Educational Support
This is a non-fiction book that tells how I beat an incurable, terminal disease known as amyloidosis. Amyloidosis turned my heart, literally and figuratively, into…
It is now nearly four years since my husband, Doug, was diagnosed with an extremely rare disease called Amyloidosis.
It came out of the blue, though we now…
Rare Disease Day takes place on the last day of February each year. The main objective of Rare Disease Day is to raise awareness amongst the general public and…
Due to the global COVID-19 (Coronavirus) pandemic, the American Academy of Neurology has no choice but to make the necessary decision to cancel the AAN's Annual…
The annual Corvettes for Chip Show will be held in conjunction with the Carlisle GM Nationals for 2022! Corvettes for Chip will operate as a "Show within a Show" at…
Come join the Chip Miller Amyloidosis Foundation (CMAF)external link, opens in a new tab and local NJ pro, Rob Kelly on July 21, 2023 for the 19th Annual Chip…
