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…
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…
‘NMO Biomarkers and You’ is part one in a new series titled ‘Do You Know NMO’. Test your knowledge with the interactive quiz at the end of this article….
Providence, RI – Creator of Dining for NMO, Gabriela Romanow, guest blogs about her most recent event and how you can join the program. Last…
Alexander City, AL – In June 2016, the University of Alabama at Birmingham’s (UAB) Center for Pediatric Onset Demyelinating Disease (CPODD) hosted its annual retreat…
Guest blogger and NMO Support Group leader, Erin Miller, writes about the first-ever NMO Pregnancy Support Group teleconference she hosted in June. I started this…
Western Pennsylvania NMO Support Group Meeting recap, with guest blogger and support group leader Heather Sowalla. I had the opportunity to host the first Western…
NMO Caregiver Support Group Meeting recap by guest blogger and NMO Advocate Lisa McDaniel. The NMO Caregiver Support Group was amazing. The group was very…
We at The Guthy-Jackson Charitable Foundation are excited to launch new updates to our website in order to offer you easier ways to take action…
Since it’s initial launch last fall, the Guthy-Jackson Charitable Foundation’s mobile app has been a breakout success with 5 star ratings both the Google and…
Let’s take a brief look at some of the common questions about NMO. You can read our full list of NMO FAQs here. What is…
Fast Facts about NMOSD
