As part of our Rare Disease Day podcast series, Emily speaks with Michelle Robinson about the rare condition MELAS, a mitochondrial disease which Michelle and her family live with.
 
To learn more about mitochondrial disease and support available, contact The Mito Foundation Support Network at <a href='mailto:info@mito.org.au'>info@mito.org.au</a>.
 
To find out about peer Support Groups in WA, contact ConnectGroups at <a href='mailto:info@connectgroups.org.au'>info@connectgroups.org.au</a>.
 
Music: <a href='https://www.purple-planet.com'>https://www.purple-planet.com</a>

As part of our Rare Disease Day podcast series, Emily speaks with Michelle Robinson about the rare condition MELAS, a mitochondrial disease which Michelle and her family live with. To learn more about mitochondrial disease and support available, contact The Mito Foundation Support Network at info@mito.org.au. To find out about peer Support Groups in WA, contact ConnectGroups at info@connectgroups.org.au. Music: https://www.purple-planet.com

As part of our Rare Disease Day podcast series, Emily speaks with Michelle Robinson about the rare condition MELAS, a mitochondrial disease which Michelle and her family live with.
&nbsp;
To learn more about mitochondrial disease and support available, contact The Mito Foundation Support Network at <a href="mailto:info@mito.org.au" rel="noopener noreferrer">info@mito.org.au</a>.
&nbsp;
To find out about peer Support Groups in WA, contact ConnectGroups at <a href="mailto:info@connectgroups.org.au" rel="noopener noreferrer">info@connectgroups.org.au</a>.
&nbsp;
Music: <a href="https://www.purple-planet.com" rel="noopener noreferrer">https://www.purple-planet.com</a>

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Rare Disease Day Series: MELAS

Rare Disease Day Series: MELAS