Showing posts with label vitamin C. Show all posts
Showing posts with label vitamin C. Show all posts

Tuesday, 14 February 2012

Dickens, vitamin D & Prof B

Probably a jailable offence but I'm not a huge Dickens fan, I still recall having to read Martin Chuzzlewit at uni, it ruined my Easter holidays. Of course, he has great characters, the names stay in your head, Mr Pecksniff, Magwitch, Miss Havisham (and we've all had our Miss Havisham moments), but given the choice, I would not choose Dickens (though I know I am probably missing out). And I have failed spectacularly (again) to finish The Hare with Amber Eyes, meant to at weekend (started it Jan 2011). I have however started Dirt Music by Tim Winton on my Kindle. Still getting used to Kindle, and though I can now see the point, when I see someone on  the bus reading one I get annoyed, it still feels they are showing off a bit. Am at page 55 of the paperback of Eric-Emmanuel Schmitt's Lorsque j'étais une oeuvre d'art, it reminds me of Candide, the absurdity. And I downloaded his Oscar et la dame rose onto Kindle. So I'm still primarily a reader of paper  books but am slowly nudging myself into the e-zone.

I've stopped blogging about ME for the time being but this is an interesting article about vitamin D and Scottish ill health due to lack of sun. I am going to start taking a supplement of D, I already take 1 gram of C daily.

*update Just saw this news about Prof Behan. He is to become a patron of MEA.


Thursday, 26 May 2011

Narratives of illness

I've been thinking recently about what books I read when I first got ill. I didn't read about illness, I simply read what I was already reading: novels. I struggled to read French, my huge dictionary clunked beside me in bed, I was trying to hang onto myself, the person I was. I never finished Voyage au bout de la nuit, it's still on my shelves. I persevered and persevered with Midnight's Children. My copy is yellowed now and I cannot open it or smell it without remembering being very ill. And yet it's one of my favourite books.

The only book on ME I had was Dr Melvin Ramsay's slim The Saga of Royal Free Disease (1986) - it is still my bible. I had a couple of 'self-help' books by Drs Anne MacIntyre and Charles Shepherd, but that was not 'til the early nineties - I can't recall exactly (I gave one to a boyfriend, I still have one on my shelf). It was in the nineties that I actually read most illness books, a good few years after getting ill. I borrowed  from an American friend (and still have it, I'm a bad person) Norman Cousins' Anatomy of an Illness (1979) - he used intravenous vitamin C, a treatment I'd also tried with positive results. In a more spiritual phase, I bought a book called The Alchemy of Illness (1993) by Kat Duff. My brother sent me Osler's Web (1996), which I still dip into and refer to. And I still love and dip into Susan Sontag's Illness as Metaphor (1978) - who doesn't?

These days, when diagnosed with an illness - any illness - you have a treasure chest of books to try - self-help and memoir - not to mention the stories, some gems, that the internet can unearth. Naturally, you devour this information, you need to know exactly what has punched into your life, derailed you. You are sustained by others' narratives. You need reassurance; you need confirmation (certainly in the case of ME, so great has our fear been of not being believed). Of course, the quality of all of these shared narratives - online and off - varies greatly. There have been one or two ME 'self-help' books I couldn't get to the charity shop quickly enough.

The misery/illness memoir really took off in mid-late nineties and by the time I was writing about my own illness the genre had - in my opinion - been done to death so I veered as far away from it as I could. This did not stop some editors from trying to pigeonhole my novel as 'sicklit'.

There are, I think, many more works of fiction on mental illness than physical illness. Perhaps mentally ill characters are seen as more interesting, they are more likely to behave 'badly' (if you are physically ill for a long time you are dull and boring, not taking part. Or you die.). I did read Helen Garner's novel The Spare Room (2008) - about friendship and cancer - I enjoyed it but didn't think it lived up to the hype (the ill character also has intravenous vitamin C, and she is definitely not dull).

Now, when I read about illness (non-fiction), I want to read about other things, not just the illness. Last year, I loved Elisabeth Tova Bailey's The Sound of a Wild Snail Eating, it is very much about other things. And I'm currently reading The Vagabond's Breakfast by Richard Gwyn, I saw Me and My Big Mouth review it. I don't always share Scott's taste in books - he hates Midnight's Children! - but I'm very much enjoying this. It is about other things.

And the writing has to engage me, always the writing.

What I am trying to say  is that when you are  ill in a life-changing way - and you have stopped being stunned by the event - you will probably hunger for illness narratives; but, later, you simply don't need or want them (unless they stretch out beyond the illness and tell you about the world). I know that people who are not ill will see things differently. The world of illness is new to them, unusual and strange.

***A lovely quote from Kat Duff, which I just found underlined in green pen (can't help wondering how long ago I did this and why green pen): ... Frankly, from the point of view of illness, healthy people seem ridiculous, even a touch dangerous, in their blinded busyness, marching like soldiers to the drumbeat of duty and desire.

Thursday, 8 June 2006

Too Much Babbling

I can hardly listen to the radio because it's all just babbling and makes me crazy. A few days ago I turned on to hear a woman who'd had ME for four years saying she is completely cured after having lightning therapy. She has thrown away her wheelchair and cancelled her disability benefit. I am happy for her that she has recovered more or less instantly from whatever was wrong with her, but I just can't listen to this bullshit . . . you wouldn't attempt to cure MS or lupis with life coaching and NLP, so please stop peddling all this nonsense and giving false hope to people who are horribly ill! The lightning therapists concede that ME is physical, claiming we are stuck in an adrenaline loop of 'fight or flight' and that this is what is making us ill - and by retraining the way we think, we can stop the loop, and lo and behold, mow the lawn and climb a mountain. I agree that our adrenaline production is fucked (I am easily alarmed, constantly feel on red alert), and that conventional medicine still has nothing to offer, and that complimentary therapies can sometimes help alleviate symptoms (intravenous vitamin C helped me through a horrible spell), but talking about negative thought patterns to some well-meaning therapist is NOT going to cure you of ME. Over twenty years I've had a plasma exhange with steroid therapy (made me more ill than ever), anti-viral drugs, ACTH injections (they helped a bit), and God knows how many complimentary treatments, but the reality is, nothing yet shifts this illness, you can have remissions, your symptoms can vary wildly day to day, week to week, but in my experience, the illness dictates, always. They have uncovered an ME gene at Glasgow University, that sounds promising, that is honest research that could lead to a cure, it is worth media attention. But lightning therapy, fuck that for a game of soldiers, as we say in Scotland when something displeases us. (But having said all this, I do understand that people will try anything that might help them.)

© 2006 NMJ