Three Share Their Life With MG in Online Documentary Series, ‘A Mystery to Me’
Three people living with myasthenia gravis (MG) tell their stories in the three-part online documentary series “A…
Articles by Forest Ray PhD
Melatonin Supplements May Worsen MG Symptoms, Case Series Suggests
Melatonin supplements usually used to treat insomnia may aggravate the symptoms of myasthenia gravis (MG), possibly…
App-based MyRealWorld MG Study Seeks Patient Insights
Argenx is looking for participants in an app-based international study of the impact and burden of myasthenia gravis (MG)…
1st Participant Dosed in Phase 1/2a Trial Testing Potential MG Therapy NMD670
The first participant has been dosed in a Phase 1/2a trial evaluating NMD670, NMD Pharma‘s investigational therapy…
Same But Different Photo Contest Celebrates People With Rare Diseases
Same But Different, a U.K. nonprofit that uses the arts to bring communities together, is holding a calendar photography…
Xperiome Platform Aims to Streamline Searches for Rare Diseases, Gain Patient Input
Raremark, an online rare disease patient community, has launched a digital platform called Xperiome, aimed at streamlining the…
Stress and Depression Linked With Relapses in MG Patients
Stress and depression are associated with higher relapse rates in people with myasthenia gravis (MG), according to a recent…
National Survey Seeks to Assess Full Social, Economic Burdens of Rare Diseases in US
The EveryLife Foundation for Rare Diseases has launched a nationwide National Burden of Rare Disease Survey to measure…
Alexion Charitable Foundation Giving $1.1M to Assist Rare Disease Community During Pandemic
The Alexion Charitable Foundation has awarded $1.1 million in grants to programs that support those with rare diseases during…
Coalition Will Address Racial Disparities in Rare Disease Communities
The Black Women’s Health Imperative (BWHI) recently created a Rare Disease Diversity Coalition focused on reducing racial disparities in…