Showing posts with label kids. Show all posts
Showing posts with label kids. Show all posts

Thursday, May 16, 2013

Summer Heat Safety Tips

Summer Heat Safety Tips

By Lee Vander Loop
CP Family Network Editor
Summer is nearly here! Kids are anxiously awaiting the end of the school year and families are beginning to plan summer outings, vacations and outdoor adventures. It’s a time of sports, outdoor play, family gatherings, and warmer weather.
With the additional sun exposure, we as parents have the responsibility of keeping our kids safe during the long, hot days of summer. We’ll highlight some of the risks the summer heat poses and what you can do to protect your children and family for an enjoyable, healthy and safe summer.

Protecting Kids from Sun Exposure

Many of us are all too familiar with the pain of sunburns. For parents of children with special needs, extra vigilance is needed. A non-verbal child cannot communicate to you when they are thirsty or feeling the effects of excessive sun exposure. Kids don’t have to be at the pool, beach, or on vacation to get too much sun. Their skin needs protection from the sun’s harmful ultraviolet (UV) rays whenever they’re outdoors. The American Academy of Dermatology estimates that kids get 80 percent of total sun damage by the age of 18. Sunburn also affects your body’s ability to cool itself and causes a loss of body fluids. Follow these tips to keep your family safe this summer.

Timing is Everything

  • Seek shade. UV rays are strongest and most harmful during midday, so it’s best to avoid outdoor activities during this time. If this is not possible, seek shade under a tree, an umbrella, or a pop-up tent. Remember, it’s important to take precautions before a sunburn occurs, not once the damage is done.
  • Cool and cloudy? Children still need protection. UV rays, not the temperature, do the damage. Clouds do not block UV rays, they filter them—and sometimes only slightly. Make sure to take proper precautions even when the sun isn’t shining.

Cover Up

  • Protective clothing. Clothing that covers your child’s skin helps protect against UV rays. A T-shirt, long shorts, or a beach cover-up are good choices—but it’s wise to double up on protection by applying sunscreen or keeping your child in the shade when possible.
  • Get a hat. Hats that shade the face, scalp, ears, and neck offer the best protection. Baseball caps, although popular among kids, don’t protect their ears and neck. If your child chooses a cap, be sure to protect exposed areas with sunscreen.
  • Wear sunglasses. Sunglasses protect your child’s eyes from UV rays, which can lead to cataracts later in life. Look for sunglasses that wrap around and block as close to 100% of both UVA and UVB rays as possible.

Sunscreen

  • Apply early and often. The CDC recommends the use of sunscreen with at least SPF 15 and UVA and UVB protection every time your child goes outside. For the best protection, apply sunscreen generously 30 minutes before going outdoors. Since no sunscreen is truly waterproof, reapply again after they’ve come from the pool or other water sports activities. Don’t forget to protect ears, noses, lips, and the tops of feet. Keep in mind, sunscreen is not meant to allow your kids to spend more time in the sun than normal, it’s meant to reduce damage from UV radiation.  It doesn’t eliminate the threat.
  • Protecting infants. Although babies younger than 6 months should be kept out of direct and indirect sunlight because of their increased risk of heat stroke, The American Academy of Pediatrics now advises that sunscreen use on babies less than 6 months old is not harmful on small areas of a baby’s skin, such as the face and back of the hands. Your baby’s best defense against sunburn is avoiding the sun and staying in the shade.

Precautions for Special Needs Children

  • Medication precautions. Children on a variety of prescription medications are especially vulnerable to heat related illness.  Check your child’s prescriptions for warnings in relation to sun exposure. The risk for heat-related illness and death may increase among children using certain medications such as drugs: (1) which affect psychic function or behavior; (2) medications for movement disorders or seizures, because some medications can inhibit perspiration; and (3) diuretic medications or “water pills” that affect fluid balance in the body.
  • Wheelchair users. For children who are non-ambulatory and stroller or wheelchair dependent, extra caution is needed. Seek shade for your wheelchair dependent child and take all other necessary precautions listed here.  Wheelchairs make heat even more unbearable. The cushions heat up and the plastic covers may cause excessive sweating, which can lead to dehydration and skin breakdown. Also be mindful that the metal portions of a wheelchair or stroller can become extremely hot in a very short period of time when exposed to direct sun. Protect your child from contact burns by covering any accessible arm rests and metal frame portions of the chair that your child may come into contact with. Wheelchair umbrellas are one way to provide added protection.
  • Be prepared. If you plan on an extended outing, be sure to pack a cooler of ice and cold drinks. If you have a child who is tube fed and will need to be fed during the course of your outing, packing formula in a cooler with ice is a safe way to prevent spoilage. You’ll also want to keep small bottles of water in a cool place for any needed tube flushes, before or after feeds.

