Donate

In honor of the life and death of Peggy Ragan, tax-deductible donations to the ALS Association’s DC/MD/VA Chapter via the Peggy and Bernie Project can be made as follows:

PLEASE MAKE CHECKS PAYABLE TO:
ALS Association – DC/MD/VA Chapter

* please write “In honor of Peggy Ragan” in the For / Note area on the check

PLEASE MAIL CHECKS TO:
The Peggy and Bernie Project
c/o Christopher Ragan
9006 Ribbon Falls Loop
Bristow, VA 20136

About The ALS Association’s DC/MD/VA Chapter
The ALS Association’s DC/MD/VA Chapter was founded in 1991 to serve the needs of those living with Amyotrophic Lateral Sclerosis and their caregivers.

ALS Association is the only national not-for-profit health organization dedicated solely to the fight against ALS. The ALS Association covers all the bases — research, patient and community services, public education, and advocacy — in providing help and hope to those facing the disease.

The ALS Association (National Office and the DC/MD/VA Chapter) operates under a shared mission: to help people living with Amyotrophic Lateral Sclerosis and to leave no stone unturned in search for the cure. On a daily basis staff and volunteers are working diligently to develop programs to make sure that our ALS family can count on the caring, compassionate support of people who understand the daily challenges of living with this disease.

The DC/MD/VA Chapter focuses primarily on helping patients and families who live with ALS in the District of Columbia, Maryland and Virginia.

WHY?

The cause of ALS is unknown and there is no known cure.

The average life expectancy of a person with ALS is two to five years from time of diagnosis.

You can make a difference in allowing someone suffering from ALS live a fuller life!