Photography, Art, Books, Music, Music and more Music, Live Music and Music and poetry, here is a poem i wrote called
The Dance
Tiny fishes dance inside me...
Muscular partners waltz.
Theres a tango in there somewhere...
Waiting to join the dance.
A full time hokey cokey...
A can can and a bellydance.
But I'd turn the music off completely,
If given half the chance.
Foxtrot in my waking...
Polka in my sleep.
Let the music play...
Heart Felt and Skin deep.
A Hippy Hippy Shake...
And a Funky Gibbon.
Now I’m a champion dancer...
And I won a BLUE RIBBON....
But I'd turn the music off completely,
If given half the chance.
MY NEW RIBBON IS A NEUROFERRITINOPATHY RIBBON A RECENTLY DISCOVERED DISORDER OFTEN CONFUSED WITH DYSTONIA AND MISDIAGNOSED TAKE A LOOK AT THE PROFILE IN MY FRIENDS
Music
Rock'n'Roll, Rockabilly, Western Swing, Jump Jive, R'n'B, Skiffle, Bluegrass and on occasion a touch of very high class Psychobilly!!!! Love all the old crooners and a few very select new ones........
Movies
Bus Stop, The Butterfly Effect, The Green Mile, The Wizard Of Oz, Gentlemen Prefer Blondes, Dorian Grey, On The Waterfront, The Fisher King.
Television
NO THANKYOU GOT ONE AND ITS RUBBISH!..
Apart from the extraordinary people series, excellent viewing!
Books
GOT LOTS TEND TO READ THE SAME ONES OVER AND OVER....
TO KILL A MOCKINGBIRD (ALL TIME FAVE)
LOVE AUTOBIOGRAPHICAL BOOKS
NOTHING SCARY EVER ..
Heroes
NAN & MUM
STRONG SENSIBLE WOMEN WITH HEART AND SOUL AND LAUGHTER
SPIKE FOR REASONS IM NOT PUTTING COS ILL HAVE TO KILL HIM
MY CHILDREN FOR TAKING MY ILLNESS AT ITS WORSE IN THEIR STRIDE AND COMING OUT THE OTHER SIDE STRONG AND DETERMINED
..
Linette Southend at xmas Sun 20th at the castle The Sundowners free, 24th the rat pack 2 quid, sun 27th the koolkatz free new years eve at foresters route 56 5 quid Posted 8 hours ago view more
Linette or Lil to my friends and family, married to a complete nutter, Spike my first love, married to his first love rock'n'roll/rockabilly, divided between four rugrats and four step rats a lunatic dog and several fish.
I suffer with paroxysmal dystonia and most of my blogs relate to this.
Dystonia - Brain to Muscle Disease
Paroxysmal dystonias are a group of rare conditions where attacks of dystonia occur, in between which people are usually completely normal. Sometimes there are triggers to these attacks such as sudden movement, fatigue, coffee and alcohol.
In some types of paroxysmal dystonia the attacks are very brief (seconds to minutes), whereas in others the attacks can be much longer (minutes to hours). Some people have many attacks per day, whereas others have very infrequent attacks.
During an attack, people do not lose consciousness, and are completely aware of their surroundings. Paroxysmal dystonias do not affect the mind or the sense. Paroxysmal dystonias are not the same as epilepsy, and therefore do not necessarily disqualify one from driving (although advice should be sought from the driving licence authority, DVLA).
In most people the condition has no known cause and usually starts in teenage years. Sometimes the condition can be caused by damage to the brain, for example following a head injury. The condition can occasionally run in families.
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How can paroxysmal dystonias be treated?
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To date, no cure exists for people with paroxysmal dystonias, although a great deal of research is being undertaken around the world, with significant progress. The condition is not life-threatening but treatment is essential and usually available using drugs.
