In the fall of 2013, the losses of ALS - or paper cuts, as Bruce called them - kept coming.

Two recent photographs of Bruce Kramer illustrate his frame of mind. In one, he didn't recognize himself at first and then saw what he calls the "ALS look." In another you see his pure joy at becoming a grandfather for the first time.

September 2015 audio highlights from the publisher.

Bruce Kramer faced some important decisions as his ALS progressed. He contemplated whether he should get a diaphragmatic pacing system which would help him breathe. And he wondered about the value of checking things off a "bucket list."

Bruce Kramer believed that researchers need to rethink the way they test new drugs on ALS patients like him. He argued that the double-blind testing model doesn't work for a devastating fatal illness like ALS. In this episode of Living While Dying, we also hear from a bio-ethicist about the decision to deny some patients access to an experimental drug.

Bruce Kramer helps medical students understand the patient's point of view. He has advice about how doctors should deliver bad news.

After being diagnosed with ALS, Bruce Kramer learned to appreciate the value of yoga. He found it to be a freeing and emotional experience. It helped Bruce reconnect with parts of his body that were affected by the disease.

August 2015 audio highlights from the publisher.

Bruce Kramer reflects on how having ALS has affected his belief in God. He says it has not shaken his faith. He thinks ALS proves that there is something greater than us.

Bruce Kramer participated in a drug trial to determine if Dexpramipexole could slow the progression of ALS. Kramer felt the drug was working for him and was frustrated when the trial was terminated.

Two years since being diagnosed with ALS, Bruce Kramer re-evaluates his priorities. As Christmas approaches, he has the time and solitude to appreciate the season more than ever.

People who've been hit hard by a very serious health challenge wrestle with a lot of questions right after their diagnosis. One of them is, "can I, should I, keep working?" Bruce Kramer talks about his battle with this question.

Bruce Kramer talks about participating in a drug trial, and how it led him to question the bureaucracy of the medical care system.

July 2015 audio highlights from the publisher.

Bruce Kramer describes how he adjusts mentally to the changes in his physical capabilities brought on by the progression of ALS. He likens it to a snake shedding skins.

A conversation with Bruce Kramer and his wife Ev Emerson about their evolving relationship. As his ALS progresses, she is becoming a caregiver.

When he was diagnosed with ALS, Bruce Kramer was a dean and professor in the University of St. Thomas School of Education. As the disease weakened his body, it made teaching more difficult. It also helped him focus on what was important in his professional life.

June 2015 audio highlights from the publisher.

May 2015 audio highlights from the publisher.

April 2015 audio highlights from the publisher.