Dad. The Jokester. The Savior. The Forgotten One.

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Dad. My Forgotten Carer. For best results, and to watch all the videos - read this on the website.

I've talked a lot over the last few weeks and months, and years as well, about how much I'm thankful for my family; my carers. But though I've talked a lot about what my amazing mother has done; her sleeping by my bedside, being there for me, every day of my life, even before diagnosis (no matter how badly I treat her) and though I've dedicated an article to my amazing brother, who also despite all the jokes, the trolls and sometimes abuse I hurl at him, is always the first at my side when I'm screaming out at night in pain; I haven't really talked about my Dad as much. 

I guess it's hard sometimes for men to express one anothers' appreciation for eachother. I'm fine with it... I love the fat bugger, and though I love hearing his dismissive, embarrassed reaction when I sneak in a little "I love you" over the phone, or as he hands me something, I really do mean it. 

One of my favourite Youtubers showing how awkward it can be at times for many Dads to hear those three little words.

So why haven't I thanked him yet? As he rightly deserves? Well... I guess it's harder to describe his role and make it seem really meaningful. Mum - well, she was a MACHINE, the brain, the torso of this movement. Always keeping us going. Keeping us protected in advance, booking appointments, looking after me most of the time; all the while somehow working and keeping the house in order too. Nirav, my brother, the limbs. Since he could drive, in the middle of his last year in high school, he was given the keys and made to dart around Sydney, moving bags of clothes, delivering boxes of food, taking me to appointments, and, more recently, events where I could have fun (when the parents were unable or unwilling); all at the expense of HIS own desires. 

But where would dad stand? What would he be in this, the body section of my life? 

Well... I've got to say. He's been the heart. 

It's not that he doesn't do the practical stuff. Oh no - he's there when we need him most, taking his fair share, often more, of the shifts when I was in hospital, or when I needed to get to an appointment (and couldn't get myself there). He's there for me when I need him too... catching me, both literally, and figuratively, whenever I fell. I still remember the words he said to me one night, when he cradled me, like a baby in bed again, and I asked, I pleaseded softly, "What's the meaning of this all? Why do we live? Why do we do this?" He didn't know it at the time... But I was in severe, clinical depression, struggling to come to terms with the loss of a friend. And it was those words that got me out of it. 

But I'd say the most important, most impactful role in this journey was his relentless quest to keep me smiling. 

And by god he did that part of his job well.

Always making light of any situation. Dad constructs a shrine, with offerings to boot, for himself as he wins Sunday morning tennis (for once). 

When you feel like you're at complete bottom in life... Humour can be a great way to distract you from your troubles. Or even make them feel trivial. And there were MANY instances where he managed to do that.

I remember almost straight after diagnosis, the day after I think, when I was allowed home for the last time before chemo. One of the things you gotta do before you start any (well most) chemos, as a young man at least, is store sperm for the future. Many chemos can leave you temporarily, or even permanently infertile.  

So there I was, still shocked, still in denial, still afraid of what was to come the day after these  scary doctors told me I had a tiny chance of staying alive; a 17 year old, shy, somewhat repressed kid sitting in the middle of this waiting room with 3 or 4 other dudes, holding a small little cup in my hand with my Dad next to me. 

I still remember the weird, slightly disgusted look the receptionist gave me as she handed me the cup. I can still feel the judging eyes of the others in the room as I looked down, avoiding eye contact. In my mind, I was picturing them shaking their heads, muttering, softly, about the sin I was about to commit. 

To be honest, I didn't know what to expect myself. Was I just supposed to awkwardly excuse myself and somehow find the inspiration, amidst all that, to, to put it bluntly, blow a load in a cup? 

But then Dad leaned over and whispered this joke in my ear. 

"The Queen was inspecting London General H0spital one day, when suddenly she noticed a man in his room, masturbating furiously..."

I shook my head slightly, amused. The Usual. Dirty. Dad joke was incoming...

"In shock, she turned to the doctor and asked, 'What the hell is this? How dare he do this in front of ME!'

But the doctor replied. 'Oh no Your Highness, this man has a condition where he produces too much sperm. He needs to release himself every few hours or his organs may fail!' 

