Saturday, 6 January 2024
Letting The Music Find Me...
Wednesday, 4 August 2021
So here I am once more... Musings on another redundancy.
“Changes aren’t permanent, but change is…” (Tom Sawyer – Rush)
Sunday, 6 December 2020
Fading Light?
As I type this, I have just passed the end of my 51st year on this planet. It feels like time is passing quickly – too quickly, but I know full well that it is passing at the same pace as ever – one second at a time, one breath at a time, one heartbeat at a time. My perception of the passing of time, however, is a whole different sock full of custard. It seems to pass ever faster as I grow older. To quote Neil Peart:
“Summer's going fast
Nights growing colder
Children growing up
Old friends growing older
Freeze this moment
A little bit longer
Make each sensation
A little bit stronger
Experience slips away...
Experience slips away...
The innocence slips away...”
And mentioning Mr Peart makes me
realise that growing older is not a problem, though it may bring with it
various issues (yes, I am looking at you creaky knees!) - over all it is a
privilege, and not one afforded to everyone. This year indeed has perhaps
brought mortality into somewhat clearer focus – not just because it started
with my 50th birthday (and thus with a certain amount of reflection,
but that was viewed through a lens tinted by a beautiful, shiny new Les Paul,
and also, more importantly, a wee gathering with as many as possible of my even
more beautiful and shiny friends and family!)
In the time since that gathering, a
lot has changed in the world partly due to a certain “c” word, but also due to
another even more malevolent “c” word that has stolen a couple of my musical
heroes (the aforementioned Mr Peart, and of course, more recently Eddie van
Halen), but also some more “Everyday Heroes” in my life.
My friend Alan “BY” McWilliam was a
talented musician and a genuine nice guy – known throughout Dundee for his
busking and being in quite a few local bands over the years. I had known him
for a long time through being out and about on the Dundee rock scene, and it was
always good to see him because of his generosity of spirit and supportiveness
(there was also the eternal fellowship of being Rush fans!). I had lost touch
with him – mainly due to my moving to Edinburgh – but I was delighted to make
contact again a couple of years ago though Mally, another old friend, who was
playing keyboards in his latest band Bravado. It just so happened that one of
their gigs coincided with a trip to Dundee, so Freya and I went along. It was a
great night, I saw quite a few other familiar faces, and I got a chance to
reconnect with BY – and it was as if there had been weeks since we’d last
spoken, not years… Little did I know that that would be the last time that I
would speak to him in person. I am even more glad now than I was at the time to
have shared that little time with him – with the added bonus that I had
genuinely enjoyed the gig too.
Going back to my 50th, I
had been really glad to share it with a good number of people that I hadn’t
seen as much as I would have liked, and none more so than my friend Colleen. I
had first met her through friends in Glasgow, and then had met her often through
the Edinburgh goth scene, and rather more prosaically, through shopping in Cameron
Toll often with her daughter. Collen was simply a beautiful person – kind,
generous and gentle. I can’t think of particular “special” memories in her
company, since she had a knack of making any meeting special in some way. That
said, seeing her at my birthday do was rather special – I already knew that she
was ill, so the fact that she was able to come was amazing. Fate is rarely kind
in my experience, but in Colleen’s case, it feels like it was particularly
cruel. She was a trans women, finally finding her path towards truly becoming
herself, if that makes sense, when she fell ill. I don’t think that the
pandemic affected her treatment negatively, but it made it a lot more difficult
to visit her in her final days. Thankfully some friends were able to spend time
with her, and her ex-partner and daughter made it over from France in time to
spend a few days with her too. It also brought a group of her friends together
online, to arrange things and share stories. Small mercies. (Probably the only
ones that we can realistically hope for in these times.)
When she passed, it hit hard. The
particular cruelty of her fate, her bravery and her gentleness of spirit
probably made her passing, though expected, harder to take. Sometimes, these
moments can bring special things into being though, and I have gained new friends
through Colleen and my frequently errant muse returned. Words formed in my
head, and spilled onto the page with a fluency that I have lacked for a long
time. It rapidly became a full song/poem, which after a moment of self-doubt, I
shared with the group… I was amazed, humbled and terrified in roughly equal
measure when Arielle, Colleen’s former partner, asked me to read it at the
funeral. It was an emotional moment, but I guess that I was glad to in some way
do something for Colleen, who had given all of us so much. We have to remember,
especially in these times where we are forcibly separated from those we need so
much, that we have to make sure that they know how much they mean to us. Don’t contemplate
your mortality so much that you forget to live. Be kinder. Love Everyone. Be
More Colleen!
