This website is a labor of love dedicated to our first Son, Harrison Cain, who was diagnosed with Branchio-Oto-Renal Syndrome shortly after birth in 2003.
We have found that there is very little information regarding Branchio-Oto-Renal Syndrome, so our hope of starting this website is that we can start a forum to help educate ourselves and others by sharing experiences and information gathered by all those that have been touched by this rare condition.
This Website is a work in progress and will be maintained in our spare time. Please email me any information or links that might be useful and I will post them on this website.
Thank You, Fiona Cain.
BREAKING NEWS
Transplant conference - Sydney
Welcome to
The Cain Foundation for Branchio-Oto-Renal Syndrome
The Cain Foundation for Branchio-Oto-Renal Syndrome
The information contained on this website is provided in good faith. While the contents are obtained from various sources that are deemed reliable, it is not guaranteed as accurate or complete and should not be relied upon as such. It is recommended that you seek independent, professional advice before implementing any of the suggestions to ensure that it is appropriate to your needs and circumstances.
ABN: 14 437 033 250
Produced in 2007 for The Cain Foundation. Site design by D-2 Design
ABN: 14 437 033 250
Produced in 2007 for The Cain Foundation. Site design by D-2 Design