A B.C. lady says she feels deserted by the well being care system, because the province by which she lives is the one one in Canada to not fund what she calls a “life-changing” medicine.
Joey Kerr beloved being lively.
“I did a variety of mountaineering. I did a variety of biking. I biked on daily basis,” she advised International Information.
However six years in the past, the now 81-year-old’s life modified drastically.
Kerr was recognized with myelodysplastic syndrome, or MDS, which is a uncommon blood dysfunction the place bone marrow fails to provide wholesome blood cells.
“I get nauseated, I get breathless, I get dizzy, the whole lot will get weak as a result of there’s no oxygen going by my physique,” Kerr mentioned.

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She now depends on common blood transfusions, with every one taking hours and leaving her drained.
Kerr is urging the province to fund a drugs referred to as Luspatercept, offered as Reblozyl, which is authorized by Well being Canada to deal with MDS and is proven to cut back how usually sufferers want transfusions.
“I’ve heard of somebody going 18 months,” Kerr mentioned concerning the drug.
“That’s a yr and a half. I’ve heard of somebody going a yr.”
Nonetheless, in response to the Medicines Entry Coalition, B.C. is the one province in Canada that doesn’t cowl Reblozyl for MDS sufferers.

“That is certainly one of many situations the place many times we will’t get the BC NDP authorities to cowl the price of these medication,” Ian Paton, the BC Conservative MLA for Delta South, mentioned.
Paton mentioned the drug can value round $200,000 a yr per affected person.
An announcement from the Ministry of Well being mentioned Luspatercept will not be eligible for Pharmacare protection for MDS and funding selections should stability proof and cost-effectiveness.
However for Kerr, she mentioned she feels just like the province is simply letting her die.
“My age on paper is previous, however I’m younger at coronary heart.”
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