The Malveaux Mission supports an aggressive approach to raising awareness of ALS: highlighting scientific research into the causes, treatments and eventual cure of the disease; promoting the important need for ALS research funding; and ultimately helping to bring hope to patients and families affected by this disease.

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In November of 2011, Mom was diagnosed with ALS, or Lou Gehrig’s Disease.  Since that time, I’ve set out to learn all I can about ALS.  Meet my family and watch our story….

The Malveaux Story
About Suzanne Malveaux

An Update on Myrna Malveaux

Myrna Malveaux: 1941 – 2018

It is with great sadness that we announce the passing of Myrna Malveaux after a long, brave battle with ALS. She passed away peacefully on Friday, April 13, 2018. She was the devoted and loving wife of Floyd J. Malveaux, … Continue reading

Mryna Malveaux Appears on ABC2 News

Myrna and her family recently appeared on ABC2 News in Baltimore to show she makes the most of everyday – even when living with ALS.  Check it out…  

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From the Blog

I Have ALS, No Need to Shout!

By Randy Pipkin.  Reprinted with permission. Ever since I was diagnosed with ALS (Amyotrophic Lateral Sclerosis) in 2005, I have noticed that people are 100 percent confused about the deadly disease.  I need to set the record straight: having ALS … Continue reading