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the Zara McRae Benefit Fund

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Links to Related Sites

The Children's Cardiomyopathy Foundation has a wealth of information on all types of Cardiomyopathy specific to children.  Founded by Eddie Yu & Lisa Yue who lost both of their children to Cardiomyopathy, this site contains very detailed information on all areas of Cardiomyopathy from symptoms, diagnosis, treatment to prognosis etc.  A must read for any parent with a child suffering from Cardiomyopathy.

HeartKids Australia website covering information on all areas of Heart Disease and Conditions in children including Cardiomyopathy.

Cardiomyopathy Association of Australia provides support by matching up families.

The New England Journal of Medicine 2003 article on the Epidemiology of Childhood Cardiomyopathy in Australia.

International Health Insurance Danmark, the McRae's Insurance provider which will cover a portion of the costs involved in the USA

The Heart Foundation Australia with information focusing on Heart Disease in Adults

The American Heart Association, the reciprocal organization in the USA

Centrelink's Carer Allowance which you may be entitled to if you have a child suffering from Cardiomyopathy, ask your doctor

The Children's Hospital Westmead, formerly the Royal Alexandra Hospital for Chidlren, in Sydney, where Zara has received most of her treatment so far

The Morgan Stanley Children's Hospital of New York Presbyterian Hospital where Zara will eventually get her heart transplant

Information on the drug Dilatrend Carvedilol, the beta-blocker drug that treats Heart Failure

Visit the website of Nick & Nate, identical twin boys in America who were both born with Dilated Cardiomyopathy, and are undergoing heart transplants, read their amazing story.

COTA, the Children's Organ Transplant Association, is a US charitable non-profit group who assist families with children requiring organ transplants to raise funds necessary to cover medical costs.  The McRaes have applied for their assistance as Zara is a dual national citizen and eligible for their services.  Hoepfully, with COTA's assistance, the McRaes can raise enough funds to cover her transplant costs in full.

http://pmj.bmjjournals.com/cgi/content/full/75/881/157

http://www.justgiving.com/transplanttwins

http://www.cardiomyopathy.org/homepage.htm

http://www.organdonor.gov/

http://www.transplant.org.au/

http://www.transweb.org/

http://www.unos.org/

http://www.anzdata.org.au/

http://www.uktransplant.org.uk/ukt/default.jsp

 

The use and copying of any material, photographs, or personal details of the McRae family without written permission is not permitted by privacy and copyright laws, and shall be dealt with in accordance with the law.  The information on Cardiomyopathy should be digested as a guide only, as individual circumstances may render various symptoms/results and the information on the disease has been based on a number of the McRae family's own research and resources; and is outlined purely for the general public to have an understanding of Zara's own individual condition, and no other.  In the event we are fortunate enough and Zara miraculously no longer requires a heart transplant procedure or in the worst event she does not make it before the procedure occurs, all donations received and monies raised will be donated to research into Paediatric Cardiomyopathy as required by law under policies relating to Non-Profit Charitable Fund Organizations, Australia.  Copyright © 2006