DTDS Foundation
Raising awareness for Dopamine Transporter Deficiency Syndrome.
DTDS Foundation Website
DTDS Foundation Website
Discover comprehensive information on Dopamine Transporter Deficiency Syndrome, including symptoms, resources, and how the DTDS Foundation supports families through research connections and specialized care guidance.
Latest Blog Post - DTDS Foundation
Latest Blog Post - DTDS Foundation
Discover latest news, resources, and updates on DTDS. Support research and connect with families impacted by Dopamine Transporter Deficiency Syndrome.
Get DTDS Foundation gear on Bonfire
Get DTDS Foundation gear on Bonfire
We support patients and families diagnosed with Dopamine Transporter Deficiency Syndrome to raise awareness and fund a cure!
Social Media
DTDS Foundation Facebook Page
DTDS Foundation Facebook Page
DTDS Foundation Instagram
DTDS Foundation Instagram
DTDS Foundation Pinterest
DTDS Foundation Pinterest
For Patients / Caregivers
PROMS NTD
PROMS NTD
DTDS Family Registry: Contact information
DTDS Family Registry: Contact information
Are you a parent or caregiver of a DTDS patient? Help us collect some very basic demographic and contact information. This data will not be shared with anyone and will give us a more effective way to communicate with the DTDS community about research updates, new treatments, and ways you can get involved in the DTDS cure. By filling out this form you will be added to the DTDS organization and be assured of receiving important updates.
DTDS + RARE-X Data Collection Program
DTDS + RARE-X Data Collection Program
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