The queen nodded, still shaken, and walked further down the ward, and noticed another man in his room, this time, getting a blowjob from a nurse.

'And what's this then?' the Queen said furiously. 

'Same disease. Better insurance.' " 

A typically crass, typically DAD joke, in a typically awkward situation. 
But that one joke eased that tension, and amazingly... it made me  smile. 

That was the first time I'd done that since diagnosis. 

And then with a pat on the backside and a whisper in my ear, "Time to spill it" he left me walking, still embarrassed, still self-conscious, but still, trying to smother a smile, into that room. 

And since then he, and I, as I've learned (some may say, been corrupted) from his antics, have done SO much more. 

If you thought that joke was dirty... you should see some of the chain emails he sends me. He always happens to have a perfectly suited joke f0r any moment. But some of the more spontaneous moments we've shared have been the most hilarious. The ones that made me forget the pain, the ones that got us AND the doctors and nurses laughing, the ones that picked me up. At least half the "Humour in Hospital series" features him - check em out if you still want a laugh after all this. 

But of all of the funny moments over the years, this would have to be on of our favourite, and one of my brother (Nirav)'s least favourite. I'd say it just narrowly trumps the time Dad and I cracked up in the lifts (once we were safe), after smuggling a 40 inch TV into the hospital without anyone noticing. 
One morning after a doctor's appointment, this was not too long after my second bone marrow transplant in 2013, we got a call from Nirav asking us for Red Rooster, his favourite fast food joint. So we decided to get him some. 

Moral of the story... be careful what you wish for. 

Trollin the bro - What Cancer Patients Do In Their Spare Time #4
So we went out for a hospital appointment and got a text from my bro to get him some Red Rooster.Moral of the story... Be careful what you wish for...We actually picked out red ones for this purpose ahahahaha
Posted by Nikhil Autar on Monday, 9 September 2013

So we went out for a hospital appointment and got a text from my bro to get him some Red Rooster.Moral of the story... Be careful what you wish for...We actually picked out red ones for this purpose ahahahaha
Posted by Nikhil Autar on Monday, 9 September 2013

Poor Nirav was sick at the time, and so keen to get some good food into him, I almost feel bad for doing this looking back. But then I watch it one more time, and see his typical, "I-want-to-be-mad-but-I-can't-believe-they-did-this", smothered smile, and laugh again.

Unfortunately Nirav ends up on the butt end of a lot of our practical jokes...

Trollin the bro - What Cancer Patients Do In Their Spare Time #2
Hey guys - we have a new hammock!!Had...
Posted by Nikhil Autar on Wednesday, 15 May 2013

That was actually an accident. But still, no regrets. For best results - keep your mouse clicking at halfway through that video and replay his face as he gasps over and over again.

Disclaimer... no children were harmed in the making of this production. 

Dad would also keep me busy, and exercising a lot of the time. And part of his job as chief entertainment officer (CEO he calls himself) was to get me out and doing normal stuff. For a long time in my recovery phase, he and I would go watch a movie every Monday night, when the tickets were cheap. He was the one who'd urge me, drag me to start exercising after a chemo of Bone Marrow Tranpslant; starting from me on wobbly feet, only managing to walk laps in the pool, to full blown runs and games of tennis every afternoon. That's nothing when you think about the hours of training he put in with me to prepare me for that amazing 200km ride we did to raise funds for cancer research. 

But the thing I looked forward to most was when he took us out on the boat to fish. 

What Cancer Patients Do In Their Spare Time #1
Deep sea fishing on a chartered boat!The fish is a morwong (aka sweetlip, deep sea bream) - this was after pulling up other fish and 500g sinkers in 50 - 100m of water all day haha. It's tiring stuff but fun nonetheless!
Posted by Nikhil Autar on Wednesday, 23 January 2013

This was me about a few weeks after the second toughest chemo I'd gotten, a mere month after I had seizures and consequent hallucinations that left me in Intensive Care for 2 weeks, a few weeks before I started work-up for my second transplant. Some would say it's a bit rash to be out on a boat, in the middle of the ocean, then. But hell. Dad's training, juicing (well, he did the whole juice thing for a week before deciding it was too much) and motivation got me to a stage where I was ready for it! 