Fading Light
Fading Light
It means too much to
let it fade away
Have to keep it close
for the future days
So much bravery
Shining from your
smiling eyes, selfless.
And even as you faded
away
You made the rest of
us stronger
Even as you drifted
further away
You brought the rest
of us closer
Cruel Fate
As you finally found
your own way
Cruel torrents washed
the path away
So much bravery
Worn with a humble
coat of kindness
Falling tears
They’re all I seem to
have today
No real answers are
coming my way
So much bravery
But I seem to have
none myself
And the beauty in
your soul
Is an honest story
simply told
The gentle kindness
That should be
obvious
Your warmth that
soothes us all
As we walk onwards,
with a piece of you in our soul.
The light isn’t
fading at all…
Wednesday, 10 June 2020
Caring In A Time Of COVID... (And other times too)
I was standing in the middle of a busy hospital, in
Edinburgh at the height of the Festival; most of my family were within 5 miles
of where I was, but I felt lonelier then I ever had before – or have since. I
was outside of one of the operating theatres in the Royal Hospital for Sick
Children, or Sick Kids as it is more commonly known. I had just kissed my 2-day
old son on the forehead and watched him wheeled into theatre.
There are many books and websites dedicated to parenting, not
that I had read many of them, but none of them prepare you for this. To be fair,
I have my doubts as to how much they actually prepare you for any of parenting,
but that’s a whole other story. Actually, nothing prepares you for this.
Looking back, I feel like I got through all of it mostly intact. Perhaps only
by the skin of my teeth, but I guess that I did get through it.
How did I come to be standing outside of that operating
theatre?
My son, Christopher, had been born two days before in the
Simpsons Maternity Unit in Edinburgh. The birth could have been less traumatic
(an emergency C-Section), but all seemed to be well and fatherhood was a happy
place. Early afternoon on the day after he was born my in-laws persuaded me to
tear myself away from the wee man and his mum and go for some lunch. Halfway
down Leith Walk ‘the call’ came – some routine tests had shown up something
unusual. Back at the hospital I heard a diagnosis that has become part of our
lives ever since. Tracheo-Oesophageal Fistula with Oesophageal Atresia (TOF/OA).
When the doctor told us, I felt like my entire being had been flushed into the
void. So many questions flooded into the vacant space. Not least “What is it –
and can you fix it?”
The answers to those questions came at Sick Kids – TOF/OA is
a congenital anomaly where the oesophagus doesn’t quite form correctly and the
upper part finishes at a dead end in the upper chest (the OA bit) and the
stomach end is attached to the trachea (the TOF bit), and yes, with a bit of
radical re-plumbing, it is usually fixable. Fortunately for us, Sick Kids is
one of the leading centres for repairing TOF/OA and one of very few at the time
that were doing the repairs using ‘keyhole’ surgery. Some light was creeping
into the darkness.
After the longest afternoon of my life, back at Simpsons
with my wife, family and some friends, the phone rang, and we got the news that
the surgery had gone well, and that Christopher was in recovery. The collective
sigh of relief almost blew the windows out of the rather overcrowded side room
that Freya had been moved into by the thoughtful midwives.
Thus began a long journey, which we are still on. Medically,
this has included numerous trips back to Sick Kids, some planned, but most not,
and a spell in Yorkhill in Glasgow for heart surgery. The physiology of a TOF
child means that food can quite easily get stuck – sometimes it can be
dislodged by judicious application of fizzy juice (Irn Bru works a treat!),
though it often requires an endoscopy to wheech it out. Along the way, we discovered
the wonderful TOFS charity, appeared on the STV evening news and in various
newspapers (they took a particular interest in the ‘medical’ applications of
Irn Bru), and generally experienced a very different baby/toddlerhood than we
expected. Now, Christopher is almost 12, and we are in a fairly good place,
relatively speaking. He still has annual MOTs, and we as parents are also still
dealing with the psychological aftermath.
