Dr. Stephen Kingsmore: "Our mission is to bring fresh hope to families who feel forgotten. That's why we come to work everyday. Our vision is for your experience to be the experience of mums, dads, and babies all around the world." #GenomicFrontiers21
"As a result of rapid whole genome sequencing, we got our answers and our baby boy was immediately placed on the right treatment plan." We're grateful to our patient families for sharing their experiences with #rWGS. #GenomicFrontiers21
Another family's experience with rapid whole genome sequencing: "If we were given the correct diagnosis earlier, it would have saved a ton of money for our insurance company and a lot of emotional trauma." #GenomicFrontiers21#rWGS
"Rapid whole genome sequencing helped us in so many ways, and we know it can help many more families." Thank you to our patient families for advocating for access to #rWGS. #GenomicFrontiers21
Baby Nathan was born with a rare genetic disease. We hope that many more CA kids like Nathan will benefit from the miracle of #rWGS, thanks to AB 114: The Rare Disease Sequencing for Critically Ill Infants Act. https://t.co/pRt90ae0c9 #ProjectBabyBear@BMaienschein@radychildrens
.@ClinicalOMICs shares the story of Baby Nathan & #ProjectBabyBear, our pilot program using rWGS® to diagnose critically ill babies with rare genetic disease. He received a diagnosis in 3 days, leading to a specialized care plan. #genomics#GenomicMedicine https://t.co/xWnZ0rpC2x
Baby Nathan’s story is one of hope. His dad says “#ProjectBabyBear is a wonderful opportunity for families like ours to seek the answers and help they deserve.” https://t.co/pRt90ae0c9
#GenomicMedicine#genomics
#ProjectBabyBear families said genome sequencing helped them by explaining why their baby was sick, or ruled out a genetic cause. This empowered them to confidently make informed decisions about their baby’s care. https://t.co/KijC4XheOM
#rWGS#GenomicMedicine@RadyChildrens
Haven’t been keeping up with Twitter, just not used to it, but to everyone who follows me here i want to let you guys know that Nathan is 3 weeks seizure free. 🙏🏼❤️
I’m a mother seeking the help of social media I need help spreading awareness about my baby’s disease. #HelpBabyNathan#CutisLaxaType3All all we ask for is a simple share nothing more 💕🙏🏼 I’m simply giving my son a voice.
"Tested positive for Covid-19" is not a joke, i know today is april fools day but that just not it chief, There's so many ways to prank your friends and loved ones, ill post a link below of ideas :)
https://t.co/3sHfW5tZgi
GOOD MORNING EVERYONE. Just wanted to remind everyone that Nathan's Awareness shirt will be released today During our LIVE STREAM tonight at 6pm PST Join Us For A HUGE Surprise.
We will be live on Facebook, Instagram and YouTube.
After months of planning, along with the help and donations from everyone, we are happy to announce Baby Nathans Awareness Shirt, a shirt made with so much love and sacrifice. It's purpose is to RAISE AWARENESS for… https://t.co/zeAum6HVKu
We introduced you to Nathan when he was 3 months old. His parents were searching for a diagnosis and treatment for their baby. A month later, they finally got that diagnosis – Cutis Laxa Type 3. The treatment for this condition still has not been found.
https://t.co/evtBEmasdB
We introduced you to Nathan when he was 3 months old. His parents were searching for a diagnosis and treatment for their baby. A month later, they finally got that diagnosis – Cutis Laxa Type 3. The treatment for this condition still has not been found.
https://t.co/evtBEmasdB
#ProjectBabyBear’s successful first year is nearly in the books. Hear how it’s helped more than 100 CA babies at #GrandRounds on 10/23. Drs. Jeanne Carroll & Ami Doshi will talk about a case at @radychildrens. #GenomicMedicine https://t.co/Sqmq3LGSLb