
let's recode relationships
patient resources
The following is a representation of organizations that offer resources and information for patients, families, and caregivers living with cerebral adrenoleukodystrophy, transfusion-dependent beta-thalassemia, and sickle cell disease.
Bone marrow transplant resources
National Bone Marrow Donor Program’s Be the Match
World Marrow Donor Association (WMDA)
Genetic & rare disease resources
ARM Foundation for Cell & Gene MedicineEURORDIS – Rare Diseases Europe
EveryLife Foundation
Genetic Alliance
Global Genes
National Organization for Rare Diseases (NORD)
The newborn screening for adrenoleukodystrophy advocacy tool kit is an empowering and educational resource created by bluebird bio in collaboration with patient advocacy organizations and advocacy leaders to raise awareness of adrenoleukodystrophy (ALD) and the life-saving opportunity newborn screening (NBS) can provide.

ALD/CALD resources
bluebird bio worked with ALD families to develop this informational site, which includes support and resources for building a care team and connecting with the ALD community. This website is for residents of the United States only.

Aidan Jack Seeger Foundation
ALD Connect
ALD Life
Associazione Italiana Adrenoleucodistrofia Onculus
Ethan Zakes Foundation
European Leukodystrophy Association
Fight ALD
Leukodystrophy Australia
Leukodystropy Family Forum
Leukodystrophy Research and Resource Organization
Stop ALD Foundation
United Leukodystropy Foundation
World Leukodystrophy Alliance
Thalassemia resources
bluebird bio sponsors this informational site for people living with Transfusion-Dependent Beta (β)-Thalassemia (TDT) - including resources for setting goals and talking to your doctor about your medical care. This website is for residents of the United States only.

Sickle cell disease resources
Association Drepagreffe
National Heart, Lung, and Blood Institute
Sickle Cell Society
Sickle Cell Warriors
SOS Globi
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