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. https://t.co/ZK1TjK2Svf
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: https://t.co/Du4wJU9Ar2
#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 https://t.co/eJw7qDNgBw.
#rareasone#quote#raredisease
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: https://t.co/V58cxzreVL
#webinar#dna#genomics#QandA
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.
https://t.co/AZfddGic2w
#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
https://t.co/0B8iOfYrig
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.
https://t.co/0lZzn12HeK
Help contribute to Epilepsy #Research by joining a community on #DNAid today!
We're building communities around genetically inherited rare disease conditions to empower patients, caregivers and families. Learn more: https://t.co/OBbsKAgTpW
#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.
https://t.co/IjzAcSwoNp
#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: https://t.co/VcwrdLKKqm
#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: https://t.co/tRRmQONkh4
#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: https://t.co/wwu1eQE3i5
#DNA#Research#RareDisease#MedicalResearch