We speak with Ellie Robertson on her thoughts and process of NDIS self management.

NDIS self management

Today's guest is Liliana Bulfone and Julie discusses the PBAC process and Spinraza. Contact us at <a href="mailto:reception@smaaustralia.org.au">reception@smaaustralia.org.au</a> or call (03) 9796 5744 Visit our website at <a href="http://www.smaaustralia.org.au" rel="noopener">http://www.smaaustralia.org.au</a> Facebook <a href="https://www.facebook.com/SpinalMuscularAtrophyAustralia" rel="noopener">https://www.facebook.com/SpinalMuscularAtrophyAustralia</a>

Today's guest is Liliana Bulfone and Julie discusses the PBAC process and Spinraza.Contact us at reception@smaaustralia.org.au or call (03) 9796 5744Visit our website at http://www.smaaustralia.org.auFacebook https://www.facebook.com/SpinalMuscularAtrophyAustralia

Today's guest is Liliana Bulfone and Julie discusses the PBAC process and Spinraza. Contact us at <a href="mailto:reception@smaaustralia.org.au" rel="noopener noreferrer">reception@smaaustralia.org.au</a> or call (03) 9796 5744 Visit our website at <a href="http://www.smaaustralia.org.au" rel="noopener noreferrer">http://www.smaaustralia.org.au</a> Facebook <a href="https://www.facebook.com/SpinalMuscularAtrophyAustralia" rel="noopener noreferrer">https://www.facebook.com/SpinalMuscularAtrophyAustralia</a>

PBAC, Lobbying Goverment

Spinal Muscular Atrophy (SMA) is a rare genetic muscle wasting disease that is the childhood version of motor neurone disease. If you are newly diagnosed, or have just come across our page for the first time, we urge you to get involved, within the SMA community here in Australia. We would love to hear from you and are happy to support you on your journey. We acknowledge that each person is different, and we endeavour to assist you and your requirements.

News

Spinal Muscular Atrophy (SMA) is a rare genetic muscle wasting disease that is the childhood version of motor neurone disease.If you are newly diagnosed, or have just come across our page for the first time, we urge you to get involved, within the SMA community here in Australia. We would love to hear from you and are happy to support you on your journey. We acknowledge that each person is different, and we endeavour to assist you and your requirements.

Spinal Muscular Atrophy (SMA) is a rare genetic muscle wasting disease that is the childhood version of motor neurone disease. If you are newly diagnosed, or have just come across our page for the first time, we urge you to get involved, within the SMA community here in Australia. We would love to hear from you and are happy to support you on your journey. We acknowledge that each person is different, and we endeavour to assist you and your requirements.

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SMA Australia

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