Conclusion

Avoiding sunburn and heat related illness is relatively straightforward if you follow these basic precautions. Being prepared, paying attention to weather conditions, and monitoring your child’s reactions to the heat and sun can help ensure your special needs child can enjoy outdoor activities this summer.

Additional Information

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Monday, May 6, 2013

Abilities Expo: Enhancing the Lives of People with Disabilities

Abilities Expo: Enhancing the Lives of People with Disabilities

By Stacey Bucklin
We recently posted an “In the News” story from CNN about assistive technology called“Rule Your Computer with a Head-Mounted Laser Beam.” The product intrigued me (who doesn’t love laser beams?), but what really piqued my interest was the event where it was featured, something called the Abilities Expo. I did a little digging and couldn’t resist sharing this resource with the CP Family Network community.
 

THE Event for People with Disabilities

The Abilities Expo, presented by Abilities365.com, plugs itself as “THE event for people with disabilities.” They even have programs targeted specifically for kids. Registration is FREE and grants you access to exhibitors offering the latest products and services, the opportunity to participate in free workshops, and world-class events and activities for all ages.
Their website states “For the past three decades, we’ve dedicated ourselves to making a better life for the 1 in 6 Americans with disabilities. This unique forum brings the Community together to learn, network and be empowered.” Expo exhibitors cater to children and adults with disabilities and their caregivers, offering products such as:
  • Assistive technology
  • Daily living aids
  • Medical equipment
  • Mobility products
  • Essential services
This video from www.karenkain.com seems to sum up the Expo pretty well. Karen is a Parent Ambassador for the 2013 Abilities Expos and has been attending the events for 17 years!
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Upcoming Expos

Abilities Expo events are held across the United States (and even abroad!) every few months. Chances are there’s an Expo coming to a city near you. Here’s a list of upcoming events:
  • NY Metro – May 3-5, 2013
  • Chicago – June 28-30, 2013
  • Houston – August 2-4, 2013
  • Boston – September 20-22, 2013
  • Singapore – November 8-10, 2013
  • San Jose – November 22-24, 2013
  • Los Angeles – February 28-March 2, 2014
  • Atlanta – March 14-16, 2014

Share Your Story

Have you been to an Abilities Expo or a similar event designed to serve people with disabilities? What did you think? Share your thoughts in the comments below!
 

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Thursday, March 7, 2013

Seizures and Cerebral Palsy

Seizures and Cerebral Palsy

By Lee Vander Loop
CP Family Network Editor
As the parent of 4 grown children, one of whom has spastic quadrapalegia cerebral palsy, I feel like I’ve experienced my share of parental stress and fears of raising 4 children and dealing with the challenges of maintaining the best quality of life possible for my daughter with CP.
I’ve experienced the heart stopping moment of having my 3rd born not recognize me after a concussion and a multitude of other parental trials and worries, but nothing could prepare me for watching my daughter with cerebral palsy experience her first grand mal seizure also known as tonic-clonic seizures.
No training, literature, insight or experience can prepare you for the heart stopping, gut wrenching experience of watching your child suffer through a seizure. Whether it be the first seizure or 50th, they all feel like the first with the overwhelming sense of fear, helplessness and frustration that comes with the inability to stop your child’s suffering.
Not all children with cerebral palsy suffer from seizures, just as not all children who experience seizures or epilepsy have cerebral palsy. Additionally, although learning disabilities are common with children who experience seizures, not all children who suffer with seizures experience learning disabilities.
Depending on the severity of the trauma and cerebral injury, infants who suffer injury due to a birthing trauma may experience seizures immediately after birth. In the case of my daughter who suffered severe global cerebral insult as a result of neonatal asphyxia, she experienced 3 days of uncontrollable seizures immediately after birth.

What is a Seizure

Seizures differ, depending on which portion of the brain is involved. Nerve impulses are constantly being transmitted from brain cells and processed by neurotransmitters. Seizures occur as a result of abnormal and excessive discharges of nerve impulses originating from certain brain cells. Some of these excess impulses reach skeletal muscle fibers and trigger the violent contractions witnessed with a variety of seizures.

