Guest guest Posted February 28, 2004 Report Share Posted February 28, 2004 I did watch the special - I thought it was a very realistic " day in the life " of a young, 26 year old woman with CF and another man, age 40, who has had a lung transplant. 3 of his siblings died earlier in life from CF, one after a double lung transplant. He lives a full life but takes over 30 pills a day (to combat organ rejection) and also 5 shots of insulin per day as he has become diabetic after the transplant. I did not realize that diabetes is very common after a lung transplant for CF patients. Another interesting fact is that the young girl was doing very well - she graduated from college and worked for Lehman brothers- then one year she MISSED HER FLU VACCINE, caught the flu, which progressed to pneumonia, and it's been downhill from there. Her doctor recommends she be listed for a transplant because her PFTs are under 30% expected capacity. I did not know this was the marker. That was a big lesson to me on the importance of the flu vaccine. The show also followed the young woman (I'm horrified that I forget her name) through her vest treatments, nebs, doctor's visit, etc., and now she is on disability. This was a great show for people who think " oh, they're doing fine, they look good " because clearly it takes a lot of work to look good. It was also heartbreaking - I definitely teared through the second part of the show - when the girl broke down because she her doc wanted her to be listed for a transplant, and also when the mother spoke of her daughter suffering. The hostess was a little too chipper for me but she did ask some very tough and sensitive questions - for that I admire her. Krishnan Mom to Santosh, 6wcf and Leela, 4wocf Quote Link to comment Share on other sites More sharing options...
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