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DiGeorge Syndrome: How to Advocate Effectively in Medical Appointments
Navigating the medical world with a child diagnosed with DiGeorge syndrome (22q11.2 deletion syndrome) can feel overwhelming. Multiple specialists, complex terminology, and evolving treatment plans make clear communication essential. As a parent or caregiver, you are your child’s most powerful advocate. Here’s how to confidently speak up, ask the right questions, and ensure your child’s…
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Williams Syndrome: Parenting with Joy and Sensory Awareness
Williams Syndrome is a rare genetic condition caused by the deletion of genetic material from chromosome 7. Children with Williams Syndrome often have a distinctive profile: exceptional verbal and social strengths, deep emotional sensitivity, and a love of music, alongside challenges like heart conditions, mild to moderate intellectual disability, motor delays, and sensory sensitivities. For…
