Hope on the Horizon: Top MDS & CMML Breakthroughs from ASH 2025 image

Hope on the Horizon: Top MDS & CMML Breakthroughs from ASH 2025

Jan 14, 2026
01:00PM - 02:00PM EST
Online Event
Overview

Join the HealthTree Foundation for this special webinar where myelodysplastic syndromes (MDS) expert Dr. Sangeetha Venugopal shares highlights from the world's largest hematology conference.

Agenda
1:00 PM
Introduction
Dalton Bean

Dalton introduces the agenda for the event and featured speaker Sangeetha Venugopal MD, MS

1:05 PM
Presentation
Sangeetha Venugopal MD, MS

Dr. Venugopal talks about ASH breakthrough

1:35 PM
Questions and Answers
Audience

Type your questions in the chat and we will answer them! 

Speakers & Moderators
Healthtree contact Dalton Bean

Dalton Bean

Dalton joined HealthTree in 2024 as the MPNs and MDS Program Manager. He is passionate about helping patients gain a better understanding of their health and treatment and sees it as a way to help empower individuals and their families who are affected by these diseases. Prior to joining HealthTree Dalton earned a Master’s Degree in Oncological Sciences while studying various different blood cancers. When not interacting with patients he is an avid snowboarder and hiker.

Healthtree contact Sangeetha Venugopal MD, MS

Sangeetha Venugopal MD, MS

Sangeetha Venugopal, M.D., is a board-certified hematologist who trained at renowned institutions, including Montefiore Medical Center and the Icahn School of Medicine at Mount Sinai in New York, and completed an additional leukemia-focused fellowship at the UT MD Anderson Cancer Center in Houston, Texas. A well-published clinician-investigator, Dr. Venugopal focuses research on improving treatment outcomes for patients with myeloid malignancies, including acute myeloid leukemia (AML), myelodysplastic syndromes (MDS), and myeloproliferative neoplasms (MPN), through clinical trials, translational investigations, and precision medicine approaches. Dr. Venugopal has a particular interest in identifying novel targeted therapies, elucidating mechanisms of treatment resistance, and developing strategies to eradicate measurable residual disease in AML.