Guest guest Posted February 19, 2003 Report Share Posted February 19, 2003 Odd, when they ordered the vest for Mallory ( already had his) we specifically said we only wanted the vest, not the machine, and they still tried to give us the machine. geez, we didn't want to pay the 60% copay we had at the time on the dang dme coverage. so, in our case, one machine, two vests. jojo is still way too little for the vest. on the vest topic, anyone else out there paranoid about it destroying lines in the ports? after joshua had two failed ports, and both were line failure, not clots or anything anyone could have done, actual holes in the line, I became suspicious that it was the vest and reverted to good ole cpt (I know where the line is tunneled under the skin) it also made me paranoid about letting anyone else (ie camp) do cpt on him. anyone else out there with these worries????? Jen Mommy of 7, 3 with CF > Hi , > > We are finding that most insurances will cover it that way. They consider a > second device as a " convenience " and not medically necessary. About the > only time they will cover a second device is when a sibling leaves the home > permanently, e.g. goes to college, moves into their own place, etc. Other > than that, we have not had any success in convincing them of the need. > > I know this doesn't help much, but I hope it answers your question. > > Randy > > vest and mult cf kids > > > I told the nurse we would like to look into getting Adam and Alec vests. > She said that we could get away with 2 vests and 1 machine. For the > families with mult cfers, is this the approach your family is taking? I > understand the cost issue, but I was hoping the time issue would > improve..After one round of Tobi and Cipro, Adam didn't culture pa this > time. The clinic's position is one more round of Tobi and if he is neg > again, Tobi will be stopped. I was told even though he didn't culture > it, they may still be there and the thoart swap didn't pick it up. Is my > clinic's approach to pa typical? > W. , mom to Adam and Alec both 7 w/cf and 2 teenage sons w/o cf > > > ------------------------------------------- > The opinions and information exchanged on this list should IN NO WAY > be construed as medical advice. > > PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR TREATMENTS. > > ------------------------------------ > > > Quote Link to comment Share on other sites More sharing options...
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