Shaping the Future of ADLD Together
We are excited to launch the ADLD Natural History Study in collaboration with leading healthcare organizations.
This study aims to advance our understanding of ADLD and shape future treatments. Join the fight against ADLD today.

Our Partners


Why Your Participation
Matters?

Help Advance ADLD Research
Your participation helps researchers gain insights into how ADLD develops and progresses over time.

Shape Future Treatments
The insights collected will be instrumental in designing future clinical trials for ADLD treatment.

Enhance Patient Care
A deeper understanding of ADLD can lead to improved standards of care for all patients.

Join the ADLD Community
By participating in this study, you become an integral part of a supportive network of patients, families and researchers united in the fight against ADLD.

How to Participate?
Please reach out to us through either of the methods below:

info@adld.center

Call
507-293-2427
What is a Natural
History Study?
A Natural History Study (NHS) is a research approach that observes and documents the progression of a disease over time without therapeutic intervention. For rare conditions like ADLD, these studies are invaluable in capturing the full spectrum of the disease, from onset to long-term impacts.


Why is This Study Important?
For ADLD, a rare condition with limited research, a well-executed Natural History Study is not just beneficial—it’s transformative. It lays the groundwork for future clinical trials, helps in developing targeted therapies, and provides a comprehensive understanding of the disease that can improve diagnosis and patient care.
Frequently Asked Questions
Any individual who has been diagnosed with Autosomal Dominant Leukodystrophy (ADLD) through a genetic test is eligible to participate in this study.
- Completing surveys and questionnaires about your experience with ADLD
- Sharing your medical records and health information
- You will be monitored on a regular basis to build out a disease progression map.
- You will be able to see a publication at the end of the retrospective study.
- Improve understanding of ADLD progression and symptoms
- Help prepare for future clinical trials
- Support research to address unmet needs in the ADLD community
- Accelerate the development of potential treatments for ADLD
