Amyloidosis is a rare disease that affects organs such as the heart, kidney, liver, the nervous system and more.
While there is no cure, there are treatments and organizations that can help. Enter, the Amyloidosis Foundation.
This month, they highlight Rare Disease Day in Indiana AND give some brief bios on two new members of their board of directors! Not to mention, they discuss the latest awarded research grants, which is always good news in the rare disease world.
Check out the Amyloidosis Foundation’s Latest Newsletter here for more information on this rare disease and stay tuned for patient stories soon to come!
