a Looking Glass into Cerebral Palsy

Hey there!

So I have been feeling like I am much more uneducated on CP than I should be, considering Im affected by it each minute I live! So here’s the deal, I did a little research and here is what I came up with, there are four types of  Cerebral Palsy…I let wikipedia break it down for ya :p I feel like they do a good job of encompassing all the FAQ’s. Hopefully it isn’t too much to take in, feel free to just skim over it…I bolded a few parts that caught my attention, as it applies to some commonalities of CP. I have a few more info to the right colums under “resources” that you maybe want to check out as well. I just thought you might want to go on here to read up on CP, as some other webs are a bit intimidating and hard to sort out. I’m not sure if you have already done any research on your own, nevertheless, this is here… who knows, maybe researching is how you came across my TCP web! :)

CEREBRAL PALSY

Spastic cerebral palsy is by far the most common type, occurring in 70% to 80% of all cases. Moreover, spastic CP accompanies one of the other types in 30% of all cases. People with this type are hypertonic and have a neuromuscular condition stemming from damage to the corticospinal tract or the motor cortex that affects the nervous system’s ability to receive gamma amino butyric acid in the area(s) affected by the disability. Spastic CP is further classified by topography dependent on the region of the body affected; these include:

  • Spastic hemiplegia (one side being affected). Generally, injury to muscle-nerves controlled by the brain’s left side will cause a right body deficit, and vice versa. Typically, people that have spastic hemiplegia are the most ambulatory, although they generally have dynamic equinus on the affected side and are primarily prescribed ankle-foot orthoses to prevent said equinus.[11] —-This is the definition of my case!
  •  
  • Spastic diplegia (the lower extremities are affected with little to no upper-body spasticity). The most common form of the spastic forms. Most people with spastic diplegia are fully ambulatory and have a scissors gait. Flexed knees and hips to varying degrees are common. Hip problems, dislocations, and in three-quarters of spastic diplegics, also strabismus (crossed eyes), can be present as well. In addition, these individuals are often nearsighted. The intelligence of a person with spastic diplegia is unaffected by the condition.
  • Spastic tetraplegia (all four limbs affected equally). People with spastic quadriplegia are the least likely to be able to walk, or if they can, to want to walk, because their muscles are too tight and it is too much effort to do so. Some children with quadriplegia also have hemiparetic tremors, an uncontrollable shaking that affects the limbs on one side of the body and impairs normal movement.

Occasionally, terms such as monoplegia, paraplegia, triplegia, and pentaplegia may also be used to refer to specific manifestations of the spasticity.

Ataxia (ICD-10 G80.4) type symptoms can be caused by damage to the cerebellum. The forms of ataxia are less common types of cerebral palsy, occurring in at most 10% of all cases. Some of these individuals have hypotonia and tremors. Motor skills such as writing, typing, or using scissors might be affected, as well as balance, especially while walking. It is common for individuals to have difficulty with visual and/or auditory processing.

Athetoid or dyskinetic is mixed muscle tone — People with athetoid CP have trouble holding themselves in an upright, steady position for sitting or walking, and often show involuntary motions. For some people with athetoid CP, it takes a lot of work and concentration to get their hand to a certain spot (like scratching their nose or reaching for a cup). Because of their mixed tone and trouble keeping a position, they may not be able to hold onto objects (such as a toothbrush or pencil). About one quarter of all people with CP have athetoid CP. The damage occurs to the extrapyramidal motor system and/or pyramidal tract and to the basal ganglia. It occurs in 10% to 20% percent of all cases. In newborn infants, high bilirubin levels in the blood, if left untreated, can lead to brain damage in certain areas (kernicterus). This may also lead to athetoid cerebral palsy.

People with hypotonic CP appear limp and can move only a little or can’t move at all.

