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VOIX DE MOGAD
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L’histoire de Nelly – Une vie colorée parce que la vie est belle
Je m’appelle Nelly, j’ai 44 ans et je vis dans un joli village dans l’Oise et j’ai la MOGAD. Sans…
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Andrea & James’ MOG Story – Love Conquers MOG
Published May 1, 2019
Anthy’s MOG Story – Advocating for Answers
It was the Friday before Halloween in 2018. Anthy was on her way home from work when she called her…
Avery’s MOG Story – Racing Against MOG
My entire life, I was always a healthy and energetic person… I have played tons of sports and never went…
Brian’s MOG Story – Life Goes On
Life was good in the spring of 2015; no, it was great! In 2012 I completed my master’s degree, which…
Brittney’s MOG-AD Story – #JaidynStrong
My beautiful 4-year-old (5 years old now) daughter Jaidyn woke up one morning in late April 2021 with a headache,…
David’s MOG Story – Father of a Survivor
When your daughter suddenly goes blind in one eyes, you feel helpless. When the doctors don’t know what it is…
Dr. Farrah Mateen’s Story – A Global Perspective on NMO
Like many physician-researchers in my field, I spend a lot of time thinking about NMO, both inside and outside of…
Dr. Michael Levy’s NMO Story – A Physician’s Quest to Find a Cure
I was an on-call intern late one night at the Johns Hopkins Hospital when I met a young woman who…
Dr. Sara Mariotto’s Story – Bedside to Bench
I was a young resident at the University of Verona’s, Neurology Unit when I met a woman with rapidly evolving…
Dr. Tracey Cho’s NMO Story – Teaching Future Neurologists That NMOSD is a “Do Not Miss” Diagnosis
My name is Tracey Cho. I am a neurologist and a teacher. I specialize in autoimmune and infectious neurology, treating…
Dr. Weinshenker’s Story – Witnessing the Transformation of Neuromyelitis Optica
My name is Brian Weinshenker and I am a neurologist at the Mayo Clinic in Rochester, MN. I established a…
Historia MOG Bożena – Życie 3.0
Drogi Czytelniku – chciałabym podzielić się z Tobą naszą bardzo osobistą historią, która zmieniła życie moje i mojego męża. Bardzo…
Julia’s MOG Story – Early Signs of a Rare Disease
Now that I have been diagnosed with Myelin Oligodendrocyte Glycoprotein Antibody-Associated disease, or MOG-Ab disease, I have met others who…
L’histoire de Nelly – Une vie colorée parce que la vie est belle
Je m’appelle Nelly, j’ai 44 ans et je vis dans un joli village dans l’Oise et j’ai la MOGAD. Sans…
Laura’s MOG-AD Story – It’s Made Me Who I Am Today
It all began with a tremor. It was September 2018, and I was off on maternity leave after having my…
Lisa’s MOG Story – Using Writing & Crafting to Cope With Chronic Disease
It was the late 1990’s. I was in my 30’s had constant pain down my left arm, and even though…
Liz’s MOG Story – In Orbit, Flying High
Liz has had NMO for 25 years now. She’s only known it for ten… Since she’d had migraines throughout…
Maureen’s Story – Experiences From the Bedside & Research
Maureen is a nurse. She worked in neurocritical care at Johns Hopkins Hospital for many years before she had ever…
Max’s MOG Story – The Luckiest Kid in the World
On a warm February evening at the University of Miami, I sat in my Music Business lecture and wondered from…
Nakeshia’s MOG Story – Finding Purpose Amidst the Darkness
Every day we wake up, we surely never expect our day to end with everything turned upside down – and…
Scott’s MOG Story – Personal Accountability to Advocating for Others
On Monday, I woke up with a slight ache on the left side of my lower back which felt numb,…
Therese Burke’s Story – IMPROVING CARE THROUGH PATIENT PARTNERSHIPS
It was over a decade ago, but I remember it like yesterday, the first patient I looked after with NMOSD.…
Virginia’s MOG story – A little child shall lead them Isaiah 11.6
Virginia was only 10 when, while checking the mail one day in April, she noticed a grayness in her vision,…
Yoka’s MOG Story – My Dutch MOG Story
Clean and clear were my glasses but still I had trouble seeing clearly with my right eye. On Easter Monday…
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