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Therapy and School Support for Children with Chromosome 22 Duplication
For families raising a child with Chromosome 22 Duplication Syndrome, therapy and school supports play a vital role in helping them learn, grow, and connect with others. Children with this rare genetic condition may face challenges in speech, motor skills, learning, and social development, but with the right team in place, they can reach meaningful…
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Therapy Planning for Progressive Symptoms in H-ABC Syndrome
H-ABC Syndrome (Hypomyelination with Atrophy of the Basal Ganglia and Cerebellum) is a rare neurological condition where symptoms such as motor difficulties, coordination loss, and muscle tone changes progress over time. While the disorder is complex, thoughtful therapy planning can support your child’s comfort, abilities, and joy at every stage. Therapy for H-ABC isn’t about…
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Real-Life Success Stories in Speech Therapy for Verbal Dyspraxia
For families of children with Verbal Dyspraxia, speech therapy can feel like a long road filled with trial and error, small victories, and big milestones. Every child’s progress looks different, but hearing how other families have navigated their journey can bring hope and inspiration. Speech therapy success is possible—with patience, creativity, and the right support.…
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Gentle Physical Therapy at Home for Mitochondrial and Basal Ganglia Conditions
Children with Mitochondrial Disorders and Basal Ganglia Conditions often have limited energy and muscle endurance. While movement is important for strength and function, too much effort can lead to exhaustion. That’s why gentle, consistent physical therapy at home makes such a difference—it helps build skills while respecting your child’s energy limits. The key is keeping…
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How Therapy and Medical Care Work Together for Dystonia
Dystonia treatment often involves a combination of medical care and therapy. Medication may help reduce muscle spasms, but therapy helps children build strength, flexibility, and functional skills for daily life. Working together, these approaches support both symptom relief and long-term progress. The Role of Therapy and Medical Care Together Children with dystonia often need a…
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Joubert Syndrome Type 6: Managing Complex Needs with Therapy and Care Team Support
Joubert Syndrome is a rare genetic disorder that affects the brainstem and cerebellum, leading to coordination, breathing, and developmental challenges. Type 6, in particular, may involve more significant medical concerns such as hypotonia (low muscle tone), respiratory instability, vision and kidney involvement, and feeding and motor delays. Families facing a diagnosis of Joubert Syndrome Type…
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Oral Motor Challenges in Children: Evaluation Signs and Mealtime Strategies
Children use more than just their hands to explore and engage with the world—they use their mouths, too. But when muscle coordination in the lips, tongue, cheeks, and jaw is delayed or disrupted, it can affect feeding, speech, and overall sensory regulation. These challenges are often referred to as oral motor difficulties, and they can…
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Chromosome 22 Duplication: Family Life, Therapy, and School Support
Chromosome 22 Duplication Syndrome is a rare genetic condition caused by an extra piece of genetic material on the 22nd chromosome. Because duplications can vary in size and location, symptoms and developmental outcomes differ widely from child to child. Some children may experience delayed milestones, speech and language challenges, learning disabilities, autism-like traits, or hypotonia…
