The Dysautonomia Center would like to provide the FD community with an update regarding the current outbreak of […]
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The urge to breathe comes from a physiological drive. Sensors inside and outside the brain are continuously monitoring […]
Guest writer Gabi Jassie describes her life at college and how she overcame the challenges of having familial […]
Our Natural History Study is currently open and recruiting patients with FD. Some patients have contacted us with […]
New treatments are coming for patients living with FD. Find out why we need a natural history study […]
Members of the Autonomic Disorders Consortium and the MSA Coalition partnered together to host the Annual MSA Patient and […]
The Dysautonomia Center blog is happy to welcome guest writer Ms. Samantha Myers, who has familial dysautonomia, and […]
Tackling rare diseases requires a well-planned strategy. The Center is kick-starting a new clinical project as part of […]
Accidents Accidents are of concern to parents of any child. The situation is especially complicated by the fact […]
Dear Friends, Multiple System Atrophy New Jersey (MSA NJ) is a non-profit organization, which provides support for patients […]
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