Showing posts with label illness. Show all posts
Showing posts with label illness. Show all posts

Friday, 17 June 2016

Gardening again


Now we write May again and although snow was forecasted for this coming weekend, the sun is out. The chalet, where I am temporarily staying in The Park has a south-facing terrace and herb bed, both yelling to be tended. The gardener in me can’t wait to respond. Weeding is the first thing that needs to be done. With the physical condition I have at the moment — amongst which vertigo with constant dizziness and distorted eyesight— it seems an overwhelming and Herculean task. I do not know how to begin gardening again! Kneeling to do the job? No! Squatting? No way. OK… sitting and moving on the ground then? That might work….  Oh my goodness! Is this something all less-able people have to go through? I never knew!

I am painfully clumsy, like a drunken sailor. For one and a half hour I try to ‘keep calm and keep on weeding’, puffing and sighing while every move of my head causes everything to swirl around. Until I have to stop from nauseousness. It is the most disappointing and frustrating experience I have had in this last half year here in The Park.
But OK, I pruned the sage. I weeded three meters of terrace tiles. I tackled a big long rooted nettle family. They’ll end up in tonight’s soup. With quite some effort I did fill more than half a brown compost wheelie bin with weeds and old branches. I did it! Now I’m proud to have gardened again.

Blog 44, text & photo © Adriana Sjan Bijman, May 2016

Wednesday, 17 February 2016

Illness: Dark & Light


I am living in the twilight, in the middle of a journey. The door of the past — with its healthy body in a very busy life— has been closed and it is not clear where the road will take me.
“Illness is a simple though painful reminder that we are not the masters of our bodies and our lives” writes Kat Duff (1).Illness is a humbling experience and as such I think, can bring some gifts in disguise. Insights wrapped up as setbacks, in the Game of Life.

After seven months of gradually increasing symptoms, discomfort and pains, instead of a slow or quick recovery, I have to accept and learn to live with this, like many people with long term illnesses have to. It has turned my life upside down, thrown me out of my comfort zone and the fulfilment of a hardworking busy life. It makes me stand apart, in another category, that of the ill, the weak, the elderly, the non-productive. It is a different journey. It feels like that, even here, in a community on a spiritual base, where most people always seem to be so busy and often are on the edge of being burned out, trying to do so well, to save the world or at least save our community. Or simply trying to earn a living and be able to control the ongoing incoming stream of bills. Like I did over the last decades.

At first this big change brought up feelings of tension, guilt and questioning “Why me?” Feeling a bit of a victim. At times I even blamed myself for it from the point of view of certain schools of psychology, that ‘with our thoughts we create our own reality’, so why did I create this? And why can’t I now immediately create a healthy body. It is easy to stumble into that pitfall of being at fault and responsible for illness ourselves. These thoughts are absolutely not helpful to me now. It does not mean I am not willing to look at a deeper personal cause of what my body is doing and how I can help to get out of this predicament; how to make my journey towards a better life. How I can make peace with the symptoms. How we can become allies instead of enemies and how we can start to work for the same goal. For me a goal of balance.

Since I was a young girl, my whole life has been an experience of learning how to have and maintain independence. Although I now know we all are inter-dependent, it is a tough journey to learn to ask for help. I can already feel grateful for and see the advantages of newly learned qualities like patience and slowing down. The ‘being dependent’ and compassion are in progress, so to speak. I’ve always been a multi-tasker, a quick thinker and doer. Slowing down, especially to prevent more accidents with my vertigo-dizziness and only partial eyesight, makes me clumsy. I walk like a drunken sailor. Out of doors with crutches, for my own safety. Constantly having to balance myself is exhausting but also contains the lesson of balancing the way of life. How to bring more balance into my, our lives?  How to bring some light in the darkness? The light of keeping up my spirit, my hope, my goals of renewed good health.

Simple but at times exhausting survival activities like washing, getting dressed, shopping nearby and cooking easily fill my days, next to time to rest.  ”How did I ever have time to work?” I grin and wonder. Too tired to pick up a pen or pencil during the daytime, texts like this only come in the sleepless dark hours of the night, scribbled on and in between the lines, which I can hardly distinguish. It does not matter: I recognised the words and pass them on to you here, as part of my journey. On my way to more light.

© text and photo: Adriana Bijman. photo in the bus at the A96 to Inverness, along the Moray First Coast, 2015.
(1) The Alchemy of Illness, 1993 p 59.
Blog 42, Winter 2015/2016

Saturday, 1 August 2015

Beauty and ugliness


Hello everybody
Here some thoughts about health, both in the garden and in my body, and the congruence I see happening between these two. Although my houseplants are thriving, healthy and growing fabulously, so I‘d like to take them as my example.

‘Fear of the unknown is an essential part of the human program', Joseph Dispenza,The Way of the Traveller,(2002)

Beauty and ugliness in the garden
More than 50 strawberry plants, there are black-and redcurrant shrubs, abundant roses, lettuces, calendula, lemon balm for my tea, and many kind of herbs for the picking. I defend my food and plants against the pests who are looking for their next meal. In essence we are all doing the same thing, looking for food to live on. The snails and slugs are enjoying an abundant wet summer in my garden.  They’ve eaten all my zucchini plants (including the yellow flowers); half my beautiful lettuces; they’ve totally destroyed an immense green striped hosta plant, and all of the dahlias; they’re doing their best with my cabbages and broccoli and now the snails are heading for my strawberries.
“No!” I told them. ”You can have the cabbages, but not the strawberries. That’s my limit.” We’re not on speaking terms anymore. So I tried to stop them, using crumbled eggshells, prickly comfrey leaves, with copper anti-slug tape and I even bought them beer. (As a coeliac, I don’t drink beer). I think they’re ugly. I wouldn’t mind seeing them drown themselves drunk in the cans with beer I placed at several strategic places. 
I still have quite some processing to do before I can be at peace with them, before I can see their beauty.

Challenges of beauty and ugliness in the human body
Like my garden, my beautiful, slim, 51 kg, flexible, strong body has its own ugly side to face, invisible to others. For years I’ve been struggling with the untreated consequences of coeliac disease. I now have it quite well under control and am at peace with it, but two months ago the right side of my body went numb. Although it still functioned normally, it is as if it was only partly present. At the same time red spots started to appear on my chest. Neither I, the doctors and nor the hospitals have any idea what is going on. I’m a guinea pig, receiving one cream and test after the other, even antibiotics, all without result; a biopsy, a lumbar puncture, an MRI brain scan; bioresonance sessions, homeopathic and Bach remedies, a thorough clean of my new house after the discovery of the fungus Aspergillus. After two month my illness is still a mystery, as both the spots and the numbness are not only not improving, but getting worse, with severe dizziness, causing me to faint in the street last week.
During good moments I am in peace with it. During other moments, the worry and the fear set in. Then I start imagining, like Don Quixote, my own dragons where there might only just be windmills. Time to face the dragons and maintain the windmills. 

No beauty without learning about ugliness, no love without getting to tackle fear.

Blog 39, July 2015, © text and photos: Adriana Sjan Bijman

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