Lou Gehrig’s disease takes a horrible toll on victims

Having recently lost my devoted and loving brother from the hideous neurological disease of ALS (amyotrophic lateral sclerosis), more familiarly known as Lou Gehrig’s disease, I feel inclined to express a personal view on the subject.

I was inspired by the numerous requests for an address to which friends and relatives could send memorial donations. I knew none, and could find none in the local or regional phone books. After some research, I finally found the address of the ALS Society in New York City, as well as one in California, where my brother resided. I’ll list them shortly.

Those who have read the best-selling book Tuesdays With Morrie, or viewed the television rendition of that story, should have a pretty clear idea of the destruction it causes to the body of a victim, subsequently rendering the patient totally helpless, as the loved ones can do nothing. A once-vibrant and independent person is reduced to total submission, with full awareness of his circumstances.

Like other neurological ailments, there has not been found any help for this disease yet. If one feels inclined to send a worthwhile donation to help in the research, the following addresses will bring your contributions to the correct source: ALS Society, 116 John St., Suite 1304, New York, N.Y. 10038. The telephone number is (212) 619-1400. The California address is: ALS Society, 27001 Agoura Road, Suite 150, Calabasas Hills, Calif. 91301-5104.

Fay Alpern

Freehold