Let's talk LHON
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Let's talk LHON
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Leber hereditary optic neuropathy, or LHON, is a rare type of mitochondrial disease, mito for short. LHON most often affects central vision.
In this episode, we talk through what LHON can look like in everyday life, including why peripheral, or side vision, may remain even when central vision changes. We explain how LHON is linked to a genetic change in mitochondrial DNA, while also noting that not everyone who carries the genetic change will develop symptoms. We also walk through how diagnosis and care can involve eye and vision tests, genetic testing, and support from low vision and rehabilitation services. We take a practical look at supports and pathways that may help, including NDIS navigation support and what kinds of information can strengthen an application.
The information in this episode is based on Mito Foundation resources, including the LHON information page and the information sheet on NDIS assistance for LHON. For support, call the Mito Foundation Helpline on 1300 977 180 or visit mito.org.au. To stay connected, subscribe and follow MitoCast wherever you found this episode.