Which brings me at last (at last!) to the actual point of
this blog – the mental toll that this has taken on my wife and I. We have not
just been parents, we have been carers too. We have learnt things that most
parents never need to know, we have had experiences that are probably the stuff
of nightmares for most parents – and still, compared to others we know, we have
had it relatively easy.
It seems to me to come in two parts, like many things in the
medical sphere – acute and chronic.
The bits I think of
as acute are the obvious stress points – the chest infections, the operations,
seeing his heart rate somewhere north of 200 bpm. The chronic is the half-life
existence – in and out of hospital, nights in camp beds on wards, wondering
“what next?”, watching him like a hawk as he eats his lunch. This makes up the
daily routine when your child has issues like this. Also, there is the guilt –
did I somehow cause this? Is there something that I am missing?
In a way, the acute parts are almost easier to cope with –
there are people there all the time, sharing the burden, watching out for you. The
chronic parts build up over time, there is often no telling when it is going to
tip over into ‘too much’. Ultimately, I think that you learn to spot the signs,
and become better at knowing when to reach out. Freya, my wife, found the guilt
side of things particularly difficult – she felt that having carried him for
nine months it must be her fault somehow. Being a maths/science geek, I took
some solace in the statistics, sought to understand what I could, and tried to
use that to support her however I could. We got through it together.
That is even more important than it seems, because ultimately,
no-one else really understands the carer’s journey the way that they do. It is
isolation. Not in an uncaring way – we have been surrounded by love, support
and care every step of the way – but because no-one else, not even other “TOF
Families” walk quite the same path as you.
Perhaps this has made our current shared, but different path
through this strange land called Lockdown a little easier.
Along with the worries that we all share in the shadow of COVID
19, there are those specific to our son’s condition. TOF children are generally
more susceptible to chest infections than non-TOFs due to an aspect of the
condition called Tracheomalacia (also known as ‘floppy windpipe’) which means that
they can’t clear infected mucus as effectively. TOF/OA can also come alongside
other conditions, so it can become quite complex quite quickly. In this, we
have been truly fortunate that the TOFS charity has been able to give support,
and act as a conduit for advice direct from some of the foremost experts in the
UK.
There is of course, also the worry that Christopher could
get food stuck (although he hasn’t had a real issue for a few years) – would we
be able to take him in? Obviously, we would not want to burden the NHS any
further either, so he has been well warned to chew carefully! While these
issues are fairly specific to our situation, these, I am sure, are the sort of
things that all carers will be worrying about.
Sunday, 14 September 2014
Super Scared...
Sunday, 13 October 2013
When the going gets TOF, the TOFs get going...
On the 7th of August 2008, my world changed completely. For the second time in 24 hours. The first was relatively easy (for me at least, for Freya, not so much) - I became a father for the first time. The second was not so easy for either of us. There were, for me, two heart stopping moments - number one was the phone call that cut short my, and Freya's parents quest for lunch and sent us rushing back to the Simpson's. Number two was the moment when a doctor there did their best to describe what was wrong with Christopher (it is a rare condition and not the doctor's area of speciality). Words cannot describe the way that I felt. It was as if someone had flushed every fibre of my being out into the void. Those are words, but they don't come close to describing the intensity of the feeling.
The rest of that Thursday is a bit of a blur. Seeing Christopher in the Special Care Baby Unit at the Royal - looking like a giant next to the truly tiny miracles that surrounded him. The trip through Edinburgh to Sick Kids with Freya's dad. Practically being frogmarched into the chippy along from the hospital by the great man that I am now proud to call my father in law, who was smart enough to know that I actually did need to eat, no matter how trivial my own welfare felt to me at the time. Hearing (with a not inconsiderable amount of relief) the much more positive prognosis for Christopher than the one that I had imagined from one of the surgeons that would be involved in his operation. Holding the Wee Man in my arms for what seemed like no time, but was actually about two hours, until the nurses persuaded me that I'd be better off going to bed in the little room that was available to me, just along the corridor. Not thinking that I would be able to sleep. but actually conking out as soon as my head hit the pillow. The dreadful wrenching pain of separation, kissing him before he went into theatre. The eternity of waiting in the side room at the maternity ward, and the explosive collective sigh of relief when we heard that the surgery had gone well. I thought that we could have blown the windows out!
