This week Facebook has blown up with videos of people dousing themselves with ice cold water in the ALS #IceBucketChallenge. The idea was an attempt to gain more awareness of the disease and to increase donations. According to reports this has happened. There has been an increase in donations by 1,000 percent in the last week. Over 1.4 million dollars has been raised for ALS research. Imagine the good things we can do with social media.
I took part in the challenge thanks to
the publisher’s twin boys who called me out. My son took great pleasure in
dumping the water over my head. I took great pleasure in dumping him into the lake,
which was too easy because we were standing on the dock at our family camp.
I followed those I tagged to make sure
they followed through, and most of them did. Thanks to Tyler DeFosse, Tony
Bessey and Jeffrey Thivierge. Still waiting for my cousin in Indiana and my
daughter at Camp Hinds to get involved. In my daughter’s defense, she isn’t on
Facebook much this summer. However, I did catch her pouring water over campers
in Pack 805 for their Ice Bucket Challenge. So she knows it’s going on. And there
is still time for her to get in on the fun.
Now I hear there’s talk about how to do
the challenge. Do you dump the ice in just before you pour it over your head?
Do you put in the ice and wait until it melts, then add a little more for good
measure? (That’s what my son did.) Or do you put in the ice, let it melt while
you call out your, three, five or many closest friends? I haven’t seen anything
that suggests there’s a right way, so if you’re “hating” on the people who are
doing this…stop. Step up to the bucket yourself. It’s about the organization
and the fun of being tagged. (I do know a few people who still have remained
untagged, if you need suggestions.)
This brings up the question of do you
donate or don’t you? In my opinion it’s a personal choice. Maybe you don’t want
to donate to ALS, but at least learn a little about it to know what you are using all the
ice in the freezer for.
Amyotrophic
lateral sclerosis (ALS), often referred to as "Lou Gehrig's Disease,"
is a progressive neurodegenerative disease that affects nerve cells in the
brain and the spinal cord. Motor neurons reach from the brain to the spinal
cord and from the spinal cord to the muscles throughout the body. The
progressive degeneration of the motor neurons in ALS eventually leads to their
death. When the motor neurons die, the ability of the brain to initiate and
control muscle movement is lost. With voluntary muscle action progressively
affected, patients in the later stages of the disease may become totally
paralyzed. From
www.alsa.org.
Bravo
for whoever started this trend. You have accomplished your mission. We should
all be fortunate to have people who love us, and who are willing to raise money
for a cause we believe in.
-Michelle Libby
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