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Your Gift of Hope

NUHS Fund - Your Gift of Hope

Learn more about how our beneficiaries benefit from your support to NUHS Fund.

 
“I'm very thankful to the donors for their generous support, which has enabled Lisa to continue receiving the necessary milk formula and feeding bags.” 

Born with multiple congenital anomalies and health conditions, Lisa* requires long-term support for fortified milk formulas and continuous PEG tube feeding to ensure sufficient nutrient intake.

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Watch how our donors and partners have touched the lives of our patients and supported NUHS’ mission of improving health outcomes through clinical care, education and research.

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First diagnosed with Congenital Heart Disease during her pregnancy 17 years ago, Mdm Ina requires long-term medical treatment to prevent further complications.

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Mdm Yanti suffers from neuropathic back pain and required support in undergoing the Spinal Cord Stimulation Treatment.

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Watch how our donors and partners have touched the lives of our patients and staff.

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The light-up of the Christmas tree signifies the kick-off of the Giving season, with the lights symbolising joy and hope. View the highlights of this year’s light-up session!

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Catch the full performance of classic Christmas carols performed by Voices of NUHS.

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Diagnosed with Duchenne’s Muscular Dystrophy and Chronic Respiratory Failure, Wee Yang requires appropriate nutritional intake and ongoing medical treatment and consumables to manage his chronic condition.

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Alex* suffers from Alport’s Syndrome (a rare genetic disorder) and required financial support for dialysis at a centre nearer home when he needed more frequent dialysis sessions due to disease progression.
*Name has been changed.

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NUHS Fund honours our donors and partners who have touched the lives of our patients and staff!

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Mastuatina suffered from symptomatic critical aortic stenosis condition and required a transcatheter aortic valve replacement implant surgery to treat this life-threatening condition.

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Alexis was born extremely premature at 26 weeks with Chronic Lung Disease of Prematurity and Pulmonary Hypertension, and required critical breathing equipment to support her underdeveloped lungs.

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Watch how our donors and partners made a difference to our patients and staff through the trying period during the pandemic.

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Syifaa was one year old when she was diagnosed with nemaline myopathy and gastroesophageal reflux in 2015. She experiences multiple comorbidities such as muscle weakness and feeling problems. 

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Born with extreme prematurity in 2014, Thinesh was diagnosed with dyskinetic cerebal palsy with failure to thrive. His condition causes multiple comorbidities such as chronic lung disease and developmental delay. 

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Diagnosed with triple negative breast cancer in 2014, Cathy faced financial difficulties and could not afford her treatment. With the support from the NUHS Fund, Cathy was relieved of her financial burden and could focus on receiving treatment. 

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“My hopes for my son are that he stays healthy and that he will be able to achieve whatever he wants in the future,” says Mdm Zubaidah, mother to Zaakir, a beneficiary of the CapitaLand-NUH Children’s Nutrition Fund.

Watch how two families have benefitted from the support of the CapitaLand-NUH Children’s Nutrition Fund.

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