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Australian cf parent

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Thank you for welcome to your group. I am mother of 24 yr old son, with

cf, in Melbourne, Australia. He has just come out of hospital after a

" tune-up " (2 weeks) and is feeling better. He is very beautiful, strong,

and wise and dearly loved. We are so lucky in Australia that treatment is

free of charge and prescriptions, even Pulmyzone, cost about $4. However

if he could work he would lose this benefit, and if he married and his wife

was employed, he would lose medicine concessions.. I think Pulmyzone cost

about $1000 per week.(Our Govt. picks up this cost) How is treatment in

other countries? ***** Forwarded Message Follows *******

>To: leonards@...

>From: cfparents Moderator cfparents-owner >

>Date: 3 Oct 2002 15:55:26 -0000

>

>

>Hello,

>

>Welcome to the cfparents list. Thank you for subscribing and I hope that

you

>find the support and information here that you've been seeking.

>I am the mother of three wonderful children, ages 9, 7, and 4. The four

year

>old has cystic fibrosis. As the parent of a child with this diagnosis, I

know

>that life can be a roller coaster ride at times, and it's good to know

that

>there are others who share your fears, concerns, experiences, and hopes.

>The email address to send list messages to is

>cfparents

>Feel free to post an introduction for us to get to know you, and any

>questions/concerns you may have. You are not alone!

>

>

>E-mail me at ma8169@... with any suggestions.

>

>This list is designed to be inclusive in nature.

>Please do not post anything overtly religious in nature,

>as we have subscribers of all faiths (and lack thereof) on this list.

>

>

>Post message: cfparents

>Subscribe: cfparents-subscribe

>Unsubscribe: cfparents-unsubscribe

>List owner: cfparents-owner

>

>Please note that responding to this email will send

>a message directly to me (the list owner.)

>If you wish to post to the list, please use the address:

>

>cfparents

>

>Thanks,

> Albright

>(The List Owner)

>

>

>

>

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