61 year old Mdm Ruhaya is lovingly referred to as ‘sayang’ by the nurses here at KDF. With a characteristic twinkle in her eye and a warm chatty personality, one would not guess that she is a kidney failure patient. Mdm Ruhaya stays positive despite…
All parties play a part in enabling a child with special needs - the system, parents, the public, as well as the child himself. When one is willing to give the child an opportunity and to accept the child, he is making a difference in the child’s…
Janet Wong (52) from Singapore has had to deal with Selective Mutism in her son from an early age, but she wishes she could have detected the symptoms earlier to make her son feel more at ease. The child in this case needs to be loved and cared for…
A touching account of how a local hairdresser volunteered to help, when others refused, to give my mother, who lived with Young Onset Alzheimer's, a glam haircut and made her look uber cool in her final years.
They say it takes a village…
Shubhrata Prakash, an officer with the Indian Revenue Service currently on sabbatical in Bangkok, went through a very long episode of depression. At the end, she was inspired to write a book The D Word: A Survivor’s Guide to Depression that not only…
Smitha Sadasivan, who is diagnosed with Multiple Sclerosis and uses a wheelchair, recounts her challenges with accessibility, toilets and medicines at airports and railway stations while travelling.
I was diagnosed with Multiple Sclerosis in 1999. I…
Deepthi Nair, who was diagnosed with Myasthenia Gravis (MG), a rare, neuromuscular autoimmune condition that leads to varying degrees of muscle weakness, finds the ‘invisible symptoms’ of the disease causes misunderstanding among people and pain and…
Joan's wish is straightforward: "My ultimate wish for Nat is for her to happy and independent, where she doesn’t need financial aid from me or my husband, is able to stand on her own and isn’t a liability to anyone else." Joan, in conversation with…
Gargi Ahluwalia is immensely grateful to the Support Group of Parkinson's Disease and Movement Disorder Society, (PDMDS), that helped her claim her independence over the debilitating disease.
I started trembling from January 2013 when my husband was…
