Cerebral Palsy and Prada Willi – syndrome – Massage and Movement with stiff and floppy babies
Cerebral palsy, also referred to as CP, is a term used to describe a group of chronic conditions affecting the child’s body movement and muscle coordination and refers to any one of a number of neurological disorders that appear in infancy or early childhood which may permanently affect body movement and muscular coordination.
It is caused by damage to one or more specific areas of the brain, usually occurring during fetal development; before, during, or shortly after birth; or during infancy. These disorders are not caused by problems in the muscles or nerves themselves, but through faulty development or damage to motor areas in the brain which disrupt the brain’s ability to adequately control movement and posture.
Cerebral palsy doesn’t always cause profound disabilities. While one child with severe cerebral palsy might be unable to walk and need extensive care, another with mild cerebral palsy might be only slightly awkward and require no special assistance.
The early signs of cerebral palsy usually appear before a child reaches 3 years of age. The most common are a lack of muscle coordination when performing voluntary movements (ataxia); stiff or tight muscles and exaggerated reflexes (spasticity); walking with one foot or leg dragging; walking on the toes, a crouched gait, or a “scissored” gait; and muscle tone that is either too stiff or too floppy.
Consequently an accurate diagnosis can take time and as time is of the essence it could be well worthwhile to observe exactly what it is that your baby is doing or not doing that is giving you cause for concern. You then have the opportunity to see what is ‘on offer’ as a means to be able to help you to help your child obtain some degree of normality while leaving the cause and diagnosis to the ‘experts’.
If your baby’s muscles and joints are stiff, floppy, or both in different areas of the body, and / or at different times, massaging and moving them gently in the right way, can bring about some remarkable improvements.
Only movement can restore and improve movement – there is no ‘magic pill’.
The magic pill is a parents love and frequent daily practice of correctional techniques
Without the correct massage movement techniques the body’s joints and the muscle groups that control them become stiffer or looser and this increases and becomes more difficult to rectify over longer periods of time through repetitive practice of the wrong patterns of movement and the increase in the child’s body weight.
At the very least massage, if practiced regularly, will improve the quality of your child’s everyday life and give you a means of expression. With an opportunity to perhaps restore the correct ‘tonus’ to the muscles, free the joints and establish a more normal /normal ‘pattern’ of movement.
What it will also do is allow you as a parent to get closer to your child and to practice massage and movement with your child at a time of day that is mutually convenient.
Prader-Willi syndrome
Prada-Willi syndrome is a complex genetic disorder, which is present from birth. Motor signs of the disorder that may be present in the first year of life include:
Poor muscle tone. Hypotonia. The baby may be very ‘floppy’’ which can cause developmental delay
Failure to thrive. Babies with Prader-Willi syndrome may have a poor sucking reflex due to decreased muscle tone. Because poor sucking makes feeding difficult, they tend to gain weight slowly.
Generally poor responsiveness. The baby may seem unusually tired and will respond poorly to stimulation. They tend to sleep more and waken with difficulty or have a weak cry.
Delayed motor development. Toddlers with Prader-Willi syndrome often reach milestones in physical movement later than do other children.
Scoliosis. A number of children with Prader-Willi syndrome develop abnormal curvature of the spine (scoliosis).
It is advisable for parents with a child affected by Prader-Willi syndrome learn techniques that can be effective in the event of the child choking.
Where ‘floppiness’ and developmental delay is evident the correct techniques using massage and movement will have a considerable effect upon restoring normal muscle tone and development.
As babies with Prader-Willi syndrome can be hypotonic a firmer touch with cool hands can help to ‘tighten up’ the muscles and joints and using supervised positions and movements that encourage strengthening rather than stretching is advisable.
Gravity assisted techniques will also assist sitting and standing and reduce the risk of scoliosis.
While Prader-Willi syndrome itself is not life threatening, the compulsive eating and the resulting weight gain can be. Many complications of Prader-Willi syndrome are due to obesity. If a child with Prader-Willi syndrome manages to follow a restricted diet and control their weight, there is no reason why they cannot enjoy a good quality of life and take part in activities such as voluntary or part-time work. However, because of behavioural problems and learning difficulties a fully independent lifestyle may be difficult.
If your baby’s muscles and joints are floppy, massaging and moving them gently in the right way, can bring about some remarkable improvements. Again, only movement can restore and improve movement – there is no ‘magic pill’.
The magic pill is a parents love and frequent daily practice of correctional techniques
Without the correct massage movement techniques the body’s joints and the muscle groups that control them become stiffer or looser and this increases and becomes more difficult to rectify over longer periods of time through repetitive practice of the wrong patterns of movement and the increase in the child’s body weight.
Practiced regularly with some gravity assisted techniques massage and movement will reduce hypotonia / floppiness and assist your child to sit and stand and redress postural problems.

Leona Gudelj, 3 years 3 months, born by Caesarean section, not walking yet. Diagnosis hypotonia generalisata, doctors haven’t discovered the cause, they want us to do the metabolic and genetic research again.
MR brain Date 1.6.2011.:Sagittal, transverse and coronal MR sections in standard display techniques.
On the series of sagittal, transverse and coronary MR section through the area of the brain can be seen in the area intratentorial neatly laid, orderly configured cerebral hemispheres that are physiological signal intensity. Fourth cerebral ventricle of adequate size, in mediosagitalnoj line.
Supratentorial are neatly laid cerebral hemispheres. The third and lateral ventricles medioponirane, enlarged, prominent left, slightly wavy outer contours. Evans index of 0.4. Reduced white matter periventricularly rear horns with posterior chamber. Gracile CC.
Myelination corresponds age.
Sellar region suprasellar area, cavernous sinus and both n. statoakustikusa not show pathomorphological changes. Extended CSF are not mutually frontotemporally based convexity and interhemispheric front.
Now: She crawls, she is stabile in kneel, she even manages to walk on knees. She stands up on her feet but when she is close to something i.e. cauch, table. Intellectually she is very smart, understands everything, copies everything, can express herself, not the long sentences example Dad work. She calls herself None. None eat. Mama give me. etc She eats on her own spoon/fork. No problems with handling the pencil.
Her feet are not in the right position when standing ie valgus both of them, and the right even more, go in the outter position, and she stands on the inner part of them, very bad to see. She practices once a week Bobath therapy, and the rest of time plays with parents, nothing else.
Please any advices, video with useful practice for a child like her. Anything that crosses Your mind.
Thank You in advance, and we are sorry that we didn’t find You three years ago.
BR
Leona Gudelj When she sits on or between her feet do her feet turn inwards?
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