But of course, not all these moments were flashy. He's not well known for sharing, both on the plate and on the boat.

What cancer patients do in their spare time #6
Sand shark that I caught today =] About 1.2m took 20 mins to pull up.
Posted by Nikhil Autar on Saturday, 25 January 2014

The fish was on MY LINE, and I was pulling it up, but dad thought my hook was "snagged"; stuck on the bottom or on the reef. In his very words, he said "Oh, it is a fish!" before deciding to reel it up for himself, taking all the glory, despite me doing all the hard work in hooking, and getting it off the bottom. To this day, we still argue about whose fish it was. 

C'MON THOUGH - IT WAS ON MY LINE!!!

(I'm sure he has a response to this coming...)

But this was one of those more memorable, one of my most favourite moments. I was cramping, a lot one Sunday morning, and just stuck in the shroud of fear, frustration and gloom that pain brings. Then I hear Bon Jovi playing in the computer room, three sets of walls away, my Dad's voice booming horribly off key over the top. After a while, and a few more '80s classics, (with a few Indian classics throwin in between of course), he barges into my room, ushers me and my sleepy brother into the next one and together he and mum serenade us with karaokes and dances of the latest and greatest Indian Pop. After a few minutes of me complaining about being dragged out of bed, that "my poor muscles were too cramp-prone to sing and dance along", I found myself belting out classics and dancing too. After a while, the playlist turned to one of Dad's favourite songs - Mumford and Son's "Little Lion Man,". As his favourite bit, the long banjo solo, came on, I had the genius idea of drawing a Guitar on his Belly. The rest is history folks.  

What cancer patients do in their spare time #5: popstar dad
What cancer patients do in their spare time #5Drew a guitar on Dad's belly... was not disappointed.#superstar #guitarhero #partylikearockstar
Posted by Nikhil Autar on Saturday, 21 December 2013

He's not perfect. He's had his share of gaffs and failed jokes inbetween. And he is NOTORIOUSLY lazy. "If you want something done, don't nag me, tell me once and it'll be done in 3 - 6 months" is his favourite mantra, to mum's constant irritation. But he, almost single handedly, has been the reason I've been able to smile, and thence been able to help others through this blog over the past few years. 

And I can't thank him enough for it.

I'm surprised I'd forgotten to officially, on here, 'til now. 

But over the last few years, the last 6 months in particular, we've started getting frustrated with eachother. I'm now 2 and a half years post second transplant. This graph that one of my transplant doctors showed me... one that showed that where I was at now was where the people surviving was essentially the same... that I was essentially cancer free FOREVER -  took me out from under my feet...

   
But though my chances of relapse are near zero now... I'm still suffering. The nature of the bone marrow transplant procedure, one that's designed to get another person's immune blood cells, and hence, immune system (as white cells are included in that, and as blood stem cells are found in the bone marrow) being produced inside me to kill off any cancerous bone marrow, means that it can, in 30-70% of cases, have long term effects. Though we're matched perfectly in terms of tissue, there are slight differences between my donor and my immune system still, so his white cells are attacking parts of my body; namely my skin, my muscles/nerves (the probably cause of the cramping) and my liver in a process called Chronic Graft versus Host Disease (cGVHD). 

The chronic nature of that disease, as well as the unexpected, yet all too real, surprise diseases that seem to come my way (a second seizing episode, my left eye being blinded, nearly followed by my right and another, completely different cancer appearing in my rib to name the most serious of those) has made it very frustrating for me, but also for everyone at home. 

I'm supposed to be getting better after all this. Getting back to real life and getting back to being me, right? But for the last few years, I've been unable to get back into study, unable to be independent for months on end (causing me, and my family grief); just unable to get into a constant rhythm as disease after disease and setback after setback came up. 

And somewhere in that time, we began to fight. Over HOW I was approaching my diseases and my life. And one key theme that keeps coming up - Why I won't believe in, and take any alternative medications or try any alternative things to treat, or at least ease my symptoms. It's not that I don't, I understand that many of our medicines came from traditional medicines, that these medicines and techniques may have an effect that hasn't been studied, or can't be studied using modern science, and often say that "I"m happy to try it. Just make sure it's safe and unobtrusive." But he tries to convince me, urges me to "believe in the medicines", and that they work. 

