Those smiles and better-than-normal state for my dad did not last long. I had gone to bed at around 12:30am. By 2:30, my dad’s ailment had taken a firm grip and gotten the upper hand. I woke up suddenly to loud yelling. Glanced at my Fitbit to check the time and rushed to my dad’s room.

Dad was in bed – clearly awake – and was yelling as hard as he could. The assistant lady was helplessly sitting beside him. And my mom was deep asleep next to my dad. My dad was trying to wake up mom with the one arm that is still functioning. But mom is so overcome by exhaustion – and as I have mentioned before, she is a patient herself – her body just could not take any more in spite of all that chaos that was happening a foot away from her.

I went by my dad’s side and started to calm him down. He was slurring all the time. Completely incoherent in his speech, there was absolutely no way to communicate with him – let alone apply reason or logic. You could sense that he was feeling very helpless and wanted my mom to be with him. As part of his brain damage – he calls my mom “mom” now!!! He does not remember her name. He just calls her “mom”. I will write about a defining moment in my life about my dad and his mom (my grandma) later.

I tried a lot of things – getting him to sit up, getting him to lie down, giving him water, just talking to him in soft voices…. He kept on going thru a phase of what seemed like a few moments of logical thinking (“Go to your bed! It is too late now!!”) followed by a few minutes of complete insanity (“Call mom! She has borrowed money!! I need to drink milk!! – and those were the words I could actually comprehend). In about 20 minutes he tired himself out and then went off to bed.

I went to mine to start writing my blog. He woke up in another 10 minutes and we went thru this cycle three times till he finally slept off at around 4am. My mom never woke up at all thru all this.

Sat in the balcony and made a few birthday calls to US. Checked the emails and realized one of my patients in hospice had “transitioned” this morning. When I went to check on him on Monday before leaving for India, I had met his son-in-law there – it was pretty evident he was not going to make it for too long.

Shut down my computer, overwhelmed with my thoughts of my dad, my hospice friend who is longer no more and my mom.

When I go to hospice, it is a volunteering thing. If I want not to deal with a situation or am frustrated by a patient, I can always walk out. Or go to another patient. I have a choice.

The caregivers in the hospice – they have less of a choice – but at some level this is their profession. They are trained for this and to some extent, they have chosen this as their calling. But still, my heart goes out to them watching them keeping their sanity amidst some of the gut-wrenching scenes. (How do you really deal with a situation when the patient helplessly looks at you and asks – “Can you speed this up?”. Yes, I have seen that happen with one of my patients)

The assistants we have here at our house – my heart goes out even more. They are not professionally trained at all. These are middle aged women who are doing this because they need a livelihood. I have found, so far, all of them extremely compassionate and incredibly patient. What they do not have in training, they make up in sincerity.

And then there is my mom. She is having to carry the biggest burden of the care giving. She has refused to sleep anywhere but next to my dad in spite of knowing that she is going to not get much rest. Dad is yelling always for her – without any rhyme or reason. She has not complained yet of her situation even once or has asked any of her kids for any more help than we are giving now.

Here is the tough reality – she was offered no choice. Life dealt her not the brain stroke itself but the biggest collateral damage it can cause.

Being a primary caregiver is much tougher than I will ever realize.

By the way, when I went back to dad’s room, mom was changing his diaper. To give them some privacy, I stepped out and came out to the balcony to enjoy the dawn break – something my dad and I often enjoyed together.

Went back a few minutes later and saw that the kitchen lights were on. Stepping in, I saw what was going on… My mom, instead of going back to sleep, was in the kitchen making tea for me!!!

Like I said, being a primary caregiver, is very very tough.
Being a mom? Much tougher, I suspect.

Being both? Beyond my level of comprehension…

Dad was sitting in his bed. The nephews were done with their firecrackers. I was wondering what to do. That is when I got a bright idea (and I take a lot of liberty when I call my ideas “bright”) to see if I can handle myself if I were a patient. The idea was to pretend that I could not move my legs and had to get myself everywhere in dad’s wheelchair only using my hands.

The initial moves within the room was easy. Dad had an incredulous look on his face but he was okay with me trying out different things. (just like in my childhood). Then the obstacles started coming. To get to the balcony, I had to negotiated an inch and a half high separation ridge (which also makes the door way watertight when you close the door). I was just not being able to push myself thru it.

It became a cerebral problem for me. What the weak forearms could not solve, I had to solve by using my wits. As I was thinking about the problem, I flashed back to our eighth grade physics teacher (we called him “Lambda”) explaining to us why pulling is easier than pushing.

And that is really how I stumbled onto the solution. I had to back into the ridge and then with a fraction of the energy was able to pull myself up. Over time I also realized that if I could do this one wheel at a time (needed a wide doorway for that), I could make the problem even easier.

Imagine the scene – totally delighted with myself, I was spinning around from room to room (I was not screaming “Wheeee” though). Then the nephews and niece showed up. That is when it got really interesting. Fortunately, they did not want to try it themselves. I was not in a mood to share my new toy, anyways. But they took a bet with me.

