Every Month I have the honor of hosting a post by someone in the the Churg Strauss Syndrome Community telling the world about what’s it like to live life with CSS.
CSS is what is called an invisible illness, we carry most of damage within our bodies and tend to look ‘normal’ on the outside. The damage is deep and I am humbled by my fellow CSSers on how they keep going on day after day. How hope burns so bright and even though our disease is considered to be an rare illness, we are all hopeful of new medical treatments in the future.
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