Wheat grass juice. One of the alternative medicines I tried while I was relapsing that failed to live up to its "miracle cure" status...

But I mean, I can't do that. I don't feel I need to. The mindset I used to overcome my whole disease in the first place relied on logic. I'd take a step back, take away all the doubts and fears with questions and analyse the options I had and take the one that seemed most promising. When I was diagnosed, that option was "Go forward, thinking and focusing on the present, what I could control, rather than the past." When I relapsed, and was told I had a tiny chance of survival, that I should consider palliative care, that option was "Look for anything and everything that could help in the literature. Analyse HOW they worked, so I could apply it to my case, and present it to my doctors convincingly, so they did do a second transplant", something only possible with a years' medical knowledge under my belt, something that's probably the reason I'm still here. 

I can't do the same with homeopathic drugs, which have never shown, in any trial, ever to have an effect, nor with meditation, herbs, tinctures or other things no-one really understands. He insists that I should look to others who have been helped by those methods - friends and family who have benefited, and copy their methods. But they haven't had the same disease at the same severity I had, most examples had no correlation with me whatsoever, and one guy who he'd gotten his "research" off for a fruit called soursop (which has been warned to cause peripheral neuropathy and 'Parkinson's like' symptoms, both things which are present in me, which could make the ALTERNATIVE MEDICINE the cause of my horrible cramps) doesn't even SEE most of his patients - he does them online... so he'd have no clue what issues I had. 

The other major point of contention is how I do TOO MUCH for others in my volunteering, blogging and charity activities... But first off... I feel I don't push myself too hard for others; I've realised and understood that to help others, first you need to be healthy yourself, second; that it's given me inlets to so many opportunities and meet so many amazing people, and finally; he doesn't understand that the purpose I've set myself, to try and do my all to help others, is THE THING THAT KEEPS ME GOING when the world seems bleak, when the pain is real, and when there seems nothing worth living for...

But it's the way that this has all been going... the time that it's taken for me to get back to "normal", the other, outside stressors that hang in the air that's made our discussions turn into arguments, turned our tones much more bitter and turned our friendship and mutual respect into begrudging acceptance that we have to co-exist, at times. We've both said horrible things to eachother. Things I wouldn't say to anyone... ever... I've said to him. He's screamed and shouted back things just as bad... 

Don't get me wrong, when things go wrong, he's still there for me, still there to help. The rib crisis a few weeks ago reminded me of that fact. 

But I'd stopped respecting him, his opinions and his thoughts over the last few weeks or months. Years, at some points, if I'm honest. He accuses me of being "egotistical", a "know it all" just like "my doctors". 

And to be honest... I have been. The way I treat my parents when they sit in on consultations with me, giving them irritated looks for asking "stupid" questions which are really just honest questions (I know if I was asked to comment on Dad's planning logistics operations, I'd draw a complete blank)... and they way I sneer, and throw death-stares at them when they bring up things infront of the doctor that made me feel foolish and less "doctorly"; alternative medicines or bad health habits I wanted concealed from them, is just obnoxious. The way I act these days when I dismiss Mum (a qualified, high achieving MBA at a high position in a multinational corporation)'s advice when it comes to starting up my own social enterprise to help charities and businesses alike make money; foolish. 

Our prides, something I don't have, or display much outside the family setting, get in the way, and and we end up butting heads over and over again. 

And in the end, it's only hurting us. Causing me to dismiss possibilities and options that may well relieve my cramping and other symptoms. Stopping us from being the good mates we are.

True. But they may still have effects we haven't been able to find yet... and at the very least... things like meditation, deep breathing and reducing meat consumption are just healthy.

So Dad... I'm sorry for being a jackass. An absolute arse and I'm sorry for not respecting you. Because YOU'VE brought me up to be the man with the values and attitude I have today. It's your belief, your teachings - "that you should leave this world in a better state than you left it in" that drives me. It's your philosophy, "that you should always smile at people. Because you never know whose rough day you just made" that I take with me everywhere; to enrich the lives of those around me, as well as mine. It's your sense of humour that compels me to add "that you could never express those sentiments this beautifully" (as your effective writing skills are nowhere near as good as mine. This bit is an inside joke I may share with you guys one day..)

