Cerebral palsy (CP) is a developmental disability that affects children’s ability to control their movements, causing issues like muscle weakness, stiffness, repetitive movements, or shakiness. It is a lifelong condition that affects how the brain and muscles communicate, affecting body movement, muscle control, coordination, reflexes, posture, and balance. CP is characterized by abnormal tone, posture, and movement and is clinically classified based on the predominant motor.
Cerebral palsy is caused by irregular brain development or damage to the developing brain, usually occurring before birth or early in life. Genetic causes, although less common, can also play a role. Cerebral palsy is the most common motor disability of childhood and is a group of conditions that affect muscle tone, posture, and movement as a result of damage to an area responsible for muscle control.
Symptoms appear during infancy or preschool years and vary from mild to serious. Children with cerebral palsy may have exaggerated reflexes and may exhibit developmental delays in physical movement, cognitive ability, communication, or emotions. CP occurs when there is abnormal development of or damage to areas of the brain that control motor function. This can happen before or during birth (congenital).
Cerebral palsy is a group of lifelong conditions that affect movement and coordination. It is caused by a problem with the brain. Cerebral palsy is the most common childhood physical disability, and it is caused by brain damage during childbirth. Comprehensive information and support are available for families dealing with cerebral palsy.
📹 Cerebral Palsy, Animation
Cerebral palsy: types (spastic, dyskinetic, and ataxic cerebral palsy), symptoms, causes, risk factors, complication, diagnosis and …
At what age is CP diagnosed?
Cerebral palsy is typically diagnosed in the first two years of life, but mild symptoms can make it difficult for doctors to diagnose before the age of 4 or 5. Doctors conduct tests to evaluate motor skills and monitor the child’s development, growth, muscle tone, age-appropriate motor control, hearing and vision, posture, and coordination. Although symptoms may change over time, cerebral palsy is not progressive.
If a child is continuously losing motor skills, it is more likely that the problem is a condition other than cerebral palsy, such as genetic or muscle disease, metabolism disorder, or nerve system tumors. Lab tests can identify other conditions causing similar symptoms.
Why do people get cerebral palsy?
Cerebral palsy is a condition that results from damage or abnormal development in the brain areas responsible for controlling movement. It can manifest at any point during the first two decades of life, with the potential for onset prior to, during, or shortly after birth. The precise etiology is frequently uncertain, and the majority of children with cerebral palsy are born with the condition, which is known as congenital cerebral palsy.
Can cerebral palsy be treated?
Despite the absence of a cure for cerebral palsy, a range of treatments is available to assist individuals in maintaining an active and independent lifestyle. Healthcare professionals collaborate with individuals to develop a care and support plan, which is subject to periodic reevaluation in accordance with evolving needs. As they age, they may require different care due to the progression of bone and joint issues, which may result in impaired mobility.
Can a child with CP talk?
Children with cerebral palsy often struggle with controlling their face, tongue, jaw, and chest muscles, limiting their ability to produce sounds and speak. Around 75 of these children have speech defects, but 50-70 can benefit from speech training. Speech therapy helps children control key muscles involved in word formation, sound production, and breath control, improving communication skills like vocal clarity and listening. It also helps children express themselves more easily, improves relationships, and boosts self-esteem, confidence, and independence.
Can a child with cerebral palsy walk?
A study involving 2, 295 children with cerebral palsy found that children who roll but do not sit without support at 2 years of age are more likely to be capable of full ambulation at 14 years old. This is defined as walking well alone at least 20 feet without assistive devices. The central nervous system lesion of cerebral palsy affects the development of children and young people with cerebral palsy in different ways according to their age, severity of activity limitation, type of motor disorder, and cognitive ability.
Growth-associated factors such as muscle tightness, contracture formation, and weakness can lead to skills being lost. Parents often want to know what the future holds for their child, but the development of key activities is usually unknown at diagnosis. Key areas of development are crucial for independence in everyday life, such as independence in transfers, meaningful communication, and effective upper limb activity for daily living activities and using mobility aids. Life expectancy is another area regularly discussed at an early point after diagnosis, particularly in children with severe impairments.
