For Rare Disease Day 2024, we travelled to New Zealand to advocate for the Immune Thrombocytopenia community. While there, we joined the Rare Disorders New Zealand Support Group breakfast.
For Rare Disease Day 2024, we travelled to New Zealand to advocate for the Immune Thrombocytopenia community. While there, we joined the Rare Disorders New Zealand Support Group breakfast.
Written by Dr Cindy Neunert, Paediatric Hematologist & Medical Advisor
The first week of December, when the American Society of Hematology (ASH) holds its annual meeting, is always a busy time for hematologists.
During November 2023, ITP Australia and New Zealand participated in the annual Haematology Conference, Blood 2023, held in Melbourne, Victoria. This marked the organisation’s third consecutive year with a presence in the Exhibition Hall alongside other non-profit organisations.
From Monday, 25th September to Saturday, 30th September, Australia and New Zealand turned PURPLE for Immune Thrombocytopenia in the annual #LightUp4ITP awareness campaign, and we kicked off the inaugural #Planking4Platelets challenge.
MEET – CONNECT – SHARE – Join us online during our regular Virtual Patient Meetings.
Danielle and Patricia from ITP Australia had the wonderful experience of attending the UK ITP Support Association’s Patient Convention on Saturday, 13 May 2023.
ITP Australia has worked to illuminate various locations across the country for the last couple of years to help raise awareness for Immune Thrombocytopenia.
In November, Danielle travelled to Sydney to attend and participate in the 2022 National Rare Disease Summit organised by the national peak body for Rare Diseases, Rare Voices Australia.
Missed the ITP Australia Virtual Patient Conference for 2022, or would like to revisit one or more of the presentations? View them here.
ITP Australia partners with Rare Voices Australia to ensure that patients living with Immune Thrombocytopenia are part of the conversation.