<div><strong>Standing Strong with Nihaal Singh, Aged 9, as He Battles Duchenne Muscular Dystrophy </strong>
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<div>Hello, we are Hetal and Ranveer, proud parents of an incredible 9-year-old boy, Nihaal Singh, who was diagnosed with Duchenne Muscular Dystrophy (DMD) in 2019.
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<div>DMD is a rare, progressive muscle-wasting condition that gradually takes away muscle strength, making everyday tasks more difficult over time. Since Nihaal's diagnosis, life has changed in ways we could never have imagined, filled with hospital visits, medical equipment, therapy sessions, emotional and physical challenges, and countless hours spent researching to better our understanding of the condition.
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<div>Each day brings hurdles that most families never have to think about, from assisting Nihaal throughout the day as mobility becomes harder, to managing complex care routines, adapting our home, and navigating a condition that continues to progress
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<div>We watch our brave boy face difficulties that no child should ever have to endure. On the outside, he is full of laughter, curiosity, and big dreams, but behind the scenes, every day is a careful balance of adapting, adjusting, and holding on to hope.
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<div>As time goes on, he will need a powered wheelchair, home adaptations (such as a stair lift or accessible bathroom), specialist medical equipment, and ongoing therapy, much of which is not fully funded by the NHS or local services.
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<div>Our most urgent need right now is to fund an electric power add-on for his manual wheelchair, something the NHS does not provide. This add-on will allow him to ride alongside his siblings when they’re out on their bikes, giving him the chance to enjoy those moments of freedom, inclusion, and independence that every child deserves.
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<div>This GoFundMe has been created to help cover:
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<div>• The electric power add-on for his wheelchair
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<div>• Mobility equipment and daily living aids
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<div>• Home adaptations to ensure accessibility and safety
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<div>• Physiotherapy and occupational therapy
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<div>• Travel costs for specialist appointments
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<div>• Quality-of-life support and care
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<div>No parent is ever prepared to hear that their child has a life-limiting condition. But we are doing everything we can to give our son the happiest, most fulfilling life possible.
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<div>Whether you can donate, share this page, or simply send a kind word, thank you. Your support means the world to us. We believe in hope. We believe in love. And we believe that with your help, we can keep fighting for Nihaal’s future.
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<div>With heartfelt thanks,
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<div>[Hetal, Ranveer &amp; Family]
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Anonymous

Jaspreet Sidhu

Standing Strong with Nihaal Singh - Battling Duchenne DMD

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