Awareness Month 2025

Switching doctors with NMOSD: When and how to do it

This is part of a series about neuromyelitis optica for NMO Awareness Month. Go here to read more. A doctor’s expertise and familiarity with a challenging condition like neuromyelitis optica spectrum disorder (NMOSD) is important, but so is having a healthcare provider who listens, understands your needs, and…

Building a strong relationship with your NMOSD healthcare provider

This is part of a series about neuromyelitis optica for NMO Awareness Month. Go here to read more. Building a strong relationship with your neuromyelitis optica spectrum disorder (NMOSD) healthcare provider may feel daunting, especially if you’re newly diagnosed or switching doctors. At first, it can feel…

Protecting autonomy, independence and finding NMOSD support

This is part of a series about neuromyelitis optica for NMO Awareness Month. Go here to read more.  All relationships require care, attention, and communication. But when living with a rare autoimmune disease like neuromyelitis optica spectrum disorder (NMOSD), voicing your needs becomes even more vital for maintaining…

How to discuss pain management strategies with your doctor

This is part of a series about neuromyelitis optica for NMO Awareness Month. Go here to read more. While neuromyelitis optica spectrum disorder (NMOSD) often causes excruciating pain that can greatly affect your quality of life, you may find that your doctor is not taking your pain as…

Why advocacy is important for the NMOSD community

This article is part of a series about neuromyelitis optica spectrum disorder for NMO Awareness Month. Go here to read more. Advocates are not chosen; circumstances force people into standing up for their rights. That’s how many people living with neuromyelitis optica spectrum disorder (NMOSD) become patient advocates.