Welcome to Signalise: a podcast from Dazzle4Rare.
Here, we signal-boost undiagnosed and rare stories, turning up the volume on their life-changing stories.
In this brief trailer, Kimberly talks about what you can expect from Signalise. You'll also hear why Signalise, and Dazzle4Rare, have been life-changing for Kimberly and many others Worldwide.
To learn more about the Ehlers-Danlos syndrome (EDS), one of which Kimberly survives and thrives with, visit the National Organisation for Rare Disease (NORD) for info on the 13 distinct types of EDS.
Don't miss an episode of Signalise! Be sure to FOLLOW or SUBSCRIBE via your podcast app of choice. You can also follow Signalise news on @Dazzle4Rare on Facebook, Instagram, Twitter, and Pinterest. You can find Kimberly on LinkedIn at @kattague.
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More about Dazzle4Rare
#Dazzle4Rare is a cross-community undiagnosed and rare disease awareness week. Unlike most awareness events, this week is meant to enable rare disease communities of all sizes to share messages for one another, signal boosting the messages to reach a wider audience. The base concept is simple – when you share for another community, they can reach your audience who may benefit from hearing their message or learning more about that. In doing so, others will share YOUR message enabling you to reach an audience you would not normally.
Official website: https://www.dazzle4rare.net/
資訊
- 節目
- 頻率每週更新
- 發佈時間2022年9月17日 下午9:55 [UTC]
- 長度9 分鐘
- 年齡分級兒少適宜