The PSP Chronicles began as a journal… a personal account of the author’s experiences with early on-set dementia and a rare, terminal brain disease. Tim decided to post his journal as a blog for the benefit of family and friends to follow online. With a miss-click of the computer mouse he ended up sharing it to an online PSP group with members throughout the world.  The project went from a blog to a book that transcends a number of genres with its continuing narrative. It is also meant to be a neurodegenerative disease awareness and fundraising effort. PSP has no treatment – no cure. Research is ongoing and requires funding to help keep hope alive for those with a brain disease and those yet to be diagnosed. Please see my “Resources” page to learn more.



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