***I feel they don’t touch on social development very much… in my opinion, I believe it is one of any parents biggest worries to see their child be socially inept. With that said, it is essential to help integrate children with CP into “normal” activities with other children, in hopes that they will feel as equally accepted, loved, and respected, regardless of their disability or insecurity. However, I do realize that there are serveral more severe cases of CP where social situations cannot be implemented in one’s therapy, or develpment program and growth, due to the severity of his or her CP. So, this could mean the simplest of activities toward progression– from learning how to tie their own shoes, to riding a bike, or painting a picture with their classmates. Anything that creates a healthy source of interaction among children will help the child feel important, and included. Yet in every human being’s life there comes a time when they just need to be told that they are loved and befriended.  Support is HUGE in the development of a child–with or without CP. A child needs nothing more than the love and acceptance of their parents, family, and peers. If you give them that– dont fret, they will grow into the beautiful human beings you always hoped they’d be. There will be times of frustration, confusion, and hopelessness, but you will get through those hardships. See that you really make an attempt to understand that person around you with CP–whether they be your child, friend, brother or mother, and know that that is all you can do. That is all they want. To be understood.***

  • Symptoms

All types of CP are characterized by abnormal muscle tone (i.e. slouching over while sitting), reflexes, or motor development and coordination. There can be joint and bone deformities and contractures (permanently fixed, tight muscles and joints). The classical symptoms are spasticities, spasms, other involuntary movements (e.g. facial gestures), unsteady gait, problems with balance, and/or soft tissue findings consisting largely of decreased muscle mass. Scissor walking (where the knees come in and cross) and toe walking (which can contribute to a gait reminiscent of a marionette) are common among people with CP who are able to walk, but taken on the whole, CP symptomatology is very diverse. The effects of cerebral palsy fall on a continuum of motor dysfunction which may range from slight clumsiness at the mild end of the spectrum to impairments so severe that they render coordinated movement virtually impossible at the other end the spectrum.

Babies born with severe CP often have an irregular posture; their bodies may be either very floppy or very stiff. Birth defects, such as spinal curvature, a small jawbone, or a small head sometimes occur along with CP. Symptoms may appear or change as a child gets older. Some babies born with CP do not show obvious signs right away. Classically, CP becomes evident when the baby reaches the developmental stage at six and a half to 9 months and is starting to mobilise, where preferential use of limbs, asymmetry or gross motor developmental delay is seen.

Secondary conditions can include seizures, epilepsy, apraxia, dysarthria or other communication disorders, eating problems, sensory impairments, mental retardation, learning disabilities, and/or behavioral disorders.

Speech and language disorders are common in people with Cerebral Palsy. The incidence of dysarthria is estimated to range from 31% to 88%. Speech problems are associated with poor respiratory control, laryngeal and velopharyngeal dysfunction as well as oral articulation disorders that are due to restricted movement in the oral-facial muscles. There are three major types of dysarthria in cerebral palsy: spastic, dyskinetic (athetosis) and ataxic. Speech impairments in spastic dysarthria involves four major abnormalities of voluntary movement: spasticity, weakness, limited range of motion and slowness of movement. Speech mechanism impairment in athetosis involves a disorder in the regulation of breathing patterns, laryngeal dysfunction (monopitch, low, weak and breathy voice quality). It is also associated with articulatory dysfunction (large range of jaw movements), inappropriate positioning of the tongue, instability of velar elevation. Athetoid dysarthria is caused by disruption of the internal sensorimotor feedback system for appropriate motor commands, which leads to the generation of faulty movements that are perceived by others as involuntary. Ataxic dysarthria is uncommon in cerebral palsy. The speech characteristics are: imprecise consonants, irregular articulatory breakdown, distorted vowels, excess and equal stress, prolonged phonemes, slow rate, monopitch, monoloudness and harsh voice. Overall language delay is associated with problems of mental retardation, hearing impairment and learned helplessness. Children with cerebral palsy are at risk of learned helplessness and becoming passive communicators, initiating little communication. Early intervention with this clientele often targets situations in which children communicate with others, so that they learn that they can control people and objects in their environment through this communication, including making choices, decisions and mistakes.

Early Nutritional Support In one cohort study of 490 premature infants discharged from the NICU, the rate of growth during hospital stay was related to neurological function at 18 and 22 months of age. The study found a significant decrease in the incidence of cerebral palsy in the group of premature infants with the highest growth velocity. This study suggests that adequate nutrition and growth play a protective role in the development of cerebral palsy.

