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NMO Video Library

NMO Video Library

 

Overview

Neuromyelitis optica
(NMO) spectrum disease
is a rare autoimmune disease.

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NMO patients describe what it’s like living with NMO and what the Foundation is doing to help.

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NMO spectrum disease doesn’t only affect patients, it affects
families and friends.

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Actor Kathy Najimy interviews GJCF Founder, Victoria Jackson about her daughter’s journey…

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Victoria Jackson talks to actor Kathy Najimy about The Guthy-Jackson Charitable Foundation.

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Victoria Jackson talks to Kathy Najimy about the role of The Guthy-Jackson Charitable Foundation.

Actor Kathy Najimy
interviews GJCF Founder, Victoria Jackson about her
daughter’s journey…

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GJCF works to create a scientific research model that will ultimately cure patients with NMO…


 

Questions about NMO

Neuromyelitis optica
(NMO) spectrum
disease is a rare
autoimmune disease.

..

GJCF works to create a scientific research model that will ultimately cure patients with NMO.

..

People living with NMO often appear to have similar symptoms as those who have MS.

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Scientists are researching many forms of treatments for people living with NMO…

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NMO treatment approvals and costs pose a challenge for today’s US healthcare system.

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Peoples’ bodies are
unique and can react
differently to any form
of therapeutic treatments.

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Two major groups can categorize people living with NMO: monophasic and relapsing.

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The current drug
treatments for NMO
have been gathered
from a rather small …

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There are many things that we do not understand
about NMO

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The current drug
treatments for NMO
have been gathered
from a rather small…

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Dr. Brian Weinshenker,
a clinician at the Mayo
Clinic, describes optic neuritis (ON)…

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People living with NMO can experience neurogenic pain, but there are treatments available.

 

Patients’ Stories

Collin’s story is about a courageous young boy and his family who have
stopped at nothing…

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Neuromyelitis optica (NMO) affects people from all over the world.


 

Foundation Events

The Second annual NMO Patient Session brought people affected by NMO together…

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The First annual NMO Patient Session brought people affected by NMO together…

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Bringing together NMO scientists and clinicians to share information.


 

Public Affairs

CIRM: NMO Advocacy

Coming Soon

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CoachArt “Evening of Champions”

Coming Soon

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Victoria Jackson talk to Tina Brown about ways she’s made a difference
in women’s lives.

Last updated 369 days ago by Steve Ornburn