Rachel Leib, Author at Neuromuscular Disease Foundation

About Rachel Leib

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So far Rachel Leib has created 51 blog entries.

It’s A Marathon, Not A Sprint – Why Is This Ultra Rare Disease So Difficult to Diagnose?

Rachel Leib2022-04-05T10:41:02-07:00April 5, 2022|

How The NDF Maintains Transparency with Patients & Donors

Rachel Leib2022-03-31T09:35:14-07:00March 30, 2022|

What Are The Most Common Neuromuscular Diseases?

Rachel Leib2022-03-14T15:02:46-07:00March 11, 2022|

The NDF Welcomes Geoffrey M. Gee, Esq. as Newly Appointed Executive Director

Rachel Leib2022-03-07T11:32:18-08:00March 7, 2022|

Rare Leader: Geoffrey Gee, Executive Director, Neuromuscular Disease Foundation

Rachel Leib2023-02-04T08:39:00-08:00March 2, 2022|

NDF Takes the Lead in Global Race to Develop Gene Therapy Treatment for GNEM

Rachel Leib2023-02-04T08:40:54-08:00February 22, 2022|

Why Rare Disease Day is So Important to the Neuromuscular Disease Foundation

Rachel Leib2023-02-04T10:00:08-08:00February 17, 2022|

Rushabh Desai Talks About the Struggles of Living with Rare Muscular Disease GNEM

Rachel Leib2022-02-08T12:34:25-08:00January 14, 2022|

THE HIDDEN CHALLENGES FACED BY DISABLED TEACHERS

Rachel Leib2023-02-04T08:43:35-08:00January 5, 2022|

The Philosophy of Giving: We Talk with Longtime Board Member and Serial Philanthropist David Haverim about Generosity and The Future of NDF

Rachel Leib2023-02-04T08:45:00-08:00December 20, 2021|

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