Showing results for "Das Syndrom" in People with Disabilities

When fourth grader Alex Schwartz first met his cello, his eyes lit up with wonder, and a smile appeared on his face as bright as the potential his new cello teacher saw within him. The cello positively impacted all aspects of his development, including focus, fine motor, and gross motor skills.

Lauren Windas is one of the estimated 250,000 people suffering with CFS in the UK. Whilst at university in 2012, she fell ill with a viral infection and was later diagnosed with CFS. Since then she has devoted herself to reclaiming her health and being able to live a full life, drawing on the knowledge of experts to help manage her often mysterious and hard-to-manage condition. In Chronic Fatigue Syndrome, Lauren recounts the highs and lows of her own health journey and experiences,.

Weeks after giving birth, Holly Frances went from being a healthy 26-year-old new mom to paralyzed and on life support—in less than 72 hours. Diagnosed with a rare autoimmune disorder called Guillain-Barre Syndrome, Holly was trapped in her body, unable to move, speak, or hold her newborn daughter. Life Support tells the story of how Holly struggled to overcome the despair, hopelessness and physical pain, to regain her health and get back to being a mother to her daughter.

Sarah’s story is one for any parent; it is not just about the highs and lows of having a child with additional needs, but also simply as a mum of three. She talks candidly about coming to terms with the decision to move Oscar to a SEN (Special Educational Needs) school, another big milestone in Oscar’s young life. Whilst Sarah may have found herself on a different path to the one she’d imagined for herself, it has not been a bad one. There is sadness, certainly; and there have been struggles along the way; but there has been so much laughter and happiness, too.

In the fall of 1961, a young girl eagerly anticipates the arrival of her baby brother, Ricky. But when he's born, the joy she expected is overshadowed by the unexpected tension that fills their home. Her mother, once lively and full of warmth, becomes distant, struggling to care for two children-especially a newborn with special needs. Raising Ricky is the poignant story of a family transformed, as a sister steps into a role far beyond her years to protect and care for her brother.

How do you find your strength when the odds are stacked against you? In Short but Fierce, Triona Keane shares her deeply personal and inspiring journey of living with Turner Syndrome—a rare genetic condition that shaped her life but never defined her. This isn’t just a story about medical challenges or fertility struggles; it’s a heartfelt exploration of self-acceptance, resilience, and discovering your true purpose. With unflinching honesty and warm humour, Triona reflects on: The loneliness of growing up feeling different. The incredible obstacles she faced on her path to adulthood.

Life with Louie is a collection of coming-of-age stories about growing up with a brother who happens to have been born with Down syndrome. For the author, Mia Rotella-White, having a sibling with a disability never created hardship. The opposite is true. Growing up with Louie meant Mia’s days were full of disco balls, group hugs, fashion shows and dance parties. When adversity struck, and it did, the siblings reminded each other how ridiculous it was to think any tragedy could ever be bigger than their love.

This memoir was written to honor my youngest brother’s influence over my life—the good, the bad, and the ugly, of living with a Down Syndrome sibling. It tells the story of the children of my family, despite our parents’ frailties, remaining committed to each other through life’s many changes and separations. Who I am today is directly related to who I needed to become.