It has been a long, winding, sometimes joyful, sometimes painful road since then, but it has been massively easier with the help of our families and friends. Many of those friends are ones we would likely never have met but for TOFS - the support charity for Christopher's condition. It is not a big charity like the ones that have ads on the telly and bus stops and the like. It is a small but dedicated group who work to support people affected by TOF, spread awareness and support research into the condition. It is a relatively small charity, but it occupies a huge place in our hearts and minds. We owe them so much.
Also important is that much maligned entity, Facebook. It is not all "selfies" and amusing cat photos - the TOFS groups on there are a vital and useful part of the "TOF family".
Now, we are in a position to offer some help and support to new TOF families - I am "TLC" (TOFS Local Contact) for Scotland, which means that I call new TOF families and welcome them to the larger "family" and offer whatever help and support I can. It feels great to be able to "give something back" - a cliche, I know, but true.
Mainly, I aim to offer friendship, an ear to listen and understanding - a real sense that there are people out there who understand some of what they are going through, although everone's journey is a little different. A feeling that you are not alone can be a powerful aid. At risk of sounding arrogant, I know that this can help; but I know that because I know that it helped us a lot to hear from other TOF families when we were just starting our own journey down the TOF road. Also, I hope that Christopher and his story can inspire and give hope to others because of how far he has come and how much he has achieved in 5 and a bit years.
To try to get to the point that I think that I am trying to make here, this week (12th to 19th October) is TOFS awareness week, so I thought that I should try to spread some awareness. If you wish, follow the link below and learn a bit more. Maybe tell someone else about it. Roughly one in 3,500 babies is born with this condition. It is rare, but that is still roughly 20 a year in Scotland alone, if my back-of-the-envelope calculation is correct. So, please be aware, understand, if you know someone affected by TOF, support them by sharing their experience and and "being there" for them. It means more than you would believe.
http://www.tofs.org.uk
Thursday, 3 October 2013
Peace for our time?
By coincidence, I am reading "Berlin Diary" by William L. Shirer, an American journalist who broadcast from Berlin and around Europe between 1934 and 1941 - seven years that saw Hitler's power grow and Europe slide inexorably into war. It gives a fascinating insight into what happened and how ordinary people came to believe in Hitler's twisted view of the world. Shirer risked arrest, expulsion and possibly worse to bring his view of the Third Reich to the outside world. He also shares his views on how America's then powerful Isolationist Lobby risked playing right into Hitler's hands.
I have long been fascinated by history, particularly military history for a long time. Not for any ghoulish reasons, it is not a morbid fascination. Reading Shirer's book has possibly helped me come to realise why I am so fascinated.
As a scientist at heart (and in my head!) boundary conditions, that critical zone between yes and no, where many of the most fascinating things in science happen - the event horizon of a black hole for one, have always intrigued me greatly. They occur on a human scale too - I feel that I have spent most of my adult life enmeshed in the grey area that is the boundary between depressed and not depressed.
That period in the late 1930's that Shirer wrote so eloquently and perceptively about was also a boundary - between war and not war. What tipped the world over the edge? What drives ordinary people to do the heroic or the horrific? These are the human boundary conditions that can make history such a compelling subject.
I have heard war described as "the continuation of politics by other means" (von Clausewitz originally, I think) - it seems to me that really, war is the failure of politics. The failure to steer us away from, or the crazed urge of some leaders to steer us towards, that most bloody boundary condition between not war and war.
Thursday, 12 September 2013
Flying through cloud,,,
I have always wanted to learn to fly, but I will probably get no closer to it than flight sims and trips on airliners. Lately, however, I have been feeling like I am flying in cloud - that stage in a flight before breaking into the glorious, sunlit paradise above the clouds, when you can see no further than the wingtips of the plane.
It seems an ideal metaphor for the dead, numb nothingness that is depression. Occasionally, there is a break in the cloud that allows one a tantalising glimpse of the sunshine or the Earth below - our familiar, comforting home, Our condition forbids us the power to climb above to that golden place above the weather.
