{"id":5351,"date":"2026-06-09T13:34:36","date_gmt":"2026-06-09T13:34:36","guid":{"rendered":"https:\/\/hypochondroplasia.biomarin.com\/en-us\/?page_id=5351"},"modified":"2026-07-20T08:19:29","modified_gmt":"2026-07-20T08:19:29","slug":"community-and-resources","status":"publish","type":"page","link":"https:\/\/hypochondroplasia.biomarin.com\/en-us\/community-and-resources\/","title":{"rendered":"Community and Resources"},"content":{"rendered":"
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community and resources\n<\/h1>\n

Discover ways to connect with the community, helpful tips for navigating care, and educational resources.<\/p>\n

Stay connected<\/a><\/p>\n \t\t<\/div>\n\t<\/div>\n\t

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These very practical things of navigating the world can make a huge difference in his life.<\/p>\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t Caregiver to a child with hypochondroplasia <\/cite>\n\t\t\t\t\t\t\t\t\t\t\t\t\t<\/blockquote>\n\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t<\/div>\n\t\t<\/div>\n\t<\/div>\n<\/div>\n\n

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Advocacy Groups<\/h2>\n

Advocacy groups and networks can offer connection, shared experiences, and helpful resources that can help you navigate your child\u2019s care with confidence.<\/p>\n

BioMarin is not responsible for the content and conduct of these organizations.<\/p>\n

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Little People of America\n<\/h3>\n

Little People of America (LPA) has been a source of connection, support, advocacy, and information for people and families living with various kinds of dwarfism. It has been instrumental in elevating and celebrating little people everywhere, and advocating for disability rights and inclusion.<\/p>\n

Visit Site<\/a><\/p>\n <\/div>\n<\/div>\n\n

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The Chandler Project\n<\/h3>\n

The Chandler Project was created to provide a safe space for those affected by achondroplasia and other skeletal dysplasias. It\u2019s a place to connect with families like yours to learn more about current and ongoing research for managing achondroplasia and other skeletal dysplasias.<\/p>\n

Visit Site<\/a><\/p>\n <\/div>\n<\/div>\n\n

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Little Legs Big Heart\n<\/h3>\n

The Little Legs Big Heart Foundation is on a mission to empower and uplift individuals living with skeletal dysplasia and their families, redefining inclusivity and acceptance for the skeletal dysplasia community and encouraging them to resiliently live life beyond height.<\/p>\n

Visit Site<\/a><\/p>\n <\/div>\n<\/div>\n <\/div>\n <\/div>\n<\/div>\n\n

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Insider tip<\/h2>\n

Self care is essential<\/strong><\/p>\n

Research shows that self care helps lower stress, helping you stay healthy and be a better caregiver. When we hear the term “self care,” we often think of spa days or meditation retreats, but at its core, it\u2019s really as simple as taking any action that helps you manage your emotional, physical, and mental health. Start small, treat yourself from time to time, and don\u2019t be afraid to lean on family, friends, healthcare professionals, or support groups when you need help.<\/p>\n <\/div>\n <\/div>\n <\/div>\n<\/div>\n\n

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downloadable resources<\/h2>\n

Find helpful tools and educational materials for a more in-depth perspective of hypochondroplasia.<\/p>\n

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Living with hypochondroplasia\n<\/h3>\n

A qualitative exploration of children\u2019s and caregivers\u2019 experiences, challenges, and unmet needs associated with hypochondroplasia.<\/p>\n

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Hypochondroplasia growth charts\n<\/h3>\n

An important tool to help track, predict, and evaluate growth specifically for children with hypochondroplasia.<\/p>\n

Download Resource<\/a><\/p>\n <\/div>\n<\/div>\n\n

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Hypochondroplasia: A guide for parents\n<\/h3>\n

A collection of insights and experiences of families living with hypochondroplasia.<\/p>\n

Download Resource<\/a><\/p>\n <\/div>\n<\/div>\n <\/div>\n <\/div>\n<\/div>\n\n

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Stay informed on upcoming events\n<\/h2>\n\t\t\t\t\t\t \t\t\t\t\t\t \t\t\t\t\t\t

Sign up to learn about future local gatherings, expert-led presentations, and other events bringing the hypochondroplasia community together.<\/p>\n\t\t\t\t\t\t \t\t\t\t\t <\/div>\n\t\t\t\t\t

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References<\/strong><\/p>\n