Physiotherapy (PT) programs are designed to encourage the patient to build a strength base for improved gait and volitional movement, together with stretching programs to limit contractures. Many experts believe that life-long physiotherapy is crucial to maintain muscle tone, bone structure, and prevent dislocation of the joints.

Occupational therapy helps adults and children maximise their function, adapt to their limitations and live as independently as possible.

Orthotic devices such as ankle-foot orthoses (AFOs) are often prescribed to minimise gait irregularities. AFOs have been found to improve several measures of ambulation, including reducing energy expenditure and increasing speed and stride length. —very helpful!

Speech therapy helps control the muscles of the mouth and jaw, and helps improve communication. Just as CP can affect the way a person moves their arms and legs, it can also affect the way they move their mouth, face and head. This can make it hard for the person to breathe; talk clearly; and bite, chew and swallow food. Speech therapy often starts before a child begins school and continues throughout the school years.

Hyperbaric oxygen therapy (HBOT), in which pressurized oxygen is inhaled inside a hyperbaric chamber, has been used to treat CP under the theory that improving oxygen availability to damaged brain cells can reactivate some of them to function normally. Its use to treat CP is controversial. A 2007 systematic review concluded that the effect of HBOT on CP is not significantly different from that of pressurizened room air, and that some children undergoing HBOT will experience adverse events such as seizures and the need for ear pressure equalization tubes; due to poor quality of data assessment the review also concluded that estimates of the prevalence of adverse events are uncertain.

Nutritional counseling may help when dietary needs are not met because of problems with eating certain foods.

Both massage therapy and hatha yoga are designed to help relax tense muscles, strengthen muscles, and keep joints flexible. Hatha yoga breathing exercises are sometimes used to try to prevent lung infections. More research is needed to determine the health benefits of these therapies for people with CP. –LOVE YOGA!

Surgery for people with CP usually involves one or a combination of:

  • Loosening tight muscles and releasing fixed joints, most often performed on the hips, knees, hamstrings, and ankles. In rare cases, this surgery may be used for people with stiffness of their elbows, wrists, hands, and fingers. —this is what serial casting did for me, yet a more mild, prolonged form of aid!
  • The insertion of a Baclofen Pump usually during the stages while a patient is a young adult. This is usually placed in the left abdomen. It is a pump that is connected to the spinal cord, whereby it sends bits of Baclofen alleviating the continuous muscle flexion. Baclofen is a muscle relaxant and is often given PO to patients to help counter the effects of spasticity.
  • Straightening abnormal twists of the leg bones, i.e. femur (termed femoral anteversion or antetorsion) and tibia (tibial torsion). This is a secondary complication caused by the spastic muscles generating abnormal forces on the bones, and often results in intoeing (pigeon-toed gait). The surgery is called derotation osteotomy, in which the bone is broken (cut) and then set in the correct alignment.
  • Cutting nerves on the limbs most affected by movements and spasms. This procedure, called a rhizotomy, “rhizo” meaning root and “tomy” meaning “a cutting of” from the Greek suffix ‘tomia’ reduces spasms and allows more flexibility and control of the affected limbs and joints.
  • Botulinum Toxin A (Botox) injections into muscles that are either spastic or have contractures, the aim being to relieve the disability and pain produced by the inappropriately contracting muscle. — Did this at age 10, more mild form of aid as well!

A new study has found that cooling the bodies and blood of high-risk full-term babies shortly after birth may significantly reduce disability or death.

Cord Blood Therapy: There are no published randomized controlled trials or meta-analysis of this treatment modality in cerebral palsy. In March 2008 a boy diagnosed with cerebral palsy appeared on the Today Show with his family. The parents noted that he could not walk on his own and appeared to be “swallowing his tongue” at times. He was eventually diagnosed with cerebral palsy and could only walk with the aid of a walker for a short time. Earlier that year he participated in a clinical trial involving his own cord blood that his parents had saved when he was born. His parents reported that within 5 days after the procedure he was walking on his own and talking, something his mother said he was not capable of on his own and it was doubtful he would ever be able to do on his own. They also reported that the doctors also told them that if his rate of progress continues uninterrupted until he is 7 he will be pronounced cured.

