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Health & Science: Gerald Ford supports therapeutic cloning
in letter to Bush

The Associated Press

WASHINGTON (April 26, 2002 7:09 p.m. EDT) - Former President
Ford agrees with advocates of cloning for medical research,
saying the effort holds "enormous potential" for treating
an array of diseases.

In a letter to President Bush dated Thursday, Ford records
his "strong opposition" to legislation that would outlaw
cloning for research along with reproductive cloning,
which is meant to produce a baby.

In both cases, an embryo is created from the cells of an existing
human being.

In reproductive cloning, the embryo would be implanted
into a womb, where it could develop into a fetus and then
a person.

In cloning for research, sometimes called therapeutic cloning,
stem cells would be extracted from the embryo a few days
after it was created in a lab and then used to develop treatments.
The embryo would be destroyed.

While various animals have been cloned, no one has cloned
a human being for any purpose.

Ford said in his letter that, like virtually all policy makers,
he supports a ban on reproductive cloning but said
"a more measured approach should be taken towards
therapeutic cloning."

"Unlike reproductive cloning, this approach will never
produce a cloned human being. But it could result in the
development of lifesaving therapies that could improve
the well-being of all Americans," Ford wrote.

He compared the cloning issue to controversy during his
presidency over research involving recombinant DNA.
This research was allowed to proceed with safeguards
in place, he said, and led to advancements in the prevention
and treatment of disease.

The Senate will soon consider a bill offered by Sens.
Sam Brownback, R-Kan., and Mary Landrieu, D-La.,
that would ban all human cloning. The House approved
a total ban last year.

Ford's letter was distributed Friday by the office of
Sen. Arlen Specter, R-Pa., who opposes the total ban.

SOURCE: The Nando Times
http://www.nandotimes.com/healthscience/story/381866p-3044961c.html

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