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National Strategic Action Plan for Rare Diseases

Susan White, MAA President, is delighted to be attending the Parliamentary Event to be held in Canberra, on Wednesday, February 26th in celebration of Rare Diseases Day.

Inform your Federal Member Please!

The letter requesting support in applying for Rituximab treatment in Myasthenia to be included on the PBS has gone to Minister Hunt.

MG Versus Mgen

An unfortunate media release occurred in July this year.