About Me

My Name is Dan Pfaff,

I was born with Cystic Fibrosis– Cystic Fibrosis (also known as CF or mucoviscidosis) is an autosomal recessive genetic disorder that affects most critically the lungs, and the pancreas, liver, and intestine. It is characterized by abnormal transport of chloride and sodium across an epithelium, leading to thick, viscous secretions.

CF is caused by a mutation in the gene for the protein cystic fibrosis transmembrane conductance regulator (CFTR). This protein is required to regulate the components of sweat, digestive fluids, and mucus. CFTR regulates the movement of chloride and sodium ions across epithelial membranes, such as the alveolar epithelia located in the lungs. Although most people without CF have two working copies of the CFTR gene, only one is needed to prevent cystic fibrosis due to the disorder’s recessive nature. CF develops when neither gene works normally (as a result of mutation) and therefore has autosomal recessive inheritance.

Cystic Fibrosis is a life-shortening disease. But thanks to research that has produced new knowledge about CF and more effective treatments, life expectancy is increasing. In 1938, when CF was first recognized as a disease, most babies with CF died before their first birthday. By the 1950’s people with CF were living a bit longer but rarely made it past early childhood. Things started to improve more in the 1980’s when people with CF could expect to live into their mid to late twenties. Since the discovery of the CFTR gene in 1989, life expectancy has continued to increase. The average life expectancy for people living with CF today is 37 year, but some people live much longer, that number is continuing to rise. because of the advances in treatment and technology, some researchers predict that babies born in the 2000’s will live into their fifties.

My life has had a large impact from having CF resulting in two double lung transplants. To this day I am grateful to have received, I have never let either issue interfere with my life. I enjoy every day as if any other person would, I have a great sense of humor and tend to pass it along wherever I go.

The purpose of this Blog is to share my life experiences so people can become more aware of CF and transplants.

One Comment on “About Me

  1. Hi Dan, just started following your blog. I too have CF and I am 20 years old. I just started blogging about my journey this past year. I have never needed a transplant, but I have had my fair share of hospital stays. I am very interested in learning about your transplant stories through reading your posts, because with the unpredictability of CF, a transplant could be something I need in my future. I havent had the chance to read all your posts yet, but I definitely will. You seem like a very strong fighter! I too try my best to bring out humor whenever I can. Thanks for sharing your story!

    Josilyn Gaudet


Leave a Reply

Fill in your details below or click an icon to log in:

WordPress.com Logo

You are commenting using your WordPress.com account. Log Out /  Change )

Google photo

You are commenting using your Google account. Log Out /  Change )

Twitter picture

You are commenting using your Twitter account. Log Out /  Change )

Facebook photo

You are commenting using your Facebook account. Log Out /  Change )

Connecting to %s

%d bloggers like this: