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📝Full show notes: https://syngap.fund/n143
BIO WAS GREAT
Multiple grants and agreements approved, wait for press releases. Thank you Aaron & Sarah, Lauren!
- Great work to MDBR - Almost $45k, that will be added to $30k! https://charity.pledgeit.org/t/jY577u7uMc Awesome Peter, Heather, Aaron, Justin Albrect & Kali Worth. Also Dr Jillian McKee!
- Blane & Ashley Dallen in Canada raised almost $15k via a tournament.
NHS UPDATE
Colorado should start seeing patients in August! Don’t cancel CHOP appointments, some people have no choice.
CHATS WITH INDUSTRY
Prevalence:
They are easily missed. The math is clear. Lots of data. 1% of ID = 35k+
1/100k at 3.6m in 2023 = 36 a year, minimum with PTV.
5/100k = 180. A YEAR.
Caren is 65.
36 x 65 = 2,340 PTVs vs 400 SRF knows about)
https://curesyngap1.org/blog/why-are-we-so-sure-that-syngap1-related-intellectual-disability-is-under-diagnosed/
CALENDAR MANAGEMENT
Rare Across America is 28 days away, register now:
https://everylifefoundation.org/rare-advocates/rare-across-america/
Conference is 170 days away & Registration is live!
https://curesyngap1.org/events/conferences/syngap1-conference-2024/
https://secure.givelively.org/event/syngap-research-fund-incorporated/syngap1-conference-2024-hosted-by-syngap-research-fund-srf
CB Blood Donation accelerates Science!
STXBP1 conference (Philadelphia, PA, July 19-21, 2024)
Myhre Syndrome conference (Philadelphia, PA, July 27-28, 2024)
HNRNPH2 conference (Seattle, WA, July 29-30, 2024)
PWS/USP7 conference (Atlanta, GA, September 26-27, 2024)
COMBINEDBrain conference (Kansas City, MO, September 29th, 2024)
SYNGAP1, SLC6A1, Cure GABA-A Variants conference (Los Angeles, CA, December 4-5, 2024)
SHOUTOUTS
- Zoe https://curesyngap1.org/blog/parents-take-action-after-syngap1-related-disorder-diagnosis/
- We need a Pavel award.
NEWLY DIAGNOSED?
New families have resources here! https://syngap.fund/Resources
- 1,030 YouTube. https://www.youtube.com/@CureSYNGAP1
- 10,421 Twitter https://twitter.com/cureSYNGAP1
- 3,652 LinkedIn. https://www.linkedin.com/company/curesyngap1/
Podcasts, give all of these a five star review!
SRF Channel - https://podcasts.apple.com/us/channel/syngap1-podcasts-by-srf/id6464522917
#epilepsy #autism #intellectualdisability #id #anxiety #raredisease #epilepsyawareness #autismawareness #rarediseaseresearch #SynGAPResearchFund #CareAboutRare #PatientAdvocacy #GCchat #Neurology #GeneChat #F78A1 #CureSYNGAP1
5
8383 ratings
📝Full show notes: https://syngap.fund/n143
BIO WAS GREAT
Multiple grants and agreements approved, wait for press releases. Thank you Aaron & Sarah, Lauren!
- Great work to MDBR - Almost $45k, that will be added to $30k! https://charity.pledgeit.org/t/jY577u7uMc Awesome Peter, Heather, Aaron, Justin Albrect & Kali Worth. Also Dr Jillian McKee!
- Blane & Ashley Dallen in Canada raised almost $15k via a tournament.
NHS UPDATE
Colorado should start seeing patients in August! Don’t cancel CHOP appointments, some people have no choice.
CHATS WITH INDUSTRY
Prevalence:
They are easily missed. The math is clear. Lots of data. 1% of ID = 35k+
1/100k at 3.6m in 2023 = 36 a year, minimum with PTV.
5/100k = 180. A YEAR.
Caren is 65.
36 x 65 = 2,340 PTVs vs 400 SRF knows about)
https://curesyngap1.org/blog/why-are-we-so-sure-that-syngap1-related-intellectual-disability-is-under-diagnosed/
CALENDAR MANAGEMENT
Rare Across America is 28 days away, register now:
https://everylifefoundation.org/rare-advocates/rare-across-america/
Conference is 170 days away & Registration is live!
https://curesyngap1.org/events/conferences/syngap1-conference-2024/
https://secure.givelively.org/event/syngap-research-fund-incorporated/syngap1-conference-2024-hosted-by-syngap-research-fund-srf
CB Blood Donation accelerates Science!
STXBP1 conference (Philadelphia, PA, July 19-21, 2024)
Myhre Syndrome conference (Philadelphia, PA, July 27-28, 2024)
HNRNPH2 conference (Seattle, WA, July 29-30, 2024)
PWS/USP7 conference (Atlanta, GA, September 26-27, 2024)
COMBINEDBrain conference (Kansas City, MO, September 29th, 2024)
SYNGAP1, SLC6A1, Cure GABA-A Variants conference (Los Angeles, CA, December 4-5, 2024)
SHOUTOUTS
- Zoe https://curesyngap1.org/blog/parents-take-action-after-syngap1-related-disorder-diagnosis/
- We need a Pavel award.
NEWLY DIAGNOSED?
New families have resources here! https://syngap.fund/Resources
- 1,030 YouTube. https://www.youtube.com/@CureSYNGAP1
- 10,421 Twitter https://twitter.com/cureSYNGAP1
- 3,652 LinkedIn. https://www.linkedin.com/company/curesyngap1/
Podcasts, give all of these a five star review!
SRF Channel - https://podcasts.apple.com/us/channel/syngap1-podcasts-by-srf/id6464522917
#epilepsy #autism #intellectualdisability #id #anxiety #raredisease #epilepsyawareness #autismawareness #rarediseaseresearch #SynGAPResearchFund #CareAboutRare #PatientAdvocacy #GCchat #Neurology #GeneChat #F78A1 #CureSYNGAP1
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