CHILDREN AND THE SUN ANCON CHI MACHINE
This weekend my Grandchildren have said they will help me make a video about the Sun Ancon Chi Machine. They have both had use of one for a few years. My Granddaughter who is 4 was introduced to it when Mum was pregnant. Not only did it help my Daughter who had SPD but it also put the baby to sleep when she was restless. Mum also used to use the Chi machine halfway through the night to get my Granddaughter back to sleep again.
My Grandson is now 8 but I remember him being desperate to try it when he was younger. I had said when he was 4 he could use it so a few days after his 4th birthday he came to the shop I was working in. The room had a wonderful light that changed colours and sheets looking like sails draping down from the ceiling. Funnily enough this has now been replicated in my own therapy room. He was so taken by the lights changing colour that he did not want to lie down for more than 30 seconds and kept raising his head to look in awe at all the colours in the room. The good news is after this he learned to stay still for more than a few seconds and uses it now when he has a headache or a tummy ache.
My Granddaughter was so eager to use the Sun Ancon Chi machine that she used to watch Mum and Brother on it and as soon as mum switched it off she would lie down and make her body move in the same way as when the electricity was switched on. The ways it makes the body move is like a figure of eight so this used to keep us very amused. As soon as she too turned 4 she was able to use it with the machine actually doing the work for her.
To see the faces of the two of them when the Chi machine switches off is fun. Unlike adults they find it really hard to be quiet and enjoy the sensation and instead we get bombarded with words of how they are feeling and usually a lot of laughter too. Don’t you just love children!
The Sun Ancon Chi machine can help with so many health issues or just to help people relax and chill out. If you want any more information about it to find out if it may be able to help either you or someone you know please feel free to contact me for further information. Contact me.
I will upload the video to my Facebook page. Please feel free to like it.
I woke up thinking about gratitude today. I especially wanted to think about some of my life experiences that had not been so good and why I should be grateful for them.
I grew up in a house where my Mother was often ill. I then found out how great my extended family were for taking care of me each time I went to live with them . This also involved going between 2 schools for a while so I had to learn to fit in with each schools way of learning. This meant accepting each time that I was moving up or down a class too as the teaching methods were so different.
I got married too young and had a problem marriage but gained 2 wonderful children from it and now my beautiful Grandchildren. I learned a lot about tolerance and patience through this period in my life and how to make ends meet on a low budget.
I suffered from serious Back problems then found Reiki and the Chi machine to help and inspire me. I am now a much more positive person than I was before. Through both of them I have been able to move on with my life and also help others who have health issues. I have also been able to use these therapies to raise money for various charities.
I had a leaking roof for years that various companies could not correct. Eventually when this was sorted a friend built me a Therapy room in this space which is awesome and was a great surprise for me.
Do you see the similarities? Out of each negative event in my life something really positive came out of it. I have also learned on the way to have respect for others and to accept what cannot be changed but also to help change what is not acceptable.
What happens in life shapes the way we will grow. We can learn from it and improve our life or we can get stuck in the “Poor me” situation. Which direction have you taken? If it is the wrong one there is still time to change your life for the better.
If you want to check out my latest or any of my aticles that I have been writing this year you will find them here http://ezinearticles.com/?expert=Joy_Fraser
This is my latest one
Developing Superior Confidence - How to Raise Your Self Esteem
By Joy Fraser
I visited a friend a few days ago who had the most gorgeous 8 week old puppy. She had only been home a few days and will build her self-confidence as she grows. I really wanted to take her home as all she wanted to do was curl up and sleep. The pup has been found to have a problem with her leg which may cause her problems as she grows older. She is lucky to live in a loving home where this was spotted quickly and with the right training she will grow to be a beautiful confident dog. It made me think that we are not all perfect but still lovable. The problem is do we know it?
Most of us have something in our lives that we are not happy with. I know I would love to lose some weight and gain enough money to have a stress free life and be able to help others more (although some stress is good for us all). Too many times in life we are looked at only from the outside by others. This can often make us feel negative about ourselves. The most important thing for us all though is to look within. What should really matter is what is inside us and how we feel -not what others want us to believe about ourselves. We all have love to share with others but do we love ourselves? We are the most important person in our life we should learn to love ourselves first to allow us to appreciate others more fully as well.
Low self-esteem can be a problem that many people have. This may be due to how they were brought up or relationships that may have gone wrong when they were younger. They may have been bullied at school because they were overweight or shy and did not make friends easily. If no one helped them through this minefield it may have continued into their adult life.
