Disclaimer: “This is a sponsored post for Self Care Catalysts. I have been compensated through the Chronic Illness Bloggers network. All thoughts & opinions remain my own and I was in no way influenced by the company.  Join the Selfcare Movement here.

(This particular letter is not based on any one instance or experience but an amalgam of many different reactions & past experiences as well as stories shared with me by other people with lung disease & those that love them.  Some of my response in the letter below is also based on things others wished they would have been able to say to other people when they had a less than pleasant experience.) 

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