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Genetic causes and symptoms (8 mins)
Genetic causes and symptoms (8 mins)
A genetic disease
A genetic disease
MJD is a genetic neurodegenerative disease, which means that it is a disease that damages the nervous system and muscles AND that it is passed on in families. It is a type of Spinocerebellar Ataxia (SCA3).
What causes MJD and what are its symptoms?
What causes MJD and what are its symptoms?
Julie Wunungmurra is an Aboriginal Community Worker with the MJD Foundation.
This video was made to educate families. In simple language, it describes the genetic cause of the disease, and how it is passed down in families.
📝 Activity
📝 Activity
Watch the video and complete the interactive activities.
This video is one of a range of resources that assist families to understand more about MJD. This video is also available in a range of Aboriginal languages. Please click on the below links to learn more.
The disease can get worse with every generation
The disease can get worse with every generation
The MJD Foundation's clients have the type of MJD that has an 'anticipation' effect, meaning with each generation or new family member it's passed down to, it gets worse. With each generation, the disease typically develops earlier than their parents and their symptoms progress faster.
In one family, several generations can be affected at the same time. Some children with MJD have to use a walker or wheelchair before their parent needs to.
This makes it hard for family members to look after each other. Sometimes there are other worries like crowded housing, other sicknesses, money and unemployment, too.
All of these challenges can cause a lot of stress for families living with MJD. It is common for parents and unaffected family members to feel guilty.
Want to know more?
Want to know more?
Select the 'Genetics' button to find out more about MJD in families, and the genetic explanation.
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