The good news if you are stuck in a negative feeling about yourself is you CAN change. Nowadays there are so many Life coaches available to listen to on the Internet that it does not even have to cost you any money. One of the people I love to listen to is. YouTube is full of his motivational videos. If any of the above rings true for you NOW is the time to take control to change whatever situation you are in to a positive one.
I chose Reiki without knowing how much it would change my life. I now feel the world is my oyster and I am stronger and more positive than before. For each of us there is a way forward and we owe it to ourselves to find the correct solution to help us change to make our lives more positive. There are many clubs nowadays for people who enjoy all different interests whether it is social, sporty or crafty. A well rounded club that I know of is Spice UK which covers all over the country. Check it out and see if it could fit into your life.
Whatever choice you make take the action now and watch your life become positive and fun. Check out the internet and find things that interest you because now is the time to build your self-confidence and enjoy the rest of your life.
Synchronicity and the Universe
A few nights ago I had been writing an article on Synchronicity. I will add a link here shortly. A few days before I had decided I wanted to make some short videos about the Sun Ancon Chi machine as I think it's awesome. I feel it's my duty to spread the word as it can help so many health issues. This week when everybody around (including me) has been getting headaches due to the weather it has come into it's own. If I wake up with a headache 10 minutes on the machine and it's gone.
The synchronicity continued on the same evening. I had been befriended a few days before by someone on Facebook and that evening he sent me an invite to a webinar on making videos. It was very interesting and gave me lots of info to get started. The very next morning I received information for a course I was about to take part in that I needed a video of myself before I started. Talk about getting the message loud and clear!
I have found more and more this year that often when I think of something the answer comes up a few days later. It can be as simple as needing x £'s and then finding that overtime suddenly comes available and I can earn the same amount.
One thing has certainly become clear-the Universe is listening. It's really important to put out positive thoughts. Don't say " I have no.... " Instead imagine that you are doing what you want to do and that whatever is needed will come in at the right time. If all you put out is that you have no money, bad health, no relationships etc then this will continue to be attracted to you. Instead whenever one of these thoughts enter your head change it to a thought that you are now at the place you are meant to be and only positives things will come your way from now on. One thing to be aware of is sometimes things happen in our life that seem negative but often when you look back on that time you will see that it taught you something that you took onboard and it changed things in your life for the better.
We all go through life learning as we grow. On looking back my life started to change when I took up Reiki but in 2012 synchronicity is speeding up!
If you would like to follow me on Facebook you can find me here. https://www.facebook.com/peaceharmonyandjoy
Following on from my posting this morning I was led to this great piece of writing by Sonia Pouton's Blog in the Daily Mail which I thought I would share with you all.
THIS week is Myalgic Encephalomyelitis Awareness Week or, as it's more accessibly referred to these days: M.E. That may not mean a great deal to you. Certainly, it didn't to me.
Oh wait, yes it did.
Based on no personal knowledge whatsoever - fortunately neither I or my loved ones have M.E. - my judgement was gleaned from how the world has portrayed the illness.
Like millions of others, I have seen M.E. through the eyes of the medical establishment, the Government and the Media. The picture has not been good.
Here is what I have previously understood about M.E. and those who have it.
M.E. sufferers are workshy malingerers. They whine, constantly, about feeling tired. They are annoying sympathy seekers.
Damn it. We're all tired. Especially those fools like me who work all hours God Sends (and even some he doesn't) to support the type of people who say they are too tired to work.
Oh, and mostly, importantly, M.E. is 'all in the head' and can be overcome with a bit more determination and a little less of the 'poor me' attitude.
That, generally, is what I thought about M.E.
Until, that is, a reader sent me a DVD of a British-made film about the illness titled 'Voices From The Shadows'.
I receive dozens of clips and films each month, and I try and see as many as I humanly can, but there was something about 'Voices...' that stopped me in my tracks.
One of the reasons the film had such an impact is because it challenged my deep-seated preconceptions about M.E.
Through 'Voices...' - and the subsequent research I have conducted - I have come to realise that what I thought I knew about the illness was a fallacy but, more importantly than that, was actually detrimental to those affected.
So, as a naturally curious individual, I'm not a journalist by mistake, I began to question why I had been furnished with one version of events - and inaccurate ones at that.
The more I began to delve into the subject the more curious it all became.
Like for example, why are records pertaining to ME locked away in our national archives in Kew for 75 years? The normal period would be 30 years.
75 years, the period generally used for documents of extreme public sensitivity and national security, is excessive.
