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G’day, My name is Kathryn,an aussie, I am a single parent with 2 children, Tristan aged 17 and jasmine aged 8 years. 8 years ago I was first diagnosed virtually straight after jasmines birth, with Osteopenia –85% density in my bones, then came Marfan’s syndrome, Bronchiectasis, Emphysema, Cystic Fibrosis and now an Ulcer is the lower throat.

The pages consist of my illnesses, my feelings, emotions, and the stress I am going through.

The Rose was chosen by Cystic Fibrosis (CF) Victoria as the Australian symbol for CF. The rose has endured throughout history as the symbol of abiding love. It is also linked to CF because of the story of a young boy who, in an effort to describe his sister's Cystic Fibrosis, mis-pronounced it as ‘65 Roses’.

On my support page, I am hoping to collect 65 roses (animated)** The roses have been broken up and put on different pages to download quicker**. If you have any or know some websites that have some please email me. Unfortunatly you can only access the "roses" via the support and guestbook page only.

Please bookmark this site, and come back often.
Take Care and have a nice day


In Memory Of :(Marfans)
Hints for the Home
Marfan’s syndrome
Other People with Marfans
Beal's syndrome VS Marfans
Cystic Fibrosis
The original "65 roses" by Lee J. Collier"
Diary Entries
My Support and GuestBook
Tristan's heart Murmur/CF
Jasmine's Marfan's/CF/Austism -

*****DISCLAIMER: None of the data or information mentioned or contained in this site is intended to be used or construed as a substitute for professional medical care and advice by your health practitioner. The author assumes no responsibility for readers use of the material and opinions expressed.*****

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My 1st WICCAN Homepage