
In Nepali, Mamata means affection, and if any word could sum up the character of this particular girl, affectionate would be the one to do it. From the moment I touched her arm in greeting to the moment - four weeks later - I plied her fingers from my wrist to leave the clinic for the last time, she never left my side.
“Some children here…maybe we can help.” confided S., a short-haired and newly retired Dutch woman who was to be my replacement. She nods towards Mamata, who was pulling at the grubby collar of my shirt and running her fingernails across my collar-bone whilst rocking on her feet. ”I give this one a look, and it’s in the eyes, you see it? Nothing there. Some children…we cannot help them, and it is a waste of energy to try.”
Epilepsy, autism, mutism, a plethora of health and developmental disorders; it was no surprise that Mamata was given up on years before her thirteenth birthday. Several weeks in, I spent an entire morning scouring the office for information on her, and came up with nothing but a photograph stuck to an brown Manilla envelope. Case file empty, progress chart blank, Next of Kin absent. In short, the perfect example of a girl so lost in the system she herself was non-existant.
The children were the ones who had not given up on her, and perhaps this was due to everyone giving up on them too. Every single child living in the centre adored her. They fought over her like the latest toy and when it came to the end of the day two of the older Down’s syndrome girls from the English class would run into Room C and flock around her like Mother Hen’s; smoothing her coarse, dark hair and pulling her up onto shaking legs with sing-song, clucking tones. To them, she was a doll to be fussed over. It didn’t matter that she never made a sound or responded to their chatter, both parties got something out of the bond regardless.
It was the smile that did it, I think. Wide, toothy, and a little bit dreamy, Mamata had the kind of perpetual smile which would melt the hearts of her peers in a moment. It never left her face, save for the handful of times her epilepsy caused her to withdraw.
Four weeks in, and while physically exhausted by her little body relentlessly draped upon my own as I went about my days, I found that Mamata’s smile was enough for me, too. In some ways, I understood the Dutch woman. She had of course earned her cynicism, a life-time spent working with difficult or impossible patients, and giving up before she began was the only thing left to do. I, on the other hand, felt I deserved my optimism, subsequently spending much of my time singing and clucking to this mysterious, hopeless case, all the while reminding myself not to expect too much of her.
The day before I left, we walked together slowly around and around the little garden. I sung and she rocked, her feet dragging out behind us as though in another place and time entirely. The sun glimmered through the dust of the city, and as her grin grew wider I wondered what it might be like inside her world.
Mamata clutched at my arm, and I clutched at my thoughts, and we walked.