27 May 2019

SMA advocate taking Pharmac to Human Rights Commission

From First Up, 5:52 am on 27 May 2019

An Spinal Muscular Atrophy advocate says Pharmac is playing a money game while patients are dying and she's now looking to take the agency to the Human Rights Commission. Fiona Tolich has SMA herself and she believes Pharmac's delay in funding certain medications is a crime against humanity. Now she's calling on other patient groups for support.