HFI Support Australia

Home
Australia
Noosa Heads, QLD
HFI Support Australia

Call Directions Website Contact the organization

An association that provides guidance & support for people with Hereditary Fructose Intolerance

09/10/2026

A huge thank you to the team ‘Silvia’s and Rodrigos’ for bringing us this podcast on Hereditary Fructose Intolerance with Prof Brouwers and Cassiman 🙏🏼 Please listen and share to help us create more awareness. It is real. It exists. There are so many undiagnosed and living with illness that need support

https://open.spotify.com/episode/3CUQslOhky1GYXeIF7hboq?si=_XiwgJNRQRWiK5oe6oi5mg

JIMD Podcasts · Episode

22/06/2026

Please help us in creating awareness so that others can be diagnosed 🙏🏼

29/05/2026

It’s official 🙏🏼 We are Australia’s first HFI SUPPORT not for profit organisation 🇦🇺

14/05/2026

Comment Below 👇🏼 Your Score -
This was posted on another page and after reading the comments, it hit hard how restrictive living with HFI actually is. Unfortunately most people don’t understand what it is like and we are often called ‘picky’ or ‘fussy’ eaters. This is not the case - we CANNOT digest Fructose (even if we wanted to) We get very sick. As eating out causes so much anxiety for people with HFI, food and meal preparation is vital. Food = Fuel. The joy if food is often lacking for someone with HFI. It is a bitter pill to swallow

10/04/2026

Our very first HFI Support Australia get together for our QLD & Northern NSW crew “Isn’t it wonderful to have company”

02/04/2026

Attention all QLD HFI’ers, family, carers and friends. Please join us for our first QLD Meet Up! Let’s mingle, share stories and connect 🙏🏼 Send us a DM and we will add you to the table

28/02/2026

Living with a Rare Disease is unbearably lonely. Connecting with others is life changing. At the age of 73, Betty Walters read an article in about Alan. A man in the UK who had been diagnosed with Hereditary Fructose Intolerance. At the age of 73 Betty was no longer alone. She was no longer a ‘fussy eater’ or ‘being dramatic’. Betty was validated. In 2026 it shouldn’t take decades to obtain a diagnosis. DNA testing should be easily accessible and affordable for all so we can prevent illness and save lives. We live with a Rare Disease and we are creating AWARENESS

Address

PO Box 2003
Noosa Heads, QLD
4567

Telephone

+61403888030

Website

http://www.hfisupport.org.au/

Alerts

Be the first to know and let us send you an email when HFI Support Australia posts news and promotions. Your email address will not be used for any other purpose, and you can unsubscribe at any time.