What is the life expectancy of a person with cerebral palsy?
Cerebral palsy typically lasts between 30 and 70 years, with the longest life expectancies characterized by increased mobility, better medical care, and adaptive equipment. However, there is no cure for cerebral palsy, and it does not worsen over time due to a one-time brain injury. Other co-occurring factors and separate conditions may impact health and life expectancy over time. Most children diagnosed with cerebral palsy can expect a relatively normal life expectancy. Severe versions of the condition may have significant mobility difficulties, seizures, or respiratory problems. Regular exercise is crucial for strong muscular and cardiovascular health.
Can a child with cerebral palsy live a normal life?
Life expectancy for cerebral palsy patients is determined by the severity of the condition and coexisting medical issues, making there no set time frame for their life. The life expectancy of cerebral palsy patients is generally the same as someone without the condition. Life expectancy is calculated based on the average age of a particular population group when they die, and can be affected by mobility issues, intellectual disabilities, vision/hearing impairments, and other coexisting conditions. Parents may have concerns about predicting and improving their child’s life expectancy.
How does cerebral palsy affect a child’s everyday life?
Cerebral palsy (CP) is a lifelong physical disability that impacts posture, balance, mobility, communication, eating, sleep, and learning. It affects one in three children and is particularly pronounced in those with spastic quadriplegia, intellectual disability, epilepsy, vision impairment, and inability to sit independently at two years of age. CP can also affect speech coordination, causing some individuals to sound “breathy” when speaking.
Pain, such as contractures, abnormal postures, dystonia, skin breakdown, hip subluxation, gastro-oesophageal reflux, and scoliosis, can lead to a person’s behavior, ability to do things for themselves, sleep, and social relationships.
People may avoid daily tasks that are essential for independence, such as attending school and social events. Pain can be relieved, but it is best to consult a medical practitioner for proper management.
Can kids with CP live a normal life?
Life expectancy for cerebral palsy patients is determined by the severity of the condition and coexisting medical issues, making there no set time frame for their life. The life expectancy of cerebral palsy patients is generally the same as someone without the condition. Life expectancy is calculated based on the average age of a particular population group when they die, and can be affected by mobility issues, intellectual disabilities, vision/hearing impairments, and other coexisting conditions. Parents may have concerns about predicting and improving their child’s life expectancy.
What is the behavior of a child with cerebral palsy?
Cerebral palsy is a motor disability caused by brain damage, which can lead to frustration and destructive behavior in children. These issues are often a response to feelings of overwhelm, stress, or misunderstood. Cerebral palsy can affect various areas of the body, including the muscles around the mouth that enable speaking and eating. Therefore, a child’s behavior may be influenced by their cerebral palsy.
Can a child outgrow CP?
Cerebral palsy is a permanent condition with no cure, but it is not progressive and does not worsen over time. However, associated conditions like epilepsy, osteoarthritis, hearing and vision loss, incontinence, malnutrition, dental problems, and speech and language disorders can worsen. Treatments can improve symptoms, functioning, and quality of life, but they cannot cure cerebral palsy.
There is no cure for cerebral palsy, but many treatments can relieve symptoms, manage associated conditions, and improve function and quality of life. Surgery can reduce pain and improve mobility, but it is unlikely to restore complete function and movement. Appropriate treatments can help manage these conditions and prevent their worsening.
📹 Cerebral Palsy – (DETAILED) Overview
I have lived with cerebral palsy for over 50 years and now understand what causes it so much better. Thank you so much. Just one thing, whilst we do know it is a static condition, we know that whilst the brain damage that caused cerebral palsy won’t progress, the motor impairments that result from the brain damage can. As a result, ageing with cerebral palsy can have a significant impact on one’s communication skills, energy levels, and physical and mental health.
