Guest guest Posted January 15, 2001 Report Share Posted January 15, 2001 , Yes I would like to find out a little more info on GSH, just another thing to ask my pead about and watch him squirm. He doesn't really approve of these sorts of things but he is willing to discuss them with me. . Pulmozyme trialling is because of the high cost of the medication, I know that before it was on the PBS there were a number of families paying around a $1000 a month to have their children on it. My understanding is that CF patients will receive a health care card, but then again politicians are politicians and who can believe a word they say. Here in Tassie they take a very " cautious " approach and don't use the Danish method, be interested to know about WA and NSW approaches, but then again I'm sure the different clinics in Sydney would do different things as well. . Earlier this year I started Ainslie on flaxseed oil capsules, with in a couple of days the night-time cough that she had disappeared. There was a 2 week break from it a one stage and she coughed every night for the second week, so I started her on it again and no nighttime coughs since. Then our naturopath recommended an Omega 3-6-9 which contains linseed oil (flaxseed) 500mg, Starflower oil 50mg, Blackcurrant seed oil 50mg, Vitamin E 33.6mg, Rosemary oil 10mg. This seems to have an even better effect on her sinuses. Again I gave it about a months break (used just the flaxseed oil) and she came down with a nasty sinus infection, since that I won't take her off this 3-6-9 even though it is double the price of the plain flaxseed oil. The doctors are fully aware that Ainslie is on this and before trying ANYTHING I always check with the pharmacy to make sure that it won't react with her other medications. Terri from Hobart mum to Ainslie 8 wcf and Connor 4 nocf Quote Link to comment Share on other sites More sharing options...
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