We have our "crew" along with us, those whom we love and who love us, our "navigators" helping us find our way home, our "radio operators" keeping us in contact with some sort of reality, our "air-gunners" keeping an eye out and protecting us from the "flak" coming up from below and the night-fighter (both real and imagined) that are out to get us...
We fly on, through the blank, featureless void, hoping for a chance to find our base to land, rest and refuel. Some flights like this are short hops, others feel like endless missions into the unknown. The cloud may often seem impenetrable, but I am glad to know that I have a top-notch crew and my "kite", while a bit clapped out and past its best, is mostly dependable, and has always got me home thus far.
Monday, 26 August 2013
No covers, no compromise...
Saturday, 3 August 2013
Who ate all the pie..?
I have been having a bit of a mixed time lately - good times with family and friends, things are good at work, and Freya and I have had a chance to go and see a bit of the Fringe with Wee C away for a holiday at Granny and Papa's in Killie. But the "Enemy Within" has also been in evidence, which is, I suppose, nobody's fault but mine. The ol' Black Dog has been chewing my brain like it was a manky old slipper. Which, in a way, it is.
I was thinking a bit about it this morning, and (being the sad old Excel-jockey that I am) I started visualising it as a pie-chart. In my life, the vast majority is good, with my lovely family making up a substantial slice, and with friends, music, books and work etc. making up most of the rest. Just now, however, I don't seem to have the whole pie - I am in possession of less than 100%. One section appears to have been substituted for dark matter - or just nothing.
This missing part is, I think, the creative part of me. And I damn well want it back. I have tried asking myself nicely, but I am not playing, so to speak. I know that it is all down to me. I want to make myself feel better by grabbing my guitar and flooding my empty parts with music. But I won't let myself. It is too damned easy to not bother.
If I do manage to get as far as picking one up, it is too damned easy for my mind to fill with the conviction that it is sounding awful and I should give up. I need to play through this, I need to get involved in some sort of musical collaboration with others so that the creativity can flow between us and be amplified like in the cavity of a laser, reflecting back and forth and growing stronger with each pass.
Of course, organising this takes the sort of energy that the depression steals away. Depression, I feel, (and may well have mentioned before) seems to have a self-preservation instinct that tries to stop you acting to lessen its effects.
There have been small signs that I remember where my creativity is - I have been experimenting with odd tunings, and tiny fragments of passably ok new music have been emerging. I have even been using my phone to keep these pieces for when my muse has returned sufficiently for them to be of use. There are embers, but the flame is not yet returned.
I will though take strength from my family and friends and try to get my fire burning strongly again, because I know that when it does, it helps to make the rest of my pie/world shine that much more brightly.
Sunday, 21 July 2013
A Long Way Away...
“You develop an instant global consciousness, a people orientation, an intense dissatisfaction with the state of the world, and a compulsion to do something about it. From out there on the moon, international politics look so petty. You want to grab a politician by the scruff of the neck and drag him a quarter of a million miles out and say, ‘Look at that, you son of a bitch.'”
― Edgar D. Mitchell (Lunar Module Pilot, Apollo 14)
44 years ago today, Neil Armstrong stepped onto the surface of the Moon, the first ever human being to set foot on another world. The last human being to set foot on the Moon left in 1972. All of the men who went to the Moon were profoundly affected by the experience - there is an excellent book, called "Moondust" by Andrew Smith which relates those experiences via interviews with the surviving Apollo astronauts. I wholeheartedly believe that we should be going back sooner, rather than later.
Not just for the challenge, we have proved that it is possible. Not just for the science, although I believe that we could learn a huge amount more about the origins of our planet, its Moon, and indeed the whole of our Solar System. A whole lot of other things too. Mostly, because I wonder if it is something like a return to the moon that could be our best hope for saving ourselves and our planet.
We need perspective, to remind ourselves just how tiny, this, our home planet is in a universal context. It is small, fragile, and so very vital to our survival as a species. Yet it seems that we don't value it, or each other anywhere near as much as we should. If we could see our planet from the moon, small enough that you could blot it out with your thumb, perhaps then we may come to realise that we need to start treating it and each other with an appropriate amount of respect and that we have to start sharing it more thoughtfully with all of our fellow inhabitants.
