Bone Marrow Registry Event on Friday, February 14, 2020

Hematology

Cure 4 The Kids Foundation’s Katherine Salkanovic along with Mary Yom appears on KTNV’s Saturday morning newscast.  Yom’s son Julian is in need of a bone marrow transplant and will need to find a bone marrow match. The public can become part of the bone marrow registry by completing a simple mouth swab.

Those who want to take part in the registry can walk-in on Friday, February 14, 2020, between 9 a.m. and 4 p.m. at Cure 4 The Kids Foundation, One Breakthrough Way, Las Vegas, NV 89135.

 

Share This Post

Explore More News

Blog

Rare Disease Advisory Council seeks input for healthier Nevada

The Rare Disease Advisory Council is seeking input from the public to help improve the health of Nevada residents. The council is focused on addressing the needs of those with rare diseases and is looking for feedback from patients, caregivers, and healthcare providers. The goal is to gather information that can be used to develop strategies and policies to improve the lives of those affected by rare diseases in Nevada.

Blog

Cure 4 The Kids Foundation Announces Senior Leadership Changes

Cure 4 The Kids Foundation is pleased to announce the appointment of Christine Tonn as its new chief executive officer (CEO), effective January 1, 2024. This promotion is part of a board of directors-supported management succession plan.