Although paroxysmal dystonia is not the same as epilepsy, many people can be very successfully treated using small doses of the same drugs used to treat epilepsy. In some people these drugs can stop attacks completely. Drugs are not universally effective, and some people do experience side effects.
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How do I live with paroxysmal dystonia?
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Paroxysmal dystonia can be a challenging condition to live with. The attacks can be quite unpredictable, and this can interrupt normal life. Paroxysmal dystonia is quite a rare condition, and therefore most people, including some doctors, will not have heard of it. People can become confused between paroxysmal dystonia and epilepsy.
What is Dystonia?
Dystonia is a very complex, highly variable neurological movement disorder characterized by involuntary muscle contractions. As many as 250,000 people in the United States and over 40,000 in the UK have dystonia, making it the third most common movement disorder behind essential tremor and Parkinson’s disease. It is a condition that knows no age, ethnic, or racial boundaries – it can affect young children to older adults of all races and ethnicities.
PLEASE TURN OFF MY MUSIC PLAYER WHILE WATCHING THE VIDEO
THE FIRST VIDEO IS OF MY ARM INT HE MIDDLE OF THE NIGHT AFTER A PROLONGED SPASM WHICH OBVIOUSLY WAS TOO PAINFUL TO VIDEO. THIS SHAKE IS FORCED BY THE MUSCLE AND DOES NOT HURT.
THE SECOND VIDEO IS THE TRAILER FOR THE DOCUMENTARY TWISTED IT SHOWS PEOPLE WITH DIFFERENT FORMS OF DYSTONIA AND SADLY THE LADY PICTURED HAS FOUND NO MEDICINE EFFECTIVE. AGAIN I THANK GOD FOR MY MEDS
Dystonia results from abnormal functioning of the basal ganglia, a deep part of the brain which helps control coordination of movement. These regions of the brain control the speed and fluidity of movement and prevent unwanted movements. Patients with dystonia may experience uncontrollable twisting, repetitive movements, or abnormal postures and positions. These can affect any part of the body, including the arms, legs, trunk, face and vocal cords.
Depending on the part of the body affected, dystonia can seriously impact daily functions. For example, if neck muscles are affected, a patient may have difficulty chewing and swallowing. Though not life-threatening, the involuntary nature of the disorder may be embarrassing, causing emotional distress or depression in some individuals. There are a number of local support groups throughout the United States that can help address some of these issues, but patients may need to be treated separately for mental health issues caused by the challenges of coping with this disorder.
Dystonia classification
Dystonia is classified by three main factors: the age at which symptoms develop; the areas of the body affected; and the underlying cause.
The chance that dystonia will affect multiple body parts is generally linked to the age of onset. The younger one is at onset, the greater the chance that symptoms will spread. Conversely, the older one is at onset, the more likely that the disorder will remain more moderate.
Dystonia classification by age
Childhood onset – 0 to age 12
Adolescent onset – age 13 to 20
Adult onset – older than age 20
Dystonia classification by body part
Focal Dystonia – is limited to one area of the body, and can affect the neck (cervical dystonia or spasmodic torticollis), eyes (blepharospasm), jaw/mouth/lower face (oromandibular dystonia), vocal cords (laryngeal dystonia), or arms/legs (limb dystonia). Other less common types of focal dystonias can cause unusual stretching, bending, or twisting of the trunk (truncal dystonia) or sustained contractions and involuntary, writhing movements of the abdominal wall (abdominal wall dystonia).
Focal dystonia more commonly affects people in their 40s and 50s and is frequently referred to as adult-onset dystonia. Women are affected about three times more frequently than men. In general, focal dystonias are classified as primary (idiopathic) and are not hereditary.
Segmental Dystonia – affects two or more parts of the body that are adjacent or close to one another. Up to 30 percent of people with focal dystonia have spasms in areas adjacent to the primary site. A common form of segmental dystonia affects the eyelids, jaw, mouth, and lower face.
