A nationwide petition initiated by a Chilliwack mom about getting access to life-saving medicines has amassed more than 17,000 signatures in one month.
The House of Commons e-petition initiated by Jocelyn James on behalf of her son, Steven, called on the federal government to repeal changes to the Patented Medicine Prices Review Board香蕉视频直播檚 (PMPRB) drug-pricing guidelines.
The campaign that closed on May 20 drew support of Chilliwack-Hope MP Mark Strahl after he heard from James about the devastating impact that lack of access to new treatment was having on her family.
READ MORE:
They now hope it will lead to action on the federal stage since tens of thousands of Canadians agreed with James about the regulatory process around approving new medicines.
香蕉视频直播淭hrough this petition to Parliament, I committed to working with Jocelyn to raise awareness of this issue,香蕉视频直播� Strahl said in a release. 香蕉视频直播淚t香蕉视频直播檚 clear that the thousands of Canadians who signed the petition share the same concerns about access to new, life-saving drug treatments.香蕉视频直播�
James wants the federal reps to think twice now, and said she is 香蕉视频直播渢ruly grateful香蕉视频直播� for the support.
香蕉视频直播淚 hope that the federal government will see this and do everything in their power to make sure the changes are right for all Canadians before moving forward with implementation,香蕉视频直播� James said.
The MP also saw the merit.
香蕉视频直播淣ew medicines can be a lifeline to those suffering from painful and debilitating illnesses for which conventional medicine has provided little help,香蕉视频直播� said Strahl. 香蕉视频直播淭hank you to Jocelyn for creating this petition and thank you to each person who added their name, sending a message to the federal government that the changes being made to the PMPRB in Ottawa could deny Canadians access to life-changing therapies.香蕉视频直播�
香蕉视频直播淐anadians who need new or novel medications, or those who do not respond to traditional or generic treatments will be left to suffer.香蕉视频直播�
The proposed price restrictions have already stopped some new treatments from coming to Canada.
Steven, the 16-year-old son of James, loves playing hockey, soccer and being a referee. He also struggles with cystic fibrosis (CF).
香蕉视频直播淗e香蕉视频直播檚 one of the people dramatically affected by this,香蕉视频直播� James said, estimating that these regulatory changes will impact more than three million Canadians.
Up until the age of 13, Steven was relatively healthy and running track competitively, as well as playing other sports, but saw a decline in the wake of a lung infection a few years ago, his mom told The Progress.
One of the meds currently unavailable in Canada has 香蕉视频直播渞evolutionized香蕉视频直播� treatment for CF patients elsewhere. Becoming known as a 香蕉视频直播淐F wonder drug,香蕉视频直播� Trikafta is one such medicine.
But this new class of meds, known as 香蕉视频直播渕odulators香蕉视频直播� won香蕉视频直播檛 get approval under the rules, even though they are designed to correct the malfunction in the gene, not just treat the symptoms of CF.
In 2019, after the release of proposed PMPRB changes, Heath Canada has seen only 15 per cent of the new medication applications submitted to the US FDA, and the number of clinical trials started in Canada declined by 60 per cent compared to same period in the previous four years.
The House of Commons petition e-2546 amassed 17,293 signatures from April 20, 2020 to May 20, 2020. See the full text of the petition:
READ MORE:
Do you have something to add to this story, or something else we should report on? Email:
jfeinberg@theprogress.com
Like us on and follow us on .
Want to support local journalism during the pandemic? Make a donation