Groups of Seizures

Focal Seizures occur in only one part of the brain or one hemisphere. Generalized seizures occur in both hemispheres of the brain.
Atonic Seizures are characterized by sudden loss of muscle tone, particularly in the lower extremities, often resulting in falls which puts the individual at risk for head injury and other physical injuries.
Generalized Tonic-Clonic Seizures also known as generalized convulsions or grand mal seizures are commonly seen with cerebral palsy.
Tonic Seizures spread throughout the brain, and are normally followed by unconsciousness, twitching legs and arms, convulsive body movements, and loss of bladder control. A child may bite their tongue during such a seizure. The “tonic phase” of these seizures is characterized by sudden muscle contractions and rigidity (hypertonia/spasticity).
Clonic Seizures – Involves recurring and coordinated jerking movements involving both sides of the body as well as rhythmic contractions of the affected muscle groups and violent and extreme gross motor movements. I’ve had the misfortune of witnessing a tonic-clonic seizure with my daughter. She was literally vibrating across the bed with the convulsive gross motor involvement.
Complex Seizures – Involve involuntary but possibly coordinated movement such as lip smacking, chewing and abnormal oral motor activity. With my daughter I called these “birdie seizures”. The oral motor involvement she exhibited involved repeatedly opening and closing her mouth, bringing to mind a baby bird in a nest waiting for food.
Myoclonic Seizures – Characterized by sporadic jerking movements, usually involving both sides of the body, that may progress to violent gross motor convulsive movements.
Partial (focal) Seizures are confined to one part of the brain and may be simple or complex. Partial (focal) seizures result from electrical impulses from one part of the brain and are usually a motor or sensory seizure that is restricted to one side of the body. The individual remains conscious. However, if the seizure progresses to a more generalized seizure, a loss of consciousness will occur.
Petit mal (absence) Seizures – Also known as Absence Seizures with this type of seizure a child may appear to be “staring off into space”, and will be unresponsive to stimulation or their environment. I’ll never forget the “vacant stare” my daughter exhibited the first time I saw one of these seizures. It was obvious, even to me, that something was wrong. I had never witnessed such a seizure. These seizures don’t pose the same hazard some seizures do, but they can put a child at risk of aspiration if they occur while a child is eating.
Fever (febrile) Convulsions- Febrile seizures are convulsions brought on by a fever in infants and small children. During the seizure a child may lose consciousness accompanied by tremors or shaking. A majority of febrile seizures are harmless and there is no evidence to suggest that they cause brain damage. However, children who have experienced febrile seizures that are lengthy or that recur within 24 hours or children with cerebral palsy are at greater risk of developing epilepsy.
The National Institute of Neurological Disorders and Stroke (NINDS) provides a comprehensive online fact sheet on Febrile Seizures, provides a detailed and informative description of this type of seizure as well as information on diagnosis and treatment.
Simple Partial Seizures - Cause muscle twitching, chewing movement and numbness or tingling. Partial complex seizures- Are characterized by a brief loss of consciousness, behavioral, emotional symptoms, loss of memory and automatisms. Temporal lobe and frontal lobe seizures are often in this category.

Diagnosis

EEG – Your child’s neurologist will probably want to do an Electroencephalogram (EEG) if they suspect seizure activity. Although EEGs are often helpful in diagnosing some types of seizures, it may not detect all. EEG’s are typically performed in the hospital’s sleep clinic and involve placing electrodes on the child’s scalp
Brain Scans and MRI – The neurologist may order a CAT scan or Magnetic Resonance Imaging (MRI) to be performed. Although these studies don’t show the electrical impulses, they may show lesions or other possible suspected causes of seizure activity.
Video EEG – This study is usually performed overnight at a hospital’s sleep clinic. It involves a video camera and constant EEG monitoring though out the study. With the video and EEG combined, the physician can collate any suspected abnormal physical motor occurrences with the EEG, better identifying the seizure activity with the physical manifestations.

