Dedicated and passionate disability advocate with a deep commitment to improving services and support for individuals with disabilities. As a parent of a child with cerebral palsy who is also part of the deaf community, I possess a unique understanding of the challenges faced by families navigating complex health and educational systems. Experience includes collaborating with multi-disciplinary teams to enhance access to resources and develop inclusive programs that empower individuals with diverse needs.
Skilled in fostering partnerships between families, educators, and service providers, I advocate for systemic change that promotes equity and inclusion. With a strong background in community engagement, I leverage personal insights and lived experiences to inform policies and practices that enhance the quality of life for individuals with disabilities. I am committed to raising awareness, driving innovation, and cultivating supportive environments that celebrate diversity and promote the rights of all individuals within the disability community.
Analyze and review proposed clinical guidelines and practices, offering constructive feedback from the family perspective to enhance quality and effectiveness of care, including reviewing guidelines for inclusive language.
Assisting families in navigating waivered CDCS programs/policies, writing CDCS and Health and Safety plans, and advocating with families to ensure their needs are being met through waivered and non-waivered services.
Perform comprehensive assessments of individuals seeking services, including in-person visits and interviews to gather relevant information about their needs, preferences, and personal circumstances.