RDNZ presented a collective response on behalf of all those with medicines access issues who live with a rare disorder to the PHARMAC Review Panel last month. 

"We consulted with our collective of rare disorder support groups to ensure we focused on the key issues, plus created a template with messages to make it easy for groups to respond themselves," says CE Lisa Foster. "In total, the Panel received 14 submissions from rare disorder groups within our collective."

PHARMAC Review panel presentation(PDF)

Here is an update by Jaime Christmas, Chief Executive of the NZ Amyloidosis Patients Association 

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From my point of view as a patient advocate, the panel is interested in understanding our viewpoints. They wanted to hear the hardships which the rare disorder community is presently facing. Their query on what PHARMAC can do better and what needs to happen to see change is good to hear. Questions posed on whether rare disease representation should sit within the PHARMAC model or be a separate entity displayed a concern on the panel's part to take actionable steps. Also, clarification on where funding should go from rare disease medicine access shows forward-looking.

However, some inquiries did highlight a lack of understanding of the characteristics, requirements and burdens experienced by people with rare conditions. Equally concerning is the inadequate knowledge of health technology and the advantage of embracing modern medicine. This short-sightedness accentuates the importance of the rare disease community to have a voice at the table.

All heavy-handed questions posed were articulately answered by Lisa Foster from RDNZ. Within the rare disease sphere, we are very fortunate to have Lisa at the helm of RDNZ together with her team. Tossed around like in a washing machine by various government entities and have had their funding vastly reduced, they keep championing for the likes of you and me. Change must happen. The length of time this would take is dependent on us supporting one another. Here's praying and hoping for a better future for all of us.

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Our Collective

Rare Disorders NZ is the collective voice of all people living with a rare disorder and their whānau. Our rare collective is made up of more than 150 disorder-specific support groups.

Our work is informed by the issues important to our collective. We work together to improve healthcare and wellbeing for everyone living with a rare health condition in New Zealand.

Learn more