July 29th 2018 – Evening

I lost my beautiful, talented, funny wife today.

She was the love of my life, my reason for living, my inspiration and my soul mate and I am utterly bereft. I don’t think Facebook is really the place to lay your broken heart on the line but I seem to have somehow got myself to this place and I need to let many of you know what has happened, so here I am.

I thank you for all those who have contacted me already; the level of compassion for someone many of you have never met is utterly overwhelming.

Give your loved one an extra hug tonight OK? Because when they go it is pain like you can’t imagine.

July 29th 2018 – Early Morning

I’m at an age, and been in the industry that created this social media monster for so long, that I think I’ve lost touch with what is right and wrong here but, somehow, as an alter-ego I’ve managed to drag my real world and real people into my fiction. I never intended this.

As a result, as well as real-life friends, I also meet here on this page with old friends and work colleagues – people who in another age I may have lost touch with – and also many ‘friends’ I’ve only met once and, staggeringly, some I’ve never met at all. All are now involved in my thoughts and life dramas.

As such, I’ve alluded to the ‘fictional’ Lady B, in reality the love of my life, my gorgeous, beautiful and talented wife Gail, being ill and referenced her ‘battling’ and being in hospital without really explaining anything as I thought it too …what? intrusive? Then why mention it at all, you may ask. A question I’m struggling to answer here right now.

The fact is, at this very moment in my real world, Gail has been moved to Addenbrooke Hospital in Cambridge, is seriously ill and in intensive care. Those who can or want too, feel free to message, call me or email me if you want to know more. I thank you for your thoughts, prayers and kindness and I hope to be back – perhaps – with better news.

I have a lot of trouble with what I wrote that morning and it haunts me still nearly 20 months later. For reasons which I can’t fully explain; reasons I have been to counselling for but still not resolved. I took time to write the above and post it before I left for Addenbrooke’s hospital on the morning of July 29th 2018. Had I not written it I may have got to the hospital in time to be with Gail at the end. But I didn’t.

I could tell you that I’d had ‘get here now’ calls before and Gail had pulled through. I could mention the comforting message from the Doctor who spoke to me as I left the hospital on the previous evening. I could tell you that years and years of battling Lupus alongside Gail  sometimes made me feel (and I know this is terribly wrong but anyone who has lived with a loved one is ill all the time will understand) that I had the illness myself and I was exhausted physically and mentally. But all that means nothing.

All I know is that I got a call from the hospital prior to Gail going into intensive care and I could have left home then, and then I got the second call to come in before which I felt the need to post a message. My inability to be there at the end is to be a recurring theme for me, but knowing I posted a blog before I left to see Gail is a source of incredulity and shame for me.    

Starting Over

To start Sign Your Name, I’ve posted each of the significant days that I logged on Facebook starting with Gail’s last day: July 29th 2018.

To put these posts in a proper chronological order, I’ve had to date this entry before she passed but, of course, in reality it was written in 2019.

Original posts taken from social media are denoted by italics. If I’ve wanted to explain something further or add comments then these are in standard font. After working on this for six months, I launched the site proper on the first anniversary of Gail’s passing. I can’t feel I can do anything else for her that will mean so much.

When I’ve caught up with what I feel are the relevant social media posts – I feel they are significant in that they reflected my moods and feelings at the time – I’ll spend some more time on grief and what I’ve learned about it.

Be aware though, this blog has no answers. As I keep getting told ‘Everyone is different’. It’s just that I found aspects that no-one told me about and no-one seemed to understand. All I want to do is document how I felt – I hate the word ‘journey’ in this context but insert it here if you wish – create a blog to honour Gail and have something to refer too if anyone asks.

This could quite easily become a blog about healthcare and the strains on the NHS but I’ll try to avoid that and just say that Gail suffered from SLE – System Lupus Erythematosus – better known as Lupus; an evil auto-immune disease for which there is no cure, in which the body fights itself thinking it has diseases it hasn’t got. I’ve written an article or two on it and I may point you in the direction of that later but, for the time being, let’s just say Gail was in constant pain but bore it with an incredible stoicism that I could only marvel at.

Part of Lupus is that it attacks various organs at will and one of the common ailments is a ‘fatty liver’. This is the liver of a heavy drinker and one with which the person having that liver had probably better stay away from alcohol. Gail didn’t. It was part of her personality to be the life and soul. She was vibrant, attractive, fun to be around and seemed to dance in a spotlight that was permanently on her.

She did – as they say – ‘like a drink’. Not in a way that would mean she came home in a wheelbarrow at 3am – she never did anything like that – nor was she ever out of control and stupid. But she might have two when I’d have one. We talked about it, of course, but she was determined to live her life to the full, aware that she had been diagnosed having ‘very low prospects for a long life’ when she was still in her 20’s. She was 56 in July 2018.

Ultimately though, Lupus attacked her liver badly in late 2017 and she was diagnosed with Cirrhosis or End Stage Liver Disease in spring of the following year. It’s then you find the person who was so desperate to live life on their own terms suddenly wants it to go on a bit longer. She’d had spells before where she’d just stop drinking – hardly the actions of an alcoholic I’d suggest – but she stopped completely in the autumn of 2017. Gail was fighting hard throughout the summer and it says much for her spirit and determination that, although she was unwell, the end came as a shock for me and also, it was confirmed later, the Doctors.

When I left her on the evening of Saturday 28th, I stopped off to speak to a Doctor and ask how she was doing. “She’s very ill, of course, but we just need to balance things and get her stable, then we can get on with improving her health”. “We’ll get there” he called out as I closed the door. It was likely had she survived this she would have had a liver transplant as the hospital were happy that she wasn’t an alcoholic, had given up when needed and could lead a normal life with a new liver.

I didn’t get to the hospital in time the following morning. I’d had the ‘You might want to get here’ call but, unfortunately, my local hospital where she’d been for the previous month, just five minutes drive away, had transferred her to Addenbrooke’s in Cambridge on the previous afternoon. Cambridge was an hour’s plus drive.

I have a reputation for never being on time. I even missed my wife’s death.