How Palliative Care Can Help IPF Patients and Their Loved Ones

How Palliative Care Can Help IPF Patients and Their Loved Ones
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The words “palliative care” often frighten those of us living with a life-threatening illness. This is because the term historically has been associated with end-of-life care due to its link with hospice care.

But the two terms were formally separated in 1990, when the World Health Organization officially recognized palliative care as a specialty focused on relieving patient suffering and improving quality of life.

Despite that shift, discomfort and stigma often still remain when patients discuss palliative care with physicians and other healthcare professionals. Unfortunately, this stigma can cause problems for patients with life-threatening illnesses such as idiopathic pulmonary fibrosis (IPF).

While it might sound strange, palliative care, legacy initiatives, and dying with dignity are all topics that interested me during my university studies, especially my master’s-level courses. My passion for talking about it has changed a little now that I live with a life-threatening illness, but I still strongly advocate for the importance of removing the stigma from palliative care.

Last week, I had a unique opportunity to address this topic with other IPF patients at a peer support group organized by the Pulmonary Wellness Foundation. We focused on understanding palliative care and its role in the management of our lung disease. During the conversation, it became clear that a better understanding of what palliative care is, and how it can help with our disease, is necessary.

When I became a patient of the transplant program at my local treatment center, staff told me that palliative care was automatically part of my care program. I reacted negatively upon learning this. Although I knew palliative care didn’t mean end-of-life, I couldn’t avoid the anxiety and fear caused by having a palliative care team involved in my care. Little did I know that eventually, this team would be instrumental in helping to maintain, and even improve, my quality of life with a progressive lung disease.

What is palliative care, and how can it help IPF patients?

Palliative care is often defined as a specialized type of treatment focused on providing relief from the symptoms and stress of a serious illness. Because anxiety is associated with an IPF diagnosis, I see value in a palliative care team getting involved in disease management as soon as possible. This is especially true if they can help improve quality of life as the disease progresses and conditions worsen.

Palliative care can help IPF patients in many other ways, too. Following are some of the unexpected ways this specialized care team has helped me since I became a patient in the lung transplant program:

Presenting options

When facing a progressive disease, not everyone chooses to fight. This is a personal choice, and deciding whether or not to seek treatment is based on a variety of factors that a palliative care team understands, especially if a patient’s quality of life will be compromised. This specialized team of professionals can present patients with all options.

Validating fears

Transplantation and living with a life-threatening lung disease are scary. While I have an amazing support network, sometimes I don’t think I can discuss my fears with loved ones. The palliative care team acknowledges those fears, validates them, and even helps me establish better coping skills. They are professional during all of our conversations and have become an unbiased sounding board for me.

Paperwork, including wills and advance directives

Wills and advanced healthcare directives are difficult to talk about. However, with the proper guidance and support, these conversations can shift from scary to comforting. This is because a palliative care team can help patients understand that preparing these things in advance gives a person some control over an uncontrollable illness. It also alleviates the stress on loved ones when that time comes, because everything is prepared in advance.

Helping family members

Living with a progressive and life-threatening illness is stressful on the entire family. Most hospitals now take a family-centered approach to care that includes the palliative care team. Team members are available to support a patient’s family members during difficult times, and to discuss options to help them navigate the loved one’s serious illness while caring for themselves.

If palliative care has been part of your lung disease management, please consider sharing your experience in the comments below.

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Note: Pulmonary Fibrosis News is strictly a news and information website about the disease. It does not provide medical advice, diagnosis, or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website. The opinions expressed in this column are not those of Pulmonary Fibrosis News or its parent company, BioNews, and are intended to spark discussion about issues pertaining to pulmonary fibrosis.

Charlene is a fiercely independent 30-something woman who can’t sit still. She loves coffee, wine tasting, playing with her dog, and spending time on the beach with her family. She’s a lover of all things travel, and never passes up an opportunity for a dip in the ocean! A proud Canadian, Charlene was diagnosed with idiopathic pulmonary fibrosis (IPF) in 2016 after 13 months of investigation into sudden shortness of breath, a chronic cough, and unusual fatigue. IPF has forced her to slow down, but she’s slowly learning the value of quality versus quantity in everything she does.
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Charlene is a fiercely independent 30-something woman who can’t sit still. She loves coffee, wine tasting, playing with her dog, and spending time on the beach with her family. She’s a lover of all things travel, and never passes up an opportunity for a dip in the ocean! A proud Canadian, Charlene was diagnosed with idiopathic pulmonary fibrosis (IPF) in 2016 after 13 months of investigation into sudden shortness of breath, a chronic cough, and unusual fatigue. IPF has forced her to slow down, but she’s slowly learning the value of quality versus quantity in everything she does.
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4 comments

  1. Maka Rebagliati says:

    Thank you Charlene for taking the time to explain palliative care. I have one question, we live in Ontario, is palliative care usually in hospitals or in assisted living facilities?
    I want to take this opportunity to thank you for sharing all your knowledge with us, my husband suffers from IPF and we learn a lot from you and other people posting comments here.
    THANKS

    • Charlene Marshall says:

      Hi Maka,

      Thank you so much for reading my columns and reaching out via the comments. I know a little bit about palliative care in Ontario, and my experience has been from others that the conversation begins in hospital or through your specialist or GP/family doctor. The palliative care team often operates out of a hospital, but if an acute need isn’t there at the time (ie. you’re not admitted) they can refer to community-based palliative care support, hopefully local to your area. I’m not sure if this helps? Let me know 🙂 I’m glad to hear my columns are helpful to you and your husband, thank you for sharing that. Wishing you both nothing but the best, please feel free to connect any time.

      Warmly,
      Charlene.

  2. Joan LaGuardia says:

    I was recently referred for palliative care, but the doctor & I agreed that I wasn’t ready for it. I am in my early 80s & recently have been on daily oxygen. I also use a CPAP at night. I was diagnosed in 2016 & had IPF for at least 6 years before that. The doctor seemed amazed that I still drive, prepare meals, & do laundry. He wanted to give me anxiety & pain meds which I don’t feel I need. He also suggested Meals on Wheels. My hubby is also in his 80s & has COPD. We aren’t done living yet. We felt like he was pushing us into an early grave.

    • Charlene Marshall says:

      Hi Joan,

      Thanks so much for reading my column and reaching out via the comments. I’m glad you had a conversation with your doctor, and that you both agreed on the involvement of palliative care (or in your case, the lack thereof). It is definitely important to be on the same page about this medical team, so I’m glad to hear you and your MD were. Really glad you seem to be doing well, and keep up the amazing things you’re doing. Thanks for writing!
      Char.

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