emotional.
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And I'm a cancer patient.
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My husband has metastatic cancer, and it's just been an hugely emotional journey.
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Some parts are traumatic, just being poked and prodded and worried about your.
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Your lifespan.
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So there's that whole emotional and existential part.
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And getting palliative care early on can help address some of that distress.
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And as the cancer, or the serious illness progresses, like with my husband, he's non-curative now.
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It's in his lungs, it's in some of his bones.
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So we are having to revisit.
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Yes, you probably have a long life.
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Yes, there's a lot of interventions, but let's start preparing ahead of time so we don't have to make those rush decisions.
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And it also helps families in the end because we've had those conversations, we have that relationship with the patient and the family.
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So that we can say, let's go back to what we talked about a year or two ago.
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Let's go back to who you were 20 years ago and what was important to you.
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And now we're in this critical thing where we say, yes, I wanna do everything.
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But let's go back to that logical piece.
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And that's where developing the relationship with the palliative care team is so important.
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'cause we can get you back.
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Let's look at that whole picture, not this critical event.
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So I'm sorry to hear that.
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about your husband and you mentioned that you also have cancer.
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I had so he was diagnosed in 2019 and then 2020 hit when Covid wrecked our world.
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And then I was diagnosed in 2021 when the world was opening back up.
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I have, stage one breast cancer.
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So I had radiation, I had surgery and I'm in, we call it no evidence of disease or in remission.
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So mine is wrapped up other than medication.
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But it's been an interesting journey 'cause I'm working with cancer.
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I.
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I've been through it and then really seeing my husband through more of a palliative care case.
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We, with palliative care, oftentimes we work with new diagnosis.
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A lot of people stay with us in the middle course of the disease.
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'cause you're dealing with the physical symptoms you're dealing with.
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Planning for the future and the emotional and the spiritual part of it.
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Can you describe what your own experience has been? As long as you feel comfortable, obviously.
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In terms of palliative care, has it been like a group of people that have helped you? So my listeners understand 'cause a lot, again, a lot of people get confused.
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And they think I'm just writing them a script of, sending them to their deathbed when I'm not Right.
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So can you share that experience? What kind of people have you worked with under that palliative care umbrella? Yeah, and that's where we get that all the time and the importance, I think for your listeners, if you have a question just.
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Get more education, just talk to a palliative care program.
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You're not gonna get jinxed.
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It's not gonna mean that, you know the universe is gonna go against you, but just really trying to understand.
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But with my palliative care patients, basically we're an extra resource.
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We don't replace any of the other physicians.
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We're just an adjunct to that.
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I don't know the Latin word, but basically the word means to cloak to provide that extra support.
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So when we're coming in, we're like, let's treat you as a person, not as a, as a patient.
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Because if most of the times when you have a physician visit, you're coming in for 15 or 20 minutes, you're very focused on the physical, you're out the door, you get in the car, you have a bunch of questions you forgot to ask.
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palliative care is whoa, let's step back.
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Who are you as a person? What do you do for a living? What's your family like? What's important to you? What are your priorities? What are your hobbies? And as we get to know you as a person, it starts to make sense what the treatment options are for you.
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So if you're 95 and.
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You maybe love your garden and wanna be at home.
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Palliative care can talk about this is the advantage of hospice maybe, or this is the advantage of not going back and forth to the hospital.
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If you're, in your forties or fifties and you're working and you have high productivity, you're taking care of your kids, you're probably gonna want.
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Pretty aggressive interventions because you know there's a good likelihood of getting either back to where you were or to at least to be able to do things that are important to you.
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So palliative care, the first part is really getting to know you as a person.
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And then based on that, what is quality of life to you? And that's different for everybody.
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A lot of my patients have, they come in with pain or high anxiety.
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And sometimes other symptoms like bowel issues or nausea or things.
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So sometimes the first priority is let's get you physically feeling better and the palliative care physicians or nurse practitioners or specialists just in symptom management.
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they're not gonna.
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Prescribe radiation or prescribe, cardiac rehab.
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They're just simply there to say, how are you feeling and how can we medically address so that the one doctor's not giving a head of medication.
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The other is I.
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Giving a different, like how are they interacting? What are, what is right for you? So managing that, and then once we get the physical part, oftentimes the emotional part comes down.
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I had a patient just last week that was all physical and the chaplain and I were also in the room and we're just sitting back like, we don't know what's going on.
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We don't know what to talking about.
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And, he physically was just talking about all this nausea and pain.
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So then the doctor and the nurse did their part and the chaplain and I start talking like, how are you feeling? Like, how is this making sense to you? So then all of us had a discussion about, wow, we didn't know you did that for a living, or, we didn't know your kids were nearby or whatever.
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Started having this conversation and at the end of the session, he was like.
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It's so weird.
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I don't feel nauseous anymore.
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Like my pain feels better, and it was like.
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Being treated as a human feeling, listened to, and heard and seen.
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To me, that's better medicine than anything that we can do in terms of prescriptions and things.
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So that's palliative care.
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We slow it down.
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We try to get to know you as a person and then find out what your goals are, what your values are, so we can say in the lens that we know your.