Document It

If you suspect your child may be experiencing seizures, keep a journal and document episodes or behaviors you suspect to be seizure related. If possible have some one video tape the episode. This will give your child’s pediatrician or neurologist insight into what you are witnessing, since it’s unlikely your child will experience a seizure during your 15-30 minutes visit with the physician.
In the case of documentation, note duration of the episode, did you child becomecyanotic (turn blue) or have blue lips which would indicate they weren’t breathing properly, what was your child doing at the time, note any abnormal behaviors your child may have exhibited that made you suspect the behavior as seizure activity.
If your child already has a diagnosis of seizure and you don’t feel that their current medication is managing their seizures effectively, again, keep a journal of any suspected break through seizure activity you may see. There are many medications and combinations of medications that can be used for seizure control. If the seizures are adversely impacting your child’s quality of life, don’t give up. Persevere and continue to question your child’s physicians until you find the right medication or combination of medications that offers a better level of control. In my daughter’s case, I was told, considering the severity of her cerebral injury, she would never be seizure free, and that she most likely experienced silent seizures even during sleep. After birth she was prescribed an anticonvulsant which seemed to do little to control the seizures. It just seemed to “zone her out.” This was not acceptable to me and I persisted with the neurologists until they changed her medication and we found a combination that proved effective, at least during her waking hours, without the side effects that she seemed to experience with her initial medication. I was amazed at her new level of awareness after the change. To this day that same combination of medications has continued to provide an optimum level of control. Never give up!

Treatments and Medications

  • Protect a person from harm during a seizure. One of the complicated risks of seizures is that further damage can occur in the brain with severe seizures. The individual can also be hurt while falling or during spastic episodes resulting from grand mal seizures.
  • Anticonvulsant medications are normally prescribed in the management of a seizure disorder. Tegretol, Phenobarbital, Dilantin, Klonopin, Valium and Topamax are several examples of medications that may be prescribed.
  • Vagus Nerve Stimulation Therapy – This therapy is relatively new and involves a surgically implanted battery, with leads threaded under the skin and attached to the vagus nerve. Vagus Nerve Stimulation involves a device which sends short bursts of electrical energy into the brain via the vagus nerve.
  • Ketogenic Diet – This form of therapy involves a diet high in fats and low in carbohydrates and makes the body burn fat for energy instead of glucose. This form of therapy has been proven effective in some children in the prevention of seizures.

Side Effects

Every medication involves side effects. Some children may tolerate one medication but another child may experience intolerance or contradictions with the same medication. In my daughter’s case, I was in a position where I had to decide what side effects were acceptable and which weren’t. With the initial anticonvulsant, my daughter seemed unresponsive to her environment and “disconnected” from the world. That was not acceptable to me, but the new medication offered its array of side effects also. I remember researching the new medication in my boss’s Physician’s Desk Reference (PDR) and calling up the neurologist almost frantic!
Our neurologist was exceptional, and we communicated with ease. When I told him of my research in the PDR and my concerns (I think I heard a slight groan) he patiently explained to me that yes, the side effects and contradictions I was reading were cause for concern but the PDR had to list every incident of contradiction so the ratio seemed out of proportion. In most cases, the incidents were more a rarity then the norm. He assured me of the safety of the new medication and told me what would constitute severe side effects or contradictions that would warrant intervention. I thanked him for his time and for taking my call. My baby was a part of my world for the first time and was showing a new level of awareness. That went far in outweighing the unavoidable side effects and possible contradictions that came with the new medication. This isn’t meant to discourage a parent’s research, just the opposite. Educate yourself on all medications. That’s the only way you make an INFORMED DECISION.
There is much research being conducted and many clinical trials occurring in the field of neurology and seizure management. Many individuals are living seizure free as a result of the advances made in Neurologic medicine.

Questions to Ask Physician

  • You may have a thousand questions in your head about your child’s possible seizures, medications, or management, but you won’t think of half of them during your appointment with your child’s physician or neurologist. Write them down as you think of them!
  • Ask your physician what side effects to expect with any medication and what contradictions you need to be aware of and what to do in the case of a serious adverse side effect.
  • Should your child take the medication with or without food? Make your child’s neurologist aware of any other medications your child may be on, whether it’s seizure-related medication or not.
  • Make sure you’re aware of any blood work or lab work that needs to be done and the frequency. Many anticonvulsants require blood work to monitor the levels of the medication in the blood and to monitor possible kidney and liver function in relation to the medication.
  • Some children experience seizures that may be triggered by different environmental or dietary factors. Ask your physician if there are any environmental factors or dietary issues that you need to be aware of.

