Guest guest Posted January 11, 2008 Report Share Posted January 11, 2008 Phoebe has cf and Down’s syndrome and we use breathing treatments and the vest as well. I am pushing to get her on the hypertonic saline treatments, but our physician told us that sometimes in very young children it can cause bleeding because their lung tissue is so fragile. But we should be getting to use it this year. Dinkins-Borkowski; Nolan(5) nocf, Phoebe(3) Ds & cf Watch Our Christmas Video, Click Here! From: Down Syndrome Treatment [mailto:Down Syndrome Treatment ] On Behalf Of jmhill46619 Sent: Friday, January 11, 2008 5:13 PM Down Syndrome Treatment Subject: Re: glutathione: capsules vs. cream now NAC () , is 12. When he was first dxd with asthma at 2yr, it was scarey, esp in the hospital. But he never fit the profile of asthma (probably because of the undxd TE fistula)He has been tested for everything from pulumonary hypertension, CF, tuberoclusis(sp?), valley fever and other fevers. He had respiratory and renal failure earlier this yr. It is really frightening when you give a child nebulizer treatment to help him breathe and it depresses his breathing further. Carol is on the right track with saline treatments. is now dxd with chronic lung disease. We have a prescription for the hospital pharmacy (can't get it at a reg pharmacy) for 7% saline that does nebulizer treatments twice a day. We also have a vest that shakes him (CF patients use this also) because he is prone to get multiple mucus plugs. He does not cough deep enough. Even the RT at hospital would suction and try to " tickle " his cough response and they couldn't. Being on this list is helpful, ask the experienced moms questions and you'll get lots of help and research to do to help your son. Janet Quote Link to comment Share on other sites More sharing options...
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