MS: Busting the Myths
June 26, 2023 | Advocacy, Carer, Carers, Life with MS, Media, Petition, Progressive, Uncategorised
Speaking in support of the Carers Alliance petition, Maxine Hall, a carer for her husband with Multiple Sclerosis, speaks of her struggles and hopes that this campaign will at least raise awareness. View original article on Otago Daily Times: https://www.odt.co.nz/news/dunedin/exhaustion-and-dread-desperate-carer-calls-change […]
November 3, 2021 | Education, Event, Life with MS, Progressive, Research
Fatigue is one of the most common, troubling symptoms experienced by people with progressive MS. For many people, it is the symptom that affects them most. Join MSIF to learn about the latest advances in treatment and research in fatigue […]
October 27, 2021 | Life with MS
Andrew Hodson was diagnosed with Secondary Progressive MS (SPMS) in 2008. “I probably had it for 20 years before that. A mixture of symptoms appeared then went away, including numb legs plus pins and needles. The initial diagnosis was very […]
June 29, 2021 | Education, Event, Life with MS, Progressive, Research, Treatments
Learn about the latest advances in progressive MS research and treatment during this 30-minute International Progressive MS Alliance webcast. An international panel of MS experts will answer questions submitted by people affected by MS from throughout the world. From symptom […]