Every year, the Center partners with the Familial Dysautonomia Foundation to host an annual conference for patients, caregivers, […]
Re: Familial Dysautonomia and Coronavirus Dear Families, It has now been 2 months since The World Health Organization […]
Several reports have emerged about conjunctivitis (pink eye) being a sign of COVID-19. We interviewed eye expert, Dr. […]
The recent coronavirus pandemic has changed the way we interact, but for patients with familial dysautonomia, this may […]
The current coronavirus pandemic has made it impossible for many patients with chronic neurological illnesses to leave their […]
According to new research over 2 in 3 patients with multiple system atrophy have depression and this influences […]
The Dysautonomia Center has put together information for the MSA community about the current outbreak of the novel […]
One of the challenges in rare diseases is creating a path for new therapies to be tested in […]
Proteinopathies are a group of disorders that causes neurodegeneration and are associated with misfolded protein deposits that are […]
Learn how our collaboration with doctors in Israel is helping educate others on the importance of a proactive […]
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