#RareOnTheHill and #SRFboard in DC were epic. It’s going to be a great, year, get some #RareBrewCoffee! #S10e135

SynGAP10 weekly 10 minute updates on SYNGAP1

Mar 5 2024 • 19 mins

DC was epic, come next year!

- Board Meeting and Leadership Team.

- Rare on the Hill - Nancy, John, Vicky, Kathryn, Marta, Suzanne, Jess Johnson!

https://www.facebook.com/suzanne.v.jones/posts/pfbid02pMjKxryjDej62FM2RRA6afyU5JPkdB37dXzVrXMLFzjsWmRTQV2wtR3BNaaFcTK4l

- Last week of Feb, don’t miss it.

#RareBrewCoffee has launched!

https://rarebrewcoffee.com/ use code SRF10

Reflecting on the latest Rick Huganir paper

- This was in part supported (as acknowledged) by our first grant, 5 years ago we funded 10x that last year.

- We are not a Rasopathy! https://x.com/cureSYNGAP1/status/1763644994685153654?s=20

- We need to have Prof. Huganir do a webinar!

#DEI #SyngapWhileBlack Nice work Petersen family

https://qcitymetro.com/2024/02/23/syngap-1-syndrome-autism-epilepsy-treatment/

State Coordinators and Advocates Sign up

- We’re looking for state representatives and state advocates - fill out this form if you’re interested - https://docs.google.com/forms/d/e/1FAIpQLSfPWiyvAPuKif-h2bbMBqUKVLMeOeK-ISehbM9PvnReXMRjZg/viewform

- Syngap1 Stories Episode 27 - guest host Jessica Johnson with guest Jackie Kancir - released 3/2. Syngap.Fund/Stories

We still do warriors, 198 is from Poland!

- https://x.com/cureSYNGAP1/status/1763006900939956252?s=20

- https://curesyngap1.org/syngap-warriors/igor/ - Are you are warrior yet? https://curesyngap1.org/syngap-warriors/

Repurposing - Thought for the week

- When you try a new molecule, any new molecule, take notes, videos and pictures.  - IF a drug increases cognition, expect frustration, at first. - Make sure you watch episode 134, even if it’s long because I really go deep on repurposing. https://youtu.be/luhVxDEXlcU?si=BUmyKmTkOvFMVN5Z

Notes, all on Youtube, make sure you subscribe there - 935 today let’s get to 1,000

https://www.youtube.com/@CureSYNGAP1

List of repurposed drugs:

Siblings - Order a kit, thank you UCB @UCBUSA

https://curesyngap1.org/sibling-support/

Ed’s notes:

- Aaron Harding guest on DeafBlind Potter Podcast - "Navigating Life's Challenges: A Journey with SynGAP - An Interview with Aaron Harding" - https://youtu.be/cagNgqmolgk?si=s9vAX1_jl07e4kOY

- Jansen Jones, daughter of BOD chair Suzanne, was one of two rare disease children featured in a Rare Disease Day article by Children’s Healthcare of Atlanta - https://drive.google.com/file/d/18lPSXcciyK3OHnSWDXxy1DDVZZvPc-sY/view

- Newsletter issue 37 (2/25) includes these and more - https://curesyngap1.org/newsletter/

Scholarship

- UCB USA Family Epilepsy Scholarship

- Blog - https://Syngap.Fund/UCB24

- Diagnosed with Epilepsy or immediate family member or caregiver

- Seeking higher education

- Application deadline March 15 https://drive.google.com/file/d/1PtAJfqOUkeXhX2NsyxvkB9A-pEHei5pc/view

Fundraising

- Get Ready for Sprint - save the date 4/27/24 - sign up your teams now; Rifton is giving away another adaptive tricycle to a team who raises $500+ - Syngap.Fund/Sprint24 https://www.rifton.com/ (12 teams signed up as of 3/2 - we had 28 teams in 2023; already have $26,000+ in donations!!! Still a ways to go before we beat last year’s record.)

- MDBR 6/8 - link to 2023 blog https://curesyngap1.org/blog/mdbr-2023-everything-we-want-to-c-happening-for-syngap1-camaraderie-community-collaboration/

- S.Carolina3rd annual Scramble 10/5 - link to past events is here: https://curesyngap1.org/events/fundraisers/scramble-for-syngap-2023/

- 3rd SYNGAP1 Conference, hosted by SRF in LA

- Pre-register to receive updated info when it’s ready https://Syngap.Fund/24Pre

- Planning committee needs volunteers; if interested in helping, contact stacey@curesyngap1.org #SyngapConf

Podcasts, give all of these a five star review!

SRF Channel - https://podcasts.apple.com/us/channel/syngap1-podcasts-by-srf/id6464522917 Episode 135 of #Syngap10 - March 3, 2024

#epilepsy #autism #intellectualdisability #id #anxiety #raredisease #epilepsyawareness #autismawareness #rarediseaseresearch #SynGAPResearchFund #CareAboutRare #PatientAdvocacy #GCchat #Neurology #GeneChat #F78A1 #CureSYNGAP1