Our expert team of clinical researchers is proud to support #RareDiseaseDay.
#RDP, #AHC and #CAPOS are rare disorders we study. If you have an #ATP1A3-related disorder, we stand with you. See why our work may help increase knowledge about these disorders: https://t.co/YiROzYbCEd
🇺🇸 Honoring our veterans isn't just a tradition—it's a responsibility. Their courage, sacrifice & service laid the foundation for the freedoms we enjoy every day. Today & every day, our team—a team that studies #ATP1A3-related disorders—remembers & respects veterans. #VeteransDay
Will your name be kept confidential if you participate in our #ClinicalStudy on #ATP1A3-related disorders? Yes. Your anonymity will be protected within the limits of the law. No medical information will be released to outsiders without permission.
More: https://t.co/TUaKmxlKpl
It’s #SocialMediaDay — the perfect time to spread awareness online about #ATP1A3-related disorders.
Learn about #RapidOnsetDystoniaParkinsonism, #CAPOS & #AHC now: https://t.co/qcR0jgA7AT
Social media has changed how we interact. Will you share our posts to spread knowledge?
On #FathersDay, let’s take time to send extra messages of support to dads dealing w/ #ATP1A3-related disorders, which cause debilitating symptoms.
Are you a father w/ a known/suspected ATP1A3 gene variant? See if you can participate in our #ClinicalStudy: https://t.co/TUaKmxlKpl
Today we honor & mourn military personnel who died while serving the U.S. To all of our #ClinicalStudy participants & anyone dealing w/ a #RareMovementDisorder, especially those who lost a beloved service member: We hope you have a peaceful #MemorialDay.
#RDP#CAPOS#AHC#ATP1A3
Does your family member have a known/suspected #ATP1A3 gene variant? You can help family members find out if they’re eligible to participate in #ClinicalResearch that has the potential to expand knowledge about #RareMovementDisorders: https://t.co/TUaKmxlKpl
#FamilyWellnessMonth
On #MothersDay, let’s take time to send extra messages of support to moms dealing w/ #ATP1A3-related disorders, which cause debilitating symptoms.
Are you a mother w/ a known/suspected ATP1A3 gene variant? See if you can participate in our #ClinicalStudy: https://t.co/TUaKmxlKpl