Friday 22 July 2016

Intelligence is in the Eye of the Beholder

Intelligence is in the Eye of the Beholder

In 2011 a group of master weavers showed their Emperors of Parliament the cloth they had made for the NHS and NICE called Cognitive Behavioural Therapy - a mind over body approach.

They warned however that you must be intelligent, that you must believe, but most of all you must not test the cloth they had so expertly weaved and they themselves had tested, the results of which you would not understand, you vexatious lot.

So it came about that all who had been diagnosed from then ME to the now CFS were treated as though they were of a lowly intellectual ability, and were told their bodies could cope with normal activity, as it were their feeble minds that were incapable of life. All but a few questioned the master weavers, and looked on at the now barefaced authority with puzzlement. Those few that questioned; though with exemplary intelligence and world leaders in all that is right and true were told they did not believe because they did not possess all those qualities to see the cloth, you have to trust the master weavers!

How the master weavers told stories of madness, depravity and deconditioning of the body and how the few nonbelievers in the cloth were ridiculed for listening to the poor people that told of their physical suffering. How the courts threw out any suggestion the Emperors could be hoodwinked, while sitting barefaced in the cloth themselves. They would not listen to the evidence before them, they wanted to show how they held the allegiance to the emperors, and the emperors basked in the light of intelligence of the mind controlling the body. They banished the truth tellers and stripped them of their authority.

The master weavers bullied, cajoled and groomed the suffering masses into believing their suffering was in their hands, and as their dysfunctional bodies gave out, the master weavers ran away to hide shouting as they ran, it was a miss understanding, that their meaning had been twisted and that the unruly mob was baying for their blood. Silly master weavers, that so called unruly mob only asked for the truth behind the none existent cloth you wove, and for you to understand what recovery meant - getting back your health, as it has always been and forevermore mean!

The little ripples of giggles started to be heard, and the truth behind the cloth was seen for what it was; red faced a mass hysteria that began to grow through the master weavers looms. Would all those fed faces ever recover from hysterical claptrap the master weavers spun?


It seems sadly unbelievable but most silly stories are based on fact and I wonder how many children are miss diagnosed as my son was with CFS/somation disorder? No numbers are kept of children harmed by the NICE guidelines for treatment of ME. It seems the so called leading paediatric Doctor is under the influence of the master weavers and does not truly understand the workings of the Autoimmune system. ME is not in the family history of mental health it is in the bodies whole system  that lets the mind down! So SMILE and MAGENTA trials are a waste of charities time and funds! These two trials should show their full findings to all that ask, but are hidden under a veil of all in the mothers heads! But truth does not seem to account for much these days of fairy-tales and madness.

Our doctors can only treat if they are taught how to heal and treatments are tried, tested and robust enough for scrutiny by other academics and the patients themselves have the last word, for we are all individuals. I would suggest patients should be taken seriously; as how many illnesses have been forged as the patients depravity of understanding and hysteria to find that in the truth of reality, they are the body’s defences in overdrive?



No one belittles how complex the body is or how difficult being a doctor is, but I do wish doctors would stop belittling their patient’s agony. Dr Ramsay in 1986 gave sound diagnosis of ME why then did we believe in the invisible and nu-provable "mind body continuum"?

Wednesday 20 July 2016

Intensive Training When You Have ME

Intensive Training When You Have ME


Even with the intensive training and grit determination Angus never made it to his last day of primary school. He had two nosebleeds and yet another infection.

It would have been nice if the school had accommodated my suggestion that he came to the last 10 minutes of school, but schools have rules and I am too busy fighting every system that is supposed to support my son to argue. Life is not fair and people are busy ticking boxes with no real understanding of the true situation and if there is one lesson my son has truly learnt is that!

My son had been on intensive training for months and months for a big event in his life! Music on the Green in Stowupland! It is a simple village event that most would take for granted and think nothing of just ambling along to and having a pleasant walk around. Simply enjoying playing a few games, talking to friends and would just be part of the rich tapestry of life. For someone with a chronic condition, it takes planning and determination on an epic scale; that only Olympic athletes would understand. It sound grandiose put that way, but it is exactly how it is with ME.

