The Story of Baby Tatev

Just a few months ago, little Tatev’s family was facing deep uncertainty. At only 6 months old, Tatev was hospitalized with troubling symptoms—shortness of breath, vomiting, weakness, and signs of delayed growth. Doctors suspected a rare genetic disorder, but without clear answers, her treatment path was uncertain.

Thanks to the kindness and generosity of so many people—and with the support of the IMAST app fundraising partnership—Tatev was able to undergo the vital Whole Exome Sequencing (WES) test. The results gave her doctors the information they needed to understand her condition better and to create a clear treatment plan.

Today, Tatev is under careful medical supervision and her health is being closely monitored by specialists. While her journey isn’t over, she now has the care and guidance she needs to grow stronger—something that wouldn’t have been possible without your support.

Baby Tatev’s story is a reminder that every act of kindness makes a difference. We are deeply thankful to each donor and to IMAST for helping bring answers, hope, and healing to her family.