REBLOG: Invisible Scars: My Life Post Transplant

While I don’t have Cystic Fibrosis myself, I have some friends who do.

I can also relate to a lot of the same heartaches faced by other young people with lung disease.  That’s why I’m re-blogging this post today even though it is a bit older.

It really resonated with me when I came across it in the CF Community Blog.

It’s one of those evergreen (good for years to come) posts that I wanted to keep here in my blog to refer back to when I need to along this journey when things are looking intimidating.

But I also hope that others will find help, understanding, & comfort in it too like I did when I first read it.

To find out more about the author, Andrew Corcoran, click here.



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