News
07
October
2014

Health Minister receives petition

Health Minister Jim Wells has received a 24,000 strong petition supporting Cancer Focus NI’s call for equal access to cancer drugs for local patients.

A wheelbarrow load of signatures was delivered by our Chief Executive Roisin Foster and cancer patients Vera Sanderson and Allister Murphy on the steps of Parliament Buildings, Stormont.

  • Click here for Minister’s comments. Read Allister Murphy’s story here and John McAllister’s here.

The campaign is calling for local cancer patients to be given the same access to 40 cancer drugs as those living in England. Over four months, more than

First Minister Peter Robinson and Health Minister Jim Wells meet
First Minister Peter Robinson has a private talk with cancer patient Allister Murphy to hear his experience first hand

 20,000 local people pledged their support online and another 6,000 sent postcards of support.

Speaking on the success of the campaign Mrs Foster said: “The Equal Access Campaign has resonated strongly with the Northern Ireland public and we thank them for getting behind it. The handover at Stormont represents the next phase of the campaign – the call for our Assembly to act now and put things right without further delay.

“England has had a Cancer Drugs Fund to pay for costly non-NICE approved drugs since 2011. Just this week, Scotland announced the creation of a £40m New Medicines Fund, paid for by the pharmaceutical industry under the Pharmaceutical Price Regulation Scheme (PPRS), effectively doubling its current special drugs fund giving patients in Scotland better access to expensive drugs.

Funding

“While we fully understand the pressures on the budget, there is a solution to this particular problem that needs to be seized. The PPRS is an avenue that would give much needed access to these drugs in NI with little or no extra cost to the Health Department.

“In the first quarter of this year, NI has already received a £2.89m rebate through the scheme, and a similar amount is to be expected every quarter for the next five years. We would ask that the Northern Ireland Executive establishes a similar fund, which could be adequately funded by the PPRS.”

Review

In May the Health Minister announced a review of the Individual Funding Request (IFR).  At the end of September an evaluation team was established with the review set to begin later this month. The findings of this review will be available at the end of the year, with potentially further time needed before recommendations are implemented.

Mrs Foster continued: “The time taken for this review to be put in place is precious time that our cancer patients do not have. As we wait for action to be taken the problem is growing – when we launched the campaign in June there were 38 cancer drugs that patients in NI couldn’t readily access; that number has increased to 40.

“We are also calling on the Health Minister to suspend the ‘clinical exceptionality’ clause within the IFR process immediately while the review is on going to allow more patients access to the drugs they need as soon as possible.”

Mrs Foster added: “The time has come for decisive action to give much improved access to drugs that can extend patients’ lives, improve quality of life and ease symptoms. We need more robust acknowledgement by the Executive that there is a major problem in access to specialist cancer drugs, and a plan of remedial action to be announced immediately.”

Changes

In May this year, Scotland suspended its ‘clinical exceptionality’ clause as part of its current drug approval system. This instantly allowed clinicians more freedom to prescribe medicines, including non-NICE approved drugs, which they believe will best help their patients.

Vera Saunderson (72), a widow and grandmother from Carrickfergus, who has advanced liver cancer, said: “My oncologist confirmed that a drug was available through the Cancer Drugs Fund in England and had I lived there I would be in a better position to access it.

“I replied, ‘Aren’t I a UK taxpayer?  Do I not also live in the UK?’ I couldn’t understand why people in England can benefit from this drug while NI patients are denied it.”

 

 

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