Life doesn’t Suck. Living with ALS SUCKS.
One year, that’s how long I’ve been blogging. One year, that’s how long I’ve been experiencing my body decaying from the inside out. Well, to be more precise, I have been living with ALS for Twenty-one months. A year ago, I started Filipendulous. Thinking that it would be my soul dangling on an ever-weakening thread. That spiritually I would be tested with every onset of a different symptom or further regression of the body. What I have discovered is that the soul is resilient, in touch with the Universe, it is instinctively aware of the energy surrounding it, living through it. With love and happiness, it gains strength to carry on. The body is however resilient only to a point. Breaking point!
Living with ALS really sucks. moving ever closer to the breaking point. Every day, more aware of your own mortality. It’ not an obsession! It’s not my focus in life. It is however a stark reality! Every passing day a random culling of motor neurons, every day less voluntary muscle movement possible. The result known, the involuntary termination of the diaphragm movement, the termination of breath! One of three essential organ functions to sustain life, lung function, heart function and brain function. Mortality is not unique, it’s the common denominator for all living organisms. Unfortunately, ALS, as with any other terminal illness gives you an insight to the end. The precise timing though still unknown. Life, our best friend until the end. Like all good friendships, to be nourished, cherished and enjoyed until the end. What we learn growing up is that we consist of body, mind and soul. What no one bothers to elaborate (unless you are studying biology, medicine or expressing an interest), we are a biochemical process controlled by genetic coding. Running on auto pilot. Very few of us question how we come to be or how we exist at all, physiologically, not spiritually or religiously. We take it for granted that we are the result of reproduction. Upon conception we start the genetic process. We start dividing, replicating, growing, mutating and programming cells. All the while oblivious to how this process is controlled. Genetic coding running on auto pilot.
If you believe scientist the genetic coding we are born with and which determines how we develop physically, mentally and to a degree even spiritually, evolved over millions of years. Our genome with a DNA super computer with machine learning capabilities involved in this process of evolution. To live, our cells need to repeat this process millions of times over every day we are alive. The only problem, at least half of the genomes found within the bodies billions of cells consist of junk, molecular parasites and retro-viruses. Unfortunately, our bodies, rather than recognizing and isolating the genetic nonsense continues to replicate autonomously. This junk can disrupt our life in a significant way. No one knows if the junk is responsible for ALS, they think there could perhaps be a retro-virus responsible for triggering ALS. It could be several other genes. No one is sure. No one has a cure for it either. I suppose it really makes no difference. Probably better that we don’t know every aspect of Life’s process, there are enough hypochondriacs self-diagnosing on the Internet already in this world. There’s nothing, on an individual level, that we can do about it. We can’t control the process of life. We attempt to influence it in many ways, we design training Programs, diets, growth hormones, plastic surgery, minerals and vitamins. Everyone tries something at some point to make us healthier, stronger, younger or prettier. To influence life’s natural selection process for better or for worst.
So, living with ALS really sucks! Not like putting in all the effort training for a marathon and then injuring yourself days before the marathon sucks. Not like a bad haircut, receding hairline or ten pounds overweight sucks. It sucks like willing your brain and body to stop producing Glutamate to toxic levels that obliterate your motor neurons! It sucks like a year of aggressive physiotherapy, three days a week, which by now would see me doing the splits Between two chairs. Instead I need Sancho and Jonathan to support my eighty-kilogram frame, with all their strength, to stumble three meters in fifteen minutes with my shorts and underwear wedged so high up, if I still had a singing voice I would sound like Sarah Brightman. It sucks knowing it’s unlikely I’ll get to celebrate Tallulah’s sweet sixteen or her twenty first birthday or walking her down the Isle on her wedding day. It sucks knowing I won’t get to grow old with Antoinette, exploring many of the magnificent destinations in this world. It sucks not being able to scuba dive and share the experience with Tallulah. It sucks not being able to walk through a construction site and experience the redolence of each stage of the construction of process. It sucks knowing you were fit and healthy one day and the next having to experience a steady decline, decaying on the inside while all your cognitive functions remain as sharp as before. Nothing sucks more though than watching your loved ones struggle more every day to support and take care of you! From being the bedrock, the family is built on to becoming the slippery clay the family rests on, displacing more every day, as more stresses are exerted on the family.
