Joint funding supports Tasmanian branch

Generous funding from the Clifford Craig Medical Research Trust, Rotary Tasmania and some Lions Clubs will support the Tasmanian branch of the Australian Genetic Heart Disease Registry for the next four years. Clifford Craig Medical Research Trust supported the establishment of the Tasmanian branch in 2010 as part of an Honours research project, which was […]

New Registry coordinator at Melbourne’s RCH

Vanessa Connell from the Royal Children’s Hospital (RCH) in Melbourne has joined us as the RCH’s new Australian Genetic Heart Disease Registry Coordinator. Vanessa is excited about working on the Registry and working with RCH families to help improve our understanding and care of genetic heart disease in Australia. “While working with children and families […]

New Left Ventricular Noncompaction (LVNC) Information Sheet Online

Our LVNC information sheet is the latest addition to our genetic heart disease series for patients and families. The new information sheet provides key information on left ventricular noncompaction (LVNC), a genetic heart disease which is less well recognised compared to other cardiomyopathies. LVNC is a rare disease, caused by a gene fault affecting the […]

Genetic Testing: Saving Lives and Cost

Genetic testing is a valuable tool in identifying gene faults in family members who are at-risk of disease.  But a new study based on data from the Registry has found it can save costs as well as lives. Published in the prestigious Heart journal, the study found genetic testing of families with hypertrophic cardiomyopathy (HCM) […]

Cardiomyopathy seminar in Brisbane

The Cardiomyopathy Association of Australia (CMAA) has an interesting line up of leading specialists to talk at their 2012 seminar in September. Cardiomyopathy – A Moving Picture 2012 Seminar will highlight recent developments and the latest research in the diagnosis, treatment and after care of people with cardiomyopathy. Professor Chris Semsarian, Dr Jodie Ingles and […]

Cuppa for HeartKids

In August and September make your cuppa count by raising funds for HeartKids Australia. During August and September 2012 HeartKids will be running their Cuppa for HeartKids campaign where people and businesses are encouraged to host a tea party and raise funds for childhood heart disease (CHD). HeartKids are a great organisation that improves the […]

HeartKids grant for gene research into sudden death in children and babies

Childhood heart disease (CHD) is one of the leading causes of infant death in Australia. Every week more than four young Australians die from CHD. Investigating the role of potentially deadly genetic heart diseases play in these heart-breaking losses will receive a boost for one research team in Sydney. The $29,000 HeartKids grant will be […]

Q&A: caffeine and heart disease

Prof Chris answers a query about caffeine for people with or at-risk of genetic heart disease. Question: As part of the dietary limitations on a person suffering from a SAD’s, what is the recommended limit of stimulants such as caffeine? Kathy C Answer from Professor Chris Semsarian: High levels of caffeine can have negative effects […]

Sydneysiders: learn more about ICDs at group meeting

Find out more about ICDs with cardiologist Dr David Whalley when he talks on Thurs 26 July at the next ICD Group Meeting at Royal North Shore Hospital (RNSH). RNSH cardiologist Dr David Whalley will give you an interesting overview of implantable cardioverter defibrillators (ICDs), how they work and how technology has progressed over the past 30 years. […]

Open your heart for HeartKids in February

Every day, 6 babies are born with Childhood Heart Disease (CHD). Learn more about CHD today February is HeartKids Awareness Month & Valentine’s Day (14 Feb) is HeartKids Awareness Day! HeartKids is trying to raise awareness and funds in Australia about Childhood Heart Disease (CHD), which is one of the biggest killers of children under the […]