Letter from Mike Armstrong
Executive Director, The ALS Association
Northeast Ohio Chapter
Two
seniors on a risky journey to fight ALS
On
Amyotrophic lateral
sclerosis, or ALS, is a degenerative neuromuscular disease with no known cause,
treatment or cure. ALS occurs when motor
nerve cells in the nervous system cease functioning and die. Although the mind remains unaffected, muscle
control becomes completely lost and paralysis sets in. The life expectancy of an ALS patient
averages two to five years. Over 5,000
people are newly diagnosed with this fatal disease every year.
Although Greg, age 56 and
Ted, age 80, both have experience in navigating rivers and canals, this
adventure will be the first time they have attempted such a trip in a
non-powered craft. Though they will make
scheduled stops in various ports to re-supply and attend local press
conferences, Ted and Greg intend to live on their craft for the duration of the
trip.
When asked why he would be
willing to suffer extreme exposure for three months living on an open raft with
no shelter or convenience, Ted simply replied, “Because I can’t forget my
wife’s last moments.” Though he promised
his wife he would not openly discuss her losing battle with ALS, Ted shared
this very personal moment. “I was whispering my love into her ear. She tried in vain to open her eyes one last
time and managed a very faint smile. A beautiful smile.”
Upon launching into the
Monongahela River at Fairmont, WV, the “Mission Cure ALS” crew of Ted and Greg
will sail and manually paddlewheel their boat 128 miles to the headwaters of
the Ohio River at Pittsburgh, PA. From
there they will challenge the Ohio
River’s 20 locks and dams, navigating through huge waves from powerful
tug-boats and barges up and down-stream for 981 miles to the Mississippi River
at Cairo, IL. The crew will follow the
“Mighty Mississippi” to
The intent of the “
Though his family worries
about Ted’s safety during this journey, his son Jim says he is not the type of
man who sits back and waits for someone to do what needs to be done. “Dad has an insatiable drive to, in some way,
fight back against the disease that took my mother from him. We are all proud of the determination and
resolve he is demonstrating in honoring her memory.”
Donations for the ALS
Association’s Research Program may be sent to The ALS Association,
Please enter - Mission: Cure ALS
on the memo line of your check.
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