Reposting from @cnbc.com
Reposting from @cnbc.com
#CNBCCures
#CNBCCures
Really wanted to hear from Gunnar. Hopefully @cnbc.com can get the video posted at some point.
Really wanted to hear from Gunnar. Hopefully @cnbc.com can get the video posted at some point.
“We’re not going to make any money on this.”
“We try not to put commercial input in what we’re developing until the very, very end.”
Damn, this hurts and really cements what those living with a #RareDisease fear the most, even if there is a treatment.
#CNBCCures
“We’re not going to make any money on this.”
“We try not to put commercial input in what we’re developing until the very, very end.”
Damn, this hurts and really cements what those living with a #RareDisease fear the most, even if there is a treatment.
#CNBCCures
#CNBCCures
#CNBCCures
#CNBCCures
#CNBCCures
#CNBCCures
#CNBCCures
#CNBCCures
#CNBCCures
We need to fix the healthcare system. Relying on AI as a fix for inadequate staffing isn’t the answer.
#CNBCCures
We need to fix the healthcare system. Relying on AI as a fix for inadequate staffing isn’t the answer.
#CNBCCures
Please, more medical professionals like these and way less political types if there is another #CNBCCures in the future.
Please, more medical professionals like these and way less political types if there is another #CNBCCures in the future.
Very true for #RareDisease. Many don’t bother with testing when there are no treatments or cures. Even with more known diseases like Alzheimer’s, very few get biomarker testing.
#CNBCCures
Very true for #RareDisease. Many don’t bother with testing when there are no treatments or cures. Even with more known diseases like Alzheimer’s, very few get biomarker testing.
#CNBCCures
Registration is free for anyone that wants to follow along.
Moderated by Becky Quick, whose daughter was diagnosed with a rare genetic brain disorder
#RareDiseaseDay is tomorrow
Registration is free for anyone that wants to follow along.