I had grown up seeing my parents’ critical illnesses. Dad had cerebral attacks twice, two years in a row, while I was in school, and later, during my CA Inter exams, he met with an accident. My mom had multiple health issues—her uterus was removed when I was in college, and she faced critical pre- and post-menopausal issues. She was seriously ill to the extent that she was on a ventilator for a couple of weeks before I got my job. Later, she was diagnosed with COPD and was admitted again due to another acute exacerbation of COPD.
Childhood, for me, was learning survival before learning life.
I worked with a multinational as a Chartered accountant that was highly demanding. I belonged to a generation that believed in hard work, respecting seniors, and staying silent even when something felt incorrect. On the few occasions when I did try to take a stand for myself, I saw the true nature of management.
In November 2015, almost seven years before her departure, my mother was diagnosed with COPD and became critically ill. One hospital even advised us to take her home, saying there were no chances of survival. However, we were not ready to give up on her and decided to try another hospital.
Hope became our only treatment when medicine gave up.
Thankfully, after more than a month of treatment, she was discharged. At that time, the doctor mentioned that her survival chances were minimal—perhaps a couple of years at most.
Due to her condition, my mother had to use a BiPAP machine—a mask covering the nose and mouth, connected to an oxygen supply, often referred to as a portable ventilator. When she was discharged, she had to use it 24 hours a day.
During the same period, my father also fell critically ill and was on bed rest. Both my support systems, my elder sisters, could not be around due to medical emergencies in their in-laws’ families. It was also my promotion year, and I was the family’s breadwinner. I arranged the BiPAP machine and oxygen machine, though I had no clue about these machines in the first place.
Every night felt like a nightmare. She developed rashes around her nose and head because of the mask, but she had no choice. Thankfully, with proper care and precautions, after six months the doctor advised that she could limit its use to nighttime only, which was the biggest achievement of my life, and my promotion at work felt meaningless. It was her willpower to get better for me that made this possible.
Even in her suffering, she chose me every day.
I remember that whenever she removed the BiPAP, it felt as if she had been freed from a cage. A few years later, I was once advised to use a nebulizer for a cough for just a few minutes. It only covered the nose, yet it felt as if death would be better than that feeling. She, however, had to use it for 24 hours, and later years, many times during the day as well. There were moments when I had to insist on her putting it on, but each time it would break and shatter me from within.
Her love was not expressed in words, but in how she managed pain silently while ensuring I was never affected by it.
One blood test was done every 2–3 months in which the needle was injected in arteries to assess her blood oxygen and co2 level and it caused intense pain for months and led to crazy blood clots. I often wondered how she mentally prepared herself for that test every single time. Why did she carry so much willpower just for me? Yet, throughout her life, she remained grateful, believing that I was responsible for giving her another life. I did not want to marry someone who would not support me in taking care of my parents after marriage or expect me to live only in the vicinity of my in-laws’ home. I was only a reflection of her love and sacrifice, not my own doing.
Her struggle was invisible, but it defined my entire existence.
My mother never gave up, perhaps especially since I was still unmarried. She continued leading a difficult life with artificial breathing for seven years, worrying about me and wanting to see me settled. To her, I was still a little child.
For her, my life was not separate from hers—it was her reason to endure.
She developed ulcers on her tongue, and even the taste of salt caused a burning sensation in her mouth, affecting her ability to taste. Yet she still cared so much about every minute detail for me. I remember how her hands would tremble due to multiple health issues, including a vitamin deficiency. Yet, with those same trembling hands, she would cut a plate full of fruits for me every day—tasting each piece first, because she knew I wouldn’t eat it if it was sour. She wanted me to stay healthy. She even cooked meals for me out of affection despite her sickness.
She was more alert to my smallest discomfort than her own severe pain.
Irrespective of our situation, she gave me the life of a princess. She was my shelter and support system at all times; even when I didn’t speak, she heard me. When I saw no hope, she assured me that better days were ahead, and they would unfold gradually, though her health kept deteriorating.
Even in her weakest physical state, she was my strongest emotional support.
I feared losing her, and I remember that in the middle of the night, I would wake up to check on her, to see if she was still breathing. I can’t even count how many nights I slept, soaked in tears, filled with the pain of seeing my mother suffer.
Her love was silent, but it filled every corner of my life more than words ever could. I never had to hear her love—I lived inside it every day.