Other types of dystonia include multifocal, which involves two or more body parts distant from one another; hemidystonia, which affects half of the body; and generalized, which begins with leg involvement, but generally spreads to one or more additional regions of the body.
Dystonia classification by cause
Primary (idiopathic) – dystonia is the only sign, and secondary causes have been ruled out. Most primary dystonias are variable, have adult onset, and are focal or segmental in nature. However, there are specific primary dystonias with childhood or adolescent onset that have been linked to genetic mutations.
The majority of early-onset primary dystonias, which may appear during childhood or early adulthood, are due to mutations of a gene known as DYT1. This gene has been mapped to the long arm of chromosome 9 at 9q34.1. In about 90 to 95 percent of cases, symptoms begin in a limb and then spread to other regions of the body. This form of dystonia has an average age of onset of 12 and seldom develops after age 29.
DYT6 dystonia is an autosomal dominant primary dystonia that has been mapped to chromosome 8 (8p21q22). It is rarer than DYT1 dystonia and has been studied in two Mennonite families in the United States. In nearly all individuals with this form of dystonia, the disorder begins at an initial site but spreads to multiple body regions, most commonly the limbs, head, or neck. Severe difficulties with speech articulation have been noted.
Other familial primary dystonias identified are DYT7, DYT2, and DYT4, all of which have been noted in specific ethnic groups, primarily of European descent.
Secondary (symptomatic) – dystonia that results primarily from secondary causes. These include environmental, such as exposure to carbon monoxide, cyanide, manganese, or methanol; underlying conditions and diseases such as brain tumors, cerebral palsy, Parkinson’s disease, stroke, multiple sclerosis, hypoparathyroidism, or vascular malformations; brain/spinal cord injuries; inflammatory, infectious, or postinfectious brain conditions; and specific medications.
Dystonia-plus syndromes – dystonia that results from nondegenerative, neurochemical disorders associated with other neurological conditions. Dystonia-plus syndromes include dopa-responsive dystonia (DRD) or Segawa syndrome, rapid-onset dystonia-parkinsonism (RDP), and myoclonus-dystonia.
Heredodegenerative dystonia – dystonia that generally results from neurodegenerative disorders in which other neurological symptoms are present and in which heredity plays a role. These include numerous disorders such as certain X-linked recessive, autosomal dominant, autosomal recessive, and/or parkinsonian syndromes. Included in this category: X-linked dystonia-parkinsonism (Lubag), Huntington's disease, Wilson's disease, neuroacanthocytosis, Rett’s syndrome, Parkinson's disease, and juvenile parkinsonism.
Symptoms
Dystonia is sometimes misdiagnosed as stress, a stiff neck or a psychological disorder. The intermittent character of the disorder may lead medical practitioners to conclude that a psychological disorder is either the primary cause or a contributing factor. Diagnosis is difficult because dystonia symptoms are similar to those of many other conditions and are so variable in nature.
Dystonia initially arises after specific movements or tasks, but in advanced stages it may occur at rest. It usually affects the same group of muscles, thus causing a repetitive pattern of movements over time. It generally develops gradually, with localized symptoms suggesting the presence of the disorder. Eye irritation, excessive sensitivity to bright light, and increased blinking may be an indication of blepharospasm. Subtle facial spasms, difficulty chewing, or changes in speech cadence may indicate oromandibular dystonia. Cramping of the hand during writing or fatigue during walking or other manual activities may indicate limb dystonia.
Dystonia is also variable in its progression. For some patients, the disease steadily worsens; for others, it plateaus. For some, dystonia stabilizes at a relatively minor stage and progresses no further. The advanced stage is marked by rapid and involuntary rhythmic movements, twisting postures, contortions of the torso, abnormal gait, and, ultimately, fixed postural deformities.
