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Get Cureageous

Enhance Wellness Experience Through Education & Advocacy

Every person affected by NMOSD or MOGAD has a unique journey.  Immune systems change over a lifespan, therapies affect people differently, and disability is not a simple yes or no question.

 

Beyond any symptom or serology - beyond any treatment or trial - patients are people first. In this respect, no two people affected by NMOSD or MOGAD are the same.  Each has a life story and identity that makes them unique.  Each of us is going through something.

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Well being is a balance of many different aspects of living, including mind, body, and spirit.

 

A GJCF mission priority is to help personalize & enhance well being through education and advocacy.  The best information is essential for the best outcomes, and we are stronger when we act together.

We study disability. We promote resilience.

Disability

Immobile

Painful

Incontinence

Unemployed

Stigmatized

Loneliness

Depression

Uncertainty

Lower QoL

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Resilience

Mobile

Pain Free

Continence

Employed

Included

Relationships

Optimism

Preparedness

Higher QoL

Enhancing Ability

GJCF believes that the best approach to wellness is to focus on the person not the disease.  Through our CIRCLES program, we have pioneered new studies to flip the script:  we study disability but we promote resilience— and everyone can use a little help through advocacy. With our interactive workshops including very popular Artistry iNMOtion sessions, Hear My Voice patient & caregiver story telling and other programs, we focus on ability not disability. GJCF promotes advocacy for all.

Contribute to the Cure

Together we are stronger. Join us in our mission to accelerate research and advance awareness. Every day we work to solve NMO, the closer we are to a cure.

Make a Direct Impact

All financial donations are directed to The Guthy-Jackson Research Foundation, Inc.

Share Your NMO Story

A rare disease is not rare if it affects you or your family. We understand the rare journey of NMO. All patients, family members and caregivers are welcome to share their experiences with NMO.

Siegel Rare Neuroimmune
Association (SRNA)

The MOG Project

The Sumaira
Foundation

International

NMO Organizations

SUPPORT THE NMO COMMUNITY

DISCOVER MORE NMO ADVOCATES ONLINE

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Devica.pl

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Fast Facts about NMOSD