As a Person that suffered a Moderate Level of Cerebral Palsy I had a communication device After school when I was in first grade, That surgery wasn’t until December a year later in 2016, My Condition of Cerebral Palsy is now Mild but I still couldn’t do things like most people can do which is, Tying My Shoes, Carrying a Dog or a person or other animals like Guinea Pigs, ETC and using Chopsticks, I Don’t talk that much and I feel that this may come back to me due to my communication. I’ve lived with Cerebral Palsy ever since I was born 16 years ago. So I’m happy my parents took care of me while I still have this disability, Today I can walk better and go safely and peacefully.
You deserve a clap 👏👏👏 What a good and fantastic explanation with an easy and creative way . Literally I have understood and memorized everything in just 13 min,🤓 seriously it is very effective than just attending a lecture for 2 hours . if our college hire people like him, I will literally attend the lecture without complaining. (A lot of thanks for making this overview)
I write the following remarks as a person with Cerebral Palsy and a Rehabilitation Counselor (like an Occupational Therapist for the mind of people with disabilities). 1. This is a good article with a lot of important information in a short period of time. 2. Be careful in referring to any disability as non-progressive or static. I understand this is an accepted medical term. However, this gives the impression that Cerebral Palsy cannot get worse. The condition cannot get worse in and of itself. The ability of the individual with the condition to handle the disability will certainly change because of aging, changes in the physical environment surrounding the person, other psychosocial realities, (e.g. families, relationships, employment, other co-occurring conditions- PTSD, Autism, etc.), and sociopolitical framing of the term disability and what having a disability means to society. All of these factors (and more) will impact a person’s ability to handle CP. A better term to use when discussing any disability that may be considered non-progressive and/or static would be dynamic. An individual’s disability and how they cope with that disability will change according to the dynamic factors above. 3. For many people who use wheelchairs, Dermatologists are a crucial member of the support team. The human body is not meant to sit the majority of the time, and yet this is a reality for many people with CP. Dermatologists are key members of the treatment team when seeking to address the skin problems sure to follow someone who must use wheelchairs for mobility.
I think what people don’t understand is that you can have this and not be disabled at all, maybe your foot turns in and you limp slightly, or you can be as disabled as people can get. Which is really tough for people with extremely mild versions. People treat us weird like we’re disabled and we’re not at all. I walk a few miles a day and I’m incredibly healthy. I’m not disabled.
I have the mixed CP hemiplegia type. If I don’t consciously think about it, my right arm and hand and shoulder will do whatever it wants and is incredibly painful when I don’t control it. I have a little bit of dyskinetic movements in that arm as well. My right foot goes down and inward to the left. I do you have tremors on my left hand as well. This was so incredibly helpful to learn what CP entails. Thank you!!
I am a home care nurse and most all of my cp patients are late birth related cp. I know as a mother I was 40 weeks and my doctor was in clinic when time to push. Nurses begged me to not push. Luckily my son was born with no defects. I truly think it has a lot to do with birth difficulty and time in the birth canal.
Wow got a bit shocked when you discussed the whole team of folks around one CP sufferer. I’m very mild, but as a child with my CP I had a physio I saw 4 times a year and a pediatrician I saw once a year and that was it. I did have some one off treatments (and wore splints only for a few years), but nothing regular aside from physio and once I hit 18 the NHS completely cut me off from anything like I’d just be fine. I’ve had physio once as an adult because I had one specific problem that cropped up and that has been it.
My foster baby was recently diagnosed with CP. Her biological mother regularly abused heroin (and possibly other drugs) during the first trimester and some of the second trimester. Biomom was incarcerated when she was almost 5 months pregnant and was put on methadone. My foster baby was born at 6.5 months and had methadone in her system but no symptoms of withdrawal or drug dependence (addiction). I was wondering if the history of drug usage would be a contributing factor to the baby’s CP diagnosis?
