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Indhold leveret af Siegel Rare Neuroimmune Association (SRNA). Alt podcastindhold inklusive episoder, grafik og podcastbeskrivelser uploades og leveres direkte af Siegel Rare Neuroimmune Association (SRNA) eller deres podcastplatformspartner. Hvis du mener, at nogen bruger dit ophavsretligt beskyttede værk uden din tilladelse, kan du følge processen beskrevet her https://da.player.fm/legal.
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ABCs of NMOSD

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Indhold leveret af Siegel Rare Neuroimmune Association (SRNA). Alt podcastindhold inklusive episoder, grafik og podcastbeskrivelser uploades og leveres direkte af Siegel Rare Neuroimmune Association (SRNA) eller deres podcastplatformspartner. Hvis du mener, at nogen bruger dit ophavsretligt beskyttede værk uden din tilladelse, kan du følge processen beskrevet her https://da.player.fm/legal.
ABCs of NMOSD brings together the latest information and research about all things NMOSD, from diagnosis and treatment to quality of life and what it’s like to live with NMOSD. We invite medical experts and researchers, to share the latest up-to-date research and clinical knowledge. We have conversations with individuals who have been diagnosed with NMOSD, their caregivers, and allied health professionals. We give tips on how to advocate at school and at work, where to find help and support, navigate health insurance, and work with a team of medical experts.
  continue reading

34 episoder

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ABCs of NMOSD

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Manage series 3240321
Indhold leveret af Siegel Rare Neuroimmune Association (SRNA). Alt podcastindhold inklusive episoder, grafik og podcastbeskrivelser uploades og leveres direkte af Siegel Rare Neuroimmune Association (SRNA) eller deres podcastplatformspartner. Hvis du mener, at nogen bruger dit ophavsretligt beskyttede værk uden din tilladelse, kan du følge processen beskrevet her https://da.player.fm/legal.
ABCs of NMOSD brings together the latest information and research about all things NMOSD, from diagnosis and treatment to quality of life and what it’s like to live with NMOSD. We invite medical experts and researchers, to share the latest up-to-date research and clinical knowledge. We have conversations with individuals who have been diagnosed with NMOSD, their caregivers, and allied health professionals. We give tips on how to advocate at school and at work, where to find help and support, navigate health insurance, and work with a team of medical experts.
  continue reading

34 episoder

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