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Your illness is going to progress.
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Let's plan for this.
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So we don't lose the humanity in the process.
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The nature of your practice, do you work independently? Do you work with a group or a hospital system? I'm just trying to understand how you function.
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And then also educate us.
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What kind of specialists would you be seeing in a palliative care team? so palliative care exists across settings.
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So in the beginning stages of palliative care, it was a lot of inpatient medical making critical decisions.
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And then it really evolved to my team we're outpatient.
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So you would get a physician and, physician order, and then you would see us the first visits like for an hour.
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And then we do monthly follow ups for a half hour.
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Sometimes our patients are getting more and more sick and it's hard to get out of the home.
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They're needing more eyes on.
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So then in home palliative care becomes an option.
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so it's various settings.
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And then there is palliative care in nursing homes too.
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My team in the outpatient setting, we have a physician we have a.
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Director who's a nurse practitioner.
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I'm a social worker therapist.
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We have a chaplain on the team and a nurse.
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And so we all have our own specialties, the nurse and the doctor or the physical.
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I'm more of the emotional, the chaplain is spiritual and existential, but we overlap because if we're gonna have four different meetings, different things are gonna come up and they don't always connect, but like with the patient with nausea.
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And pain, I'm guessing he had some anxiety about meeting with us, meeting with this four people on a team.
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one minute we're talking about pain.
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The next minute we're talking about anxiety or depression, and then we're going into, I feel punished by God that this is happening to me.
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Or how do I make meaning because, I feel like my life has changed because of this.
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So it's like these wormholes that are constantly, talk about one thing we get to somewhere else, and then as things come up in a more natural conversational flow, then you get to the bottom of it.
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Like people won't even know what to ask or what to say, but then there's certain clues that we'll say oh, okay.
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Maybe this is the issue and then we can present it and cross work together on that.
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So all of us have our specialties in within that group, but we also have training so that we overlap.
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So if the nurse isn't there, I have enough knowledge to say, okay, this sounds medical.
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Let me get the physician, the nurse involved, or if it's emotional, like trouble caregiving burnout or trouble accessing resources.
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Okay, let's move that to them.
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But there's a basic knowledge.
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Some of the.
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Teams in larger groups and things have palliative medicine, not necessarily the social worker or the chaplain involved.
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And so sometimes people get a referral to palliative medicine and it's important to ask are there other resources like either embedded in the team, the social work and the chaplain, or at least have some adjunct resources outside of that group.
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So we've talked a lot about palliative care educate us as to what hospice care is.
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So hospice is a service that really you're bringing the medical piece into your home.
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A lot of people think that hospice is a place that you go to.
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In some states, in some places there's hospice homes that you can pay for, usually privately.
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But generally hospice comes to you wherever you're at, whether if you're in a nursing home, if you're in assisted living, or you're in your own home.
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So hospice is generally prescribed based on Medicare guidelines as having a prognosis of six months or less.
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I have patients that have been on hospice for a couple years or even longer.
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But generally if we say the patient has a prognosis, if they had no curative focus treatment, it wouldn't be surprising that they would be at the end of life in the next six months.
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Hospice comes in where, like palliative care, you have a physician, you have nurse practitioner, social worker, chaplain nurse, and they come in and provide the care.
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They also provide, it's a bundled rate.
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Hospice comes in as a bundled rate, so they provide everything.
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So you have a crisis in the middle of the night.
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You don't go to the hospital.
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The nurse comes to you within an hour or so.
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They provide all your medications.
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They provide equipment like a commode or hospital bed or things, so that the goal is to keep you as comfortable as possible in the home.
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this is a really helpful benefit for people that are really like, I'm just going to the hospital all the time, or I'm having a hard time getting outta bed, but I need to go to all these specialists and it's not changing.
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I'm still on a trajectory where I'm at the last chapter of my life.
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So how can I have the best quality without trying to chase things that aren't gonna be cured? So it's an excellent benefit.
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And my frustration and probably yours, is that people don't.
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Allow for hospice until it's so late that they are in the dying process.
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Because I don't want hospice.
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This means I'm giving up.
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It means I'm gonna die.
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And so people wait to get on hospice and then they die within seven to 14 days.
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Every time I have a patient that starts.
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Sooner when hospice is recommended, they say, I wish I would've done this sooner.
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This is what I want.
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This is what's meaningful to me.
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And then that's where we're making the right decisions to have a peaceful death for that person.
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Rather than like my patient I discussed before where you're in the ICU and escalating care that probably they didn't really want.
245
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Thank you so much for sharing that, because I think that will actually help people understand the difference and also practitioners, because I think, there's confusion amongst people who see patients about what the difference is and when it can be useful for people.
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Obviously the palliative care provides.
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A holistic approach for patients.
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You were mentioning a patient that, you visit who had, who wanted everything and ended up having a tracheotomy and is now in a not so great situation.
249
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How do you talk to your patients about quality of life? Because this can be a very sensitive topic and.
250
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I often run into confusion, not just from the patient but from the family members as well, because the definition of quality of life can be different for the family member who is taking care of the patient possibly.
