DNA ID is a rare disease patient registry platform to connect researchers with the people and data 🔬they need to accelerate cures
New York, NY
Joined March 2018
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Very exciting to see this level of participation in #DNA sharing for the #allofus research allofus.nih.gov/news-events/…
Trials And Tribulations: Turning #ClinicalTrials Virtual During #COVID-19 news.crunchbase.com/news/tri… via @crunchbasenews
The #coronavirus pandemic is impacting critical #research in #rarediseases fortune.com/2020/04/28/coron…
Living with a rare disease doesn't mean you have to live without hope. #CareAboutRare #RareDisease #DNA #DNAResearch
We're coming down to your LAST chance to invest in our #crowdfunding campaign!
Help us connect researchers, patients, & advocacy groups to accelerate medical #research treatments by creating a #data platform that puts control back in the patients hands. bit.ly/33O9mo0
Lupus has a wide range of symptoms and can impact each individual differently. Here's a look at how even explaining lupus can be a challenge: lupus.org/blog/sharing-the-j…
#Lupus #DNAResearch #DNAid #LivingWithLupus
Not everyone will understand your journey, but finding a community that shares your experience can help you make sense of yours.
Find you community on dnaid.com.
#rareasone #quote #raredisease
No matter your struggle, it's so much easier to get through it with others. Join a community on DNAid today to utilize your data to help others just like you.
dnaid.co
#RareDisease #DNA #DNAResearch #Community
Download our Mobile App on the Apple Store today and start contributing your data to medical research communities. Alone we are rare, together we are strong. #DNA #RareDisease #MedicalResearch
apps.apple.com/bn/app/dna-id…
What a powerful story on living with #Epilepsy and the power of #community to keep pushing forward in life. Thank you for sharing, Christina & @myepilepsystory.
myepilepsystory.org/real-lif…
Help contribute to Epilepsy #Research by joining a community on #DNAid today!
The DNA ID crowdfunding campaign is now live on MicroVentures! app.microventures.com/crowdf…
Join us in helping researchers and patients combat some of the rarest diseases we face!
#dna #dnaresearch #raredisease #crowdfunding #crowdfundingcampaign #investment
Through community we can empower patients, caregivers and families. 💪#RareDisease #DNAResearch
We're building communities around genetically inherited rare disease conditions to empower patients, caregivers and families. Learn more: dnaid.co/advocacy
#DNA #RareDisease #MedicalResearch
Sickle Cell Anemia is often a misunderstood disease. This blog interview done by @pickereurope shines a light on the real world struggles that come with disease.
picker.org/news/blog/sicklec…
#SickleCell #RareDisease
1. Reduce the time for drug development.
2. Connect your de-identified health information to multiple research
projects.
3. See new clinical trials as they come out.
Register Today: dnaid.co/register
#DNA #DNAResearch #RareDisease
Danielle shared her journey with MS with @Healthline. Here at DNAid we're striving to bring patients like Danielle together to accelerate research to find a cure through sharing DNA data.
Read more about Danielle's journey: healthline.com/health/multip…
#MS #MultipleSclerosis
Really excited about partnering with Yourdna to connect rare disease patients to genetic researchers in a safe, secure, and more efficient way and provide educational resources in the process!
Read more: clinicalomics.com/topics/pre…
#DNA #Research #RareDisease #MedicalResearch