The bet was that I had to get out of home, get inside the elevator, go downstairs, open the complex gate and go out in to the street. No putting my foot down. Only the wheelchair and my hands.

The biggest challenge was squeezing myself into the elevator. The wheelchair barely fit in – the door was so narrow. And then I had to back myself in – because there was a difference in the level of the elevator floor and the building floor.

Long story short – as you can see from the pictures taken by my eldest nephew, the lunatic did escape the asylum. What is more, once on the streets, he put on as high speed roll. Worse, he went “Wheeeee”!!!

You see my sister looking at dad and laughing her heart out? Well, this has not happened in the last month ever since dad had the medical incident.

To understand what is going on – and remove any doubts that my dad was feeing much better after the walk – first note my mom. I will write about her a little later. But you will notice that she is absolutely exhausted taking care of dad and having to deal with all the visitors (not to forget, she has been a psychiatric patient herself for six years and she is supposed to be sedated most of the day) – and had fallen asleep in her chair as the rest of us were talking.

Let’s go back to why my sister was laughing so much.

My dad – having noticed mom doze off – was imitating how she had slept off in her chair. This, from the guy, who can’t think rationally or speak coherently for more than a few seconds!!!

Jet lag had gotten the better of me. Plus I had had no sleep last night because of my flight times. Thus, I had inevitably gone off to sleep after lunch having spent some more time with my dad and the nephews.

When I woke up, daylight had started fading. Walked over to dad’s room and saw that he was surrounded by the domestic helps and my mom. I asked him if he would like to go out. He promptly shook his head signaling he had no interest.

Well, a good guess would have been that I would have left matters there. But, we are talking about me here. A few minutes later, I had put him in his wheelchair and in about another minute, I was out pushing him in the streets. Behind me were my brother and my nephews.

First, he kept on admiring the lights. If I had not mentioned before, it was Diwali day. Every house was decorated with colorful lights. Dad just kept saying how beautiful those lights were. What he did not realize was that there was a particular place I was taking him to.

Before long, we had reached the spot where he used to get together with a few other old people when he was stronger and had the ability to walk. I placed him in that off-the-street-corner location and we all stood around him and started chatting.

And then a funny thing happened. An innocuous looking old man who was peacefully shuffling along suddenly looked at my dad and with clear surprise in his voice, yelled – “Roy-babu?” Once he realized that it was my dad, he sat down there too.

And then came along another old gentleman. Slowly there was a small get together of the old folks that started forming there. At one point (you will see my nephew holding a phone to my dad’s ear, one of those elderly person called up another of their old friends and had him talk to my dad!

At that point, my brother mentioned something. It is then that I realized that my father was saying multiple words together. So far, he had been mostly grunting one or at best two words and then everything else would be a slur.

As I tried to follow what they were talking about. I realized that I was still not following dad’s words much!! Actually, I was not following very well the other gentlemen’s words either. Turns out all of them had had brain strokes or heart strokes before (even multiple). All of them have difficulty in speech. But among them, they were chatting along – seemingly effortlessly!

In all this confusion, my sister and niece showed up with some tasty fritters from a street side vendor. We all had some nice snacks standing there and chatting idly.

Eventually, we all left and I took my dad to a few more streets to see the bright lights before going back home.

That was quite a surprise sprung on everybody. In fact, most had not noticed me even when I walked in straight to the inside room where my dad was. The two assistants were on the bed holding him up and my mom was feeding him. She had her back towards me – she had no idea I was there. And the two assistants had no clue who I was either. I stood there for a couple of minutes or so when my mom looked back and got the shock of her life!!!

My dad’s condition is pretty much what you would expect from somebody who has had a brain stroke. He was able to recognize me but telling my name was quite an effort. For the next hour or so, I realized that he had lost his ability to lay down or get up by himself (his right side is paralyzed) and quite some of his faculties around memory and speech are gone.

But most painful is his realization that he has lost complete independence. His deep sense of helplessness – even simple things like he inability to express himself – is visibly driving him to tremendous frustration and anger.

I finally remembered something that I had learnt while visiting my friend – Samaresh’s dad. He was totally quiet till I had shown him a picture of his granddaughter in Atlanta in my phone.

As an aside, every December, I make one of those large twelve month Apple calendars – with pictures of Natasha, Nikita, Sharmila, Jay Jay (the dog) and myself (especially of our vacations) from that year and send them to my parents. And my dad, dutifully, puts them on the wall and often asks me about those pictures.

This morning, I brought down all those calendars and then started showing him one picture after another and asked them to recognize the people. Each picture was an effort. Many times he gave up (his choices were restricted to only five names). He missed me most of the time!! Recognized Sharmila, Natasha in all and then after an initial struggle with Nikita’s pictures, started consistently recognizing them.

Took us almost an hour to go thru one calendar!!!

And that was how the first couple of hours with him went…