Wednesday, March 6, 2013

National Cerebral Palsy Awareness Month

National Cerebral Palsy Awareness Month


March is National Cerebral Palsy Awareness Month, a month designated to bring attention to this all-too-common disorder and the ongoing research efforts to find new treatments and possibly, a cure. At the Cerebral Palsy Family Network, we are proud to promote these efforts and be a part of such an important cause.
In 2011, the United States Senate designated March 25 as National Cerebral Palsy Awareness Day. The day was created to encourage all people in the United States to become more informed and aware of cerebral palsy. According to the resolution:
  • Cerebral palsy is caused by damage to 1 or more specific areas of the brain, which usually occurs during fetal development, before, during, or shortly after birth, or during infancy
  • The majority of children who have cerebral palsy are born with the disorder, although cerebral palsy may remain undetected for months or years
  • 75 percent of people with cerebral palsy also have 1 or more developmental disabilities, including epilepsy, intellectual disability, autism, visual impairment, and blindness
  • Cerebral palsy is increasingly prevalent, occurring in about 1 in 278 children
  • Approximately 800,000 people in the United States are affected by cerebral palsy
To celebrate this special month, we’ve created a “Faces of Cerebral Palsy” video series showcasing children with cerebral palsy from across the United States. The photos were collected during our “What Works for CP Kids” iPad contest held late last year. Cerebral palsy is such an all-encompassing term, and our videos represent the many different types of CP and the wide range of abilities these precious children possess.
We hope these adorable kids bring a smile to your face and brighten your day! To see your child in an upcoming “Faces of Cerebral Palsy” video, submit your photo on our Facebook page.

Thursday, February 28, 2013

Joint Contractures in Children with CP

Joint Contractures in Children with CP

By Drew Dillard
Joint contracture is the abnormal and essentially permanent shortening of a muscle resulting in the loss of normal joint movement. It is an especially prevalent condition in patients suffering from spastic cerebral palsy. Learn how to recognize joint contracture in your child and what treatment and therapy options are available to help alleviate the condition.

Definition

Normal muscles work in pairs. When one contracts, the other relaxes. This allows for conventional movement in the desired direction. In children with spastic CP, because brain-to-muscle communication is compromised, muscles have a tendency to work against each other, thus inhibiting effective movement. Over time, the pathological result of this muscular conflict (hypertonic spasticity) is a tightening or shortening of the joint. When muscle fibers are shortened (dystonia), the nearby joint can remain fixed in one position.  This, in part, is what causes the abnormal gait and postures seen in some spastic CP patients.
Hands, wrists, elbows, shoulders hips, feet, the back and even the jaw can be affected. Sometimes it affects only one or two joints, but in more extreme cases it can affect nearly every joint in the body. Untreated, it can lead to extreme pain and frequent bone fractures. Although spastic CP is not thought to be a progressive disorder, as brain damage does not get worse over time, spasticity in muscles can increase over time.

Symptoms and Diagnosis

In children with spastic CP, the process of growth often acts against them, making contractures more problematic. Symptoms may include a loss of motion in one or more extremity, joint inflammation, abnormal movements, disrupted growth (especially longitudinal growth) or an inability to stretch.  Discomfort is another symptom, as pain can result even without voluntary joint movement.
A healthcare professional skilled in joint mobilization will be able to test your child for indications of restricted structures within the joint. They might use a goniometer to measure the motion capabilities of a particular joint or use X-rays to reveal visible decreases in joint space, which could be an indication of a tight, contracted joint.

Prevention

As with anything, early detection is key. The best way to increase and maintain joint elasticity and prevent joint contracture is through joint mobilization and stretching. This can best be done with the guidance of a qualified physical or occupational therapist. Your child’s treatment regimen will depend on the severity of the condition and the child’s prior physical development. The sooner physical therapy is introduced into the child’s routine the better, because once joint contracture has taken place, it cannot be stretched or exercised away.
All physical therapy for cerebral palsy patients should include activities and education aimed at improving flexibility, strength, mobility and function. Cerebral palsy patients suffer from increased muscle tone (in the correct use of the term, muscle tone is an unconscious, low-level muscle contraction while the body is supposedly at rest). Tight muscles are the enemy of CP patients.
A physical therapist can also work with a client on “positioning” (placing the body in a specific position to attain long stretches) or suggest or provide adaptive equipment. A good physical therapist will teach the care-giver how to continue exercising, stretching and positioning at home.
Newer techniques, such as aquatic-based rehabilitation, have achieved impressive results in recent years. In addition to its restorative and detoxifying properties, water provides buoyancy that makes aerobic and anaerobic exercises easier and, in many cases, safer. Some of the documented benefits include improved neuromuscular responses, better muscle synchrony and improved range of motion in joints.

