Welcome!
NMO STORIES AROUND THE GLOBE
Rare to the Rescue
From MS to NMO – a mysterious journey
My name is Kimberly. I started this journey in the summer of 1996. Water from the sprinkler felt hot on…
Read MoreI am an NMO miracle
Eight years ago at the age of 52 I was diagnosed with NMO. I became fully quadriplegic before I was…
Read MoreAnnie’s NMO Journey
Our 13 year old daughter, Annie, was diagnosed with NMO almost a year ago. Her first visit to the hospital…
Read MoreStem Cell Transplant
I am 28 years old, a single mom to a beautiful 3 year old daughter and I own my very…
Read MoreAnnabelle Moult – My NMO Story
“Congratulations Lucy Mutton and Annabelle Moult for raising approximately £3,000 for GJCF and NMO research at London’s Blenheim Triathlon in…
Read MoreNMO Patient seeking Clinical Trials and a place to live
I am a 50 y.o. living with NMO for the last 13 years. Was not getting good treatment in California…
Read MoreMy journey with NMOS
My journey began October 4, 2012, but let me back up to three days prior to my symptoms. It was…
Read MoreThey Should Of Known
Misdiagnosed for almost 10 years and was taking wrong medication that could harm me. Was told years ago instead of…
Read MoreThings I have learned
” My first symptoms of NMO was on Dec 22, 2013 with optic neuritis. I was eventually diagnosed in April…
Read MoreMy Independence Day….What you need to know!
It has been over 2 years now when i became diagnosed with Neuromyelitis Optica (NMO). I like to refer to…
Read MoreMy NMO Diagnosis in Canada
Sometimes I think I could write a book about my story with NMO. I was 21 years old at the…
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