I have problems with vision, pain, movement and my bladder, every time i drink a cup of liquid i have to urinate urgently, and I still wet the bed a little bit, I struggle with urinary frequency and urgency several times a day and at least twice a night and i still leak sometimes, and I have to wear eyeglasses because of my visual impairments, and I struggle with neck and back pain also
My son has been diagnosed with hereditary spastic Paraplegia through genetic testing..I and several of my family members have it. My daughter however has been diagnosed with spastic diplegia CP. I thought CP required some sort of scarring on the brain. My daughter, son, and other family members have had that brain scan and show no scarring..could it be that my daughter doesn’t have spastic diplegia but hereditary spastic Paraplegia. She has not had genetic testing. Also is clonas a type of involuntary movement? It can be stopped by situating the foot in s different position, but still is that considered involuntary and therefore be considered a different type of cp? I ask because we all have clonas in our family, my son and daughter have balance issues in various degrees…
CAC Panchasakar churna is an Ayurvedic formulation that consists of mainly five ingredients as its name describes. This medicine is known to have properties like laxatives and purgatives etc. The Churna contains ingredients such as Shunthi (Zingiber officinale), Haritaki (Terminalia chebula), Trivrith (Operculina turpethum), Pippali (Piper longum), and Sauvarchala lavana. It decreases the abdominal pain, bloating, constipation that maintains a healthy colon and supports the overall health of the body.
Does this mean my 3 year sister with cp will she ever be normal and act like a normal kid she can’t walk or anything but she can say certain word but she doesn’t understand her surroundings but she do a little but but can’t necessarily really talk or say how she feel but she responds with no words she also watch coco melon a lot and when she says wants too watch it we put it on she also sings the songs in coco melon as well so she does have intelligence so what’s wrong with her when can I do is it treatable will she be normal and ever walk instead or the doctors putting braces on her and potentially putting her in a wheel chair ?
Got an MRI and the Neurologist still doesn’t know if my son is having seizures or not. Seems like I need a second opinion. The pediatrician has been no help. i have to tell her what to do in order for her to write referrals. Then most of the time they do not write them the correct way which prolongs my son getting help. I just don’t understand the incompetency.
Hi i would love to understand more of this condition. My daughter she is 1 year old and she born without the cerebellum, thin corpus callosus, enlarge ventricules, smooth cortex and other malformations. She suffers high muscle tone, muscle and bone contracture, tremors, seizures, she is not able to eat by mouth since birth, her right arm and her left leg is the most affected areas but is totally noticiable in all her body. Her sight is affected too. Also she’s diagnosed with colpocephaly, microcephalic, hydrocephaly, short stature baby, poor weight, and cromosomal abnormalities, she have a change in her adn chain. Is all of this conditions cerebral palsy?
I was born with CP. I went from deploying as a contractor to Afghanistan Iraq and Qatar in my 30’s with mild CP. To excruciating chronic pain and weight gain by 45. This is no Joke. Doctors want to diagnose every problem and pain as CP related. I started declining when the apartment had a saver black mold infestation. Overnight I went from what was my normal. To falling 3 times a week on the way to work. There were even days I was furniture walking to keep my balance. I even had physical and visual hallucinations of bugs and lice infestation. To this day I have chronic pain and inflammation. I keep a recumbent bike, an elliptical trainer a starch machine, a 60-up balance trainer and recently got a treadmill for what I call “the little gym” in my home. I moved to a dyer climate to get away from the mold and got a job where I can work from home. I work in IT. I figured out that the full body vibration machine really really really helps. So did getting away from the black mold. I am Leary of walking in public. I brace myself against vehicles or reach for objects when climbing curbs. I use curb cuts and ramps . I climb and descend stairs slowly. Holding on to railings. Most of it is fear. I would fall 2-3 times a week going to work in Washington DC. And I did not know what was making me worse. I will say. I figured out the music benefits by the time I was 9 years old. Music also helps calm all the spasticity and thus the pain associated with muscle tightness.. An also pretty sure I have a lot of undiagnosed micro fractures from falling and an undiagnosed hernia.
