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/precisi… #DNA #Research #RareDisease #MedicalResearch

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/multipl… #MS #MultipleSclerosis

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

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/sick… #SickleCell #RareDisease

We're building communities around genetically inherited rare disease conditions to empower patients, caregivers and families. Learn more: dnaid.co/advocacy #DNA #RareDisease #MedicalResearch

Through community we can empower patients, caregivers and families. 💪#RareDisease #DNAResearch

The DNA ID crowdfunding campaign is now live on MicroVentures! app.microventures.com/crowdfunding/d… Join us in helping researchers and patients combat some of the rarest diseases we face! #dna #dnaresearch #raredisease #crowdfunding #crowdfundingcampaign #investment

What a powerful story on living with #Epilepsy and the power of #community to keep pushing forward in life. Thank you for sharing, Christina & My Epilepsy Story. myepilepsystory.org/real-life-epil… Help contribute to Epilepsy #Research by joining a community on #DNAid today!

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-…

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

This Thursday, DNA ID will be hosting a webinar Q&A to discuss their genomics research marketplace and answer your questions. Reserve your spot today: register.gotowebinar.com/register/46577… #webinar #dna #genomics #QandA

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

Happy Thanksgiving from all of us here at DNA ID! #Thanksgiving #HappyThanksgiving

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-t… #Lupus #DNAResearch #DNAid #LivingWithLupus

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

Living with a rare disease doesn't mean you have to live without hope. #CareAboutRare #RareDisease #DNA #DNAResearch

Merry Christmas from all of us here at DNA ID! #MerryChristmas #HappyHolidays

The #coronavirus pandemic is impacting critical #research in #rarediseases fortune.com/2020/04/28/cor…

Trials And Tribulations: Turning #ClinicalTrials Virtual During #COVID-19 news.crunchbase.com/news/trials-an… via Crunchbase News

Very exciting to see this level of participation in #DNA sharing for the #allofus research allofus.nih.gov/news-events/an…