September Named Tay-Sachs Awareness Month
The Senate this July voted unanimously to name September National Tay-Sach’s Awareness Month. The resolution was introduced by Senator Sherrod Brown of Ohio and co-sponsored by Senator Evan Bayh of Indiana. At this point, Tay-Sachs, a hereditary degenerative neurological disease, has no cure. The National Tay-Sachs & Allied Diseases Association, Inc., the oldest genetic disease organization in America, has endorsed Brown’s resolution.
The initiative was set into motion by an Ohio family with a daughter suffering from the disease. The Bihns of Olmsted Falls wrote to Brown and proposed the measure as a way to increase awareness and raise funds for research. Tay-Sachs is always fatal in children, with many not living beyond the age of 5. Dakota Bihn is 9. September is seen by the Bihns as a starting point for 12 months of fundraising — with a goal of $1 million.
“Tay-Sachs is a devastating disease that is often overlooked and misunderstood,” Brown said. “This disorder requires our close attention. The more people who are aware of the risk posed by Tay-Sachs, the more lives we can potentially save.”
"Why I became the Forward’s Editor-in-Chief"
You are surely a friend of the Forward if you’re reading this. And so it’s with excitement and awe — of all that the Forward is, was, and will be — that I introduce myself to you as the Forward’s newest editor-in-chief.
And what a time to step into the leadership of this storied Jewish institution! For 129 years, the Forward has shaped and told the American Jewish story. I’m stepping in at an intense time for Jews the world over. We urgently need the Forward’s courageous, unflinching journalism — not only as a source of reliable information, but to provide inspiration, healing and hope.
