SRNA
The Siegel Rare Neuroimmune Association (SRNA) is a not-for-profit international foundation dedicated to the support of children, adolescents, and adults with a spectrum of rare neuroimmune disorders including: ADEM, AFM, MOG-Ab disease, NMOSD, ON, and TM.We support individuals living with rare neuroimmune diagnoses and their families, promote awareness to empower patients, families, clinicians and scientists, build a collaborative and dedicated clinical care network and help advance scientific understanding and research.
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The Power Of Community: Teaser
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502. Men and NMOSD
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- 14 күн бұрын
The Power of Community: Francisco
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- 14 күн бұрын
1211. Community Spotlight | Kim Harrison
- 29:31
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1210. Community Spotlight | Paula Jones
- 35:22
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2024 ADEM Together | Community Q&A
- 18:58
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1209. What is ULTOMIRIS?
- 58:30
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2024 MOGAD Together | Community Q&A
- 49:26
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2024 NMOSD Together | Community Q&A
- 1:00:23
- 3 ай бұрын
1208. MOGcast | Understanding Cortical Encephalitis
- 33:21
- 4 ай бұрын
1206. Voices of SRNA Volunteers | Part 2
- 17:48
- 4 ай бұрын
2024 Stronger Together | Raising Funds for Rare
- 37:01
- 4 ай бұрын
1205. Voices of SRNA Volunteers | Part 1
- 43:48
- 4 ай бұрын
1204. Community Spotlight | Ilona Williams
- 22:01
- 4 ай бұрын
102. Dr. Paula Barreras
- 42:59
- 5 ай бұрын
1203. Community Spotlight | Rick Telander
- 29:16
- 5 ай бұрын
501. Transitioning from Pediatric to Adult Care with NMOSD
- 2:13
- 5 ай бұрын
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