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Re: nasal cannula O2

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heidi,

My DD is 6 and we have had oxygen her most of her life. As an infant/toddler

it was tough to keep the cannula on. Now it is no big deal. has given me

some hints on making it more comfortable for her. First we use a cannula like

the Salter because it tends to be a bit stiffer than the other brands.

still

used the infant size most of the time. She weighs about 41 pounds. Then, we

cut off the prongs. We cut them totally off. She may need a bit more oxygen

this way but it is worth it. We also use humidity because it is more

comfortable

for her. Giving her some control in this situation helps compliance a whole lot.

We have let her help us put the cannula on, etc. since late infancy.

sleeps with a continuous pulse ox. For our family, it is more convenient

than waking up and having to check to make sure the oxygen is on. It does

go off three or four times a night but I still sleep better with it than

without. She

has been taught to wiggle her toes if she needs help and can't speak (as in an

asthma attack). also hypoventilates and has hypercapnia and

hypercarbia. is also pretty fair but I can't always tell when her sats are

low. She can be pretty blue and have decent sats and be pink in the 80s.

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