This video I made about doctors needing to care about their patients more is embodied, essentially on your beliefs. Ones that are strikingly similar to great people like Patch Adams. 

I will try to be more accepting, more respectful, more patient with you and promise to take your advice and apply it at home (instead of just outside the confines of it, as I've been doing), and, as you say, "listen to anything said about you or your ideas without emotion or bias, for there may be wisdom, or an idea in there waiting for you to grab it". I'll listen to any advice you give me and take it to heart, and try to not let bitterness stop me from becoming a better person. Something you've taught me to do, and be. 

But one pearl of wisdom I've heard elsewhere is that often the ones that make us laugh the most are the saddest inside. 

One thing I also want to ask on this Father's day is, Are You Okay? It's not just because R U OK day is coming up this Thursday, but because for all the times you've asked me that question over the years, I've never asked you that back... I've forgotten to...

Maybe no-one has... 

The things you've said to us, the anger you release at times... it doesn't make sense. Once or twice... you seem to have hinted that you're hurting too. Something you don't like to show. 

You've had to watch a person you love go through hell and back. You've had to sit by silently and watch as doctors inserted needle after needle into me, while I lay strapped down in bed in ICU twice (perhaps more times, I can't really remember), watch in horror as my face, in your words, for I can't remember, "distorted, to the point where your right eye was where your mouth should be"; you've had to watch me wither away into this hobbling, pained creature as these cramps and my disease has gotten worse... YOU'VE been through hell and back... And I don't know how you've done it. 

I know you're strong, I know you've also gotten strength from my brother, and his reaction, as well as mine to this whole thing, but to you, and any man reading on who may think this way, it's not weak to admit, or wanna talk about how you're feeling. It's weak to hide it inside; it takes strength to put it out there, at first. But once you do, you're taking the first step to being a happier person. And when you put it that way... it doesn't make sense not to do it, if you are feeling that way. 
You may think you're strong enough, smart enough to do it on your own. But hell, if someone else could help you do it in half the time, you've just saved yourself more time to enjoy life as you want, and deserve to. 

If you do think talking about it may help - please do so. Find a good mate, someone older, someone who you respect, or someone you trust; or else find someone who you never have to see again who is obliged to keep everything you said to them a secret - a psychologist, perhaps to do it with. And if you, or any man is stuck for people to talk to - check out these guys who may be able to help: 

Australia: http://softenthefckup.com.au/
http://www.mensshed.org/home/.aspx
America: http://www.mentalhealthamerica.net/find-support-groups
International: https://www.beyondblue.org.au/resources/for-me/men/depression-in-men

Lifeline: (+61) 131114

Whatever you may or may not be going through - I'll always be here for you dad, as you've always been here for me. And we'll be together forever. Happy Father's day. Enjoy these moments!

Dad and I after chemo #1

Dad and I after finishing the Ride to Conquer Cancer

Dad and I about a week ago tearing up the party as usual!

Categories: Carers Carers Support Dad Dad's shed Father Carers Humour in hospital Man's Shed My Hilarious(ly annoying) Dad Red Rooster Prank

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Losing Independence and Feeling Like a Burden. But a Kind Gift's Gonna Get me Some of it Back.

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Cancer, as a young person, can affect your life in SOOO many more ways than people imagine. It's not just the brutal, life-threatening treatment that leaves scars, physically (pick any picture of me and you can see it), psychologically (I still get nightmares, that I'm back in hospital getting treatment, every now  and then) and emotionally (coping with the loss of your looks, physicality, and sometimes self is hard, especially when you're meant to be "at your peak); it's the little seen, but all too present loss of independence that can REALLY get to you. 

As a young adult, you're expected to live life "To the max", having started to come to grips with who you are as a person, you're expected to go out, stay in, explore the world and do things, pursue the dreams, and start to live the life you've envisioned for yourself... but when the long term effects of cancer stop you from doing that... it SUCKS. 

But what sucks more though is the fact that you have to rely on others to help you. Because another thing that's expected as you leave your teens and hit your 20s is that you go out and become your own man. Or woman. 