First he has to get his body in tiptop condition. He has to eat the right diet for his gut flora and fauna to keep the bad toxins out of his system. A lot of food he takes on is because he has to, not because he enjoys eating them. Inevitably the foods he most enjoys are the ones his body becomes sensitive to. Eating no longer becomes a simple pleasure, but a war zone.

Next comes muscle stretching, he can’t move in the normal sense because of the lactic acid his body produces and his unstable and hypermobile joints. But stretching those tight muscles will help ease the day to day pain; well we hope, allow him some comfort when he moves - that’s the plan. Each day we gently go through these small stretches and have to take account of the energy it requires, even though I’m doing most of the work. It sounds absurd I know, but it is fast becoming the world we have to live in as one by one the normal becomes abnormal to his body. Someone with ME produces 20 x the normal lactic acid, so where a normal person can walk for miles before their muscles become tired and feel that familiar lactic burn, people with ME will feel it after a short distance. When they sit to recoup that lactic burn can last for days if not weeks. The acid does untold damage to their connective tissue. This connective tissue damage then affects their internal organs and we are only now beginning to piece it all together.

Car training, because his body has a hard time staying upright, he has to travel in strange positions to elevate the travel sickness he feels; so far he has not found a position that elevates his suffering. His heart does strange palpitations and his rhythm is all over the place and it is the same for his blood pressure. This work horse of the body is like an out of control stallion and runs away with any normality.
With true grit and determination to cope with whatever his body throws at him we made the very short journey to Music on the green. He took control of his excitement as best he could which is not easy when you are 11 and not often out and about.

The first part was held at one o’clock and was a track event of charitable stalls and fairground rides. He won two hammers, a smiley bouncy ball on a string and beanbag in bucket competition, Whoop Whoop! He then rested for four hours on his bed to recover his energy, while his heart rate and blood pressure went back to normal. Then with extreme effort he picked himself up for the big event!
We got there and his friends came to say hello which cheered him on no end bless ya all xxx the heavens opened and cold and wet and bitterly disappointed we went home!!! You can't win everything in life!

We are back in training so that he can attend the last day of primary school! The pain and training will be hard but he is one brave fighter!!

After music on the green he came down with two infections and suffered nose bleeds. Unperturbed we carried on training but a visit to the doctors has put him back yet again. He has suffered nose bleeds and being tested yet again for infections. His body is not recovering in any tangible way at all.

It is one of the hottest days of this year and instead of his normal resting pulse of around 96 he is back to a resting heartbeat of 115. So tomorrow we are faced with a dilemma that we face on a day-to-day basis-that is to say what does he need to do and what state will his body be left in after.


Does he have to go to school? Well I think to say goodbye to a class of children who he has no contact with for the last year is one of those situations that it’s hard to give an answer to, it is the conundrum that ME always puts you in.

25th July 2017

We have to accepted training does not work, nothing allows his body to sustain energy. A year on and even with our best efforts car travel is very difficult. 

I have lost faith in NICE, they are just a front. They refuse to review the guidelines and would rather take the word of research that is both harmful and flawed with vested interests. Even though there are 9000 papers login the damage in the body, there are no random trials so they don't listen? Makes no sense. If it is hard to work out what is happening maybe it is too early for trials? You cannot fix a car if you don't know the problem?

The NHS is just a commercial concern, that turns its back on difficult issues and bullies others.

Angus would love to see his brother off to Australia, but the journey would hold him back so that the beginning of the next school year he will not be ready to have his weekly lesson.

He does not want to make plans for when his brother comes home; because this illness takes all life away from you, disappointment is hard to live with, when it is all you have. But he wants more! More than anything he want to travel to London and go to Harry Potter world with his family. It might as well be outer space to him.

I sit cutting out pictures of a life I once had, for a party we are throwing to wish my eldest son all the best in his placement in Melbourne. I think how to get the best out of the time we have before he leaves. Angus is preparing himself for the fun he has lined up for his brother involving Nurf guns and water bombs and I breath, you have to learn to float with what ever you have, to keep you from sinking.

I have to accept training does not work, and not until we know how the body fails, can we begin to piece back together the energy pack that is need to live.

Until then we are learning to float in a pool of hope and love






Friday 15 July 2016

The Freedom to Work - Yes Please



This short story still in its rough form is dedicated to Nicki  and Cathy and all those that have to chose to suffer in silence.

