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NCD Chronicles #24: Living With A Disease With No Known Cause

NCD Chronicles #24: Living With A Disease With No Known Cause

Shawn Sharif, Living with IIH | Dr Nazima Shadaht Ali, Consultant Ophthalmologist | Professor Datin Dr Norlinah Ibrahim Mohamed, Consultant Neurologist

Spinal Muscular Atrophy: From Carrier Screening To Life After Diagnosis

Spinal Muscular Atrophy: From Carrier Screening To Life After Diagnosis

Dr Sangita Dharshini Terumalay, Consultant Paediatric Neurologist | Yap Sook Yee, Parent and SMA Advocate

NCD Chronicles #20: “I Would Bleed Even While Sitting Down” (Living With Haemophilia)

NCD Chronicles #20: “I Would Bleed Even While Sitting Down” (Living With Haemophilia)

Hariee Prabakaran, Living with Haemophilia | Premalatha Narayanan, Hariee’s mother | Dr Zulaiha Muda, Consultant Paediatric Haematologist-Oncologist

Because Feelings Matter #31: Diary of a Work-From-Home Dad

Because Feelings Matter #31: Diary of a Work-From-Home Dad

Mohammad Yazid Kamal Baharin, Comic Artist and Father

Doctor in the House: Disability Days - Are We Getting Anywhere in Advancing Disability Rights?

Doctor in the House: Disability Days - Are We Getting Anywhere in Advancing Disability Rights?

Dr George Lee, Consultant Urologist | Dato' Dr Amar-Singh HSS, Consultant Paediatrician

Because Feelings Matter #27: “Tak Ada Peluang Langsung Untuk Bernafas”

Because Feelings Matter #27: “Tak Ada Peluang Langsung Untuk Bernafas”

Dr Nurul Izzaty Hassan, Mother and Lecturer

Because Feelings Matter #25: World Children’s Day Special (Part 1)

Because Feelings Matter #25: World Children’s Day Special (Part 1)

Branden Lim, 13

NCD Chronicles #11: Finding Hope in Motor Neuron Disease

NCD Chronicles #11: Finding Hope in Motor Neuron Disease

Albert Koo, Living with Motor Neuron Disease | Dr Loh Ee Chin, Consultant Palliative Care Physician

Doctor in the House: A New Treatment for Neurofibromatosis in Malaysia

Doctor in the House: A New Treatment for Neurofibromatosis in Malaysia

Professor Dr Thong Meow Keong, Consultant Paediatrician & Clinical Geneticist | Carol Lim, Living with Neurofibromatosis

Rare Disease Day 2023: The Story of Baby Athif with Spinal Muscular Atrophy

Rare Disease Day 2023: The Story of Baby Athif with Spinal Muscular Atrophy

Nur Azizah Zamri | Mohd Farhan bin Mohd Sait

Budget 2023: We Need To Invest in Rare Diseases

Budget 2023: We Need To Invest in Rare Diseases

Nadiah Hanim Abdul Latif, President, Malaysian Rare Diseases Society (MRDS) | Professor Dr Thong Meow Keong, Consultant Paediatrician & Clinical Geneticist, University Malaya Medical Centre

Doctor in the House: Can Patients With Mucopolysaccharidosis Get Treatment?

Doctor in the House: Can Patients With Mucopolysaccharidosis Get Treatment?

Dr George Lee, Consultant Urologist | Prof Dr Thong Meow Keong, Consultant Paediatrician & Clinical Geneticist | Rubee Ahmad, Parent

Brain Waves: Identifying Rare Disease Genes

Brain Waves: Identifying Rare Disease Genes

Dr Azlina Ahmad Annuar, Neurogeneticist

Rare Disease Day 2022: Young People Living With A Rare Disease (Part 2)

Rare Disease Day 2022: Young People Living With A Rare Disease (Part 2)

Jaden Lim, Living with Growth Hormone Deficiency and Pituitary Microadenoma

Budget 2022: Did We Get A Budget that Puts Health First?

Budget 2022: Did We Get A Budget that Puts Health First?

Dr Khor Swee Kheng, Independent Health Policies Specialist

Brain Waves: The Promise of Gene Therapy

Brain Waves: The Promise of Gene Therapy

Dr Azlina Ahmad Annuar, Neurogeneticist | Assoc Prof Dr Cheah Pike See, Department of Human Anatomy

 
 




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