The reason given, that of data protection, is a nonsense as it is perfectly acceptable, and easy, to omit names on official documents. The excuse, supplied in Parliamentary questions by the Department of Work and Pensions, didn't wash with me.
Why, I thought, were they making such an exception?
It got me thinking about what information the files actually do contain. And, seeing as the topic of M.E. is still beset with misunderstanding, we could all benefit from some enlightenment on the subject.
So, to this end - and seeing as it M.E. Awareness Week - here is my personal guide to shattering the myths and blatantly-pedalled untruths about M.E.
Myth No. 1: ME is a mental illness
Not so. It is a neurological one. It is not a case of 'mind over matter' despite many GP's and health professionals still thinking it is. Psychiatrists have bagged it as 'their thing' and the General Medical Council has been somewhat remiss in suporting it as a physical condition.
I spoke with one ME sufferer, who asked to remain anonymous for fear of upsetting the medical professionals who are currently treating her. She said a new GP at her practice had suggested she take up meditation to help her combat her decades-old condition.
Thankfully there are some doctors, few and far between admittedly, who really understand the physical nature of M.E.
Dr. Speight, a medical advisor for a number of M.E. charities does. Commenting on the wide-ranging debilitation of the illness, he has said:
"The condition itself covers a wide spectrum of severity but even the mildest cases deserve diagnosis and recognition because if they are given the wrong advice or don't handle themselves correctly they can become worse.
"At the more severe end of the spectrum there's a minority of patients who are truly in a pitiable state...some of them in hospitals, some of them at home...and this end of the spectrum is really one of the most powerful proofs to me of what a real condition this is and how it cannot be explained away by psychiatric reasons."
Sadly, there are still many health professionals who buy into the notion that M.E. is a psychological disorder and should be treated as a form of insanity.
In Denmark, only last week, The Danish Board of Health sought to remove a 23-year old woman, Karina, from her family home on the grounds of mental illness despite the fact that what she really has is M.E.
Karina, bed-bound, light and sound sensitive and too weak to walk is considered to be insane, rather than physically sick, and her family has been repeatedly told by Danish doctors that the diagnosis of M.E. is not recognised.
Myth 2: ME is just extreme tiredness, right?
Wrong. Despite falling under the Chronic Fatigue Syndrome category - as does Fibromylgia which has its own Awareness Day next week - it is entirely wrong to assume that M.E. is merely about lack of energy.
This confusion arose over the past 20-odd years and is due to the condition being re-classified as a Fatigue Syndrome.
The result of this has been to trivialise the illness which has served as fodder for ill-informed public commentators who have used M.E. and Fibromylgia to talk about 'scroungers' in the benefits system who are 'too lazy' to get out of bed.
For those who know about the illness, this type of commentary is viewed as dangerous rhetoric that deserves to be classified as a form of hate crime.
Myth No. 3: M.E. is just like a bad flu
Oh, if only. M.E. is a complex, chronic, multi-system illness that affect the body in similar ways to Multiple Scelerosis. In addition, inflammation of the neurological system can lead to heart disease, extreme muscle pain and other debilitating and life-threatening conditions.
As one doctor put it, comparing M.E. to an illness like flu is like comparing Emphysema to a chest infection. It seriously undermines the truth extent of M.E.
Myth No. 4: M.E. sufferers should just 'pull themselves together'
Many sufferers have found themselves abandoned by health professionals, struck off of registers and even rejected by their own families when they have failed to respond to 'tough love'.
Too many people assume that M.E. can be overcome with the right mental attitude. This consequently leaves M.E. sufferers even more vulnerable to issues like depression as they are further isolated.
M.E. is not a case of the mind being able to heal itself with determination. M.E. breaks the body down and that also includes the brain.
Myth No. 5: Only adults have M.E.
Children have M.E. and their childhoods are destroyed as a consequence.
Margaret Rumney of Allendale, Northumberland.watched as her 11-year-old daughter, Emma, was reduced to a shell of her former self when she was struck down with M.E. nine years ago.
"Since then it has been a continual rollercoaster of emotions and has been one fight after the other," says Margaret. "It is very hard for my daughter being ill, she is virtually housebound, often reliant on a wheelchair, and to have to cope with disbelief and ridicule on top of this makes this illness even harder to bear.
"Our experience of my daughter's school was an awful one. When my daughter was receiving home tuition organised officially by the Education Welfare Officer we were threatened by one professional that if my daughter didn't return to school that it would be classed as a psychological issue and social services would get involved."
