Australia MS News: Expensive MS drug (Mavenclad) to be on PBS next year

 · Dec 23, 2018

When Australian Paralympian Carol Cooke is on #Mavenclad, she almost forgets that she has multiple sclerosis.

The cyclist and rower says that going on the medication has made “all the difference in the world” and changed her life.

Now, thousands of Australians who, like Cooke, are affected by the most common form of the disease could save about $54,000 a year thanks to the drug’s listing on the Pharmaceutical Benefits Scheme.

With the PBS listing, sufferers of relapsing remitting MS will pay just $40.30 a script or $6.50 if they are concessional patients.

“This is Christmas a few days early for those who live with MS … it’s a gift from the Australian people, but it’s a gift that is absolutely deserved,” Prime Minister Scott Morrison told reporters on Sunday.

The plight of MS patients is close to Mr Morrison’s heart as his brother-in-law Gary Warren has a different form of the autoimmune disease.

While there’s no cure for MS, the federal government says the drug listing means patients will face fewer relapses, less disease activity in the brain and less progression of disability.

Carol Langsford, the chair of the Trish Multiple Sclerosis Research Foundation, said she believed her daughter Trish could still be alive if the drug was available in time.

Her daughter, a keen athlete, was 30 when she died in 2002 after spending four-and-a-half years in a nursing home.

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