Sophia Cacciatore (@secacciatore) 's Twitter Profile
Sophia Cacciatore

@secacciatore

Advocate for rare disease families, asker of many questions, and just happy to be here.

ID: 523547272

calendar_today13-03-2012 18:46:23

1,1K Tweet

375 Followers

871 Following

FamilieSCN2A (@familiescn2a) 's Twitter Profile Photo

During the SCN2A Family & Professional Conference, we will recognize 4 professionals for their extraordinary efforts that align our Core Values. The deadline for nominations is June 21st. For more info & to nominate today: docs.google.com/forms/d/e/1FAI…

Gillian Sapia RN (@gillianhsapia) 's Twitter Profile Photo

“Mommy can I tell you something? I’m scared.” I always tell her it’s ok to be scared. It’s ok to cry. We flew into Atlanta to go to her drug trial clinic, hopefully for the last time if FDA approves govorestat. What we thought we be six months turned into years. It’s way too much

“Mommy can I tell you something? I’m scared.” I always tell her it’s ok to be scared. It’s ok to cry. We flew into Atlanta to go to her drug trial clinic, hopefully for the last time if FDA approves govorestat. What we thought we be six months turned into years. It’s way too much
Courageous Parents Network (@courageouscpn) 's Twitter Profile Photo

Courageous Parents Network had the pleasure of presenting Dr. Zeena Audi-Saba from Hassenfeld Children's Hospital NYU Langone Health with the Margaret S. Lindsay Courageous Provider Award. Congratulations Dr. Audi-Saba and thank you for your leadership in pediatric palliative care.

Courageous Parents Network had the pleasure of presenting Dr. Zeena Audi-Saba from Hassenfeld Children's Hospital <a href="/NYULangone/">NYU Langone Health</a> with the Margaret S. Lindsay Courageous Provider Award. Congratulations Dr. Audi-Saba and thank you for your leadership in pediatric palliative care.
RARE Revolution Magazine (@rarerevolutionm) 's Twitter Profile Photo

June is #CDKL5Awareness month and @cdkl5_ifcr is taking over this channel to shout out about #CDKL5 Deficiency Disorder all day long! Want to learn more about this rare disease? Check out the information available at CDKL5.com.

Gillian Sapia RN (@gillianhsapia) 's Twitter Profile Photo

This mom needs your help. In order for my daughter to get life changing treatment. I need Protect Rare HR 6094. If you have time, please tag your Congress and Senate member in this post. Email them on their website with this one liner “I support Protect Rare HR 6094” or call

This mom needs your help. In order for my daughter to get life changing treatment. I need Protect Rare HR 6094. If you have time, please tag your Congress and Senate member in this post. Email them on their website with this one liner “I support Protect Rare HR 6094” or call
Ana Mingorance (@cnsdrughunter) 's Twitter Profile Photo

This was such a great meeting! 🗽 It was a privilege to attend the INSYNC-AS meeting representing the Loulou Foundation (#CDKL5) and to meet FAST and stxbp1 and RSRT and FamilieSCN2A and so many experts from academia, industry and the regulatory world. Thank

Yssa DeWoody (@yssadewoody) 's Twitter Profile Photo

Headed to UPenn Million Dollar Bike Ride by ODC and Riding for Ring14 USA. Want to know what it’s all about? Watch this short video. This was the first event I did after losing Marie - I was raw. But this was important! Link to donate in the comments. youtu.be/tN-ziuZW22k?si…

CURE Epilepsy (@cureepilepsy) 's Twitter Profile Photo

Did you know there are phases of a seizure? Dr. Kristen Park, Pediatric Neurologist at Children’s Hospital of Colorado, explains the basics of seizures in Epilepsy Explained. Watch the full episode: bit.ly/3YKT8eS #epilepsyexplained #seizure #epilepsy

Dennis Lal (@laldennis) 's Twitter Profile Photo

In the past two months I attended six rare #epilepsy and #neurodevelopmentaldisorder conferences and rearch round tables. Attached what I learned.

In the past two months I attended six rare #epilepsy and #neurodevelopmentaldisorder conferences and rearch round tables. Attached what I learned.
Effie Parks (@onceuponagene) 's Twitter Profile Photo

If you are newly diagnosed or finally coming up for some air, this episode is for you. Please send this episode to a family whose child was recently diagnosed with a #RareDisease effieparks.com/podcast/episod…

Effie Parks (@onceuponagene) 's Twitter Profile Photo

It's an opportunity to connect with fellow advocates & friends, to learn from the top experts and revel in meaningful connections. You'll find friends that will feel like family and leave feeling inspired, empowered and ready to take on the world. There's something for everyone!

It's an opportunity to connect with fellow advocates &amp; friends, to learn from the top experts and revel in meaningful connections. You'll find friends that will feel like family and leave feeling inspired, empowered and ready to take on the world. There's something for everyone!
EpiCARE (@epicare_ern) 's Twitter Profile Photo

📤New call on the Collaborative Genetic webpage! DECADE-Deciphering the CACNA1E developmental and epileptic encephalopathy, from Dpt. of Neurology and Epileptology, University Hospital Tübingen, Germany (Prof. Holger Lerche). epi-care.eu/collaborative-… Do not miss it!

Rare Epilepsy Network (@rareepilepsy) 's Twitter Profile Photo

Thanks to our friends at TSC for sharing this opportunity open across the epilepsies. REN members check this out and share with prospects.