Threats and intimidation of this nature at the hands of the authorities are a constant feature of those in the M.E. community, and particularly those caring for children with the illness.
Naturally, this pressure merely adds to the overall anxiety that sufferers are already experiencing. Education is key. Bullying is not.
Myth No. 6 - You can 'catch' M.E.
Absurd. It is no more infectious than a broken leg is. M.E. appears to follow various viral infections, including meningitis, although the true cause is still a hotly debated topic among professionals.
Myth No. 7: Real M.E. sufferers are few and far between.
There are currently 250,000 recognised cases of ME in the UK. That's 1 in 250 so that's hardly an insignificant amount, is it?
Myth No. 8: Only severe cases of M.E. are worth acknowledging.
Terrible misconception. M.E. ruins people's lives even if the patient is not entirely bedbound.
The media tend to concentrate on the worst case scenarios but this does not help the full situation as it leaves others, who are still able to move at times, with the stigmatisation of 'not being ill enough'.
Claire Taylor-Jones, a mother of one from Rhyl in South Wales, has been unable to pursue her ambition of becoming a solicitor after she was diagnosed with M.E.
In common with other sufferers, Claire has good days and bad days but she is not consistently well enough to pursue her goals and she is left in a type of limbo land. Her plans are on hold.
Myth No. 10: Children with M.E. have neglectful parents
There's the notion that children with M.E. are actually victims of mothers who have Munchausens by Proxy – the illness where parents act as if the child is sick to further their own need for attention.
This is a particularly dangerous belief system as it leaves the true M.E. sufferer without sufficient support and diagnosis and the carer is treated as the problem.
Myth No. 11: Phyiscal exercise will benefit M.E. sufferers.
Absolutely not true. Worse, still, enforced 'graded exercise' can escalate the condition to dangerous and irreparable levels for the patient.
During the research of this subject, I have watched footage of hospital physiotherapists literally bullying M.E. patients to stand and walk. It is pitiful to witness.
The physios say things like 'Come on, you can do it. You just have to put your mind to it' and, at worst, 'You're not trying hard enough.'
Julie-Anne Pickle, who has had M.E. for the past seven years has experienced a serious deterioration in her condition as a consequence of wrong diagnosis and ineffective medical response. She is now 90 per cent bedbound and has been diagnosed with depression, diabetes and Angina.
She told me:
"Cardiology phoned me with an appointment the other day and they told me to wear trainers because they want me running on a treadmill while on an ECG! I said: 'You do know I have M.E.?' They said they did but not to worry as I won't be running for more than five minutes! Running? I crawled on my hands and knees to the loo this morning!"
This idea among some of the medical professional that enforced exercise will help the condition of a M.E. belongs to a darker time in our history. A period when we thought that autistic children were a result of being born to cold and detached women or 'refrigerator mums' as they were heinously and immorally labelled.
Myth No. 12 - M.E. is not life-threatening
It is, although the true mortality rate of M.E. is mired in great confusion.
Recently, Labour MP George Howarth asked Paul Burstow, Minister of State for Care Services, to supply details of deaths to arise from M.E. Mr. Burstow replied that 'this information is not available and is not collected centrally'.
As with so many issues regarding our sick and disabled, the Coalition had this wrong, too.
According to figures obtained from the Office of National Statistics, there have been five deaths listed as the cause of M.E. in recent years.
For campaigners this is nothing less than a fudge of the true scale.
Figures are easy to massage with M.E. because it triggers so many other illnesses, such as heart disease. Given that many health professional still deny that M.E. is a physical condition, they are unable to list it as a cause of death even if it is.
Myth No. 13: M.E. is an excuse not to work
Despite recognition from the World Health Organisation in 1969 that M.E. is a neurological disorder, many Governments - including our present Coalition - have chosen to ignore this.
Consequently, M.E. sufferers are subject to a battery of controversial fit-to-work assessments. The anxiety and physical exertion this requires generally worsens the condition.
When the M.E. sufferer is unable to work, because of their illness, they are removed from disability benefit and are plunged into poverty.
So, for M.E. Awareness Week, let us be clear. M.E. is comparable to AIDS and Cancer and all the other vicious and uncompromising diseases that savage the body and, in some extreme cases, kill it completely.
The fact that it is still so widely misunderstood is a modern day travesty that must be addressed without further delay. Or is it convenient that we still view M.E. as being 'all in the mind'?
I believe that we, as a nation, deserve to know the truth. Not only for those still battling the disease, but for those poor souls who have already been lost to it.
* For further details on Voices from the Shadows: