Community Health Leaders
In order to stay up to date on latest treatments, drug discovery, clinical studies and how to manage neuromyelitis optica every day, Neuromyelitis-Optica.net brings you frequent articles, blogs, points of view, and advice from leading health leaders and professional medical experts.
Current Health Leaders
Sandra is 53 years old and has been living with NMOSD for 15 years. A native of New York, she has spent most of her life in Florida, where she was a senior sales marketing associate for a Fortune 500 company until the day that her life changed forever. Read more.
Hello my name is Avery and I’m 24 years old. I was diagnosed with NMOSD in 2017, then quickly learned I actually have MOGad. I am a former college track runner and due to the severity of my attack at the time, I gave up the sport I loved. Read more.
I am not an expert on NMO or MS or any of the many diagnoses I had received over the time I’ve dealt with symptoms, but I’ve got my little bag of tricks that have helped me normalize the new me that comes home slightly different than the person who went into the hospital with a flareup. Still, every step I take as I walk reminds me that I have NMO and my abilities have changed. Read more.
My name is Teaira Daniels. I am 38 years old and from Cincinnati, OH. I am a Licensed cosmetologist; I have 1 child my daughter Amariyah who passed away July 1, 2009, 13 days from turning 2 from Pompe Disease. Read more.
Shekita Green is the mother of 2 teenagers, the wife of an Army Vet and an entrepreneurial spirited businesswoman. In January 2013, she first began experiencing terrible nerve pain, back pain and numbness in her fingers and toes along with piercing headaches. Read more.
Monica Jones, affectionately known as “Mo” to those close to her is an NMO warrior and a Type 2 Diabetic. Having been a diabetic for over a decade Mo was used to hitting bumps in the road, but it was the NMO diagnosis that knocked her off her feet. Read more.
Chelsey studied immunology at Case Western Reserve University, completing her PhD in 2016, and further studied immune mechanisms involved in HIV as a research fellow at the Ragon Institute of MGH, MIT and Harvard. Read more.
My name is Daniel but go by Dan or Danny. I'm 33 and living in North Carolina, originally from upstate New York. I am a happy cat dad who loves his fur baby. She is my world and cuddle buddy. I am a pretty big Marvel and horror movie nerd. Sadly, nothing scares me anymore. I also enjoy all kinds of music and love to dance and be silly. Read more.
Haleemah is a 19-year-old Law Student in Scotland who has been advocating for NMOSD since diagnosis. She was diagnosed with NMOSD in late September of 2021 after a three-month-long fight to get diagnosed. Read more
Chelsey Tucker resides with her husband, 5 children, and 3 goldendoodles in Nashville TN. Most people would agree that Chelsey Tucker lives anything but an ordinary life. Diagnosed with Multiple Sclerosis at the age of 21, Chelsey began a course of disease modifying treatments in hopes that the MS living inside her body would slow in progression. Read more.
My name is Aldelly and I’m fabulously living with neuromyelitis optica (Devic’s disease). A rare demyelinating inflammatory disease that has changed my world. I’m in my early 30’s, a mother of two young active boys, a proud daughter of immigrant parents, a sister and so much more. Read more.
Regular contributors and moderators at Neuromyelitis-Optica.net are offered compensation for their contributions to the Neuromyelitis-Optica.net community. If you are interested in joining our team, please contact us at email@example.com.