ATTENTION MEDIA & OTHERS SEEKING INTERVIEWS!
If you represent a media company, are a student writing a report or anyone interested in interviewing our visitors, please seek permission (see email address at the bottom of the page) before posting your requests or emailing solicitations for any talk show, magazine, thesis, census or other interview on any message board on this site. If not, your posts WILL be removed. Please respect the privacy of our members.
I am the mother of Kaela, she is five and was diagnosed at birth. We live in Geraldton and had been seeing Dr Byrne who has since retired. We now see a Dr Liz Davies & Dr Tony Lafferty who are both wonderful. I too was overwhelmed when first told of Kaela's condition, and trying to take it all in and understand it is hard. There is so much information! We have had a few ups and downs but generally I have found that I have been able to completely rely on the endocrinologist's and Princess Margaret, just make sure your local G.P is fully up with what is going on as I have found that to be a huge problem in Geraldton in case of an emergency, though Perth should be better. Hopefully all will sort out for you over the next weeks - Take care
