Rachel Leib, Author at Neuromuscular Disease Foundation

About Rachel Leib

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So far Rachel Leib has created 47 blog entries.

The Neuromuscular Disease Foundation Leads in Patient Resources and Grant Funding in Service of Rare Disease GNEM Patients Worldwide

Rachel Leib2023-07-25T05:47:28-07:00July 24, 2023|

New Patient Care Partner Support Group Programs

Rachel Leib2023-06-06T11:18:30-07:00June 6, 2023|

Is Your Confidence Affected by Your Disability?

Rachel Leib2023-04-12T11:49:59-07:00April 4, 2023|

How Two Young Disability Inclusion Advocates Are Building a More Inclusive World, One Lesson at a Time

Rachel Leib2023-03-31T14:20:40-07:00March 28, 2023|

Celebrating Female Scientific Achievement with One of Our Own: NDF Scientist Dr. Kelly Crowe Awarded $20K Grant and Named an Uplifting Athletes 2023 Young Investigator Draft Pick!

Rachel Leib2023-03-01T14:23:05-08:00March 1, 2023|

In-the-News: Suma Rao-Gupta, Izabella Tyszler and Navid Rachman to Join the Neuromuscular Disease Foundation (NDF) Board of Directors

Rachel Leib2023-02-23T19:18:10-08:00February 22, 2023|

Using Her Rare Disease Diagnosis to Fuel Patient Advocacy – Tara Voogel Steps into Her Role on The Board of The Neuromuscular Disease Foundation

Rachel Leib2023-02-10T07:47:17-08:00February 9, 2023|

Rare Disease Day 2023: A Celebration of The Promise for a More Equitable Society

Rachel Leib2023-02-10T07:43:00-08:00February 8, 2023|

‘I live a beautiful life’: What wheelchair users wish you knew – and what to stop asking

Rachel Leib2023-02-04T08:49:54-08:00February 4, 2023|

Neuromuscular Disease Foundation’s Dr. Kelly Crowe Presented with $20,000 Research Grant from Uplifting Athletes

Rachel Leib2023-01-14T20:09:34-08:00January 14, 2023|

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