Signalise: a Dazzle4Rare Podcast

Kimberly explores September’s awareness days, upcoming webinars, conferences, and industry resources. She also highlights the inspiring ”Life After Diagnosis Day” on The Disorder Channel. Stay tuned for news, voicemails, and more!

Show Notes

In this rare and relevant episode Kimberly delves into various awareness days and months in September. We also talk about upcoming webinars and conferences, share industry resources, and highlight the inspiring "Life After Diagnosis Day" follow-up available on The Disorder Channel.

 

Stay tuned for voicemails from our listeners, news about Weill Cornell Medicine and New York-Presbyterian Weill Cornell Medical Center, and San Diego-based Crinetics Pharmaceuticals' promising results in the development of an oral medication for acromegaly. So much to hear in one episode! 

 

Links ⬇️

http://dazzle4rare.net/awareness_days](http://dazzle4rare.net/awareness_days 
https://www.hopeforhh.org/get-involved/](https://www.hopeforhh.org/get-involved 
https://rarediseases.org/rare-diseases/usher-syndrom](https://rarediseases.org/rare-diseases/usher-syndrome 
https://www.childrenshospital.org/conditions/microvillus-inclusion-disease

https://rarediseases.org/event/nfed-advocacy-day/](https://rarediseases.org/event/nfed-advocacy-day 
https://globalgenes.org/event/rare-health-equity-forum/](https://globalgenes.org/event/rare-health-equity-forum

https://www.hlth.com/2023event 
https://mmpharmasciences.pathfactory.com/l/integrated-perspectives

https://news.weill.cornell.edu/news/2023/09/national-organization-for-rare-disorders-designates-weill-cornell-medicine-and-newyork

 

Reach Daniel De Fabio at daniel@rarediseasefilmfestival.com

 

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What is Signalise: a Dazzle4Rare Podcast?

The Dazzle4Rare event and Signalise podcast amplify the voices of rare disease and associated communities by sharing their stories, new, events, and more. Working together, we have strength in numbers, amplifying our critical messages.

We feature guests and discuss relevant topics for rare disease patients, caregivers, and those in the URCIID community.