The most amazing thing though, if you have a sound mind, the mind and Soul accept the onslaught and you find ways to nourish and cherish Life. Together the family experience the external changes and learn new ways to adapt Life changes forever but, memories are made, and lessons learnt. Life has given me an opportunity to imagine, in some way, what the future may hold for Antoinette and Tallulah. It’s like sketching an image from a camera obscura, the pin hole my imagination, their future the perfect Image upside down and inverted. As long as the light shines bright I will be able to add more details. My eyes to the keyboard recording my thoughts, in some way I will continue to be a small part of their Life in future. As Shakespeare said “Let me embrace thee, sour adversity, for wise men say it is the wisest course.”
#ChallengeALSDXB
Jackie
Dearest Peter , you are so , so brave and we have so much to learn from you . Thank you for sharing and for reminding us to enjoy each breath. Sending you so much love. Jackie and Peter
Sancho
A simple thought can bring about an inspiration in the right moment and the right circumstances. Let your soul continue to flow in your blogs. As some people say, what is written on the net is written on ink. Your blog will be a part of a legacy in the making that will continue to inspire others. Never let ALS pull you down from being the great man that you are.
Pieter
My beloved son…
As i read thhis expression from your soul, i realise the tremendous strength and character that radiates from your being…So much love and wisdom that you share to make us aware of what your world feels like from your perspective….I am so grateful for the memories that we have shared and are still being allowed to share by the grace of our heavenly father…
I salute you my son …I truly salute you
I must honestly admit that i seriously lack understanding when it comes to matters of the soul…You my son are letting me in by making it possible for me to have a glimps (albeit a small glimps) of your wonderfull soul!!!
Jan Bronkhorst
Dear Peter
We had breakfast with Evangelist and Sister Smith a few months ago. It was a good two to three hours for us because we reflected on many things, but mostly the good old days when life was different. We spent time with an extremely proud oupa who couldn’t stop talking about his granddaughter, her influence on him and her achievements. We also spoke about you and the state of your health and how everyone is coping and dealing with it.
We are extremely sad that ALS has crossed your road and stayed. It was a shock when we first heard about it, because like with everything else, human nature seems to freeze moments, and we remember you and Antoinette the way you were the last time we saw you, young, full of life and energy and ready to take on the world. In the meantime, life has happened to all of us, we moved on and things have changed. Fortunately, we have also grown and matured in understanding, and even though we cannot help you physically we would like to share some thoughts with you.
1. For everything that happens to us, there is a purpose and a reason. We do not always understand why, but if we believe in God and trust him with our lives, he will bring to us the understanding of why certain things were placed on our road.
2. God also teaches us that he will never test us beyond our abilities, we must therefore believe that when we face a challenge, we will have the ability to overcome or beat the challenge. (1Co 10:13 There hath no temptation taken you but such as is common to man: but God is faithful, who will not suffer you to be tempted above that ye are able; but will with the temptation also make a way to escape, that ye may be able to bear it.)
3. We were never guaranteed that we will live for ever (or long for that matter) naturally, but God did give us the promise of everlasting life, that is not for the body, but a promise unto the soul of man. That means that part of you that is disgruntled about the ALS happening to your body can live forever in the glory of God’s kingdom.
In a strange way an Angel of God crossed your road today. Her name is sister Lizzy. She said “Please help me, I want to write something spiritual to Peter”. I answered “What do you want to write to Peter?” Her answer – “I don’t know, but he was our youth member”. Indeed you were our youth member, feels like yesterday, but I think it is something close to thirty years ago! How time has flown!
You and your family are always in our thoughts and prayers.
Love Elder and Sister Bronkhorst