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

Rare Voices CEO, Nicole Millis, will be supporting this initiative also.

We request that you make an appointment with your local member to raise awareness of the current community inequity that exists and the practical need to make key drugs more accessible to people with a rare disease.

Call Susan on 1800 802 568 for additional details.