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In This Issue:

Drug Trinity Shows Unexpected Strength
Jean-Pierre Julien—his “cocktail” does wonders for ALS mice.

From Iceland: A New Way to Decode ALS Genes
In Iceland, a country of roughly 300,000 citizens, ALS is pretty much unknown. If you wanted to find genes tied to that disease, it’s an unlikely spot for a search. But from that country may come, if not the genes themselves, a superior way to track them down.

Getting to the
Heart of It

With ALS, many of the simplest questions remain unanswered. ‘That just won’t do,’ say Center scientists.

One Step Closer to the Bedside
The Basics Bolster Stem Cell Therapy.

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About ALS Alert


Rich Soil for a Blooming Friendship

photo - Laura Murphy and daughter Sarah.  
Laura Murphy and daughter Sarah.
   

Elizabeth Coleman knew Laura Matlaw Murphy because they were both lawyers in Atlanta. “We were acquaintances,” Coleman says. “Women lawyers’ paths tend to cross.”

It would’ve been difficult not to know about Murphy: Her incisiveness and keen mind made her one of the best law clerks to serve the Georgia Supreme Court. Equally focused in her spare time, she was a nearly unbeatable runner, a star in Atlanta track circles. She and her daughter were a familiar sight, flying past course markers.

“About six years ago, I ran into Laura and I could tell something wasn’t right,” says Coleman, who now directs the New York State Trial Lawyers Association. “When I heard later she had ALS, I felt a bit strange in writing a personal letter out of the blue, but I sent it anyway.”

And in the way ALS has of cutting things to the quick, Coleman and Murphy became friends. “Laura just flowered after her diagnosis,” Coleman explains. “She made everyone around her open up, including me. But she wasn’t sugary—just ask her about the chewing-out she got from a cashier who thought her slurred speech meant she was drunk.”

At times, Coleman says, Murphy could push aside the scrim of human misunderstanding:“With decreased time and mobility, I’d have thought I wouldn’t be interested in spending time with any but close friends. But I’ve been delighted to have found friendship and love in unexpected places. For my cynical soul, that’s been enough to push me into something like faith.”

When Murphy died last September, The Coleman Foundation donated $12,000, in her name, to support the Center’s hallmark investigators’ meetings.

Next > Insider's View
Noah Lechtzin, M.D., is a Hopkins pulmonologist who sees ALS clinic patients regularly.


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Special Features:

Vantage Point
With approaches to ALS therapy, progress seems to move one step forward and a half step back.

On Center
Runners, Walkers Make Feet Fly to Help the Center.

Rich Soil for a Blooming Friendship
“About six years ago, I ran into Laura and I could tell something wasn’t right,” says Coleman, who now directs the New York State Trial Lawyers Association. “When I heard later she had ALS, I felt a bit strange in writing a personal letter out of the blue, but I sent it anyway.”

Insider's View
Noah Lechtzin, M.D., is a Hopkins pulmonologist who sees ALS clinic patients regularly.

From the Clinic
Lora Clawson, M.S.N., C.R.N.P., manages Johns Hopkins’ ALS clinic, including its clinical trials. In this column she answers typical patients’ questions.

A Friend Indeed
Ride for Life Keeps Center Rolling.

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