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And the individuals quality of life.
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How do you approach the patient and or their family members with that? And sometimes it's the same and sometimes it's different when you have a patient that's able to speak for themselves.
253
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I have a lot of patients with neurological issues like dementia, and so the burden is on the loved ones, the caregivers, to make those decisions about what quality of life is.
254
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But I think it goes back like today, what is quality of life to me as a 56-year-old? When I look at my future, how do I wanna live my final days? And then when a person gets to a place where their illness is really advanced, really evaluating.
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Who was Anne when she was 56? What was important to her? What things have changed? I imagine the end of my days watching prices, right? Eating potato chips, doing whatever I want.
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I do not wanna be in a rehab, exercising.
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I don't even wanna do that now.
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So that's I'm guessing that'll be my course as much as if that's a possibility.
259
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So remembering again, like who is that person? I have people that I.
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They're like, we just like being in the house and looking at the garden and I'm not asking for a lot.
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And other people that are like if I can't go to the gym, if I can't go to the senior center, be around other people, be talking, be connecting, then that's a different qual quality of life to consider.
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Because if I have a stroke and I am laying in bed and I can't communicate, I can't recognize my family.
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Would that be quality of life? And so having those conversations and just reflections as family members or the patient helps remember, let's put this in context of a person, not the patient, not the interventions.
264
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Because when you go to the hospital, when you're dealing with a lot of doctors, you're looking at what can we do to cure you? What can we do to extend life? And then you become a body, not a full, fully rounded person, right? That's where we look at what the quality of life is.
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And then within that, what's the story of your illness? Where your treatments, how is this looking if I take chemo and radiation, what does that look like for me in six months? Am I going to be.
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So sick that I'm gonna go in the hospital and I'm still not gonna be cured.
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That my illness is gonna get worse and maybe even more painful because of all the side effects.
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Or is it gonna be really bad now? But if I, white knuckle it through in a few months, I'm gonna be back to where I wanted to be.
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That, it's understanding.
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The medical perspective of where we're going.
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And then the other part, what's important, I had a, an oncologist that would say, let's just kick the can down the road a little.
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And I was like people aren't cans.
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And then, so then offline, the palliative care said what does that mean to kick the can down the road? Very.
274
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Very bad symptom issues.
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It'll give her another month.
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how do I want my last month to look like? If I know that either way I'm going to die? Do I wanna be in all this craziness of treatment and not feel well? Or do I want something like hospice and be comfortable and have time to say goodbye to my family in my home? quality of life just shifts as we get older, as our issues change, I have people that say, I want everything.
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I want every intervention possible.
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I have a I think he's about 60.
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He has a teenager.
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I wanna stay here till she graduates from high school.
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But as his condition changes, it's I don't know if I'm gonna live long enough for her to graduate.
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And so what do I do? To have the best quality of life, to have the best treatment I can to stay longer, but not suffer and not have her suffer watching me when, it's just, it's hurtful to everybody.
283
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I think, you touched on two that different things.
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One is that, and I don't come from a medical family.
285
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I'm the only doctor in my family, and so the world of medicine, When I finally started residency there were so many things that it was like an entirely new world for me.
286
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And one of the things that I learned is oncologists love to keep their patients alive.
287
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Oncologists And to the dismay of the cardiologist and the neurologist, It's true.
288
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Who already talked to them about advanced care planning and what they may or may not want.
289
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And it all goes out the window.
290
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And that's the hard part 'cause they're relying on, tried and true interventions or clinical trials and I don't know what it would be like to be a doctor.
291
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I think it's incredibly hard because a lot of people, especially the older generation, I.
292
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Doctor is God.
293
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And so if you tell me what to do, I'm gonna do it.
294
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My mom's a nurse and sh I grew up saying, being told, do not talk to doctors.
295
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Do not speak back.
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Don't ask questions, what they say do.
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And so it was this very patriarchal, kind of relationship.
298
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the newer doctors as they're coming up, it's more no, we're all kinda.
299
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On equal playing field.
300
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Yeah.
301
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this is your life.
302
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So let's have a conversation.
303
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Yes.
304
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I don't like that kind of role.
305
00:29:05,873.05 --> 00:29:11,88.05
So I don't necessarily take on that role that you just mentioned.
306
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And I understand that's probably a different generation of doctors that you're referring to.
307
00:29:16,58.05 --> 00:29:20,878.05
But I think also patients there's a whole lot of information that they have.
308
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And I tend to have smarter patients, so they do a lot of reading before they come in.
309
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So for me to say, I'm the boss of this, I'm the captain of this ship and you will do whatever I tell you to do, that would be a hardship to navigate.
310
00:29:35,643.05 --> 00:29:45,553.05
Yeah I think we need to be mutual partners, especially when it comes to certain obviously when quality of life and end of life issues start happening.
311
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So the other part of it is I come from two different backgrounds.
312
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I was born in the States, but I also have an eastern background.
313
00:29:54,83.05 --> 00:30:07,673.05
One of the things I've realized having studied a little bit of medicine in England was that the approach to end of life is very different when it comes to different countries.
314
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And I think in America, that's the other part.
