I am proud to be a voice for people living with Cystic Fibrosis and other rare diseases. I have had the opportunity to share my story – and my beliefs at times – with major news outlets.
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*Nothing contained in these blog posts, podcasts, images, or any other posts should be considered medical advice. Such advice can only be given by a physician who is experienced with cystic fibrosis. The contributors on this blog/podcast cannot be held responsible for any damage which may result from using the information on this blog/podcast without permission of their medical doctor. Furthermore, the views expressed on this blog are solely those of the contributors and do not represent the views or opinions of the writer's employer(s) unless explicitly mentioned.