The Patient Services program was
initiated formally in the fall of 2008, as the students of AMND desired
scheduled monthly visits with ALS patients in the immediate area. The students
are welcomed into the homes of ALS patients and spend time visiting them in
hospitals and rehabilitation centers all over Long Island.
The students have formed invaluable relationships with every ALS patient they
have come in contact with, and are grateful for the opportunity to help in the
daily struggles families of ALS patients face. In addition to helping around
the house, playing with the kids and easing many physical challenges patients
face, the committee members have gotten to know every ALS patient they visit on
a very personal level. They interact with them and learn first-hand what it
means to face a terminal illness with strength, courage and grace. With every
visit, the students become even more energized and determined to find a cure
for this terrible disease.
Pictures from our Patient Servives Program
ALS RESEARCH
The ALS Research Program was
developed at the 2006 AMND event, after a Dr. Ratnesh Lal, from the University of California,
Santa Barbara led
a Science Research Symposium before the event. His talk was titled, “Can Nanoscience and Technology Accelerate our Search for a
Cure for ALS?” This meeting created opportunities for Northport High School
students to become active participants of ALS Research in both the clinical and
laboratory setting. In the summer of 2006, four students performed ALS
research at the following research centers: The Robert Packard Center for ALS
Research at Johns Hopkins University
with Dr. Jeffrey Rothstein, The
University of California at Santa Barbara with Dr. Ratnesh Lal, ALS Therapy
Development Institute with Dr. Ken
Thompson and Columbia
University with Dr. Serge Pzerborski. Again in
the summer of 2007, four students gained first hand experience with ALS
research at The Robert Packard Center, Columbia University
and the newly opened, Jenifer Estess Stem Cell Lab. The lab, founded by
Meredith and Valerie Estess of Project A.L.S., is the first privately-funded
stem cell lab focused exclusively on the study of stem cells to treat ALS and
related motor neuron diseases. Project A.L.S. is at the front-line of both stem
cell theory and research surrounding ALS and was recently recognized by Time
Magazine as “The Number One Medical Breakthrough of 2008” for their work in
reprogramming iPS cells.
For all of the fortunate students able to conduct ALS
research over the past three years, their experiences, both invaluable and
rewarding, have shaped many of their career plans and changed the way they view
the disease. To have been a small part of the journey towards a cure is
certainly an experience unmatched by any lesson taught in a classroom and one
our students will never forget.
Pictures from our Research Program
ASSEMBLY
INITIATIVE
The Assembly Initiative was created after the students of
AMND were invited to speak at the 2007 National Honor Society convention in Atlanta, Georgia.
After preparing an assembly for the other National Honor Society students in
attendance, the committee was met with an outpouring of enthusiasm and passion.
Their assembly was so effective that a high school in Carson City, Nevada,
took the “Challenge for a Cure” offered by AMND, and raised over $2,000 for ALS
in a little less than 2 months. AMND invited these remarkable students to the 4th
annual A Midwinter Night’s Dream and honored them at the event. After
witnessing the inspiration that had come from their first assembly, the
students decided to spread the Assembly program to other schools in the area.
The committee has organized two successful assemblies at local elementary
schools and is currently in the planning stages for two more to take place in
the coming month. The students are working to inspire others to believe that
their efforts can change the world and to never stop dreaming big!
Pictures from our Assembly Program
If you would like to get more information about our three programs, please contact Don Strasser. We are always looking for more ALS patients to visit, new labs to place students and more schools to tell our story to. Thanks for your time.