Freedom To Work
Yes Please!

I’ve been living in this flat now for almost six months, and each and every day I get a quick hello from my neighbour, who then decides to come round for coffee, unannounced, with her cat!

Now for some with the simple freedom of choice and with a “normal ability to live”, they would think this innocuous and what appears to be friendly, neighbourly thing to do, a charitable and much needed contact with the outside world, especially for someone who is chronically ill like me. So do I, well in a way. You see the problem I have is that I don’t have the freedom to walk away. I’m pinned down by a body that can’t. I have to say and be lectured everyday about how working could improve my spirits – I don’t need to be told this, I know this. My mind craves difference and when I give it a go, something pulls the plug on my neurons and I am left with intermittent thinking, of the fuzzy kind, no crystal clear thoughts for me.

She explains how the money would give me the ability to live so that I no longer live in squalor! Yes she actually used the word squalor! As if I am some complete moron who never gave that a thought! What makes it so awful and wretched is that she is right, it is a squalid flat! What can you say to that, how can you defend yourself? You see, each night someone, while I am asleep pumps my body with lead, seriously I’m not kidding! Some days just looking after my own hygiene is all my body can take. Innately I am a very organised and tidy person, squalor makes me depressed.
Anyhow I bet even a saint would lose their patients under this much scrutiny, and believe me I’m no saint, nor would I want to be. I’m more of – live life to the full type of gal, why walk when you can dance, why dance when you can rock?
I’m rocking now, although I’m not entirely sure if I’m rocking to get out of the chair Sam sees me as she walks to work or in pain. I just don’t want to face that encouraging smile this morning; I’m not in the mood! My halo has gone missing! But I’m too late; her face is at the window of my bedroom.

‘Morning Katie, How are you this morning?’
‘I’m fine, and you?’

‘Oh I’m loving the spring, perhaps we can go for a walk when I get home - blow a few cobwebs away, make you feel better?’ I slap a smile on my face and she is gone. I know what I would like to blow away.

‘I don’t want to think how I am Sam!’ I grumble and groan as my body adjust to the upright position. I close my eyes as the dizziness kicks in. It makes it real, and I don’t want my reality to be all there is thank you very much – I want to live in a dream world of fluffy clouds for as long as I can. I look across at the time on my phone, ‘I bet a get a shimmy on, my mum will be around in two hours and I haven’t even brushed my teeth yet!’

As I had feared Sam came round that evening, she promised she was on a flying visit. I know though she is trying to get me out of the house as promised this morning. I told her I was waiting for company so now she is waiting to see who that could be. She sips at the coffee that I have just made her. Which means: I won’t be able to finish the prep for my evening meal – I simply won’t have enough energy to do it now!

Sounds stupid doesn’t it? You can’t explain it to anyone who has no difficulty in moving, their blood flow, breathing, with their energy all being normal. Looking at me I don’t look disabled. I ponder on that thought as the devil cat winds her tail lazily and lovingly around my leg. I tense up, not because I hate cats but because I know what is coming, but I don’t know when. The pounce of the Duchess the devil cat is always unpredictable and unprovoked.
‘I saw you out at lunch time with your mum. That must have been a nice change for you? Made you feel better?’ Duchess devil cat jumped upon my legs and purred comforting soft velvet purrs the kind that makes you sleepy. Her warm soft fur comforted my knee joints and a connection was made between animal and human.

‘Yep’ I false smile into my hot chocolate, no point telling the truth. I remember my mum’s face when she took the full force of abuse hurled at her this morning. You see I have a disability badge; it took two years to get it! Even though I am house bound, I still have to go to see the GP, and there is no parking nearby, and the journey alone will make me so sick it will render me bed bound for the next week or more, apparently I still did not constitute a badge! I refuse to use the wheelchair, so it makes it worse. You see the whole process of getting the badge and Department Work and Pensions forms and interviews; they insisted I attended, not only put my health in jeopardy but made me feel worthless.

The process of losing all your function after you do any daily living, is innocuously called Post Exertional Malaise; PEM for short. It is more a kin to having a heart attack or stroke though; as my body closes down to conserve the precious oxygen my body craves. Because my brain is constantly starved of oxygen when I over do things. My body just cannot utilise oxygen or energy, every system in my body is compromised. It is a hard concept to get your mind around. My mum has been a rock for me and she has got her head around it, but we are all allowed to lose it from time to time, my mum lost it big time today.

