 |
 |
 |
|
|||||||
| Pediatric Tracheostomies For parents and caregivers of children with tracheostomies. Please limit discussion to seeking and sharing of information pertaining to tracheostomy care, medical issues, special needs, disabilities, networking and moral support. |
 |
|
|
Thread Tools | Display Modes |
|
#1
11-20-2009, 10:57 PM
|
|||
|
|||
Does anyone use helios o2 I think that is how to spell it!
We have always used portable tanks for on the go , but we offered helios with our new DME! ANy complaints! What do you all use or think!
__________________
Amy, Mom to Brionna (9) , and to Jarriell Jr better know as JJ (born 10-27-08) trach since 02-10-09, diagnosis Severe chronic lung & BPD. Nissen fundo also lower pyeloplasty & Mic-Key button all done 03-09. 2 Prolapse rectum repairs. Right & left ignueal hernia repairs. JJ decanned himself aug 2010 and has been doing great!!! Sleep apnea resolved with toncilectomy! 
|
|
#2
11-20-2009, 11:17 PM
|
||||
|
||||
|
Never used it, but sounds great!
 Just make sure it supplies continuous - I just assume since it's liquid O2. The downfall of liquid O2 is that it evaporates... in case you aren't familiar with it.
__________________
Dawn  former 26 weeker -- 4/2006 -- trach, g-tube, nissen; came home 1/07 vented 24/7; Successfully decanned 8/8/2008 -  Follow decan at: http://sleepy-dogs.blogspot.com/
|
|
«
Previous Thread
|
Next Thread
»
| Thread Tools | |
| Display Modes | |
Linear Mode
|
|
All times are GMT -5. The time now is 02:15 AM.