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Rare Disease Day is Monday! And here at SRF we can feel it all happening…
COOL START TO THE DAY
https://twitter.com/cureSYNGAP1/status/1496855893324926977?s=20&t=S7QHkcWewhu0hi-I_XlQBA
Grief in convo with Kali about Rare Disease Diagnosis.
NEWS
We dropped the Zempleni Presser! How cool is this? Cool enough for the Exosome Industry News to write about it https://twitter.com/ExosomeRNA/status/1496907785535049729
Zempleni Webinar: Milk exosomes to increase the expression of SYNGAP1 in SYNGAP1 mice March 3, 2022 @ 9am PT/12pm ET https://syngap.fund/zempleni
More is coming soon. We have a few press releases in the hopper! One just made possible by a $70k donation from Unlock Defi https://www.unlockdefi.com/ thank you so much. Learn more about that via this interview we did in November https://www.youtube.com/watch?v=A840uoG1Wj0
PRESENTATIONS
Jess is presenting on SRF to the UK Community this weekend at Edinburgh, congratulations!
Marta gave a presentation at one of our Pharma partners all-staff for Rare Disease Day. Thank you to her and congratulations. It is powerful to talk about our disease.
The Data Sharing Panel was exceptional, if you missed it, watch the recording here:
https://syngap.fund/data
Get your EEG Tracings! In EDF format. Just ask them at the lab, remember you have a right to your data in all Geographies.
AMAZING ASKS
Profs at Oxford and McGill have reached out with exciting opportunities. Rarebase is getting noisy. I’m told to expect a proposal from WCM and we have one from Finland. We need more funding… start talking to families now. We are asking Leon and Overcome to co-fund with us too.
FUNDRAISING
Suzanne in GA on Sparks of Hope
Julie in NC on Scramble
Nancy in NJ on Gala
YOU where you are on Sprint eg. Tavilla
2nd Annual #Sprint4Syngap is coming April 30, 2022, help us raise funds by starting a team and/or donating!
Sign up now: https://syngap.fund/sprint2022
Get a shirt: https://www.bonfire.com/sprint-for-syngap-2022/
This is a podcast: subscribe to and rate this 10 minute #podcast #SYNGAP10 here https://www.syngapresearchfund.org/syngap10-podcast
Apple podcasts: https://podcasts.apple.com/us/podcast/syngap10-weekly-10-minute-updates-on-syngap1-video/id1560389818
Episode 49 of #Syngap10 - February 25, 2022
#datasharing #biorasi #EEG #ciitizen #SYNGAP1 #Syngap #epilepsy #autism #intellectualdisability #id #anxiety #raredisease #epilepsyawareness #autismawareness #rarediseaseresearch #SynGAPResearchFund #CareAboutRare #PatientAdvocacy #GCchat #Neurology
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Send in a voice message: https://podcasters.spotify.com/pod/show/syngap10/message
View all episodes
By Syngap Research Fund, 501(c)(3)
5
8383 ratings
COOL START TO THE DAY
https://twitter.com/cureSYNGAP1/status/1496855893324926977?s=20&t=S7QHkcWewhu0hi-I_XlQBA
Grief in convo with Kali about Rare Disease Diagnosis.
NEWS
We dropped the Zempleni Presser! How cool is this? Cool enough for the Exosome Industry News to write about it https://twitter.com/ExosomeRNA/status/1496907785535049729
Zempleni Webinar: Milk exosomes to increase the expression of SYNGAP1 in SYNGAP1 mice March 3, 2022 @ 9am PT/12pm ET https://syngap.fund/zempleni
More is coming soon. We have a few press releases in the hopper! One just made possible by a $70k donation from Unlock Defi https://www.unlockdefi.com/ thank you so much. Learn more about that via this interview we did in November https://www.youtube.com/watch?v=A840uoG1Wj0
PRESENTATIONS
Jess is presenting on SRF to the UK Community this weekend at Edinburgh, congratulations!
Marta gave a presentation at one of our Pharma partners all-staff for Rare Disease Day. Thank you to her and congratulations. It is powerful to talk about our disease.
The Data Sharing Panel was exceptional, if you missed it, watch the recording here:
https://syngap.fund/data
Get your EEG Tracings! In EDF format. Just ask them at the lab, remember you have a right to your data in all Geographies.
AMAZING ASKS
Profs at Oxford and McGill have reached out with exciting opportunities. Rarebase is getting noisy. I’m told to expect a proposal from WCM and we have one from Finland. We need more funding… start talking to families now. We are asking Leon and Overcome to co-fund with us too.
FUNDRAISING
Suzanne in GA on Sparks of Hope
Julie in NC on Scramble
Nancy in NJ on Gala
YOU where you are on Sprint eg. Tavilla
2nd Annual #Sprint4Syngap is coming April 30, 2022, help us raise funds by starting a team and/or donating!
Sign up now: https://syngap.fund/sprint2022
Get a shirt: https://www.bonfire.com/sprint-for-syngap-2022/
This is a podcast: subscribe to and rate this 10 minute #podcast #SYNGAP10 here https://www.syngapresearchfund.org/syngap10-podcast
Apple podcasts: https://podcasts.apple.com/us/podcast/syngap10-weekly-10-minute-updates-on-syngap1-video/id1560389818
Episode 49 of #Syngap10 - February 25, 2022
#datasharing #biorasi #EEG #ciitizen #SYNGAP1 #Syngap #epilepsy #autism #intellectualdisability #id #anxiety #raredisease #epilepsyawareness #autismawareness #rarediseaseresearch #SynGAPResearchFund #CareAboutRare #PatientAdvocacy #GCchat #Neurology
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Send in a voice message: https://podcasters.spotify.com/pod/show/syngap10/message
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