There are many ridiculous arguments about economical effects and the rest. I feel that if there is a plausible risk that we are poisoning the planet sufficiently to make it uninhabitable, then that risk is too much, and we shouldn't be quibbling about the minutiae of it. We should aim to make our world safer and better for all. A renewed space programme could create a lot of jobs, potentially. Both directly and indirectly through technology spin offs. I would argue that it is possibly more cost effective than baling out investment banks that should be allowed to fail. In addition, nowadays you could get a lot more buy-in from commercial interests without necessarily jeopardising the scientific worth of the missions.
Fact is, if we let the planet die by our actions or inaction, there will be no "standard of living", no industry, no economy - there will be no human race to create or need them.
Sunday, 7 July 2013
Mibbes aye, mibbes naw...
I am genuinely undecided on which way I will vote when it comes around. I am proud to be Scottish, but have no real problem with being British and am proud of the things that Scots and people from the other British nations have achieved over the years.
Nationalism troubles me deeply however - far too many terrible things have been done "In the name of a piece of dirt, For a change of accent, Or the color of your shirt" to quote Rush's song "Territories" - which pretty much echoes my feelings on the topic. I try to judge people (if I need to) based solely on the person that they are - where they happen to have been born is irrelevant.
However, my real issue with the current Independence "debate" is not anything to do with Nationalism. It is simply that I have seen nothing yet that can be reasonably described as debate. Childish yah-boo yeah-but-no-but squabbling, yes, reasoned, adult debate, no.
All of it seems to be "if you vote yes, we'll do..." followed by something great that they probably can't guarantee that they will be able to carry out. Or "If you vote no, then maybe..." followed by some dire apocalyptic consequence. Neither side seems to be able to back these statements with anything even resembling hard facts. Surely someone, somewhere is able to provide us with actual, definite answers to these sort of questions? What we really need, I think is an independent (irony, we do that, yes!) assessment of the key issues, so that we can make a realistic and informed decision as to which box we want to check.
Maybe we could even extend real, grown up, sensible debate into the rest of politics too? Nah, it'll never happen...
Saturday, 22 June 2013
Just a Spanish Minute...
While we were there, we headed off on a day trip to the Alhambra in Granada for our token bit of culture. And it is indeed a stunning icon of the medieval Moorish culture of Southern Spain. Our guide pointed out a feature of it's decoration that got me thinking a wee bit (oh no not again, I hear you cry!) The outside of the Alhambra is quite plain, but the inside is beautifully decorated with intricate designs - as our guide put it, they "kept it to themselves"...
It made me think about how much is to be gained from sharing our creations - be they arts, scientific discoveries or even just daft blogs by depressive weirdos! The thing is, I suppose, that you don't know what other people will gain from or do with what is shared - in work, for instance you can share something that you have learned and save your colleagues from having to discover it themselves. Another way that I have seen this bear fruit is by sharing our experiences with Christopher, we have hopefully given other TOF parents, who are earlier in their journey, some idea of what they can expect. I know that we have gained from the experiences of others.
I suppose that there is a risk sometimes of "oversharing" or perhaps becoming self-obsessed (which seems to be quite common these days) but I think if you can foster a sensible "interrnal editor" and a reasonable degree of self-awareness, hopefully you can realise what to share and when to have as positive effect as you can. (Or you can put it in a blog that people can read or ignore as they see fit!)
The "Spanish Minute" idea is another thing that I encountered on holiday - it is like a less extreme version of "manana"- as in "the show will start in 5 minutes... 5 Spanish minutes, that is". I remain unsure of the exact correlation between "Spanish" and "normal" minutes but I am pretty sure that it is always a ratio greater than one!
Saturday, 1 June 2013
Skin Deep
I am talking about the fiendish scourge that is eczema - the demon itch that can drive even the most disciplined soul to scratch themselves in a frenzy. I, myself have suffered from skin complaints, as has Freya - we both know the impossibility of resisting the urge to tear at your own skin until you bleed in an ultimately futile attempt to make that damned itch do away. So it is difficult for us to tell Christopher to stop scratching, though we must.