315
00:30:11,333.05 --> 00:30:19,123.05
And I didn't realize this until I went to another country, and also understanding a little bit of how healthcare is in India.
316
00:30:19,633.05 --> 00:30:23,563.05
We tend to keep people alive for a long time.
317
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And yeah, with that, that comes, a whole different set of issues comes about.
318
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So you have to wonder why we do that.
319
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I'm not necessarily sure what the answer is.
320
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So I was mentioning to you that.
321
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Advanced healthcare planning.
322
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One of my struggles is even when I do address it, I'm not saying it happens all the time, but there are times when I address it and I don't say do you want everything? 'cause I'm like, what does that mean? right exactly.
323
00:30:51,753.05 --> 00:30:55,663.05
You have to be a little more specific, as to what questions you're asking.
324
00:30:56,63.05 --> 00:31:05,203.05
pull the plug So I often go through all these painful questions and sometimes I have to spell it out, okay, this is what's happening to you.
325
00:31:05,243.05 --> 00:31:07,103.05
This is a hypothetical situation.
326
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This is what's happening to you.
327
00:31:09,23.05 --> 00:31:15,753.05
What would you want us to do? And if they were like, okay, what do you mean? Do you want us to do chest compressions? Do you want us to.
328
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Put a tube down your airway.
329
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Sometimes it's not fun to have to talk to people that way.
330
00:31:21,558.05 --> 00:31:25,368.05
It's a crucial component though, of palliative care.
331
00:31:25,558.05 --> 00:31:34,8.05
What are some of the challenges that you experience when you talk to patients Talk to about advanced healthcare planning, who are facing this process.
332
00:31:34,8.05 --> 00:31:46,748.05
Maybe they're completely healthy or maybe they've been newly diagnosed with something, and how do you assist them during this process? I think like you're saying, the earlier the communication, the better.
333
00:31:46,748.05 --> 00:31:56,858.05
And my kids went off to college and we did an advance care directive because the number one thing I think is that you have to have a person that you trust that can speak for you.
334
00:31:56,858.05 --> 00:32:02,528.05
And if you go to the hospital and your neighbor is there and says, Hey, I'm the decision maker.
335
00:32:02,768.05 --> 00:32:05,948.05
And then the mom comes in and says, no, I'm the decision maker.
336
00:32:05,948.05 --> 00:32:10,968.05
It's like you're left to, your treatment provider's trying to figure that out.
337
00:32:10,968.05 --> 00:32:21,258.05
So it's really important to have a designated person and a person that you feel like will have your best interest, that can speak in your voice, not what they want, but what you want.
338
00:32:21,648.05 --> 00:32:23,388.05
And it's really a conversation.
339
00:32:23,388.05 --> 00:32:25,398.05
It's hard to have that one and done.
340
00:32:25,933.05 --> 00:32:31,723.05
And as, especially with my patients that have serious illness, their condition gradually changes.
341
00:32:31,723.05 --> 00:32:35,833.05
So quality of life changes, types of intervention changes.
342
00:32:35,893.05 --> 00:32:40,363.05
And so really revisiting that I know a year ago we talked about.
343
00:32:40,943.05 --> 00:32:42,623.05
Let's do chest compressions.
344
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Let's do everything because it's likely that your illness is gonna get better.
345
00:32:47,273.05 --> 00:32:59,573.05
But now we're in a different spot where your cancer's now in your bones, and if we do CPR, it means it's gonna crush your bones or you're gonna be in a lot more pain and your cancer's gonna continue to progress.
346
00:32:59,573.05 --> 00:33:06,593.05
So it's having that ongoing conversation and then also building up just a general trust and.
347
00:33:07,313.05 --> 00:33:19,913.05
I think the primary care physicians outpatient, even if you're not on palliative care, just you having that good relationship with your doctor so that in an emergency you can go back and say, Hey, doctor.
348
00:33:20,458.05 --> 00:33:22,318.05
I'm scared, I don't know what to do.
349
00:33:22,708.05 --> 00:33:28,258.05
And the doctor can go back and say we've had this discussion and this is what's really going on.
350
00:33:28,258.05 --> 00:33:32,338.05
When you have five different specialists telling you all these different things.
351
00:33:32,938.05 --> 00:33:41,978.05
What I see and I think it requires bravery on the treatment team's part to be able to lean in and to tell the truth.
352
00:33:42,8.05 --> 00:33:46,718.05
And I think a lot of times the medical profession, it's hard to tell the truth.
353
00:33:46,798.05 --> 00:33:49,78.05
My husband, we were, he's still.
354
00:33:49,528.05 --> 00:33:54,748.05
Figuring out the chemotherapy stuff, but the doctor said, probably chemo's on the table.
355
00:33:54,748.05 --> 00:33:58,648.05
And I've been doing this for years and my gut reaction was, it's okay.
356
00:33:58,648.05 --> 00:34:00,118.05
Chemo isn't gonna be that bad.
357
00:34:00,238.05 --> 00:34:01,288.05
It's the good chemo.
358
00:34:01,738.05 --> 00:34:05,28.05
And I just wanted to protect my husband you're not gonna get sick.
