Posts tagged Disabilities and the Disabled
Making Sense of Bioethics: Column 187 : The “Quality of Life” Error

Our focus should be on the benefits and burdens of a proposed medical intervention rather than on trying to impose our own conclusion that certain individuals no longer have enough value or meaning in their lives.

Read More
Making Sense of Bioethics: Column 173: Medicine and a Sense of the Sacred

We need to attend carefully to the graced realities we regularly handle lest we end up squandering or losing our sense of the sacred.

Read More
Making Sense of Bioethics: Column 163: The Welcome Outreach of Perinatal Hospice

This approach seeks to set up a particular supportive environment in which all the members of the family can receive the child following delivery, hold and name the newborn, and fully acknowledge his or her brief but meaningful life.

Read More
Making Sense of Bioethics: Column 135: Leaving Our Values at the Door of the Strip Club

Good parents never drive their children to strip clubs, and neither should any institution entrusted with a protective parental role; on the contrary, such institutions should erect appropriate boundaries and limits on harmful behaviors, so their residents can grow and flourish...

Read More
Making Sense of Bioethics: Column 078: Unconditional Parental Love

A husband and wife are called to give themselves to each other completely and unreservedly, and to accept each other unconditionally in the marital embrace. Every child of theirs, whether entering the world with a handicap or not, is an expression and fruit of themselves and their acceptance of each other.

Read More
Making Sense of Bioethics: Column 064: Defending the Dignity of Those with Dementia

When our ability to think rationally or choose freely becomes clouded or even eliminated by dementia, we still remain at root the kind of creature who is rational and free, and the bearer of inalienable human dignity.

Read More
Making Sense of Bioethics: Column 031: Feeding Our Loved Ones: The Modern Anathema of Living With Brain Damage

Our duty is to provide loving care and strong support to those whose “quality of life” may be less than perfect, including those who are sick or those who may be disabled like Terri Schiavo, rather than targeting them for an early demise through the withholding of food and water.

Read More