‘Where did you go?’ Sam asked. I didn’t want to say disability aids, so I lied.
‘We fancied getting so good underwear but we were naughty and brought the most glamorous frilly knickers’. I wish my life could cope with frilly knickers I privately thought. ‘We are fed up with the Polk Dot bloomers we normally get’. She had to gulp down the coffee; she had been daintily and slowly sipping! I lowered my eyes as I smugly smiled into my hot chocolate.

My mum’s beleaguered face haunts me, her frustration hurts me. I had just finished my degree you see when I was struck down with a virus that left me this way; I was diagnosed with Chronic Fatigue Syndrome, the most hated condition of modern time, with I have to say the most stupid and misleading name. Fatigue, everyone has fatigue and I wish it was just a case of fatigue.

My mum was so so proud of me at my graduation; all those struggles to get me through Uni were worth it she told me. My job was to die for, and I would have if my body had let me. We value ability is highly prised; I have no ability, so I am worthless? Today for the first time I felt worthless to my mum. All her dreams had been shattered, they had splintered like a mirror, we only caught glimpses of our former happy self’s. Mum had to give up work to look after me; she lost most of her friends and a life she loved.

Sam drew out of her bag my latest prescription, it was a trial medication and I could see she was itching to ask questions. Sam worked at the Health Centre; she was the softly spoken dragon that refused to help in a helpful manor that mirrors her personality. This job perpetuates her belief that she is a most helpful and understanding person. I’ve seen people staring at her in disbelief at the reception with the comments she comes out with. It makes me smile; I am not the only person she does this to so now I don’t take it so personally.  

‘Would you like to take the cups in the kitchen, I’ve finished my coffee.’ Sam encouraged me to move. I bit my tong but –

‘No that’s Ok Sam, just put it on the coffee table next to you’ Duchess digs her claws in very painfully. As I knocked her off my lap and Sam was about to protest the door opened, and in walked in Peter and his crew followed by Dr Burns.

The suit was amazing, worn under clothes you could not tell you had it on. Even I was impressed with my design and I don’t get impressed with myself very often. The head band was the same and I marvelled at the lightweight and complexity of it all. A small app was transferred to my phone and Sam was bristling with pride that she knew me, which was a first! She was visibly astounded when the whole team congratulated me and said they were in ore of me, considering my disabilities and how much thought had gone into the concept.

‘We have all had a go with it, and boy - were we pleased with the function. Not all of us could cope with wearing it though’ He looked over to Dr Bures. ‘Possibly a couple of tweaks would be needed after someone with a non-biased opinion could be found.
Well what would you do if you were in my position? Would you take full advantage of it, and put your neighbour forward - an ability to get the truth over let alone some well-earned revenge? Well I didn’t have to worry about that, as though by magic with Sam jumped up and offered herself as a guinea pig.

‘Although there is nothing that could compare with what you go through on a day to day basis’ Tom looked at me with such earnest eyes that it made me bloom inside. ‘I think if we did anymore it would be torture for torture sake, and not research practical.’ I have always loved Tom, from our first lecture together. His like a universe of possibilities.
‘Dr Burns was going to take part and as kindly agreed to ask his staff, if they would like to take part in the trial.’ Tom sparked interest in Sam in more ways than one and she took the suit and bristled up to her full height of 5ft nothing, patient high heels, formal skirt and diamanté hairclip in her perfectly plated blond hair, leaning into Tom.

“What a splendid idea Dr Burns”, Sam’s smooth as treacle and sweet as acid voice oozed something like sincerity; which she may later regret. I understand how this illness is.’ Dr Burns looked over to me puzzled. ‘I live next door to Kate; I’ve taken her under my wing’
‘Smother me more like’ I grumpily whispered out of earshot of Sam.
‘I think we should all have a go with the suit, so we can truly understand how it is for these poor people.’ Big mistake lady I thought to myself, as her condescending ways got stuck in my throat so no worlds came out. She had asked no further questions, silly woman.

‘If I try it on now and give it a go, then you can tweak it and the sooner we can start to trial it out’.
‘Splendid beamed Tom.’ I opened and shut my mouth. I should warn her?