359
00:34:05,298.05 --> 00:34:09,548.05
Even though knowing what I know that it can be pretty brutal.
360
00:34:09,548.05 --> 00:34:11,348.05
So it's hard.
361
00:34:11,348.05 --> 00:34:12,158.05
It's really hard.
362
00:34:12,158.05 --> 00:34:16,898.05
And I think as healthcare professionals really leaning into our own.
363
00:34:17,648.05 --> 00:34:26,828.05
Our own, feelings about mortality and maybe our own knowledge that we're not, God, we can't save, we, we can't fix everything.
364
00:34:27,158.05 --> 00:34:33,363.05
And so learning that, how do we keep the humanity in the healthcare? But I think it, I.
365
00:34:33,423.05 --> 00:34:37,623.05
It's not a one and done conversation, it's something we keep needing to talk about.
366
00:34:38,433.05 --> 00:34:48,588.05
I think I, when I was a young resident versus now I think the priorities of not the priorities different word the.
367
00:34:49,643.05 --> 00:34:56,303.05
The goal if you wanna use that word, initially it was to save as many people as I could.
368
00:34:56,303.05 --> 00:35:02,123.05
And as I got older, I realized, okay, first, obviously, those words do no harm.
369
00:35:02,633.05 --> 00:35:04,313.05
Definitely come more into play.
370
00:35:05,138.05 --> 00:35:12,818.05
Then secondly, I was, I'm always about, making sure that people are their healthiest and happiest.
371
00:35:13,268.05 --> 00:35:19,248.05
And my goal is not always to, make you live the longest that you can.
372
00:35:19,348.05 --> 00:35:23,338.05
If that happens and you also stay healthy and happy, that's awesome.
373
00:35:23,738.05 --> 00:35:27,528.05
As we're not always in command of how that goes.
374
00:35:27,988.05 --> 00:35:46,268.05
The other difference that I see is that the cultural aspect is that it, I think in America, I think I, I think, how do I say this? there's, I think even amongst people, we, as a society I think there's like this.
375
00:35:48,443.05 --> 00:35:51,573.05
This belief that we're invincible.
376
00:35:51,573.05 --> 00:35:51,633.05
Yeah.
377
00:35:51,963.05 --> 00:35:54,213.05
And that nothing will happen to us.
378
00:35:54,213.05 --> 00:36:01,578.05
Whereas I think on a more Eastern, if you subscribe to this, you realize that we're not invincible.
379
00:36:01,873.05 --> 00:36:02,953.05
there's a finite.
380
00:36:03,248.05 --> 00:36:05,408.05
Aspect to everything.
381
00:36:05,838.05 --> 00:36:08,198.05
And I straddle both of those things.
382
00:36:08,318.05 --> 00:36:14,778.05
And I try to incorporate both of that with my patients, but it's often very difficult.
383
00:36:15,78.05 --> 00:36:37,488.05
So how do you teach? Doctors such as myself about how to effectively communicate with patients when it comes to these difficult conversations that we often need to have with people, I think it goes back to helping people or doctors to get in touch with their humanity.
384
00:36:37,918.05 --> 00:36:39,363.05
There's studies that show that.
385
00:36:40,23.05 --> 00:36:45,483.05
What the doctors prescribed to another patient that I would go to the ICU, I would do all these things.
386
00:36:45,933.05 --> 00:36:51,513.05
If you asked them what they would do for themselves, if they were in that situation, they would say, no, I don't want all that.
387
00:36:51,963.05 --> 00:37:05,703.05
As a, putting yourself in the other person's shoes, looking at the bigger story and what does that come up for Me as a professional that I am not able to fix everything, that I am not able to be that superhero.
388
00:37:05,703.05 --> 00:37:08,943.05
Not that I think most doctors go in that way.
389
00:37:09,398.05 --> 00:37:12,498.05
But there's just the, you're trained to, to heal.
390
00:37:12,498.05 --> 00:37:24,928.05
You're trained to fix things and when you can't, sometimes, physicians feel that's something on them that they didn't do enough and I think the other part is it's just really hard to sit and be in the room.
391
00:37:25,288.05 --> 00:37:31,728.05
And I see this when I work with the doctor and the nurse, I'll see a patient crying or really emoting and being scared.
392
00:37:31,728.05 --> 00:37:33,498.05
And the doctor and nurse are let's do this.
393
00:37:33,498.05 --> 00:37:35,418.05
Let's give medica, let's do something.
394
00:37:35,838.05 --> 00:37:44,778.05
And sometimes something is sitting back and just holding a hand or just letting the person cry and not feel like you have to fix it.
395
00:37:44,808.05 --> 00:37:50,368.05
And so helping, I guess doctors go to that softer place that it's okay.
396
00:37:50,758.05 --> 00:37:56,928.05
And I have, our doctor even gets frustrated sometimes and he is I feel like I'm just sitting there not doing anything.
397
00:37:56,928.05 --> 00:38:00,618.05
And it's okay, maybe the patient just needs to be heard.
398
00:38:00,978.05 --> 00:38:09,108.05
And that's where sort of the social work, the therapist, the chaplain part comes in because we are talking more what you're saying that.
