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The exact cause of many of the 7,000+ diagnosed rare diseases is still unknown today. It’s estimated that between 25-30 million Americans live with a #raredisease. Stayed tuned to learn how to join #7KMC and help us rally support for those 30 million Americans. #WeTackleRare

⁦@rarebasepbc⁩ launches FUNCTION 🧠 💊🔬 #drugdiscovery w/15 #raredisease orgs. ADNP kids⁩ is proud to be an anchor ⚓️ partner alongside outstanding groups like FOXG1 Research stxbp1 ⁦⁦SynGAP Research Fund (SRF)⁩ HereditaryNeuropathy & #Hope4Harper prnewswire.com/news-releases/…

I’m excited and humbled to share our next step in helping to find treatments for patients with rare genetic disorders. Thanks to all our collaborating partners and families, and the amazing team at @rarebasepbc for being part of this to make this happen. prnewswire.com/news-releases/…

2021 RARE Champions of Hope Nominee ⁦Global Genes⁩ This has been an epic year but I should have 2 others listed w/me - ⁦@[email protected]⁩ & @mattdavis. Im so grateful & proud to be included. #globalgenes #adnpkids #championofhope #susanlucciofcoha globalgenes.org/2021-rare-cham…

Excited to see #syngap1 as one of the 13 proteins in this study. Along with other friends ADNP kids CTNNB1 Syndrome Awareness Worldwide Effie Parks PTEN Foundation US MED13L_UPDATE CureSHANK Kris Pierce COMBINEDBrain

CDRC 2021 Annual Meeting: Repurposing Ketamine from Club to Clinic youtu.be/nv570EUyXeg via YouTube thank you @[email protected] for suggesting me as a presenter. Can’t wait for the Q&A! Register today!

The most wonderful time of the year, which means #leekleekgiveaway is back! Whether you are a cowboys fan or a fan of myself listen (read) closely. This is how you enter below for a chance to win a signed football, custom cleat (left or right) designed by Sean Vergara

.Lynsey Chediak, MSc. is Rarebase’s Head of Partnerships. In our first episode of Rarebase Remarks, learn about Lynsey's own experience with #raredisease and her hopes for research and treatment. anchor.fm/rarebase/episo…

Thank you ADNP Kids Research Foundation and Simba Global for funding an ambitious $4 million program at the MIND Institute to test #GeneTherapies for #ADNPSyndrome! Sandra Sermone Fink Lab @jill_silverman_ UC Davis Stem Cell health.ucdavis.edu/mind-institute…

We are so excited to start this amazing project that we hope will help our children. Rare Disease research is funded by families - because we are desperately trying to save our children. Read about how we are stepping into gene therapy for ADNP.

LIVE on Gene Fixers w/⁦ ⁦@[email protected]⁩ to discuss drug repurposing, specifically the repurposed drug #ketamine for #ADNP found using Dr. Might’s ⁦NCATS⁩ funded AI tool. . 1st #raredisease to start #fda #RepurposedDrug trial using #AI linkedin.com/posts/sandra-b…

mRNA display makes billions of macrocyclic peptides in one round (🤯) - dramatically impacting drug discovery. ACS Med Chem Lett highlights Merck’s PCSK9 inhibitor which is the first clinical candidate from this technology! pubs.acs.org/doi/10.1021/ac…

New Study Suggests Ketamine May Be An Effective Treatment for Children with ADNP Syndrome First-ever clinical trial for rare disorder that is a leading genetic cause of autism also identifies path for a ketamine clinical development program mountsinai.org/about/newsroom…

What the……….? Amazon is “ending” #AmazonSmile? Small #raredisease grassroots nonprofits like ours ADNP kids need every penny we can get, and our family & friends sign up to help us, no you are shutting it down. #AmazonFrown this sucks!

Thank you KOIN Extra AM for doing a live interview with me today on Rare Disease Day in DC, and for sharing the challenges faced by parents of children with rare brain diseases. koin.com/news/health/mo… #RareDiseaseDay2023 #cureADNP

Check out Seattle Eras Tour Taylor Swift's video, 22 Hat Day 1! #TaylorSwift #ErasTour #TaylorSwiftErasTour tiktok.com/t/ZT8NXU8dC/

The moment 72000 fans cause a 3.2 earthquake! #TaylorSwift #ErasTour tiktok.com/t/ZT8NXJUmH/