Welcome to the Utah Chapter

The Utah chapter of the FSHD Society is a local group of people, families, and advocates working together to support those living with facioscapulohumeral muscular dystrophy (FSHD). Whether you join us in person or virtually, our chapter offers a place to connect with others who understand what you’re going through.

我们为您提供支持、共享当地资源，并让您了解最新的研究和护理信息。无论您是刚被诊断出患有前列腺增生症，还是已经与前列腺增生症共同生活了多年，我们都将为您提供支持，帮助您走好人生的每一步。.

加入当地分会 了解我们如何在您的前列腺增生症之旅中为您提供支持。.

认识我们的团队

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  Allison Calder

  Allison is proud to be part of the strong FSHD community in Utah. FSHD became a part of her life in 2013 when her husband, Curtis, was diagnosed at age 29. As a nurse, she immediately started learning about the disease and how it would affect their family. The FSHD Society has been an invaluable resource, and being part of this community has supported her family in many ways.

  Allison and Curtis live in Salt Lake City with their four children, where they founded Anson Calder shortly after Curtis’s diagnosis. The business creates high-quality leather goods and helps fund the mission of the FSHD Society, making a positive impact on the community.

  Contact Allison directly or visit the Utah Facebook page.