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orphan diseases

Are you ready for 2023?

Are you prepared for 2023? Make 2023 a health-focused year for you and your family. An FD annual […]

zenithkhan January 19, 2023 Uncategorized

Success in treating high blood pressure surges

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Within the brain exists a network of nerve connections that allow us to process emotions, like fear, and […]

dysautonomialab August 14, 2020 familial dysautonomia, research papers, Studies, Uncategorized

Progress in a rare disease: Highlights from the 6th International Congress on Multiple System Atrophy

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New York City, 2018 The 6th International MSA Congress (https://msa-congress-nyc.com), held recently in New York City, marked a […]

dysautonomialab April 24, 2018 Lab News, multiple system atrophy, orthostatic hypotension, palma, Parkinson disease, Uncategorized

MSA NJ organizing a fund-raiser picnic for families in the tristate area

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Dear Friends, Multiple System Atrophy New Jersey (MSA NJ) is a non-profit organization, which provides support for patients […]

dysautonomialab September 1, 2016 Uncategorized

New article marks research progress in FD

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Familial dysautonomia is rarer than most rare diseases, but this little known genetic disorder has become a gateway […]

dysautonomialab August 22, 2016 Uncategorized

FD Day 2016: Everything you need to know

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At FD Day 2016, patients and family members came together for a 1-day intensive conference in New York […]

dysautonomialab June 20, 2016 Dr. Lucy Kaufmann, dr. mendoza, familial dysautonomia, FD Day 2016, horacio kaufmann, Lab News, palma, Studies, team, Uncategorized

RESULTS: The World Through my Eyes Photography Competition for People with FD

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  History The photography competition began in 2009 when we set the challenge for people with familial dysautonomia […]

dysautonomialab June 8, 2016 familial dysautonomia, FD Day 2016, Uncategorized

What’s new for FD Day 2016?

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You either heard about FD Day or came to FD Day. Every year we tell you what is […]

dysautonomialab May 5, 2016 familial dysautonomia, FD Day 2016, team, Uncategorized

THE WORLD THROUGH MY EYES: A photo competition for people with FD

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Only you know how what it feels like to grow up with FD, and this is a chance […]

dysautonomialab May 4, 2016 familial dysautonomia, FD Day 2016, team, Uncategorized

An update from the 5th Congress on MSA

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At the 2016 International Congress on MSA, over 130 experts in the field came together for a 2-day […]

dysautonomialab April 27, 2016 horacio kaufmann, Lab News, team, Uncategorized

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