Meet gorgeous Ariella Italiano, the smiley little girl who is one of only 100 people in the world — and the only person in Australia — who has the gene mutation TBC1D24. 🔒 bit.ly/2Pv8Ysr #wanews #perthnews

1st Tweet has to be about the $100k grant! See link for information on how to apply! static1.squarespace.com/static/5fbd2cd… UPenn Million Dollar Bike Ride by ODC Penn Medicine #Neurology #RareDisease #tbc1d24mutation

Since it's the 1st day of Fall & we're planning some new things... seemed appropriate 🍂

Notice from our other SM platforms - we're back and making some upgrades! #tbc1d24 #rarediseases

Join us at 7pm (your local time) tomorrow! #NeverBeStill #tbc1d24 #RareDisease

#tbc1d24

Tweet us your purple pumpkins and help spread awareness! #epilepsyawareness #purplepumpkinproject #tbc1d24

nytimes.com/2022/10/19/hea… This is disheartening and will only change with raising awareness and understanding. We can do better. #disabilityinclusion #tbc1d24 #RareDisease

Calling all US based persons living with rare epilepsy. Gathering inputs about multidisciplinary care clinics. Please share your POV by 10/28. Patients: forms.gle/ZF7j9i5fQwbvzz…

FDA is hosting a #patient-focused drug development listening meeting on November 15 & seeking perspectives about the following #GeneTherapy topics: •Risks and benefits •Clinical trials •Patient experience data •And more Learn more here: bit.ly/3REqGEo

I’m riding with tbc1d24foundation this year! Please consider supporting if you can 💜 charity.pledgeit.org/f/CThJBWOE8R

Read REN's Mar newsletter and share it with a colleague! rareepilepsynetwork.org/so/72ORCkn4G?l…

charity.pledgeit.org/t/qE4x2LRWK4?f…. Need more cyclists/need more donations 💜🤞🏼 But we’re getting there ! 88 days left ! 🚴‍♀️🚴‍♀️🚴‍♀️

#WednesdayWhy Support our ride here: charity.pledgeit.org/t/qE4x2LRWK4

Autism Awareness Day !

Check out her blog post here- epilepsygenetics.net/2023/05/05/tbc…