Olympian Tim Jecko Dies

MADISON, NJ, January 17. TIM Jecko, 66, a member of the 1956 U.S. Olympic swim team, an NCAA champion at Yale University and an actor on Broadway and in regional productions, died Jan. 11 at his home in Madison, N.J. He was diagnosed with amyotrophic lateral sclerosis (ALS), or Lou Gehrig's disease, 18 months ago.

Born in Washington and raised in Bethesda, Mr. Jecko began swimming as a young teenager for the Amateur Athletic Union at the Walter Reed Army Medical Center pool and at Edgemoor Country Club in Bethesda. Until restricted by failing health, he continued swimming several times a week.

Tim graduated from the drama school at Yale University, where he was captain of the swim team. He won no Olympic medals, but in subsequent years, he held world, U.S. and NCAA records.

In a 1992 letter to the editor and a 1996 op-ed article for the New York Times, he reviewed his Olympic experience and urged the public to give up its fixation on gold medals.

"I made the Olympic team four years later [in 1956], and had the thrill of swimming at the Games in Melbourne, Australia. Not the thrill of victory — I didn't win a medal. But not the agony of defeat either. As a reserve on the 800-meter freestyle relay team, I helped qualify the United States for the finals, and then four faster swimmers took over to win a silver medal," he noted.

After his military service in the Navy's 7th Fleet, he began a professional life that included both acting and teaching.

Mr. Jecko performed on Broadway in "Annie" and in "Woman of the Year" with Raquel Welch. He appeared in primetime and daytime television programs and in network television commercials. Until shortly before his illness, he continued to act in regional theater.

As deputy director of performing arts for the Smithsonian Institution, Mr. Jecko developed national and international performances, including U.S. entries in the cultural festival of the 1968 Olympic Games in Mexico City. He wrote articles for the performing arts journals Spectacle and the White Tops. He was a contributing editor for the recently published Encyclopedia of New Jersey.

Until his illness made it necessary to retire, Mr. Jecko was teaching writing and communication skills to undergraduate and graduate students at Fairleigh Dickinson University in New Jersey.

His marriages to Mary Louise Long and Margaret Oksner ended in divorce.

Survivors include his wife, JoAnn Jecko of Madison; two sons from his first marriage, Christopher Jecko of Hamden, Conn., and Nicholas Jecko of Chatham, N.J.; a daughter from his second marriage, Sarah Jecko of Madison; and a brother, Michael Jecko of Rockville, Maryland.

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Meyer Odette
Meyer Odette
7 months ago

I am a CALS of my 68 year old Husband who suffered from muscle tiredness brought on by chronic fatigue in its early stages. Neurologists first had difficulty diagnosing it until multiple examinations indicated ALS, for which there was no known cure other than the prescription of riluzole medications, vitamins, and therapies. More advancements in breathing difficulties, difficulty pronouncing words, and difficulties eating occurred before we made the decision to try different medications, which significantly enhanced his condition. He received treatment for ALS/MND at vinehealthcentre. com from the U.S approximately four months ago; since then, he has stopped using a feeding tube, sleeps well, works out frequently, and has become very active. Although it doesn’t cure his ALS, it has improved his quality of life. .

Maggie Patel
Maggie Patel
9 minutes ago

I was diagnosed with MND. I had weakness in my arms, legs, and hands. I lost all of my strength. I had to keep pliers and wrenches scattered around to open things. I couldn’t walk very far, and I lost my balance easily. I had trouble swallowing and drooling sometimes. It impacted all my voluntary moves. My hands shake when I eat or write. This year my family doctor decided I try alternative treatment as Riluzole caused side effects for me. I started on the ALS/MND protocol from the Uinehealth Center. Since starting the treatment, my symptoms have greatly improved. I now write and eat without my hand shaking, I can feel my strength again with no case of muscle weakness, I’m getting active again. This is a game changer for people with motor neurone disease. This protocol has truly transformed my daily life, allowing me to reclaim activities I once thought were lost forever. I encourage anyone facing similar challenges to explore their options and seek support, as there is hope beyond the diagnosis. Reach them at uinehealthcentre. com

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