The disorder is usually not associated with pain, but it certainly may lead to pain in affected areas. Cervical dystonia can be particularly painful due to degeneration of the spine, irritation of nerve roots, or frequent headaches. Limb dystonia may not cause pain initially but may become painful over time. Uncontrolled muscle movements may cause the joints to deteriorate, possibly leading to the onset of arthritis.
Treatment
There is a three-tiered approach to treating dystonia: botulinum toxin (botox) injections, several types of medication, and surgery. These may be used alone or in combination. Medications and botox can both help block the communication between the nerve and the muscle and may lessen abnormal movements and postures.
Botulinum toxin type A was developed in the 1980s. In 2001, the U.S. Food and Drug Administration approved botulinum toxin type B for treatment of cervical dystonia. Researchers created the new drug after some patients began developing resistance to the type A form. The type B drug has mild to moderate side effects such as dry mouth, dysphagia (difficulty swallowing) and indigestion.
Surgery is considered when other treatments have proven ineffective. The goal of surgery is to interrupt the pathways responsible for the abnormal movements at various levels of the nervous system. Some operations purposely damage small regions of the thalamus (thalamotomy), globus pallidus (pallidotomy), or other deep centers in the brain. Deep brain stimulation (DBS) has been tried recently with some success. Other surgeries include cutting nerves leading to the nerve roots deep in the neck close to the spinal cord (anterior cervical rhizotomy) or removing the nerves at the point they enter the contracting muscles (selective peripheral denervation).
The benefits of surgery should always be weighed carefully against its risks. Although some dystonia patients report significant symptom reduction after surgery, there is no guarantee that surgery will help every individual
Who I'd like to meet: Anyone into the lifestyle and music of the 1950's, musicians and anyone who suffers from dystonia.
Join Yeller Bellies as we celebrate the release of our new album “Here to Suffer”! Marvel at the lineup, which includes The Clydesdale, Voodoo Organist, The Mad Caps, and The Slow Poisoner!!
Gasp at the relatively early start time of 9PM!!!
SATURDAY, DECEMBER 12th @ 9PM
Boomers Bar 3200 Sirius Avenue Las Vegas, NV 89102 702-368-1863
Take Valley View south, past Sahara to Sirius (north of D.I.).
Pick up your copy of Catch That Rockabilly Fever today.
Makes the perfect Christmas gift. For U.S. customers, you can buy it at www.mcfarlandpub.com for $39.95 plus $5 shipping or Amazon.com for
$35.95. Outside of the U.S.,
Amazon.com
is your best bet for the lowest price in shipping. You may also order it from
your local bookstore.
A few weeks ago I backed up Don Woody at the 1st Rockabilly Bash. I did that with the Tri-Tones from Estonia. Here’s a video clip with his song “Barkin’ Up The Wrong Tree”.
At the same evening I released my 2nd album ‘Mixed Up”. I recorded this album with The Neva River Rockets from Russia, the Tri-Tones from Estonia and did two duets with U.S.A singer Karling Abbeygate.
Hi there,thanks for your friendship and for the ad.I hope you dig my music too?Please have a listen and send me your comments. BEST WISHES TO YOU,DARREN JUVIE
BACK TO THE GRAVE KLUBNIGHT presents MOJOKINGS+THEE CHILLS live at Satans Hollow Manchester. +BACK TO THE GRAVE dj's. Doors open at 9pm, music until 3am!! A night of Rockabilly, Garage, Psychobilly, Rock'n'Roll...
Hi Yall get down to the Dev on Saturday night , rockin little club,Dance floor , great atmosphere,good beer , car park and some serious rock n rollabilly music from yours truly ye ha
Hello my dear friend. What is going on? Sorry I have been side tracked here lately but I am hopefully getting back to the norm. I have not forgotten about you. Love ya!
Hope to meet you at one of our concerts in the UK,France or somewhere else in Europe real soon.
You can go on our page and also on youtube to watch 5 videos taken from one of our last gig.Hope you’ll like them and will come back from times to times on our page to watch them.
Online Now!
