CHARCOT-MARIE-TOOTH DISEASE
CHARCOT-MARIE-TOOTH DISEASE
What this diagnosis means
BEING DIAGNOSED WITH CMT DISEASE
For many people, the diagnosis of Charcot Marie Tooth (CMT) comes as a complete shock.
CMT is a disease caused by genetic faults. In some cases they are inherited, in others the fault is a new mutation in the gene.
Different people respond in different ways to the news that they have CMT. There is no right or wrong way to respond. However part of your coping mechanism will probably be to gather information regarding your condition to help you understand its impact on your health and more broadly, your life.
This page aims to give you that initial information.
What is CMT?
About, Symptoms, Good News
CMT is an inherited neurological disease. Research indicates that as many as 1 in 2,500 people in Australia could have the disease.
The severity of the disease can vary a great deal from person to person.
New Diagnosis
What Type, Who Can Help
More than 100 different genes causing CMT have been identified, and the list continues to grow.
Your GP, Occupational Therapists and Physiotherapists can help. A Genetic Counsellor is a good source of information.
Have Diagnosis – What Next?
Questions, Research, Knowledge
How to find medical and allied health professionals to assist you, and how you can manage your CMT.
Will it impact other members of your family?
Are researchers close to finding a cure?
Latest News from CMT Aust
Fundraising, Events, Research
Articles and news from CMT Australia including how you can help research into the disease by fund raising.
