“But I do know that it is my life, it is my death, and it
should be my choice” said a physician with ALS or Lou Gehrig’s disease after he
received a prescription for drugs that he could use to end his life.
This was part of an excellent story on the front page of the
New York Times by Katie Hafner titled: IN ILL DOCTOR, A SURPRISE REFLECTION OF
WHO PICKS ASSISTED SUICIDE, August 12,
2012.
Opponents of the death with dignity law painted frightening
scenarios where poor people would be forced to commit suicide by their families
when they could no longer afford end-of-life care.
It is important to see what actually is happening in states
where you can die with dignity; law in place since 1997 in Oregon
and 2009 in Washington
State . People who have
used the law are white, well educated and financially comfortable and they are
not in excruciating pain; they just want to control their deaths as they
controlled their lives…make sense?
The laws stipulate that two physicians must certify that the
individual has six months or less to live and the lethal medication must be self
administered which can be tricky for ALS patients who cannot control their
muscles.
Having gone through a long and tortuous death of my
father-in-law (92) who begged me to let him go, I can see value to such laws
and most of all humanity. We all deserve a “good” death if possible and this
law makes that possible.
I realize that the Catholic Church considers suicide a sin
but I do not look at death with dignity as suicide in the normal use of the
word; death is imminent anyway but you get to choose the time when you want it
to come.
I hope the real-life experience in states like Oregon and Washington
will show critics that the law is actually a very humane law and is not being
misused as they so vehemently warned would happen.
It is time to allow us the option of a death with dignity.
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