I would like to contact those people who
are ventilated mechanically due to an
obstructive pulmonary desease. How do
they cope with the infections ? Do they
know ways to reduce their frequency ?
Are these people living at home ?
For the time being, I am in the Prolonged
Care Unit of a Chest Hospital but would like,
of course, live at home. Has anybody some
useful ideas ?
Thanks a lot.
B. Ilie