Judy Siegel-Itzkovich, The Jerusalm Post 18.5.2025
A NONPROFIT group established in 2014 – Caregivers Israel – was a promoter outside the Knesset that had a vision to give family caregivers recognition and support, rights, and tools to make it possible for them to continue in their role while maintaining their health and quality of life. Through the lobby, it views its major role as providing education and outreach among the public and elected officials, promoting legislation and policy, and developing evidence-based services.
Its founder and CEO Rachel Ledany told The Jerusalem Post that the caregivers have only a few benefits, lack government recognition and no budget except for those who take care of the demented. Many are embarrassed to ask their employers for time off or other help, and some have to leave their jobs.
Laws have to be changed, she continued. A caregiver for a patient with ALS (amyotrophic lateral sclerosis – a fatal neurological disease that gets worse over time) is entitled to five extra sick days annually, compared to 60 for those caring for cancer patients, many of whom recover. All who care for people with serious illnesses should get many more days, she insisted.
