Her petition, which is available on the Parliament website, is calling for a series of amendments to the bill.
Those include allowing patients to import prescription medications, and changing the definition of “advertisement” so that people can continue to talk about unfunded medicine without risk of penalty.
As of this morning the petition has clocked up more than 3500 signatures.
“I got the idea for the petition because I was trying to get hold of Members of Parliament and I was having no luck,” she said.
“It’s tracking well, considering it’s just a mum in Gizzy.”
Theresa has been supported in her fight by Patient Voice Aotearoa chair Malcolm Mulholland, who has labelled the bill “badly drafted”.
He previously told Local Democracy Reporting the Government was trying to prevent New Zealand patients from receiving medications that weren’t fit for purpose, even though there wasn’t evidence to suggest this was an issue.
“The Government isn’t aware of the consequences of what it is they’re proposing.”
Theresa and Mr Mulholland plan to take the issue to Parliament in person on June 7 with a march.
He has also prepared an open letter backed by a number of groups and organisations concerned about the proposed changes.
Health Minister Ayesha Verrall is in charge of the bill but has turned down a previous request for comment, with her office saying it would not be appropriate while the bill remains before the Health Committee.
The minister will get a report from the Ministry of Health on submissions and proposed amendments in June.
Theresa’s petition, which closes on Sunday, May 30, can be accessed at tinyurl.com/3svc6amr
A Gisborne woman living with terminal lung cancer is continuing her fight against proposed changes to the country’s medicine legislation one signature at a time.