399
00:38:09,573.05 --> 00:38:14,673.05
It's a life cycle and not everything is, gonna be, there's not a pill for everything.
400
00:38:14,673.05 --> 00:38:18,3.05
So let's step back and just be with the person.
401
00:38:18,33.05 --> 00:38:22,233.05
And oftentimes patients know how their illness is going.
402
00:38:22,233.05 --> 00:38:23,733.05
They know what's ahead.
403
00:38:23,733.05 --> 00:38:31,23.05
They might be scared, they might not wanna talk about it, but there's this weird codependence between the physician and the patient.
404
00:38:31,73.05 --> 00:38:35,813.05
I don't wanna tell you that I know my illness is getting worse and that I'm probably dying.
405
00:38:35,893.05 --> 00:38:41,623.05
Because I don't wanna disappoint you, the doctor who's invested so much time and energy on me.
406
00:38:42,13.05 --> 00:38:45,133.05
And then the doctor's saying, I don't wanna tell you that.
407
00:38:45,998.05 --> 00:38:58,98.05
This isn't going well because I don't want you to lose hope or I don't want you to be sad, or, and a lot of times I can speak for you, but a lot of the doctors I work with just, they have a hard time with the emotions.
408
00:38:58,98.05 --> 00:39:00,588.05
It's when the emotions get soft.
409
00:39:00,588.05 --> 00:39:01,68.05
It's ooh.
410
00:39:01,188.05 --> 00:39:02,928.05
I wasn't trained to do that stuff.
411
00:39:03,358.05 --> 00:39:04,528.05
Let's go back to science.
412
00:39:04,528.05 --> 00:39:09,848.05
Let's go back to the hard knocks, I still have, it's, I'm more used to it.
413
00:39:09,848.05 --> 00:39:10,593.05
I should say.
414
00:39:10,653.05 --> 00:39:15,33.05
Because I realize that I can't make everyone live forever, nor do I want to.
415
00:39:15,513.05 --> 00:39:18,983.05
But I still feel that I've.
416
00:39:19,383.05 --> 00:39:19,983.05
Failed.
417
00:39:20,313.05 --> 00:39:27,283.05
It's almost this feeling of failure that, and I'm like, okay, but this person, and then the other side of me is okay, that person was 95 years old.
418
00:39:27,843.05 --> 00:39:29,13.05
99 years old.
419
00:39:29,13.05 --> 00:39:36,148.05
What were you trying to do there? Not that I was actually trying to make them live longer than that but it's just It's It's very difficult.
420
00:39:36,148.05 --> 00:39:40,718.05
And often their family members, even if they're not my patients, often they are.
421
00:39:40,768.05 --> 00:39:46,258.05
You see it in their eyes and it's like, how do I look at them with the compassion and still.
422
00:39:46,918.05 --> 00:39:47,938.05
Telling the truth.
423
00:39:47,998.05 --> 00:39:48,28.05
Yes.
424
00:39:48,113.05 --> 00:39:49,73.05
It's really hard.
425
00:39:49,163.05 --> 00:39:49,253.05
Yes.
426
00:39:49,253.05 --> 00:39:56,603.05
I think it's about saving their dignity and their grace in their lifecycle because we can't fix everything.
427
00:39:57,83.05 --> 00:40:04,223.05
And if we're talking about saving to the nth degree when a person, if they knew better, they may not make those choices.
428
00:40:04,583.05 --> 00:40:08,783.05
It's really about how can we preserve the humanity so that people.
429
00:40:09,483.05 --> 00:40:14,753.05
Whatever the course of illness is they're feeling like human beings and not just Yeah.
430
00:40:14,753.05 --> 00:40:16,73.05
A science experiment.
431
00:40:16,223.05 --> 00:40:16,583.05
Yeah.
432
00:40:17,303.05 --> 00:40:30,123.05
I don't and I'm thankful for it because I don't think it's meant for me to see, but it often sometimes comes up like, is this how you want to remember? Your parent or your loved one? Yeah.
433
00:40:30,153.05 --> 00:40:34,253.05
Is this how, let's say that person can't make those decisions anymore.
434
00:40:34,253.05 --> 00:40:35,963.05
Is this something that you want to.
435
00:40:36,478.05 --> 00:40:37,408.05
Continue.
436
00:40:37,458.05 --> 00:40:48,398.05
And have you ever had conversations with them as to what they would or wouldn't want? Sometimes even after the, in the aftermath, you're still having those kind of discussions.
437
00:40:48,808.05 --> 00:41:03,438.05
With family members I often see multiple generations of people in a family, I'm still having those conversations even though I'm not in the hospital because I'm taking care of that person's son or daughter, or even right.
438
00:41:03,708.05 --> 00:41:04,608.05
Grandchildren.
439
00:41:04,858.05 --> 00:41:09,268.05
And you're probably the one that they trust the most because you've had that relationship.
440
00:41:09,318.05 --> 00:41:15,478.05
Trusting your outpatient doctor is really an essential part because you're the sort of the neutral person.
