SRNA @[email protected]
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The Siegel Rare Neuroimmune Association (SRNA) is a not-for-
140 Videos
SRNA "Ask the Expert" Podcast Series
13 Videos
SRNA "Ask the Expert" Podcast Series - Season 12
7 Videos
The Power of Community
1 Videos
2024 TM Together
31 Videos
"ABCs of NMOSD" Podcast Series
1 Videos
2024 ADEM Together
1 Videos
2024 MOGAD Together
1 Videos
2024 NMOSD Together
5 Videos
2024 Stronger Together | Rare Disease Day
2 Videos
"Community Meets Clinic" Podcast Series
10 Videos
2023 RNDS en Español
15 Videos
SRNA "Ask the Expert" Podcast Series - Season 11
5 Videos
2023 Virtual RNDS
12 Videos
2023 RNDS
2 Videos
2023 AFM Together
2 Videos
2023 TM Together
2 Videos
2023 ADEM Together
2 Videos
2023 MOGAD Together
1 Videos
2023 NMOSD Together
3 Videos
"ADEM Academy" Podcast Series
17 Videos
This is Me
2 Videos
2022 RNDS | Day 2 | Track 3 | Pediatric
2 Videos
2022 RNDS | Day 2 | Track 2 | Diagnosed more than two years ago
2 Videos
2022 RNDS | Day 2 | Track 1 | Recently Diagnosed
10 Videos
2022 RNDS | Day 3
14 Videos
2022 RNDS | Day 2
2 Videos
2022 RNDS | Day 1
11 Videos
SRNA "Ask the Expert" Podcast Series - Season 10
10 Videos
2022 Pre-RNDS
12 Videos
COVID-19
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About
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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