Americans With ALS Look to Canada for Promising Drug the U.S. Hasn’t Approved

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Some ALS patients in the U.S. are weighing a trip to Canada to obtain Albrioza, a newly approved drug for fatal disease. “Getting more months with my family is worth a trip.”

William Woods, a retired doctor in Atlanta who has ALS, says he needs to go to Canada for Albrioza ‘sooner rather than later’ because of the disease’s relentless progression.Updated June 22, 2022 5:55 pm ET

Canada approved Amylyx Pharmaceuticals Inc.’s new drug for amyotrophic lateral sclerosis last week. Now some U.S. patients with the fatal neurodegenerative disorder—also known as Lou Gehrig’s disease—are considering a trip north to get the medication, Albrioza. The drugWilliam Woods, a 75-year-old retired doctor in Atlanta who was diagnosed with ALS in 2019, is contacting Canadian doctors who might help him get Albrioza.

 

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They won’t approve a drug for people on their last legs but happily approve a experimental vaccine for toddlers who don’t need it. It has to be a money issue. The ALS drug is obviously a money loser.

America the great where medical tourism for procedures and meds is a thing. Cheaper to fly over, stay, get TX and come back than to sit here dying to get partial if anything covered by insurance for life extending or saving procedure.

Risking a trip to Canada is almost like going to North Korea based on the recent Prime Ministers actions. But the food is more interesting in North Korea.

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