441
00:41:15,958.05 --> 00:41:25,858.05
But then I think for doctors also, like when you're describing these really complex relationships and intergenerational, there's grief, I think for the doctors too, that Oh, yeah.
442
00:41:26,298.05 --> 00:41:28,278.05
I don't wanna lose this person.
443
00:41:28,278.05 --> 00:41:32,638.05
I'll with my patients, we've seen patients for years and it's oh, that hurts.
444
00:41:32,638.05 --> 00:41:33,598.05
That one hurts.
445
00:41:33,648.05 --> 00:41:35,238.05
And you move on.
446
00:41:35,718.05 --> 00:41:39,258.05
But it's allowing space for yourself too, that it's o okay.
447
00:41:39,258.05 --> 00:41:40,788.05
That we have feelings about it.
448
00:41:40,788.05 --> 00:41:40,848.05
Yeah.
449
00:41:40,878.05 --> 00:41:42,378.05
We're, it's just human.
450
00:41:42,388.05 --> 00:41:44,698.05
We should be connecting on that level with people.
451
00:41:44,748.05 --> 00:41:46,98.05
That's what good care is.
452
00:41:46,518.05 --> 00:41:49,848.05
I, in New Jersey, we do have medically assisted suicide.
453
00:41:50,388.05 --> 00:41:50,778.05
Yeah.
454
00:41:50,878.05 --> 00:41:55,258.05
So I do have one patient and she ultimately decided not to do it.
455
00:41:55,658.05 --> 00:42:05,178.05
But when I got a letter saying that this was the step that she was going to take, I was the one who was like, oh, no, don't do it.
456
00:42:05,228.05 --> 00:42:05,828.05
yeah.
457
00:42:07,718.05 --> 00:42:09,188.05
Not knowing anything.
458
00:42:09,238.05 --> 00:42:11,698.05
But yeah, I was like, please don't do that.
459
00:42:12,898.05 --> 00:42:14,368.05
Like you're my baby.
460
00:42:14,368.05 --> 00:42:14,818.05
Keep going.
461
00:42:17,848.05 --> 00:42:18,268.05
It's hard.
462
00:42:18,598.05 --> 00:42:19,293.05
It's really hard.
463
00:42:19,358.05 --> 00:42:27,878.05
But I think it's just, it's such a complicated relationship 'cause you're holding bodies to put them together to live longer.
464
00:42:28,298.05 --> 00:42:38,228.05
But then you're also holding the hearts that these are people like, these people, like wedge into your heart where they matter and so it's a lot of responsibility.
465
00:42:38,278.05 --> 00:42:48,470.05
That doctors have, and it makes sense to me that sometimes it just, it's really hard to have those complex discussions because we don't wanna be the ones, to, We don't.
466
00:42:48,475.05 --> 00:42:53,118.05
But it, it's a burden that comes, if you wanna call it a burden.
467
00:42:53,118.05 --> 00:42:54,83.05
It's a responsibility.
468
00:42:54,233.05 --> 00:42:54,523.05
Yeah.
469
00:42:54,763.05 --> 00:42:59,982.05
A responsibility that we have, to make sure that if we can give a person.
470
00:43:00,672.05 --> 00:43:05,952.05
The best end of life, then that's a responsibility that we should take.
471
00:43:05,952.05 --> 00:43:06,12.05
Yeah.
472
00:43:06,162.05 --> 00:43:07,92.05
It's not a burden.
473
00:43:07,92.05 --> 00:43:07,152.05
Yeah.
474
00:43:07,477.05 --> 00:43:10,957.05
'cause we are not always lucky enough to have that.
475
00:43:11,387.05 --> 00:43:16,637.05
But if we can provide that for someone that's actually a privilege and an honor.
476
00:43:16,637.05 --> 00:43:21,647.05
And so when, there are times when I know that, okay, my patient, who I've known for.
477
00:43:21,912.05 --> 00:43:27,557.05
God knows how long and they passed away peacefully and they lived the best life.
478
00:43:28,242.05 --> 00:43:29,82.05
That they can.
479
00:43:29,242.05 --> 00:43:32,192.05
It's an honor to be able to say, okay, I was a part of that.
480
00:43:32,762.05 --> 00:43:33,602.05
It really is.
481
00:43:33,722.05 --> 00:43:34,22.05
Yeah.
482
00:43:34,72.05 --> 00:43:37,102.05
But then also knowing, and I find this with palliative care too.
483
00:43:37,102.05 --> 00:43:45,322.05
Obviously we're dealing with a lot of complexities but really holding space for ourselves in each other that this is hard work that we're doing.
484
00:43:45,322.05 --> 00:43:57,892.05
And I think for most of us, for me, it's a calling This is what gives me meaning, but it doesn't mean that I'm not human and that the cumulation of patients and special ones that they're not gonna hit me.
485
00:43:57,892.05 --> 00:43:58,642.05
They are.
486
00:43:58,972.05 --> 00:44:10,152.05
And so how do I take care of myself so I can maintain that objectivity? 'cause it weighs on you if you don't provide yourself the compassion and space to let those feelings out.
487
00:44:11,132.05 --> 00:44:11,882.05
Of course.