Conductive education (CE) was developed in Hungary from 1945 based on the work of András Pető. It is a unified system of rehabilitation for people with neurological disorders including cerebral palsy, Parkinson’s disease and multiple sclerosis, amongst other conditions. It is theorised to improve mobility, self-esteem, stamina and independence as well as daily living skills and social skills. The conductor is the professional who delivers CE in partnership with parents and children. Skills learned during CE should be applied to everyday life and can help to develop age-appropriate cognitive, social and emotional skills. It is available at specialized centers.

Biofeedback is an alternative therapy in which people with CP learn how to control their affected muscles. Some people learn ways to reduce muscle tension with this technique. Biofeedback does not help everyone with CP.

Neuro-cognitive therapy. It is based upon two proven principles. (1) Neural Plasticity. The brain is capable of altering its own structure and functioning to meet the demands of any particular environment. Consequently if the child is provided with an appropriate neurological environment, he will have the best chance of making progress. (2) Learning can lead to development. As early as the early 1900s, this was being proven by a psychologist named Lev Vygotsky. He proposed that children’s learning is a social activity, which is achieved by interaction with more skilled members of society. There are many studies, which provide evidence for this claim. there are however, as yet no controlled studies on neuro-cognitive therapy.

Patterning is a controversial form of alternative therapy for people with CP. The method is promoted by The Institutes for the Achievement of Human Potential (IAHP), a Philadelphia nonprofit, but has been criticized by the American Academy of Pediatrics.[The IAHP’s methods have been endorsed by Linus Pauling, as well as some parents of children treated with their methods.

Ok so that pretty much covers the mechanics of it, I think. Haha… I bolded some stuff I found interesting, as it applies to my life with CP. Seeing as Spastic CP ( I have that!) is the most common, I found this other article:

http://www.indianchild.com/CerebralPalsy/spastic-cerebral-palsy.htm

On a less informative note, I had another soccer game today! It was pretty awesome if I do say so myself. :) I almost scored a goal, except one girl got in my way. My my my it was such an inconvenience. :p I stretcheed really well afterwards, hopefully I’ll stay this limber, otherwise this running will do no good for me in the future. I feel like I have really kicked up the gears lately, I can run about 3 miles now at a steady pace without stopping, I am so happy. :) My parents, a few others ( and my sister!!) are doing a 200 mile relay race from Santa Barbara to Dana Point, alllll down the Pacific Coast Highway for about two days non-stop! It is a 12 man team, and each runner has 3 legs of different times and milage. I am so excited for them to kick some butt! I will be waiting for them here as they travel down the coast. Yay! :) I sometimes wish I could run that much, but it is just too hard on my body and I dont want to risk my health at this point in my life. Trying to be smart about it is all! Life is about keeping everything in moderation.

Hope all is well! Can’t wait for spring break, are you all counting down the days or what!?  Be on soon,

-Katy

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Category: Exercising, Random, Teen Cerebral Palsy | Tags: , , , , , | 11 comments

  • Wikipedia Talk makes up for the lack of social information in the article.

    Also I have read a lot of information on HemiHelp. (This is a British organisation for and by those with hemiplegia).

    I think the soccer game may actually be the most informative.

    Thanks, too, for all the great information on therapy. I’ll probably have a few questions about HBOT and the various surgeries.

  • Courtney says:

    This is great :)

  • Katy Fetters says:

    Hmm i will be sure to look up Hemihelp.

    Haha well soccer is certainly my favorite form of exercise, so maybe thats the informative explanation :p

    Courtney– glad you like it :)

  • Greg says:

    I found this post by googling, “Running with CP”.

    “I sometimes wish I could run that much, but it is just too hard on my body and I dont want to risk my health at this point in my life.”

    If you decide you want to do it badly enough, I wouldn’t be surprised to see you out running most of your friends in a few years. Especially as you get older, your friends will get fatter and weaker.

    I too have mild CP. However, I can tell you from direct personal experience that the only thing that has made mine better and less noticeable was pushing my body too hard. Stretching has never done a thing for me. But, all I needed to do to see improvements in balance, strength, and all the areas in which I lacked was to take up weight lifting and running.

