He had acquired syringomyelia in a freak accident during a thunderstorm in 1929. His symptoms became noticeable in 1948 and finally diagnosed in 1950. Over the ensuing years, he would go from leg braces, to a cane, to a walker, to a wheelchair, and, finally, to a bed. As his condition deteriorated, his physical symptoms became too much to hide. Yet, even in the face of increasing disability, he continued to carry on as much as he could with the normal activities of life. After all, as he would say often, “In life, as in golf, you play the ball where you find it.”
That attitude, that spirit of sportsmanship, was what endeared him to golf fans on both sides of the Atlantic. It was the same spirit that touched the many friends and family members who watched him wrestle this implacable foe. His courage, good humor, and grace did not go unnoticed. Bobby Jones would die from his disease twenty-one years later in December of 1971, leaving behind a legacy of excellence, honor, and integrity, that remains unmatched to this day. His family has been committed to preserving and enhancing this precious heritage since then.
To that end, the Bobby Jones Family is proud to announce a new partnership with the Chiari Syringomyelia Foundation, now known as The Bobby Jones Chiari & Syringomyelia Foundation. With every person that our foundation touches, the legacy of Bobby Jones lives on. From our partnerships with medical centers around the world, to our invaluable work with the National Institutes of Health, to providing information to patients and family members, the Bobby Jones CSF offers hope and understanding. It brings the values of the greatest athlete of his day to the modern world, because
hope never goes out of style.