488
00:44:11,882.05 --> 00:44:27,752.05
And I think, for those of us who deal a lot, and I think that includes primary care physicians, oncologists, there are certain specialties where we're frequently seeing this and dealing with patients who are closer to the end of life.
489
00:44:27,932.05 --> 00:44:36,637.05
I think it's important that we, have professional care ourselves where we have an outlet where we can talk to someone.
490
00:44:37,782.05 --> 00:44:43,122.05
Objectively and in a safe space where we can let out our emotions and be safe.
491
00:44:43,842.05 --> 00:44:43,932.05
Yes.
492
00:44:45,102.05 --> 00:44:50,232.05
So we've learned a lot from you, Ann, and honestly, it, I think this will be a.
493
00:44:50,957.05 --> 00:44:59,507.05
great listen for anyone who wants to learn about palliative care and hospice care and how we can, really help people.
494
00:44:59,807.05 --> 00:45:22,417.05
What haven't we talked about that you would like to include in the podcast? I think the only thing I would say is that, even as much as we've talked about it, there's just so much confusion and just being okay to ask questions to I'm on TikTok, so a lot of times I'm like, there's so much information on there or on YouTube where social media, just to get like basic.
495
00:45:22,792.05 --> 00:45:33,647.05
Put the questions out there and see but then also talking to professionals that it doesn't hurt you to call a hospice company or to call a palliative care and just say, I don't really know if this.
496
00:45:34,652.05 --> 00:45:37,652.05
It was helpful to me, but just wanted to get more information.
497
00:45:38,42.05 --> 00:45:45,92.05
And if you for instance, called me and said, I don't really know, and I say, you're seem like you don't need palliative care.
498
00:45:45,452.05 --> 00:45:51,942.05
I have enough experience to know what, maybe you need chronic pain or maybe you need some other avenue that we have.
499
00:45:52,592.05 --> 00:45:58,112.05
A lot of experience and the doctors have a lot of experience to know where to plug you in.
500
00:45:58,112.05 --> 00:46:09,732.05
So just not being afraid to take the risk and especially we're talking about palliative care, how much of a support it is that just don't be worried about the semantics of it.
501
00:46:09,732.05 --> 00:46:11,352.05
Just go in with an open mind.
502
00:46:11,352.05 --> 00:46:24,892.05
If my listeners did want to find you on TikTok or Instagram or on your website where should they go to get that information? my website is ww w ann a NE front.com.
503
00:46:24,892.05 --> 00:46:26,572.05
So ann front.com
504
00:46:26,932.05 --> 00:46:30,192.05
and then the TikTok is the palliative therapist.
505
00:46:30,192.05 --> 00:46:41,622.05
So you can find me there I started the TikTok because I keep answering the same questions over and over again, and it tells me there's so much information that's wanted, but not out there.
506
00:46:41,622.05 --> 00:46:44,932.05
whatever you can do to educate, ask the questions.
507
00:46:44,932.05 --> 00:46:50,602.05
There's a lot of help out there and with serious illness, people feel so isolated and alone.
508
00:46:50,702.05 --> 00:46:51,842.05
that breaks my heart.
509
00:46:51,842.05 --> 00:46:52,682.05
I would rather.
510
00:46:53,17.05 --> 00:46:56,567.05
Connect people so that you feel like we're all in this together.
511
00:46:57,167.05 --> 00:46:59,327.05
Thank you so much for joining us today.
512
00:46:59,687.05 --> 00:47:00,317.05
Thank you for having me.
513
00:47:01,7.05 --> 00:47:07,817.05
Yes, this is a great topic and I think it really will help a lot of people in terms of understanding.
514
00:47:08,67.05 --> 00:47:11,337.05
what palliative care is and how important it is.
515
00:47:11,387.05 --> 00:47:12,197.05
To healthcare.
516
00:47:12,747.05 --> 00:47:13,857.05
Thank you for all you do.
517
00:47:13,907.05 --> 00:47:18,467.05
You're on the front lines, so I really appreciate all the work you do.
518
00:47:19,737.05 --> 00:47:22,167.05
Honestly I enjoyed talking to you so much.
519
00:47:22,347.05 --> 00:47:25,17.05
So you're always welcome to come back and Thank you.
520
00:47:25,272.05 --> 00:47:26,307.05
You can talk more.
521
00:47:26,602.05 --> 00:47:26,992.05
I'd love that.
522
00:47:27,82.05 --> 00:47:27,292.05
Yeah.
523
00:47:27,342.05 --> 00:47:31,592.05
This will be available on Apple Podcasts as well as YouTube.
524
00:47:31,962.05 --> 00:47:32,982.05
Thank you for your time.
525
00:47:32,982.05 --> 00:47:35,112.05
It was really nice to have this discussion.
526
00:47:35,112.05 --> 00:47:39,212.05
And don't forget to like, share and review my podcast.
527
00:47:39,762.05 --> 00:47:43,552.05
Remember, it's always ladies first on Soma Says.
528
00:47:43,852.05 --> 00:47:47,512.05
Let's make a difference one conversation at a time.