The last few months, as I've had those eye; let's call them "episodes" (1/10,000 complications happened in EACH of my eyes, a few months apart), as I've started further chemotherapy based treatment for the chronic graft versus host disease that lingers in my body, and as those awful cramps I keep talking about have gotten worse and worse, I've had to rely on others A LOT. My Mum, Dad and Brother, the most. But others too. 

I remember the day before I lost my left eye, I was cramping so bad that I needed a friend to escort me from the full lecture theater of concerned looking medical students (the dean herself was lecturing, and looking worried too), and look after me as my brother pulled up to take me home. I was thankful. As hell. Touched, at not only his, but also the whole's grade's obvious concern for my welfare. An amazing trait to see in a room full of people who are gonna be looking after our, and our children's well-being in the near future... 

It restored my faith in what I said here. That doctors DO care. And that they DO want to help others. But that sometimes... they feel they can't. And that's what gets them down.

But despite the gratitude I felt for that act, and despite the occasional kind comments and well wishes I get from people, often strangers, when I tell them my story, I can't help but feel... pity for myself every-time I have to lean on someone else's shoulder, or say those things. 

That self-pity can easily turn to self-loathing. 

Especially in the context of home. 

My parents and my brother are the most amazing people I know. They've not only looked after me, caught me when I fell (literally and figuratively) and on top of that, also looked to help others  (this amazing interview my mum did to let other carers know they're not alone was beautiful. You may not know this, but often, when people approach me through there, I "refer" mothers, fathers and other family members to her, and she gives them support) - they've kept me happy in these, the most frustrating times of my illness too. Which is just as important. 

When there's a party or an event on at uni, they usually offer to drive me. There, and back (no matter how late I end up home). When I went to Adelaide last year for a medical conference, and Canberra, just a week ago, for the International Youth Ag Summit, they called everyday, readied everything, picked me up from thousands of miles away - Dad, for last week's conference, actually took a week off work to stay and care for me. He did everything, from helping dress me (it's been hard to do that, with the recent rib-tumour surgery. Don't worry - I'm fine and recovering now), lugging around my bags and stuff, and being forced to stand inconspicuous, mostly bored in the background during lectures and breakouts, to make sure I was fine and could attend. 

And my poor, besotted brother is usually the one to pick up the slack. He's been tasked with taking me to poker games every night, often the only thing that takes my mind off things when I'm cramping really bad, the last few months where I couldn't drive. And he's had to do that, as well as all the other things; taking me to appointments, putting cream on my back, running after me and doing all the things I couldn't do normally for all those reasons, AT THE EXPENSE OF HIS SPARE TIME and holidays... At the expense of HIS youth. 

I'm grateful for all they do. But at the same time... they get frustrated. Over time, as their acts of kindness becomes expectations  for the boorish, annoying person that is me (I take them for granted and treat them like crap, WAY too much), they can't help but snap back at me. Or give me frustrated looks. And do those amazing things they do for me everyday begrudgingly. 

And I can't help but be frustrated by that either. 

I HATE the fact that I have to rely on them so much. I HATE the fact that I can't make all those things I want to; half the time because I'm not up to it, half because I can't bring myself to beg my family for a lift.  I HATE that when I look at the kids playing in the street, or when I see my friends posting pictures of their birthdays or trips overseas, or THAT when I JUST see other people WALK AROUND, MOVE FREELY AND PICK UP THINGS WITHOUT FEARING PAIN, I feel a surge of jealousy overcome me... 

I wish I could do all those things. I wish I could just be normal. I wish I could do thing myself... and not feel like a burden all the time. 

And I've felt this way for ages... As do many others struggling with things like this, or chronic illnesses or disabilities and even depression... my age, younger and older. 

   

But recently... one extremely kind act has changed that, just a tiny bit, for me. 

I recently got a message on my personal Facebook from a stranger. Not too uncommon an event due to this blog. But this was an offer to give me money. 

Now I've been offered money, gifts, even flights to America being paid for through this blog and through my speaking a few times now. I always tell them to donate it to a good, effective cause, one that helps the most people possible, or to donate to one of my own fundraisers, if I have one running, if they insist. And so far, they've acquiesced. But this lady kept insisting. 

