When to Consider Professional Help While Dealing With PF

It would likely come as no surprise to others that patients diagnosed with a life-threatening illness, such as pulmonary fibrosis (PF), have many intense emotions and valid fears associated with their disease. These emotions can manifest themselves in many different ways. For example, even the emotions associated with a positive medical appointment can physically impact a patient by keeping their mind from restful sleep. A patient might be busy thinking about whether or not something was missed in their appointment, or if they asked their specialist all the questions they wanted to, or what their next appointment might show. Lack of sleep due to emotions and fears is something that most patients have to deal with.

MORE: How to help yourself and let others help you when you have PF

There are several physical signs that may indicate you’re dealing with something more than just worrying or feeling sad. Below are four symptoms that might indicate depression, and if you are experiencing these regularly, it might be beneficial to seek professional help.

Loss of appetite
This is often a classic indicator that something is wrong. A sudden loss of appetite usually accompanies stress and anxiety, but  if the feeling persists, it’s important to address it. Being chronically under-oxygenated due to a lung disease does enough damage to your body, but avoiding food doesn’t give your body the fuel it needs to keep going. This should be especially concerning if you’re someone who usually eats well.

Turning inwards and avoiding previously enjoyed social activities
This can be common, as everyone needs their alone time. However, if suddenly you’re regularly canceling plans to spend time alone or you find yourself anxious in social situations, it’s important to seek professional help. It’s nearly impossible to face a chronic illness alone, and everyone needs support from his or her friends and family. Suddenly losing interest in activities can be an indicator of depression.

Trouble sleeping
This is a hard one because so many patients with PF lose out on sleep due to excessive thinking, worrying or even due to physical symptoms like a dry cough. However, if attempts to improve sleep are ineffective, it may be time to seek professional help.

Excessive crying
Some patients dealing with a lung disease are on steroids for the treatment of their symptoms, which can lead to excessive emotions and lots of tears. Based on other columns and social clips, this has been a shared experience among many patients. However, excessive crying without reason may be a cause for concern.

For those living with a life-threatening illness, seeking help is important for survival. Considering professional help is an important way to help with that emotional pain, especially if you are experiencing symptoms for prolonged periods of time. If you aren’t already connected with a social worker or some type of counselor, your doctor can make a referral and point you in the right direction.

MORE: The benefits of sleep for pulmonary fibrosis patients

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 another 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.

Thanks for stopping by my column! My name is Charlene Marshall and I was diagnosed officially with Idiopathic Pulmonary Fibrosis (IPF) on April 7 2016 after 13 months of various tests, hospitalizations and misdiagnoses, such as bronchitis and asthma. Due to my age, the specialist disclosed that he was unsure how the IPF would manifest itself in terms of progression, and whether it would be fast or slow and what the course of my illness might look like. Not much has changed since then, meaning there is still a lot that remains unknown, which is largely due to my age and how “rare” it is for someone under 30 to receive a diagnosis of IPF. That being said, a lot has changed for me in the time since diagnosis and I am looking forward to sharing some of those changes with you through this online platform, and I invite you along for the ride! Throughout this column I intend to chronicle the experience of living with an invisible, yet fatal disease as a young adult and share some stories about how IPF has impacted every aspect of my life, both good and bad, thus far. I plan on highlighting the challenges (and where I can, the positives…) that come with living with IPF and the impact on social and intimate relationships, finances, family dynamics, facing mortality, infertility, travelling, medication side effects, career goals and so much more as it arises for me as a “new” patient. I hope others’ with similar experiences will reach out as no story trumps any other, nor should any go unheard. For now, let me leave you with some personal details about who I am, outside of my IPF diagnosis. I grew up in a small town in south-western Ontario and still live within Ontario, although in a much bigger city. My favorite sport is/was underwater hockey (yes, it is a thing: look it up on YouTube), I love working with people, I work full-time in the Social Work/Social Services field, I am an avid learner filled with heaps of curiosity for the world, which lead me to start my Masters Degree in 2014. I am in the last few months of my Masters Degree and am looking forward to an upcoming trip to Australia more than I’ve looked forward to anything before. Welcome to the shambles and chaos that is my life!
×
Thanks for stopping by my column! My name is Charlene Marshall and I was diagnosed officially with Idiopathic Pulmonary Fibrosis (IPF) on April 7 2016 after 13 months of various tests, hospitalizations and misdiagnoses, such as bronchitis and asthma. Due to my age, the specialist disclosed that he was unsure how the IPF would manifest itself in terms of progression, and whether it would be fast or slow and what the course of my illness might look like. Not much has changed since then, meaning there is still a lot that remains unknown, which is largely due to my age and how “rare” it is for someone under 30 to receive a diagnosis of IPF. That being said, a lot has changed for me in the time since diagnosis and I am looking forward to sharing some of those changes with you through this online platform, and I invite you along for the ride! Throughout this column I intend to chronicle the experience of living with an invisible, yet fatal disease as a young adult and share some stories about how IPF has impacted every aspect of my life, both good and bad, thus far. I plan on highlighting the challenges (and where I can, the positives…) that come with living with IPF and the impact on social and intimate relationships, finances, family dynamics, facing mortality, infertility, travelling, medication side effects, career goals and so much more as it arises for me as a “new” patient. I hope others’ with similar experiences will reach out as no story trumps any other, nor should any go unheard. For now, let me leave you with some personal details about who I am, outside of my IPF diagnosis. I grew up in a small town in south-western Ontario and still live within Ontario, although in a much bigger city. My favorite sport is/was underwater hockey (yes, it is a thing: look it up on YouTube), I love working with people, I work full-time in the Social Work/Social Services field, I am an avid learner filled with heaps of curiosity for the world, which lead me to start my Masters Degree in 2014. I am in the last few months of my Masters Degree and am looking forward to an upcoming trip to Australia more than I’ve looked forward to anything before. Welcome to the shambles and chaos that is my life!
Average Rating
0 out of 5 stars. 0 votes.
My Rating:

Leave a Comment

Your email address will not be published. Required fields are marked *