You’re not alone. 💙

At Love Never Sinks, we know how important it is to have someone to reach out to — whether you’re a family member, caregiver, or researcher or anyone touched by Lesch-Nyhan Disease.

Please don’t hesitate to contact us with your questions, ideas, or ways you’d like to get involved. We’re here to connect, support, and help however we can.

A young boy with short brown hair and freckles sitting in a motorized wheelchair outdoors on a trail surrounded by grass and fallen leaves, smiling and making a gesture with his right hand while wearing an orange long-sleeve shirt and dark pants.

Our Mission is to support families affected by Lesch-Nyhan disease by addressing their unique needs. Through raising awareness and contributing to research initiatives, we strive to provide assistance and comfort to loved ones living with this disease

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You’re not alone. 💙

At Love Never Sinks, we know how important it is to have someone to reach out to — whether you’re a family member, caregiver, or researcher or anyone touched by Lesch-Nyhan Disease.

Please don’t hesitate to contact us with your questions, ideas, or ways you’d like to get involved. We’re here to connect, support, and help however we can.