
Connor B Judge Foundation
Raising global awareness of #NMOSD & #MOGAD, building community, supporting research, advocating for rare disease patients/caregivers. Illuminating the darkness of NMOSD & MOGAD

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Bay Village
NMOSD & MOGAD | Sumaira Foundation The Sumaira Foundation is a 501c3 organization dedicated to generating global awareness of NMOSD and MOGAD building communities of support for patients and their caregivers supporting research and patient advocacy NMOSD Neuromyelitis optica spectrum disorder NMOSD is a rare neuroimmune condition in which the immune system attacks cells in the central nervous system CNS mistaking them for foreign invaders. Common symptoms include vision loss color vision deficiency paralysis paraparesis weakness numbness spasticity vomiting hiccups and bladderbowel dysfunction. MOGAD Myelin oligodendrocyte glycoprotein antibodyassociated disease MOGAD is a rare neuroimmune condition that targets the MOG protein which is located on the surface of myelin sheaths in the central nervous system. Common symptoms include vision loss color vision deficiency paralysis paraparesis weakness numbness spasticity vomiting hiccups seizures and bladderbowel dysfunction.
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Join us on October 18th for Seattle Patient Day for Rare Neuroinflammatory Disorders where you'll learn from the experts, be inspired by patients and caregivers and make new friends. Meet our fabulous patient and caregiver panelists: π¦ Alicia π¦ Bryce π¦ Jill π¦ Ken π¦ Lisa & Bravo π¦ Melinda π¦ Melody π¦ Michael π¦ Michelle π¦ Rachael π¦ Tara π¦ Taylor π¦ Teri π¦ Tracy π¦ Wennie π¦ Vanessa If youβre impacted by AE, CNS Vasculitis, MOGAD, neurosarcoidosis, NMOSD or SPS and are from the Pacific Northwest region, join us for a day of education, connection and impact. To register, visit www.
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