Marcus was diagnosed with amyotrophic lateral sclerosis (ALS) in 2016. For the past four years he has been committed to raising awareness about the underfunded disease and the path to finding a cure.
mnd
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November 02, 2020Read more »
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September 27, 2019Read more »
I’m lucky. It's been 4 years since the first MND symptoms, only my voice has been impacted.
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September 10, 2019Read more »
Two and a half years after his diagnosis, David found a medicine with off-label application for MND.
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July 29, 2019Read more »
After 3 years of living with ALS, Marc found a new medicine on the other side of the world.
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July 22, 2019Read more »
With tears, laughter and hope, Mark and his family find their own way to cope with ALS.
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July 22, 2019Read more »
Diagnosed with ALS only 6 months ago, Peter went against the current to find more options to treat his disease.
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June 17, 2019Read more »
Still walking and talking after 4 years with ALS: we share Bakr's experience of living with a rare disease in the UAE to further his goal of creating awareness and to connect with other ALS patients.
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February 05, 2019Read more »
Teresa's husband was diagnosed with ALS. She spent 11 years as his caregiver and discusses her experiences.
