Following on from our informative National Zoom Coffee and Chat, here is your opportunity help our leading researchers to help you and our "CMT family". Are you interested to participate in our research? Do you have CMT that is genetically [...]
Did you know that 40% of those who have been diagnosed with CMT don’t know what specific CMT gene they have? Professor Marina Kennerson PhD, from our own world leading ANZAC Research Institute, will be giving an informative and encouraging presentation regarding a major [...]
The Sord Deficiency Webinar recording, from Hereditary Neuropathy Foundation in America, would be highly relevant for patients with a positive SORD mutation genetic test. This mutation is only reported in families with recessive inheritance. The therapies in the webinar would [...]
Teens Tri for CMT. Lachie McNamee is a lively 14-year old in Grade 9 at Toowoomba Grammar School. With a family history of CMT, Lachie was diagnosed with the disease a couple of years ago, but only his closest friends knew. Last year he [...]
An excellent overview of Genetic testing that assists us in understanding more of the "pros and cons" involved Read more
Sydney Morning Herald article about CMT (Charcot-Marie-Tooth)disorder, the most common inherited neurological condition, that is poorly understood. Read more
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