I made a promise when I began this blog-the ramblings of an ageing female-that health issues would not be at the forefront of every post. Every now and then, however there is bound to be some blot on the fitness horizon and this particular blot appears to have eclipsed normal life like a blackout curtain.
In an ironic curve the disease I have eventually been diagnosed with is not at all age related, more an unfortunate plague of a far younger demographic. What is it? It is ulcerative colitis; nasty and incurable, yes, life threatening-well no, supposedly not, except that the odds of more sinister complaints are increased.
Whilst Fiction Month was running its [highly satisfactory] course the writer was undergoing many weeks of initial terror followed by exhaustion and desperation as the slow wheels of our UK health service ground along; well-meaning and efficient but over-stretched and ponderous.
During the past two months life has shrunk back within the walls of the house, where access to bathroom facilities provides a secure reassurance-for now, the only factor that matters. This disease, as all inflammatory bowel diseases [Crohn’s is another] is neither romantic nor noble, reducing us, the sufferers to the most basic of needs- a toilet and means of cleaning up. A walk, shopping trip or evening out becomes an activity to be undertaken with trepidation and vast amounts of planning, but mostly not at all.
With Christmas rearing up I fall eagerly on the reassuring presence of the internet while fantasising about strolling around Christmas markets, choosing ‘real’ items, stopping for coffees, enjoying the ambience of the ‘Alpine Bar’ that popped up in our local town [according to Facebook].
Between sojourns enclosed within the shiny, tiled cell of the lavatory I have enjoyed the luxury of unlimited research time, during which I have discovered the unfathomable ocean of misery that is undergone by those who suffer chronic illness. I am castigated by the small but dedicated carers that are my immediate family for doing this, but to me, ignorance can never be a pleasure. The more I know, the better I am prepared.
The GP [local doctor] who was my first port of call has kindly followed up with inquiries regarding diagnosis and progress but clearly is at a loss to know how to provide cheer amid the gloom. ‘You are on a journey’, she tells me and I refrain from advising her that my travel plans have reduced down to the few steps it takes to achieve the safety of the loo. She does mean well.
In all I have not failed to recognise that I am extremely lucky to have Husband-supporting without false cheer, and Offspring-resilient in her newly acquired nurse’s knowledge. Messages, however brief, from some of those who I’ve plucked up the courage to inform are more appreciated than they can know.
So far treatment cannot be described as an unmitigated success, although I recognise it is still ‘early days’ and that there are further options along what the doctor calls the ‘journey’.
I am learning to appreciate home comforts and I am catching up [via the wonder that is ‘Blinkbox’] on TV and film I missed when I was engaged in more worthy activities.
One tragic casualty has been my writing, the pursuit of which has escaped me. This may change-who knows? What a blessing we none of us know what lies ahead!