SEE MY TRANSPLANT ON YOU TUBE

To see CNN video of my transplant go to http://www.youtube.com/. Then search " Susan Burroughs".

Are you on FACEBOOK? If so, send me a friend request so we can be friends! "Susan Crenshaw Burroughs"

What is Cystic Fibrosis?

Cystic fibrosis is an inherited chronic disease that affects the lungs and digestive system of about 30,000 children and adults in the United States (70,000 worldwide). A defective gene and its protein product cause the body to produce unusually thick, sticky mucus that:
clogs the lungs and leads to life-threatening lung infections; and obstructs the pancreas and stops natural enzymes from helping the body break down and absorb food.
For more information visit http://www.reachingoutfoundation.org/

Monday, January 26, 2009

Medical Update

It has been a while since I gave an update on my photopheresis treatments. I had two treatments in December (one trip) and I also went to lung transplant clinic. The transplant docs were pleased at how my photopheresis treatments are going and my lung function was up!! 87% FEV1... WBC (white blood count) is good and Kidney function good.
But... there is always a but... isn't there... BUT.... they want to do a couple of new things as well to save my new lungs.

1. Start taking Azithromycin every Monday, Wednesday and Friday
2. Get some Esophagus Studies to see if I have acid reflux. (Acid reflux will destroy your lungs)Italic to be done in February.

I had 2 photopheresis treatments (one trip) in January. The first day went great. The second day I had a few problems with blood clots but my A number 1 photopheresis team took care of that and the treatment went fine.

Thursday, January 1, 2009

New Year's at Sea World


Leah wants to become a marine biologist so we went to Sea World for New Years. Here we are having dinner with Shamu. Notice I have on a wet suit. That is because Shamu came right up to our table! (No we were not eating fish)