All posts tagged: Living Breathless

Posts about my odyssey with Sjӧgren’s Syndrome and Interstitial Lung Disease, including information about treatment, changes and how I live a normal life with busted lungs and oxygen.

My Sjogren’s Story

I’m not one to jump on bandwagon decorated with colored ribbons, or start plastering social media with awareness campaigns. Usually, I’m of the opinion that all the ribbons and campaigns and marches and walks and fundraisers do less to raise awareness of something and more to annoy me. Don’t get me wrong, I think the intentions behind these efforts are fantastic. I just get inundated with them and therefore tune them out, making the entire point of an “awareness campaign” moot. But I digress. I’m going to make an exception and pay attention to at least one of these campaigns. April is Sjogren’s awareness month.

A New Look, A New ME!

Whew. I don’t know about you, but that last blog entry got a bit to real for me. I’m not all into talking about my feelings or even really talking about myself – especially not on this blog. But I’m going to keep with this personal vein here and there on the blog, even though adventuring is waaaay more interesting than stupid autoimmune diseases. Notice anything different about this site? I’ve gone through I-don’t-know-how-many redesigns over the years, each time getting further away from my original purpose: To showcase my fine body of work when I was in college and “networking.” (I use the term “fine” loosely here. I look back on all that and cringe now, a lot like how I will reread this in another five years and do the same.) I have tried to move my blog from being about me – because, lets face it, I’m boring – and focus on adventures! Formerly called “Curious Adventurer,” I’ve now dubbed myself the “Breathless Adventurer” complete with a new banner photo and URL. I …