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Anyone living with NMOSD/ Devics Disease? We want to hear from you 💚

jadahu

Hey there! Jada here, I help run Neuromyelitis-Optica.net and where we support so many living with NMO. We know SO many people have had the NMO misdiagnosed as MS.

Sadly, lack of awareness can mean unnecessary suffering, ineffective treatment, and undue stress on the part of the patient. If you or anyone you know has NMO please consider sharing and/or taking our NMO in America Survey.

Your voice matters, and we want to hear from you! Please check out the link below. Or feel free to message me. 💚

https://healthunion.az1.qualtrics.com/jfe/form/SV_agURAPsnl0UfhJA?Source=MultipleS

Have you heard of NMO?