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Why Doing Things For Others Feels Good as a Patient with PF.
As a patient living with a life-threatening illness such as idiopathic pulmonary fibrosis (IPF), it sometimes feels like we take more than we can give to others. This is not by preference, it is simply because our disease forces us to require the assistance of others (“taking”) more often than allowing us to do things for others (“give”). As a result, when we can do something for someone else it often feels so good, since we’re used to people doing so much for us due to our lung disease. At least, this is the case for me.
I have always enjoyed doing things for others simply because it made them happy. I never felt as though I had to do something for someone “in exchange” for what they did for me, even though I know healthy friendships or relationships are reciprocal like this naturally. Since my IPF diagnosis I still enjoy doing things for others for the sake of it making them happy, however, sometimes I also feel it necessary to do things for people who help me so often with my disease.
Regardless of why I choose to do things for others, there are ample reasons why doing so makes me feel good. Below are just a couple of those reasons:
- It gives me an opportunity to feel as though I can “give back”: while my friends and family do not expect this when they help me with tasks, sometimes it can feel as though the equilibrium of reciprocal support feels off balance. To me, it often feels like I take more than I give so when I can do something for others, it brings that equilibrium a bit more into balance.
- Enables a sense of normalcy vs. life with a chronic illness: I believe that as human beings most of us have this innate desire to help and support others. When living with a life-threatening illness such as IPF, it often feels as though normal life for us as patients no longer exists. This due to the constant threat to our health and having to cancel or re-schedule plans around our illness. Offering to do something for others helps enable a feeling of normalcy in our lives, as this is something most healthy people would also do.
How does being able to do things for others make you feel since your IPF/PF diagnosis? Does it make you feel good, and if so, why is that? I’d love to hear from you!
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