![Once Upon A Gene artwork](https://is5-ssl.mzstatic.com/image/thumb/Podcasts123/v4/13/87/f3/1387f351-a21c-4837-d86d-52cd7a00c2a8/mza_9714266795295838361.jpg/100x100bb.jpg)
Ciitizen - Take Control of Your Own Medical Records and Advance Research with Nasha Fitter
Once Upon A Gene
English - September 10, 2020 11:00 - 30 minutes - ★★★★★ - 258 ratingsParenting Kids & Family advocate caregiver disability genetherapy genetics inclusion parenting raredisease rarediseasepodcast raredisorder Homepage Download Apple Podcasts Google Podcasts Overcast Castro Pocket Casts RSS feed
Ciitizen - Take Control of Your Own Medical Records and Advance Research with Nasha Fitter
Nasha Fitter is the mother of three daughters, one of which was diagnosed with a rare disease called FOXG1. After her daughter's diagnosis, she got to work and co-founded the FOXG1 Research Foundation. She's dedicated to leading the research strategy and finding a cure for every child in the world with FOXG1 syndrome. She's here to talk to us about her work as the Director of the Rare and Neurological Disease Division for Ciitizen, a technology company that enables fast and seamless access to patient data. In this episode, you'll learn about the most innovative medical record platform that will be open and accessible to parents, caregivers, clinicians, academics, bio pharma and researchers. Their goal is to eliminate the slow, manual and expensive processes that are currently used to collect data.
EPISODE HIGHLIGHTS
Tell us about you, your family and how you came to be a part of the rare disease community.
Tell us about Ciitizen and your role there.
How do you get started if you want to have medical records digitized?
Can doctors, geneticists and scientists access the platform and perform their own search?
If all these medical records are in this database, how do we protect our privacy?
How can parents and caregivers help move this platform forward?
What is a natural history study?
What final thoughts do you have for parents and caregivers?
LINKS AND RESOURCES MENTIONED
What is FOXG1 Syndrome? https://foxg1research.org/foxg1syndrome
Ciitizen
https://www.ciitizen.com/
EPISODE 041 - Time is Brain: SYNGAP Research Fund with Mike Graglia
https://effieparks.com/podcast/episode-41-syngap-research-fund
The Patient Record Scorecard
https://www.ciitizen.com/scorecard/
EPISODE 043 - David Fajgenbaum - Chasing My Cure - A Doctor's Race to Turn Hope into Action
https://effieparks.com/podcast/episode-43-david-fajgenbaum
CONTACT NASHA FITTER
[email protected]
[email protected]
TUNE INTO THE ONCE UPON A GENE PODCAST
Spotify
https://open.spotify.com/show/5Htr9lt5vXGG3ac6enxLQ7
Apple Podcasts
https://podcasts.apple.com/us/podcast/once-upon-a-gene/id1485249347
Stitcher
https://www.stitcher.com/podcast/once-upon-a-gene
Overcast
https://overcast.fm/itunes1485249347/once-upon-a-gene
CONNECT WITH EFFIE PARKS
Website
https://effieparks.com/
Twitter
https://twitter.com/OnceUponAGene
Instagram
https://www.instagram.com/onceuponagene.podcast/?hl=en
Built Ford Tough Facebook Group
https://www.facebook.com/groups/1877643259173346/
Ciitizen - Take Control of Your Own Medical Records and Advance Research with Nasha Fitter
Nasha Fitter is the mother of three daughters, one of which was diagnosed with a rare disease called FOXG1. After her daughter's diagnosis, she got to work and co-founded the FOXG1 Research Foundation. She's dedicated to leading the research strategy and finding a cure for every child in the world with FOXG1 syndrome. She's here to talk to us about her work as the Director of the Rare and Neurological Disease Division for Ciitizen, a technology company that enables fast and seamless access to patient data. In this episode, you'll learn about the most innovative medical record platform that will be open and accessible to parents, caregivers, clinicians, academics, bio pharma and researchers. Their goal is to eliminate the slow, manual and expensive processes that are currently used to collect data.
EPISODE HIGHLIGHTS
Tell us about you, your family and how you came to be a part of the rare disease community.
Tell us about Ciitizen and your role there.
How do you get started if you want to have medical records digitized?
Can doctors, geneticists and scientists access the platform and perform their own search?
If all these medical records are in this database, how do we protect our privacy?
How can parents and caregivers help move this platform forward?
What is a natural history study?
What final thoughts do you have for parents and caregivers?
LINKS AND RESOURCES MENTIONED
What is FOXG1 Syndrome? https://foxg1research.org/foxg1syndrome
EPISODE 041 - Time is Brain: SYNGAP Research Fund with Mike Graglia
https://effieparks.com/podcast/episode-41-syngap-research-fund
https://www.ciitizen.com/scorecard/
EPISODE 043 - David Fajgenbaum - Chasing My Cure - A Doctor's Race to Turn Hope into Action
https://effieparks.com/podcast/episode-43-david-fajgenbaum
CONTACT NASHA FITTER
TUNE INTO THE ONCE UPON A GENE PODCAST
https://open.spotify.com/show/5Htr9lt5vXGG3ac6enxLQ7
https://podcasts.apple.com/us/podcast/once-upon-a-gene/id1485249347
https://www.stitcher.com/podcast/once-upon-a-gene
https://overcast.fm/itunes1485249347/once-upon-a-gene
CONNECT WITH EFFIE PARKS
https://twitter.com/OnceUponAGene
https://www.instagram.com/onceuponagene.podcast/?hl=en