The doctors played around with my kid and continue to do it. I have to constantly stay on top of every doctor and try to get therapies. This is really frustrating. Especially since most therapies are via zoom when most kids need hand on and active therapies. I have been thinking my kid had this but the doctor didn’t want to test until almost 2. I asked if there would be pain and he said no; but other sources say otherwise. Since my kid is non-verbal; I have to pay attention to make absolutely sure. I wish the therapies in my area were more hands on and active. All I see are a lot of people making money off of my child because he has these problems. He has not been able to benefit as he should as of yet. I am going to continue to advocate for him as best I can but it is really exhausting. Pray for me.
hi good evening… i usually watch your articles and learn alott from them. they are really very helpful… you are a life saver…. is there any way that you can post the full chart as a link or on end of article so we can have a look collectively whenever we want…so we can keep in safe in our phone or laptop… thank you so much love u
I look up to them and appreciate them . In this imperfect world certain amount of people must suffer the imperfection. They are b burdening huge deep sufferings we would have burdened if they hadnt. They are being crucified. People should treat them polites and governments should protect. their life.
I have cerebral palsy I am 36 years old and I developed bipolar manic depression at 17. Thanks to good care I am doing okay. Is there a link between cerebral palsy and bipolar. As when I was ill I went catatonic. Is there a link between Catatonia the cerabalum and the frontal cortex because when I was treated on a physio ball my condition got better. Is that a correct link to make, I would love to know your thoughts many thanks, Samuel
War on buffet (jimmy), buffet’ where we know he to be the loin fruit of Justin Berry, “Boof, bauf” in the one shown in my dreams as the champion of the merger of blue and red, the royals of saturn from Asland, via the cia root in the grateful dead following of CareBears of Camelot… All these stories possess the seeds of truth with the connecting pieces unto other lore, while all possess the ommissions of the core truths that bind them all together… The chosen one, of the sword and the stone, the righteous one whom ties all stories together in one “History”, to which Wynn road on the left at the turn works eleven hour days to forever destroy the history, in the fashion of the DEA dystopian truth… What happens when you try telling a new 26 generation story beyond the safest high temperature? 425, under the guided watch of the lord of Rainier, which again only one possesses the root of their birth chart being expressly fortelling of whom it is that is lord of the western side of Washington state, the seventh heaven, heaven on earth that daily falls lower away from its true heritage. Wells Fargo (dakota)… Waterless roots… Indian reservation lands. Even their allegiances with the forefathers have been removed, where they were given life and liberty under the sworn forever allegiance to the As Land, never Oceanic underwater realm to which they could be removed of being under the light of the sun as children of it… This is the sad truth, that there is currently no AD vert i sing that truly cares about your eternal soul.
I was born with epilepsy and cerebral palsy. I have a twin brother, i was born first. My brother was born with no problems. I take phenytoin for my epilepsy, as a child I was on phenabarbatone, then at 14 i was put on Epilim 500mg. Which caused me to gain lots of weight. I went to live in Canada for a few years where I was taken off eperlim & switched to phenytoin. Which I still take today. As a child I had grand mal seizures, which doctors said I would grow out of. Which I did, but I now have petit mal. It’ feels weird when I have it, i can hear all thats going on around me, but ppl and any noise, sound much louder, plus it feels like I’m floating on water. Before the seizure I get the smell like burnt toast. I can have a seizure at any time, night or day. Unpredictable. I feel a little confused when I come round, which lasts for a couple of minutes, then I’m back with you again. Usually a cup of tea helps me recover. I read a lot of blogs where people who shared their testimonies kept mentioning Anti-seizure Herbal medication. I searched for a website I just followed the email address of Doctor Patrick that was shared on these testimonies; I got lucky when I got a reply from Dr. Patrick. I followed his instruction, used Herbal Medicine in less than 2 months, I was already cure because of the changes I was seeing. Within a period of 5 months, I was cured totally forever. I went back to my neurologist, I was checked up and marked epilepsy free. If you need his help you can Contact this herbal doctor via his email herbalmedicalhome@gmail.