Treatment

If joint contraction has taken place, physical therapy and therapeutic massage will remain major parts of the treatment. Anything that increases mobility, joint elasticity and muscle strength can prevent the contraction from worsening, prevent additional contractions and provide pain relief.
Other treatments that may get introduced include: casts or splints, medication, nerve blocks and electrical stimulation and/or surgery.
  • Casts or Splints. Casts or splints can hold a body part in place in an effort to stretch the soft tissues surrounding an affected joint and keep it in a more functional position. They need to be examined and changed regularly to reassess joint position and avoid skin breakdown.
  • Medications. Baclofen infusion, a relatively new procedure, involves inserting a pump into the abdomen that distributes baclofen (a muscle relaxant) to muscles, thus temporarily reducing spasticity. Another relatively new treatment involves botox (a muscle paralyzer) injections into overly tightened muscles. In successful cases, the botox was able to weaken the group of muscles and reduce spasticity for periods of up to 4 months.
  • Nerve Blocks and Electrical Stimulation. Because the root problem in spasticity is muscles not working in tandem as they should, in some cases, opposing muscles can be alternately blocked (anesthetically numbed) while others are electrically stimulated. This treatment is usually combined with casting.
  • Surgery. When a contracture is unresponsive to other treatments, it may become necessary for an orthopedic surgeon to surgically lengthen or release certain tendons or muscles to improve range of motion.
The treatment for spastic cerebral palsy can vary greatly depending on the condition and prior development of your child. Assembling and consulting with a treatment team, including physical therapist, pediatrician, physiatrist, neurologist and orthopedic surgeon will aid in the decision making process. Started early, a well-managed and determined therapy regimen can prevent joint contracture from ever occurring.

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Monday, February 18, 2013

Traditional vs. Special Education for Children with Cerebral Palsy

Traditional vs. Special Education for Children with Cerebral Palsy

By John Lehman
Every parent wants their child to have a well-rounded education, and parents of children with cerebral palsy are no different. However, it can be difficult deciding what educational environment will best suit the needs of a child with CP. Some parents find that a special education program, with specially trained instructors, is the best environment for their child. Other children with cerebral palsy benefit more from attending a mainstream school. Of course, every child with cerebral palsy is different, and each option has its advantages and disadvantages.

Mainstream School

This type of school is best suited for children whose cerebral palsy is considered mild, and works best earlier in the child’s education rather than later. Some parents feel that a child with cerebral palsy learns social skills and grows emotionally in a mainstream educational environment. By interacting with non-disabled children, proponents of this option suggest that children with cerebral palsy will learn routine, everyday practices faster. Including children with cerebral palsy in a mainstream school can also be beneficial for non-disabled children, who can learn to develop empathy towards those who are different from them.
Usually, parents and teachers will develop an Individualized Education Program (IEP) to ensure that a child’s needs are attended to. During your child’s schooling years, they may receive physical therapy, speech therapy and special considerations during certain classes. For example, physical educational requirements will likely be different for your child than other children, depending on the severity of their cerebral palsy. These specialized programs can also be beneficial if your child has developed learning disabilities as a result of cerebral palsy.

Special Education

This kind of educational environment is great for children whose cerebral palsy is severe. Unlike mainstream school, a special education system will often have instructors specifically trained to teach a variety of children with disabilities, including those with cerebral palsy. In a special school program, the school’s curriculum is tailored directly to each child’s needs, eliminating the worry that a mainstream school might move too fast for your child.
That is not to say that a child with severe cerebral palsy cannot utilize classes offered by a mainstream program. In fact, many disabled children in a special education program will take art or musical classes at a mainstream school while receiving math, writing and other common classes at their special school program.  Depending on the severity of their condition, some children may receive special education for only specific subjects and use a mainstream school for the majority of their education.
When deciding which educational environment is appropriate for your child, it is important to know that you are not alone. Your child’s teachers, doctors and therapists are all available to assist you and your child as best they can. By working together, you can ensure that your child receives the educational support they need.

