I am totally naive as to the FEV #'s. Aidan at age 4 just did his first and had a # of 151% so I was psyched. We are beyond compliant with his treatments and do the hour daily at top pressure everyday of his VEST, Mucomyst, Pulmozyne and a slew of others...
But as CF progresses, how low can your numbers go before transplant? If you have a FEV of only 40% or something, does that mean that 60% of your lung function is gone? Are you constantly out of breath and feeling crappy? I am in awe of how some of you manage life with low FEVs? It must be so frustrating to do all these treatments and still not get results?
Megan