Navigating Holiday Madness With NMOSDNavigating the holidays can often be difficult for those living with rare diseases like NMOSD. The holiday season can be a joyous time, but it can also be a source...
Handling A New Attack On My EyeWhat happened in March was not how I thought I’d spend my NMO awareness month. I’ve tried writing this several times but every time I write, things continue to change...
Finding the Correct Rehab Team for My NMOMy hopes and dreams of one day getting up from my wheelchair and walking freely are partly kept alive by my rehab team. Don’t get me wrong, there are other...
Navigating Holiday Madness With NMOSDNavigating the holidays can often be difficult for those living with rare diseases like NMOSD. The holiday season can be a joyous time, but it can also be a source...
Handling A New Attack On My EyeWhat happened in March was not how I thought I’d spend my NMO awareness month. I’ve tried writing this several times but every time I write, things continue to change...
Finding the Correct Rehab Team for My NMOMy hopes and dreams of one day getting up from my wheelchair and walking freely are partly kept alive by my rehab team. Don’t get me wrong, there are other...
Navigating Holiday Madness With NMOSDNavigating the holidays can often be difficult for those living with rare diseases like NMOSD. The holiday season can be a joyous time, but it can also be a source...
Handling A New Attack On My EyeWhat happened in March was not how I thought I’d spend my NMO awareness month. I’ve tried writing this several times but every time I write, things continue to change...
Finding the Correct Rehab Team for My NMOMy hopes and dreams of one day getting up from my wheelchair and walking freely are partly kept alive by my rehab team. Don’t get me wrong, there are other...
Spasm HorrorsAfter being diagnosed as AQP4+ and getting paralyzed from the waist down, my initial phase of spasms started without any pain. My muscles would get very stiff and my leg...Reactions0reactionsComments2 comments
Cozy in the Cold GiveawayThis fall season, we want to express our gratitude for the Neuromyelitis-Optica.net community. When you live with neuromyelitis optica spectrum disorder (NMOSD), it is not always easy to stay comfortable...Reactions0reactionsComments2 comments
Will you take our In America survey and help others understand the true impact of NMO?The In America survey is now closed. To better understand the patient experience and realities of NMO, we are fielding our NMO In America survey. By taking this anonymous survey...Reactions0reactionsComments0 replies
16 years misdiagnosed with MSHello, I'm Brittany! I was first diagnosed with Relapsing Remitting Multiple Sclerosis when I was 15 and have been dealing with the trials and tribulations that come along with it...Reactions0reactionsComments3 comments