Resources:


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Tuesday, February 5, 2013

Psychotherapy for Children Diagnosed with Cerebral Palsy

Psychotherapy for Children Diagnosed with 
Cerebral Palsy

By Drew Dillard
The causes of cerebral palsy (CP) are both many and unknown, and no two people diagnosed with CP endure identical situations. However, at one point or another, nearly all people with cerebral palsy will face emotional and psychological challenges regarding the limitations CP has placed upon them. Let’s explore the types of psychotherapy available and how they might benefit your child.

Psychotherapy

Psychotherapy is a general term referring to therapeutic interaction or treatment contracted between a trained professional and a patient in an effort to improve that person’s sense of well-being, coping skills, communication skills and general disposition in the navigation of life’s challenges. It is different from therapeutic disciplines such as physical, speech & language, music & dance, occupational and play therapy, but is an important part of the overall care plan for your CP child.

Behavioral Therapy

Behavioral therapy uses psychological techniques that encourage the mastery of tasks. It is rooted in the belief that responses to emotional challenges and negative behaviors are learned and can therefore ne changed through therapy. Children do not yet possess the cognitive ability to process all that goes on with their thoughts and emotions, much less the ability to clearly communicate them. Psychotherapists are trained in identifying troubling situations, helping that child explore the thoughts, emotions and beliefs surrounding that situation, then helping the them acquire skills that will allow them to respond in a more effective and beneficial manner.
The activities used in behavioral therapy vary greatly depending on the abilities of the child and the problem behavior being addressed. Activities can be designed to teach completing tasks, managing emotions, resolving conflicts, delaying gratification and any number of other basic life skills. Behavioral therapy can help alleviate depression, mood swings, sadness, loss, anger and frustration by allowing previous negative outcomes to be replaced with a more positive perspective.

Counseling or Talk Therapy

As they get older, children with cerebral palsy will likely feel ostracized by peers, isolated from friendships, embarrassed by body image and/or frustrated with treatment goals. This may be a good time to introduce them to “counseling” or “talk therapy,” where they can talk about the things that are bothering them and learn to put them in perspective. It differs from behavioral therapy in that the goals are more along the lines of learning to accept and embrace one’s individuality rather than of raw behavior modification.
Even the most “normal” young person faces daily psychological and emotional challenges. Your hopes for your child at this age won’t differ much from that of any other parent. You want your child to cultivate a healthy attitude toward his or her challenges and to acquire the basic tools that will carry them into adulthood.  Many adolescents and teens see therapists to help process these complicated years. The right therapist can work wonders.

Social and Group Therapy

Individuals with physical or cognitive limitations often face real, and sometimes self-imposed, challenges in building relationships. Difficulties in communicating, fitting in or feeling accepted can lead to delays in social, emotional and even physical development.
Social therapy, introduced in the late 1970’s, helps children learn and embrace strategies that will help them develop friendships as they grow older by participating in group therapeutic settings. This decreases their sense of loneliness, isolation and stress. Social therapy focuses on the health and welfare of the individual as an integral part of a group dynamic. This relational approach helps children integrate into society and understand their role within.

Children with Mild Cerebral Palsy

Mild forms of cerebral palsy are often more difficult to detect and diagnose. Sometimes this leads to missed opportunities to introduce early-intervention corrective treatments, including those of a psychological nature. Undiagnosed abnormalities are often more emotionally troubling than diagnosed ones. If a child’s family and doctors don’t know what’s going on, it can be frustrating and confusing for the child.
A child that only exhibits minor physical impediments, such as issues of balance and coordination, may be completely normal in every other way. This can easily affect the child’s self-esteem. Also, children with minor physical or intellectual limitations are actually more likely to be teased and bullied for it than a child with an overt disability. Likewise, recent studies have shown that children with even minor learning disabilities benefit as much from treating the emotional component of the condition as with remediation of the learning disability itself.

It Takes a Village

It is important that parents and caregivers remain fully involved in the child’s therapies, especially with pre-teens. Caregivers need to understand and practice the positive behavior modifications learned in therapy to be able to recognize attention disorders, identify stressors, prevent meltdowns and minimize triggers all in an effort to reinforce a child’s progress.
Parents, caregivers and children with CP can all benefit from the positive interactions achieved with psychotherapy to compassionately, respectfully and appropriately interact with each other in a stable, secure and happy environment.

