Arginase 1 Deficiency Foundation

Welcome to the patient advocacy website for support and information regarding Arginase 1 Deficiency (ARG1-D). We are glad you found us. Our community is made up of parents, family members, friends and caregivers who have also faced this diagnosis and understand the range of emotions and questions you may have. We are here to provide information on ARG1-D, resources to guide you on this journey and perhaps most importantly, we are here to let you know that you are not alone. We hope you find this website a valuable resource as you learn more about ARG1-D, and that you reach out to us should you have additional questions or needs.
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