What was touching about this though was the reason why she was insisting on ME having it.

Without me saying it, ever publicly before, without me having blogged or complained about it all... she'd somehow hit the nail right on the head. 

Her own words... Here they are. I "just noticed that you'd like to play poker and I wondered if I could offer you some cash for taxis to get you going independently. I figured the hardest part (well maybe not the hardest...) of being a tad sick is loosing the independence which you've just gained as a young adult so nobody need know In fact I propose you don't mention it and just take s bloody taxi" 


At that point in time, the week after being released from hospital after my surgery, that was probably the most frustrated I was feeling by this. I was otherwise healthy, I wasn't in any major pain, but I still needed help showering, putting on clothes, shoes; even getting up from bed and getting to the bathroom when those cramps came on. 

The humiliation was one thing. My parents, and brothers' frustration at me, and mine at them, another. Tension just builds around the home when someone's sick, and in our case, it was sky high, and my activities, my "running around after others' while you're still sick" and my freedom was being questioned and ground away into dust.

I was sick of it. But as touching as it was, I still wasn't going to take that gift. I do all this not for money but to help others. So I told her, after she insisted on giving it to ME for my personal use and personal use only, that if she REALLY wanted to help me, she should give it to my soon-to-come charity (a social enterprise I'm talking to a few people about and starting to develop that'll help charities gain a new source of income and help businesses out simultaneously... I'll post more about it later). 

But again, she admonished, "Nikhil, I'm probably your mums age so I'm going to have to pull rank here! You are not a charity. I give both time and money to politics and charity when I can and you are neither - you're a young man who should take a hearty offer to enjoy life and have fun with tiny help from someone offering who is happy to do so."

"Just be simple and un philosophical for the moment, push away boring old reason, humility and just take it!! Don't be shy or embarrassed. The only condition is its for you and it's for fun! I love that you play poker!"

"you should accept and should take whatever life throws your way... Just because you can! You of all people know it throws some shite... So a random stranger, eyes wide open offers you taxi cash, just take it." 

And you know what, after talking to her for a while, after learning more about her and her battles with disease, and her work with social enterprises too... I decided to do just that. 

She sent me the money just yesterday. And I'm gonna use it. For that reason only. All my poker winnings go to the Buywell Foundation (my charity's name) seed-fund anyway. Technically, she has given to my social enterprise. Technically, she has given me back some of my freedom, and technically, I am gonna be using it for poker. 

But in reality... she's allowed me to feel nearly normal and free again. 

And that's EVERYTHING. 

She's insisted this remain anonymous. And it will. It wasn't a HUGE amount - don't worry, I'm not gonna be heading off to Vegas for a weekend of debauchery anytime soon (unless I win big of course... though to be honest... I'd chuck it all in the bank and build up that charity-cum-company anyways). 

But one thing I've also realised is that TECHNICALLY.... I'm being payed to play poker now. 

So TECHNICALLY... I'm a Pro! 

Hahaha - I'll keep you updated on my progress, on if my current $4000 "career" poker earnings go up significantly... but the way I play, just for fun, in low stakes games, her donation should last me months. And hopefully by then, the medications will have kicked in, I'll be over my cramps, and back to being me. 

What will last forever though is my appreciation for her keen sense of understanding. 

And the knowledge that others in the world DO GET IT. 

Being sick, or sad sucks. But if you feel like you're a burden too, it sucks even more. 

Hopefully this allows you guys reading on to understand that, and be more aware that others in your life may feel that way. Or that you're not alone if you yourself do. One thing I've also realised from all this, the weeks of tension that's lingered in my home, is that they wouldn't be doing all this for me if they didn't love me. 

Caring is the physical embodiment of that love, and I thank everyone who's ever shown me that care in my life because it's made me the man I am today. 

Now before you guys who wanted to donate before go off in a hurry and use this as a way to get me to accept gifts... again thank you SO much but honestly... I'll be fine! You save up that money and donate it when the kickstarter for Buywell comes out; 'cause when it does... it'll go HUGE. And I truly believe, and want it to make the WORLD a better place. 

Categories: Donations Feeling Like a Burden Losing Independence Losing Independence to Disease Poker Poker star Random Acts of Kindness

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