Guest guest Posted March 30, 2003 Report Share Posted March 30, 2003 I sent the following email to ita some time ago but have had no reply so assume I made a mistake with the email address and will post the info here. The ACFA email address is www.cysticfibrosisaustralia.org.au hope this is of some help. Also Leon if I am incorrect in my assumptions could you please furnish ita with the correct info. Terri. Date: Fri, 21 Mar 2003 09:24:28 +1100 From: Therese Fox Reply-To: tmfox@... To: needa_benny@... Hi there I am Terri I live in Hobart - how much further away from you could I be - I have A daughter Ainslie who is 10 1/2 wcf and a son Connor 6 1/2 nocf. I got your email address from the CF parents list so thought I would write and say hello. Having a child with cf is " interesting " but it isn't the end of the world, just life changing. How is Brodie? 2 is such a gorgeous age, I do miss those baby times but I wont be having another.sighhhhhh. Two kids is enough. Knowing what your entitlements are is a tough question. I would recommend contacting the ACFA- I can get you their contact details but I have a meeting to go to shortly so will send them soon. I did a stint on the board a while back and I seem to recollect that you can go to a SA cf clinic - I may be totally wrong on that one. I know that here in Tassie if there is not a specialist here for a particular problem then you are sent to Melb. Have you approached the main hospital admin in Darwin - they may be able to give you some info, or even the health dept. I must go hope I've helped a little, will write again soon. Quote Link to comment Share on other sites More sharing options...
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