It is also difficult to come into his room at some obscure hour of the night, half asleep and nerves shattered by the howling that has woken us, to find him writhing about on his bed, crying unconsolably and feverishly scratching at himself, often with blood all over his legs. We seem to have every lotion, potion, cream and ointment that exists from the simple emollients to the fierce steroid creams and the positively vile icthopaste bandages. Many nights he goes to bed bandaged neck to ankle, looking like an extra from a b-movie. It is no joking matter, though we try to make light of it for him.
The hardest thing though, is hearing him say "I want to give my body to someone else" or "I don;t like my skin, daddy". These are not the sort of things that you want to hear from anyone, least of all a four year old. Once, the blood is cleaned away, the creams and bandages applied, and the tears have been soothed away - something that Freya has a particular genius for - then Christopher starts to reassert himself over his skin, and he talks about how he doesn't like the creams, but he knows that they help his skin.
I am weak compared to my boy, but his strength of character lends me strength - coffee will push the tiredness away long enough to get the working day over - but my beautiful family are my true love in this world. "Beauty is only skin deep" they say, but Christopher, to me, is beautiful to the core.
Tuesday, 21 May 2013
A modest man...
I have long had my own little theory (which I may have unconsciously plagiarised from somewhere, I really don't know) that we all spend our youth "growing up" and becoming more and more convinced that we know everything, only, if we are fortunate, to spend our adult years learning just how wrong we were. Perhaps we reach a stage where we doubt everything and know nothing... I don't have a problem with that.
Doubt is good.
Questions and the journey to try to answer them, which inevitably leads to more questions - unless you are intellectually moribund perhaps - is the joy of life in my view. And I know that I have been at stages where I have reached that point of mental rigor mortis - the darkest times, the most terrifying places in my mental landscape. Slowly, though, the way back from there has become apparent and I have gradually freed the rusted gears in the me machine, I know that I am not as mentally agile as I was back in the day, when I managed to persuade a certain seaside academic institution that I deserved a receipt for the mental effort that I had spent there.
Now though, that thought doesn't bother me as much as it did, because I have got my hunger and curiosity back, along with the humility (I hope) to realise that I can learn from anyone that I meet. Particularly from a certain small boy who, like all of his kind can reflect our conceits and self-deceit and show us how ridiculous we are sometimes.
I think that we need to recover some of our childlike qualities, stop trying to be so smart and so full of our own importance - and find as much as we can to be modest about
Thursday, 16 May 2013
Six words to drive you mad(der)...
Wednesday, 8 May 2013
Was that summer that just happened?
There is, however one particular flower (if it is truly a flower - I don't know, or much care for that matter) that I do love to see - cherry blossom. I think that there are few things more beautiful in nature than a flowering cherry tree in full bloom. I still intend to replace the poster of one of Van Gogh's studies of cherry blossom that I acquired in Amsterdam, then foolishly neglected until it was too trashed to frame.
I got to thinking about this because I noticed the first blossom emerging on the tree that is a few feet from the door of Christopher's nursery. It has evidently been conned into coming out of hiding by the random day or two of sunshine that our wondrous Scottish weather has decided to throw at us, no doubt to pull the rug out from under our over-optimistically sandal-clad feet by then hitting us with a couple weeks of rain/hail/snow/plague of frogs more befitting a Scottish May. I think though, joking(!) aside, that this is a clue to one of the reasons that I think I like it so much - it is a sign of impending (slightly) better weather. Which is generally a good thing for my (and everyone else's) mood, coming from the darkness of winter into lighter mornings and longer evenings that make life that little bit better.
On a related note, I was interested to see research (done in Edinburgh) that suggests that the health benefits from exposure to sunshine (decreased likelihood of heart attacks and strokes, it seems) may well outweigh the elevated risks (but still quite low in Scotland) of skin cancer. Particularly if you manage to avoid getting burnt - everything in moderation I suppose. Though it is quite hard to get sunshine in anything other than moderation here!
So let us rejoice in the "cherry blossom in the market square", and try to forget how soon we'll be back to "dancing in stilettos in the snow"...
Thursday, 2 May 2013
A Mistaken Perception...
