The ABL+ Foundation is dedicated to improving the lives of families living with rare disorders known as:
- Abetalipoproteinemia
- Familial Hypobetalipoproteinemia
- Chylomicron Retention Disease
Our Vision
The ABL+ Foundation works to:
- Promote education and research within the medical community
- Provide info on current treatment protocols
- Educate patients and caregivers on how these illnesses impact patients
- Advocate for our patient communities with governmental agencies, insurance providers, and the public at large
- Provide a safe space for patients and their caregivers to share knowledge about treatment, research opportunities, and nutrition