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.


Other Trustworthy Sources

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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