Now the thing you must remember of Sam, she has a condition which she equates to every other long term illness since she found out about it. Now, I would not belittle anyone’s condition, but just having one condition does not give you a right to say you understand, or give out the impression you would be able to take on any illness and work through it. You can see my dilemma can’t you? Should I go easy or should I ramp up the ‘muscle cruncher’?

They took great pains in explaining how the suit works, now that she had it on. The electrical currents to simulate the pain, the tightening and how it took impulses from the brain to collect data, how the joints had sensors to show instability and how that affects lactic acid expression, the heaviness of the thin material and how they could control it. She did try to ask how light material can make your bodies limbs feel like lead, but she was no geek and they were off the geek Richter scale. They did explain that they could only cope with 7 on the pain dial app themselves. The dial went up to 14 which is about where they thought my pain was at. I saw a flicker of I’ll show them how it’s done, dance with glee across her face.

Sam was giddy with her own importance, and eager to show everyone including me – probably more me, how she was a trouper and could carry on regardless. They explained with equal puppy dog excitement (that Duchess seemed impervious to) that their aim was to get slowly go up to a 7 while taking notes at each stage.

“It’s just like spandex hold it all up, tuck it all in and give shape underwear” she followed her shape from boobs to hip. Who could blame her with these dishy intellectual types all around you. Sadly for Sam however, her timing was off, they were too engrossed in the app on my phone. All of a sudden she squealed, and went cross eyed. I tried to stop myself from a giggle, but the corners of my mouth curled into a smirk and the giggle bubbled out.

‘Perhaps the inside thigh should be modified?’ I suggested
“What number have you got that on” Dr Burns asked suspiciously. I looked down as I was not too sure myself, they all looked at me clipboards in had for the answer.
‘Two!’ I replied blankly.
‘Two? Are you sure?’ Sam’s eyes were sort of watering. Simon and lead researcher unceremoniously stuck his hand up the sleeve of the suit.

“Yep, it’s a two; crank it up two more, than we will leave it for a while, see how she copes.”
I did as I was told, but instead of the pleasure of showing someone how it feels, I felt and pang of uncertainty as I saw the familiar pain flash over Sam’s face.

“No that’s OK turn it up to the” Another ripple of muscle contraction took the breath away and she held out her hand to steady herself against Simon.

“Just go for a walk hold onto me so your body can adjust to the sensations.” Simon suggested.
We all held on to the childish giggles and comments as Sam walked out of the flat and onto the street like a person constantly hit by a lightning bolt.

They all decided to make a cup of tea while they were out walking and adjusting. We sat drinking and nibbling while talking about the technology and what it would do for the medical staff with their teaching, about other chronic conditions. How it all brings a new dimension to care. They all thought that my idea of being able to process the information gathered by the sweat on how the lactic acid and the heart behaved was - a genius way of gathering and furthering research.

Out of the corner of my eye I could see Sam walk like a cat on hot bricks, the sharp intakes of breath, closing of the eyes and pausing to gain the will to move again.

“Perhaps we should get her out of the suit and make sure it is working properly” I suggested. Perplexed they looked over to me, then out of the window where Sam was teetering in high heels, unsteady and shaking her limbs. Duchess was following looking confused at her mistress, sitting down and looking around and I felt certain I could see the cat’s eyes roll.

Two days later they had the data from Sam’s trial in the suit and they had tweaked it, so that lower settings were incorporated with differing incremental settings for many other conditions and individual tolerance to pain.

Sam had not been round to see me in those two days since she ore the suit, and was frosty towards me as she went to work in the mornings. Today was not a good day for me the PEM had kicked in big time. Tom had been my constant companion. He had said that they had caused the relapse in my condition, the least they could do was support me back until I was better.

They asked Sam to try on the suit again. I could see the horror on her face, but she became my hero when she silently took hold of the suit again. But it was her words that grabbed me the most, when she looked at me in the eyes with determination and grit.


‘I’ll be happy to’ and as she passed me she touched my shoulder and privately stated ‘I have the freedom of taking off the suit, others don’t.They don't have the freedom to work’ She squeezed me just a little and there just right at that second I lost the ability to fly on a dream cloud, as a reality sunk in, but I gained another hero and a true friend!