Trustworthy sources

The fickle information checkerboard we navigate now requires that we know where the data we rely on is coming from and what possible agendas might driving it. This is called “information literacy” and it is crucial for patients. These are some sites I consider trustworthy places to start any MS research.

Societies

• The National Multiple Sclerosis Society (NMSS) | YouTube channel – MS Connection magazine
• Multiple Sclerosis Association of America (MSAA)
• MS Society UK
• MS Society Australia
• MS Foundation – MS Focus magazine

Other Trustworthy Sources

• Can Do Multiple Sclerosis
• The European Committee for Treatment and Research in Multiple Sclerosis (ECTRIMS)
• Healthline section on MS
• Medical Xpress section on neuroscience
• Medscape section on MS
• MS Teamworks
• MSology Canada
• Multiple Sclerosis News Today
• Overcoming MS
• Patients Like Me
• Shift.MS UK
• WebMD section on MS

This is by no means an exhaustive list. If there is something you feel should be on here, please let me know and I’ll do my best to check it out. Thanks!

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