    It might not be as easy for us to run as it is for others, but those of us who can run and do, find amazing results.

    When I started running at 24, I could barely run around the block and sprained my weaker leg by the third day. My surgeries to lengthen my akiles tendon left me with a concave calf muscle, and I’ve lost the ability stand on my right toes. However, I can run mid-strike, which I couldn’t do before.

    As a teenager I was afraid to rebuild my calf and was constantly worried about the doom and gloom all my doctors predicted for me in my “later years”. In a couple weeks I’m attempting (completing) my first marathon.

    I wrote about my first hour long race (yesterday) on my blog: http://www.thecasualvegan.com. But, I’ve never blogged about CP, because it’s not something I think about often.

    I am always curious how many of us are into serious exercise.

  • Greg the Casual Vegan:

    We love your idea of the Running Streak.

    I’m going to read your exercise story, to see if it’s the way you told it here – with extra blogging detail of course!

  • Katy Fetters says:

    Greg–
    Wow you don’t know how great it is to hear your “story!” I am so relieved, in a way to know that I’m on the right track, and that there is hope in my coming years to keep the pace I am going at now. I just did castings awhile back, yet I don’t stretch enough for how often I work out. As of late, I have been doing 9-10 min miles for 45min-1 hour at a time about 4 days a week while still being able to play halfback in soccer and weight lift three times a week. So I definitely agree with you that strength training has ALOT to do with my ability to maintain stamina while working out. Although I still feel like I am putting myself at risk at times, I know that challenging myself is more important to me at present, than waiting to see myself deteriorate in the coming years. So thanks for your input, it is much appreciated!! I am going to read up on your running experiences once I knock out this homework, but congrats on that race and training for the marathon–that is mighty impressive. Great to see another hard core advocate for physically going for it with the “just do it” mentality.
    -Katy

  • And isn’t the point of challenging yourself so you can do more?

  • katy fetters says:

    I like to think that, yess!

  • katxdan says:

    hi
    im so glad to come upon this site as im 27 and we had our xspecial lil boy on the 7th july 2009 and was diagnosed with cerbal palsey within a few days also suffers from eplipsey and visual problems also has problems eating anything other than pot shots and milk, he was diagnosed with quadlipega cerbal palsey last christmas , and i have been so worried what life will have to offer him in the future im clueless to anything about cerbal palsey havent evr spoke to anyone with a child with cerbal palsey or a person who has it and how u overcome thhe reactions from other people as mentally our boy i dont think he is affected as bad as he is physically as he fully understands and is aware of everything, and you know what really makes me upset and annoyed how people insist on calling him or saying he very spasticated hate the word i really do i get so annoyed and upset how the hell will he feel as he gets older

  • Hi Katy! So glad to come across your blog. What a breath of fresh air you are :-) I’m the mother of a 10yr old daughter with CP, and also co-founder of “Reaching for the Stars. A Foundation of Hope for Children with Cerebral Palsy” http://www.reachingforthestars.org. Don’t know if you are familiar with us. We’re the only national nonprofit CP organization in the U.S. led by parents of kids w/CP and are busy doing lots of great work in CP advocacy, research, clinical trials and education across the country. See what you think!

    Would love to connect more with you and hear about your interests, challenges & successes. We’re on Twitter http://www.twitter.com/reach4stars and Facebook http://www.facebook.com/home.php#!/pages/Reaching-for-the-Stars-RFTS-Inc/162336273809809

    It’s great to see a beautiful young lady like you speaking up and using your voice and point of view. You can be an inspiration to other teens and children! Look forward to hearing more. All the best to you.

    p.s. We’ve arranged for John Quinn to speak at our National CP Awareness Day event in March at the CDC in Atlanta :-) I saw him listed in your resources. If you’re interested in learning more about some of great CP information & research resources out there – please let me know.

  • Katy Fetters says:

    Hi Cynthia!
    Thank you! I think it is so great you and many other parents have taken an active role in improving the lives of those with CP. I will definitely take a peek at your facebook page and foundation website! That’s awesome you’re having John Quinn speak this spring, he has a great story to tell.
    Ill be in touch! :)
    Katy


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