MDA’s critical support for people with ALS
For many, amyotrophic lateral sclerosis is a fast disease. Once diagnosed, the average life expectancy for a person with ALS can be as few as three to five years. When Ben Thomas received his ALS diagnosis at the age of 29 — just three months after the birth of his only daughter, Emmerson — his world was turned upside down.
MDA vs. ALS
MDA is the world leader in funding ALS research and...
Fighting the good fight: Celebrating IAFF and all who help us battle muscle disease
As I meet and work with more and more people in the MDA community — families, staff, volunteers, donors and national partners — I’m amazed at the tenacity that drives our lifesaving mission. We are an army mobilized in the fight against muscle disease.
MDA's 2014 Clinical Conference on neuromuscular disease brings together health professionals from across the country and focuses on improving lives through excellence in care
"Optimizing Care: Improving Lives Through Clinical Excellence" is the theme of the 2014 MDA Clinical Conference, which takes place March 16-19 at the Hyatt Regency in Chicago. A secondary theme — "I am progress" — also will be in evidence, referencing the crucial role that MDA clinic team members nationwide have in providing expert medical care in neuromuscular disease and identifying new...
MDA re-launches its flagship publication, with a fresh look and the same high-quality content for people living with muscle disease
The Winter 2014 issue of Quest marks a new chapter for MDA’s flagship publication in print. Our goal with this redesign is to provide you, our dedicated readership, with a more contemporary and visually dynamic resource through which to present the research news and broader narratives that matter most to MDA families and supporters and all those affected by neuromuscular disease.
Feedback from Quest readers and the MDA community
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News and updates from the MDA community
Featured in this issue: Muscle Walk in full swing across the country; anti-bullying advocate with Friedreich's ataxia publishes new book; MDA Clinical Conference to be held in March; MDA Team Momentum hits the ground running; Shamrocks program raises millions for the cause; MDA Art Collection achieves milestone; accessible playground database now available; Muscular Dystrophy Coordinating...
A breathtaking view: Visions for 2014 worthy of the work ahead (CEO update)
As I travel from state to state, city to city, I continue to have the privilege of meeting ordinary people doing extraordinary things. They faithfully pledge their leadership and support to MDA, making it possible for us to fund worldwide research, provide comprehensive health care services and support to MDA families nationwide, and rally communities to fight back against muscle disease.