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Speakers

Jason Kohari

Genentech

Justin Abbatemarco

University of Utah

Nischay Mishra

Columbia University

Janell Routh

Centers for Disease Control and Prevention

Eileen Yee

Centers for Disease Control and Prevention

Amy Rosenfeld

Columbia University

Sammita Satyanarayan

Icahn School of Medicine at Mount Sinai

Cara Amos

Alexion, AstraZeneca Rare Disease

Dennis Tom-Wigfield

Kennedy Krieger Institute

Melissa Hutchinson

Nationwide Children's Hospital

Nathan Rosenberg

Nationwide Children's Hospital

Kim Bjorklund

Nationwide Children's Hospital

L.A. Campbell

Barrow Neurological Institute

Daniel Becker

Johns Hopkins Medicine

Paula Barreras

Johns Hopkins Medicine

Elias Sotirchos

Johns Hopkins Medicine

Kaitlin Hagen

Kennedy Krieger Institute

Sandy Hanebrink

Touch the Future

Cynthia Wang

UT Southwestern Medical Center

Rebecca Whitney

SRNA

Jim Lubin

SRNA

Debbie Capen

SRNA

Angel Simpelo

SRNA

Linda Malecky

SRNA

Krissy Dilger

SRNA

Janelle Hewelt

MEd

John Chen

Mayo Clinic

Margaret Jones

Vanderbilt University Medical Center

Jacqueline Nicholas

Ohio Health

Sara Qureshi

Billings Clinic

Ram Narayan

Barrow Neurological Institute

Lana Harder

Children's Health & UT Southwestern

Philippines Cabahug

Kennedy Krieger Institute

Cristina Sadowsky

Kennedy Krieger Institute

Eoin Flanagan

Mayo Clinic

Leslie Benson

Boston Children's Hospital

Sarah Hopkins

Children’s Hospital of Philadelphia

Kyle Blackburn

UT Southwestern Medical Center

Rohini Samudralwar

University of Texas Health Science Center at Houston

Tanuja Chitnis

Brigham and Women's Hospital

Janet Dean

Kennedy Krieger Institute

Roberta Pesce

SRNA

Stacey Clardy

University of Utah

Carlos Pardo

Johns Hopkins Medicine

Michael Levy

Massachusetts General Hospital and Harvard Medical School

Benjamin Greenberg

UT Southwestern Medical Center

Sandy Siegel

SRNA

Cody Unser

Cody Unser First Step Foundation

Julia Lefelar

The MOG Project

Jacinta Behne

Guthy Jackson Foundation

The nonprofit advocating for people with rare neuroimmune disorders. Accelerating research for a cure.⁣⁣ ⁣⁣ ADEM | AFM | MOGAD | NMOSD | ON | TM⁣

Booths

SRNA | connect. care. cure. ™

The nonprofit advocating for those with ADEM, AFM, MOGAD, NMOSD, ON, and TM

Genentech

ENSPRYNG

HORIZON

Information on HORIZON and a patient brochure about UPLIZNA

ALEXION NMOSD SRNA 2021 Virtual Conference Booth

Ready to learn about an Alexion NMOSD treatment option?

NeuFit

Putting the Nervous System First

The Sumaira Foundation (TSF)

Illuminating the darkness of neuromyelitis optica

Come chat with The MOG Project!

Meet the MOG Squad and find out more about what we do for the MOGAD Community

AFMA

Acute Flaccid Myelitis Association

The Guthy-Jackson Charitable Foundation

We are NMO.

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