Vimarsana
Biggest News Aggregation in the World

Ontario Exceptional Access Program News Today : Breaking News, Live Updates & Top Stories | Vimarsana

Stay updated with breaking news from Ontario Exceptional Access Program. Get real-time updates on events, politics, business, and more. Visit us for reliable news and exclusive interviews.

Top News In Ontario Exceptional Access Program Today - Breaking & Trending Today

pCPA announces new three-year pricing initiative agreement for generic drugs with CGPA, appointment of Douglas Clark as its first CEO | Smart & Biggar - Vimarsana News

pCPA announces new three-year pricing initiative agreement for generic drugs with CGPA, appointment of Douglas Clark as its first CEO | Smart & Biggar

The pan-Canadian Pharmaceutical Alliance (pCPA) and the Canadian Generic Pharmaceutical Association (CGPA) have agreed to a new three-year pricing initiative for generic drugs,...

As a Thunder Bay man battles a rare cancer, his family fights to get $300K treatment covered - Vimarsana News

As a Thunder Bay man battles a rare cancer, his family fights to get $300K treatment covered

The family of a 30-year-old man in Thunder Bay, Ont., who's fighting a rare form of cancer is waging a battle of their own: Trying to get funding for his treatments, which cost $9,000 each.

Source: cbc.ca
Woman with cystic fibrosis previously denied gets game-changing drug - Vimarsana News

Woman with cystic fibrosis previously denied gets game-changing drug

Sara Aldrich's application for provincial coverage for Trikafta, which lessens CF's severity and slows its progression, was just approved.

Family pinning hopes on fundraisers for toddler's $2.8M treatment - Vimarsana News

Family pinning hopes on fundraisers for toddler's $2.8M treatment

Family pinning hopes on fundraisers for toddler's $2.8M treatment A Pikwàkanagàn First Nation family is scrambling to raise millions of dollars for to provide a cure for their 14-month-old's genetic disorder, spinal muscular atrophy, before he turns two. Social Sharing Born with genetic disorder SMA2, Kevin Verch must receive one-time dose of Zolgensma before he turns 2 Posted: Jan 07, 2021 4:00 AM ET | Last Updated: January 7 Dana Pearce, 20, Brody Verch, 22, and their son Kevin Verch. The family is relying on fundraisers to pay for the toddler's $2.8-million genetic treatment for spinal m...

Source: cbc.ca