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Wednesday, January 30, 2013

Understanding and Treating Epilepsy

Understanding and Treating Epilepsy

By John Lehman
Some children who suffer from cerebral palsy have a chance of developing epilepsy, a seizure disorder brought on by brain injuries or certain neurological disorders. In fact, children and adults with cerebral palsy have a significantly higher chance of developing epilepsy than those not suffering from the disorder. Although there is still much to learn about epilepsy even today, there have been many advances in diagnosing and treating the condition.

Definition

Epilepsy is usually identified after the victim has received more than two randomly occurring seizures. When a person suffers from a seizure, the brain receives an overload of electronic signals powerful enough to disrupt normal brain functionality. This typically results in unconsciousness, involuntary muscle movements or spasms, emotional outbursts and loss of memory, though it varies depending on the person and the severity of the seizure.

Diagnosis

If you are concerned about your child having seizures, or your child has experienced his or her first seizure, set up an appointment with your doctor immediately. When children with cerebral palsy are experiencing seizures, a doctor can perform an EEG exam to assess their condition. Using a recording device, your doctor will scan your child’s brainwaves for abnormalities. Once the scan is complete, the data will be sent to a neurologist for analysis.

Types of Seizures

For those suffering from cerebral palsy, seizures associated with epilepsy are often categorized into two distinct types. Symptomatic seizures are identified as such when there is a specific, identifiable cause such as a disease or abnormality in the brain. Cryptogenic seizures, on the other hand, have no directly identifiable cause. These seizures are also known as idiopathic seizures. In these cases, doctors tend to look into the patient’s family medical history to see if the seizures are genetic.

Treating Seizures and Epilepsy

Once a seizure has begun, there is no way to stop it. Instead, the best thing you can do to help is to ensure your child is safe and comfortable. Clear the environment of potential hazards that could physically harm your child, as their uncontrolled movements could lead to cuts and bruises. Provide them with a pillow or a blanket so they may rest comfortably once the episode has passed. Contrary to popular belief, never attempt to stick anything in your child’s mouth when they are suffering from a seizure, as this could lead to serious injury (including choking or damage to teeth).
A single seizure is indeed a cause for alarm, but it may not be indicative of a seizure disorder. Remember that a doctor will likely not diagnose the condition as epilepsy if this is your child’s first seizure. In the case of a second or even third seizure, your child’s doctor will consider different forms of treatment, such as antiepileptic medications. If these do not prove effective, the doctor may recommend surgery.
There are other methods available to reduce the likelihood of a seizure occurring, including maintaining a healthy diet, keeping a balanced sleep schedule and exercising regularly. Your child’s doctor should be able to advise on which treatment is the best fit for your child’s condition.

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Thursday, December 27, 2012

Doctors Using Cord Blood to Treat Cerebral Palsy

Have you considered storing cord blood for later use? Many children with cerebral palsy have benefited from this procedure. Read more about cord blood storage and the benefits in our latest "In the News" article.
http://www.cpfamilynetwork.org/in-the-news/doctors-using-cord-blood-to-treat-cerebral-palsy

Wednesday, December 19, 2012

Don’t Hesitate to “Bother the Doctor” During Holidays

CP Family Network Medical Director Giles Manley, M.D., encourages parents to trust their instincts and contact their doctor if something seems wrong with their unborn child or infant over the holidays. He described a recent case where delayed medical intervention resulted in cerebral palsy:

I settled a case recently where a pediatrician sent an infant with severe jaundice home on New Year’s Eve with instructions to the parents to “check back in 2-3 days.” The baby had elevated levels of bilirubin in the blood, which is a sign that the liver is not cleansing the blood like it should, and is a serious condition if not treated quickly. The delayed treatment resulted in brain damage to the child.

So I always remind expectant parents, stand up for your rights as a patient over the holidays. If you think there is an issue with your pregnancy or your newborn baby, don’t let health care providers put off tomorrow what should be addressed today. If your doctor will be out of town, make sure you have his cell phone number and the name and phone number of the doctor who will be filling in for him or her. Then, don’t hesitate to use it if anything seems unusual.

To see a list of symptoms that warrant contacting your doctor, read Don’t Hesitate to “Bother the Doctor” During Holidays.


For more information please visit:

http://www.cpfamilynetwork.org