Hali's Journey with NMOSD Part 3Editor's note: This article is part of a multi-part series. To read part one, click here, and to read part two, click...reactions2comments
Shekita's NMO Life HacksHave you ever wanted some tips for coping with the pins and needles feeling that accompanies nerve pain? Are you curious about...reactions3comments
Take the Health and Media Habits Survey!The Media Habits Survey is now closed. Thank you for your interest! Managing a chronic condition is not easy and can be...reactionscomments
A Handy NMOSD Patient Information FormFrom my experience, hospitalizations and NMOSD go hand-in-hand. My relapses never seem to happen during “normal business hours," so my neurologist often...reactions3comments
Bladder Issues, Ladies?One of the most common symptoms we, women living with NMO, suffer from is recurrent UTIs (unitary tract infections) due to many...reactions2comments
My Journey with NMO Part 6: New Hopes and BeginningsEditor's note: To read part five of Dan's story, click on this link. The year was 2017 and it had already started...reactionscomments
Ask the Advocates: How to Cope with NMO-Related HeadachesWe asked our advocates how they cope with headaches. Here's what they had to say: "For as many years as I’ve had...reactionscomments
Hali's Journey with NMOSD Part 2: Feeling Afraid, Losing HopeEditor's note: This article is part of a multi-part series. To read part one, please follow this link. Mentally, I was exhausted...reactionscomments
Hali's Journey with NMOSD Part 1: No Relief, No AnswersI had just turned 19 two weeks earlier and was working as a soft playworker at my new childcare job. On the...reactionscomments
[Closed] Leisurely Self-Care Kit Giveaway!Happy NMO Awareness Month! Let's celebrate with a giveaway! This year we're focused on making sure you SHINE! Nothing helps us shine...reactionscomments
NMO Awareness Month: Our Time to SHINE!March is NMO Awareness Month! Now more than ever, let us come together and use our voices to bring more awareness around...reactionscomments
Strategies for Coping with a Rare Disease like NMOWhen you are diagnosed with a rare disease like NMO, you might feel overwhelmed about what to expect. Because few people have...reactionscomments
Moving Through NMOSD ChallengesI just need to vent about NMOSD challenges and frustrations. I need to speak my truth and say out loud what’s building...reactions1comment
Ask the Advocates: Coping with PainWe asked our advocates how they cope with the pain that comes from living with NMO. We also asked what tips or...reactionscomments
My Journey with NMO Part 5: Realizing I Had a ProblemEditor's note: To read part four of Dan's story, click on this link. This was the year that things would shape up...reactionscomments
Through Sickness and in HealthYou know that part of the wedding ceremony when you hear “in sickness and in health, to love and to cherish, till...reactionscomments
My Journey with NMO Part 4: Darker RealityLet's revisit where we left off: My vision had been diminished by an attack, after four months my disability insurance through my...reactionscomments
How NMOSD Vision Loss Has Changed MeI have always been a mover. Sitting still for too long makes me antsy. Even before I was diagnosed with NMOSD, I...reactions2comments
The Sumaira Foundation Distributes Five $25,000 Research GrantsThe Sumaira Foundation recently announced that it has awarded five grants, each in the amount of $25,000, to further research into NMOSD...reactions2comments
My Journey With NMO Part 3: When It Gets DarkI was on top of the world and was really growing as a person. I thought I beat the fear I was...reactionscomments
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