A Lifetime of Advocacy: What Individuals and Families Living with Turner Syndrome Need to Know

Authored by: Valerie A. Powers Smith, Esq

Soft cover book, 38 pages

This is a useful resource has been authored to provide families with children and individuals living with Turner Syndrome and other special need with a lifetime guide on how and when to advocate for services over one’s lifetime. Many individuals feel uneducated about disability and health insurance systems. As a result many are uninformed about obtaining benefits for themselves or their family member and appealing adverse determinations regarding the same.  This booklet authored by Valerie A. Powers Smith, Esquire with Slovak Baron & Empey LLP, serves as a Legal Advisor to Turner Syndrome Foundation.

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