The MOG Squad hit the road on July 8th for the Guthy Jackson Charitable Foundation 2022 Patient Day in Los Angeles, California! We traveled, we learned, we…
Award-Winning High School Art Student Honors Grandmother Who Has NMO “Neuromyelitis optica (NMO) is a cruel disease – and it hides,” says Bonita Melonio, whose…
April 26, 2018 – Vatican City – Victoria Jackson, Founder of The Guthy-Jackson Charitable Foundation (GJCF), was honored with the 2018 Pontifical Key Advocacy Award…
Tell Congress to Oppose the Repeal of the Orphan Drug Tax Credit! TAKE ACTION NOW: Email or Call your Senators and Representative Now! Washington, D.C., November 2, 2017—The National…
NMO Advocate asks you to join “TEN on TEN” for NMO research. Well, it may not be the ice bucket challenge, but if the NMO…
NoMOreNMO’s 5K Raises $30K for NMO Research “Mom, there are no words to tell you how proud I am of you!” Riley Reimer After her…
Race of Joy, Race of Wonder Jasmine Lellock ran in the “Race the Rhode” Providence Marathon on May 7, to honor her mother, Patti, who passed…
NMO advocate Tim Woods attended Chronic Disease Awareness Day at the Denver, CO, State Capitol on March 9, raising awareness about NMO. A collaboration of different charitable…
Mother of a son lost to rare autoimmune disease educates tens of thousands of medical professionals. Getting up to speak to an audience can be…
What is #GivingTuesday? Entering its fifth year, #GivingTuesday is a global day of giving fueled by the power of social media and collaboration. Celebrated on…
Facebook has been reinventing the way people communicate and stay informed of their favorite organizations, and now it’s reinventing the way you can contribute to your…
Providence, RI – Creator of Dining for NMO, Gabriela Romanow, guest blogs about her most recent event and how you can join the program. Last…
Fast Facts about NMOSD
