NMO Video Library
Featured Videos
Victoria Jackson, Ali Guthy and clinicians discuss the progress made in the fight against NMO (Neuromyelitis Optica).
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Victoria Jackson and Ali Guthy Appear on Ellen to discuss NMO and Saving Each Other.
Victoria Jackson and Ali Guthy Appear on Hallmark’s Marie to discuss NMO and Saving Each Other.
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Inspirational video about the progress and future of NMO.
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 how the Foundation helps.
NMO spectrum disease doesn’t only affect patients, it affects families and friends.
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Overview
Victoria Jackson
shares her quest for a
cure with Leeza Gibbons.
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Footage from Patient Day 2011
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Our Repository Study Nurse travels anywhere within the continental US to collect blood samples.
Actress 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.
Actress 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…
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Imagine being struck by a crippling, debilitating disease and then being misdiagnosed.
Questions about NMO
Neuromyelitis optica
(NMO) spectrum
disease is a rare
autoimmune disease.
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GJCF works to create a scientific research model that will ultimately cure patients with NMO.
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People living with NMO often appear to have similar symptoms as those who have MS.
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.
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
The current drug
treatments for NMO
have been gathered
from a rather small…
..
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.
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Foundation Events
The Fourth annual NMO Patient Session brought people affected by NMO together…
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The Third annual NMO Patient Session brought people affected by NMO together…
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The Second annual NMO Patient Session brought people affected by NMO together…
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.
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Public Awareness
Victoria Jackson talks to Tina Brown about ways she’s made a difference
in women’s lives.
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GJCF speaks to the CIRM governing board to raise awareness for NMO.
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Victoria Jackson and her daughter Ali Guthy Champions of Courage
Jenna promotes NMO awareness with the Guthy-Jackson Foundation at the Consortium for MS Centers in Montreal.
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The hope is that these funding approaches will accelerate the discovery of cures through more efficient collaboration.
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A talk with Dr Brian Weinshenker, Professor of Neurology and researcher at the Mayo Clinic.
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