I can see that in many cases, it seems to be one parent denying the other "possession" of the children as part of a divorce/break up. Obviously, these people are not functioning quite "normally", but the bit that confuses me most is where they get the idea that they are in whole or in part the "owners" of their children? This is certainly not the way that I think of parenthood (though I in no way claim to be an expert).
My view is that we, as parents, are merely caretakers of our children - bringing them into being, feeding, protecting and educating them and guiding them to adulthood to make their own contribution to the world. They owe us nothing, other than perhaps a little gratitude and maybe respect (assuming we have earned it) and they are in no way our possessions. I have seen my son on the boundary between life and death - at one point with a heart rate of 253 - and have had to make decisions (no-brainers really) such as signing consent forms for surgery, that no parent would want to have to make, but it is not my decision to end that life or anyone else's. His life is his own, and always should be.
This brings me to another thing that I have encountered in news stories recently that I find difficult to handle. I am an Atheist. I am very happy with that and feel more at ease with that aspect of my life now than I ever have. However, I have no real issue with people having religious beliefs. I can't really understand how they rationalise them, but fair play to them. There is a definite line in the sand, though. I think that where religious belief starts to require the suffering of others then it loses validity for me.
An example of this is the stories that I have seen where religious parents (often, it would seem, American) have failed to get their children proper medical care, preferring to rely on prayer and ultimately resulting in the death of the child ("God's Will" my arse). This is, in my eyes, one of the grossest types of dereliction of the most important duty of parenthood - to protect your child to the limit of your abilities. Any god who wants your child to die is worthless in my view.
I have decided (partly inspired by an interview with Neil Peart that I read recently, though mainly through years of contemplation of such things) that I can see only one rule I need (laws of the land notwithstanding) and the best way that I can think of to formulate it is "Wherever you can, lessen suffering".
Sunday, 21 April 2013
Three travellers, Men of Willowdale...
I have never really rated the opinion of music critics - they largely seem to be bitter wannabe musicians with an axe to grind and a desire to like the "right" bands and to brainwash the gullible would be hipsters into toeing the party line. The NME is a classic case in point - pretty much the British equivalent of the "Rolling Stone", and a prime exponent of the vile "build 'em up yo knock 'em down" culture prevalent in so much of British journalism. They infamously described Rush as "Nazi Fascists" - which is surely particularly hurtful given that Geddy Lee's parents survived the Nazi Death Camps in WWII. Think of that and listen to "Red Sector A" again...
I don't care if people like Rush or not. Equally, I don't mind if other people do like them - I am not (or at least try not to be) an elitist. I would rather like it if people gave them a chance and due credit for being a talented, innovative, hard-working and influential band. Their music has spoken to me and many others) more than anyone else's, often describing the "view from the suburbs" - a middle class geek's view of the world. "Subdivisions" and indeed many of the songs from the album "Signals" deals with this sort of theme.
They are also an excellent live band who are never anything other than well-rehearsed and respectful of their audience - something that certain other Canadian artists could do well to learn. They are now members of a club that they never really cared for, but they recognised that many of their fans cared and when inducted had the decency to turn up and thank the people whose opinions do matter to them. Now it's back to the real business for them - see you in Glasgow on May 30th, guys!
Monday, 15 April 2013
A Hielan' Laddie...
My Uncle Iain also wore it by choice, though in circumstances as far removed from a wedding as you can get. He wore it as a member of the Black Watch, having (if I recall the family stories correctly) lied about his age to join up. He then volunteered to join the Parachute Regiment, which was then in its infancy. Just over 70 years ago (28th March, 1943), he was killed in action in Tunisia.
I am glad that I have never had to join the Forces - with absolutely no disrespect to those who have - I really do not think that I am made of the right stuff for it, for a start. I am not a brave man. Then again, I have read many stories of ordinary people who did extraordinary things in extraordinary times - perhaps I could have measured up. I doubt it, but perhaps. I am glad that my Uncle, and many thousands of others did, but deeply saddened that they had to. And, because they did, I am free to choose to not join up, free to choose to wear the Black Watch tartan, and free to hope that my son will know a better world than even I have...
http://twgpp.org/information.php?id=2634521