Cancer du cerveau

There are many common types of childhood brain and spinal cord tumors. If your child has recently been diagnosed with a tumor in the central nervous system, it is essential that you work to learn as much as you possibly can pertaining to the condition. The first step is to gain an understanding of the most common tumors that affect children.

In this medical guide, you will learn just that. Childhood brain and spinal cord tumors are often quite challenging to contend with overall as far as symptoms and treatments are concerned, but with the advances in the medical field, many tumors are treatable.

CNS Embryonal

The CNS or "Central Nervous System" embryonal is a common tumor that affects children. These childhood brain and spinal cord tumors actually form in the brain cells as well as the spinal cord cells when the child is considered a fetus - before birth. There are many different types of tumors that a child may develop if they suffer from a CNS embryonal.

These include an ependymoblastoma, medulloepithelioma, pineoblastoma, and a medulloblastoma. It is often challenging to identify these tumors. However, many women participate in an ultrasound at least during pregnancy. Medical professionals are typically able to identify these tumors through this process.

Astrocytomas

When it comes to childhood brain and spinal cord tumors, astrocytomas are quite common. A child that experiences a situation in which tumors form in the cells that are identified as astrocytes is said to have this type of tumor. These types of tumors may be further classified as either a low or high grade.

Those that are considered to be high as far as the overall grade is concerned typically grow at a rapid rate and also spreads quite quickly. These tumors are also considered to be malignant. This means that they are cancerous. Those tumors that are considered to be in the grade of low are those that progress at a slow rate of speed and are not likely to be cancerous.

Conclusion

There are many different childhood brain and spinal cord tumors that kids may be affected by. If you are informed by a medical professional that your child has a tumor in the central nervous system, it is important that you learn as much as you possibly can about the abnormal growth. You should discuss the following with your child's doctor:

• It is important to know which type of tumor that your child has.

• You should inquire about the location, and general size of the tumor.

• You should ask about the types of treatments that are available for the tumor.

• It is important to understand what symptoms will be experienced as a result of the abnormal growth.

• You should become educated on each of the brain cancer treatments that are available and inquire about which are the most appropriate for your child's condition.

• You should inquire about special funding sources and other types of resources that may assist you and your family while your child receives care.

If you receive the above information, it will allow you the opportunity to make well informed decisions pertaining to childhood brain and spinal cord tumors.

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About the Author: Anne Ahira is an established entrepreneur and successful coach in her country of Indonesia. Her success story has been published in many nationwide publications in Indonesia.

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As parents, the ultimate dream we have for our children is that their childhoods will be happy ones, and they will grow up to lead long and healthy lives. Yet, every day, across America, there will be nine families whose dreams will be shattered when they learn that their child has a spinal cord tumor or some form of brain cancer. And, by the end of the year, over 3,000 families will have faced that same moment; when time stood still, the world blurred, and their lives changed forever.

From the moment their child is diagnosed, parents embark on a journey that will challenge every aspect of their being - from intellectual and physical, to mental, emotional and spiritual. It is essential that these parents have a strong support network, with family and friends taking on a vital role in that network. Along with that key component, parents also need a structured system that can provide resources to help them navigate the many challenges they will face, and assist them in making the best possible decisions for their child's health and well-being.

Once past the initial shock of the diagnosis, parents begin searching for answers to the flood of questions rushing through their minds. Knowledge is power, and early education about this disease can provide a lifeline in these dark waters.

There are several good sources for information on pediatric brain tumors and brain cancer, all of which can provide resources for education, assistance and support--

• Family doctors and pediatricians;
• Children's hospitals and cancer treatment facilities; and
• Nonprofit organizations focused on pediatric brain cancer.

Here are just a few examples of what a parent might find within the FAQ sections of these organizations:

Q: What are the causes of pediatric brain cancer and spinal cord tumors?
A: There are many different kinds of pediatric brain cancer, and their precise causes are still unknown, although research programs are making advancements towards understanding the causes, as well as improving treatments.

Q: What is the prognosis for most young patients with this disease?
A: Current statistics show that one in three patients will survive no more than five years. However, thanks to the progress that has been made in research over the past twenty years, there has been a significant decline in the overall cancer death rates, and it is estimated that there are 25,000 brain tumor survivors in the U.S. today.

Q: What are the treatment options for a child with a brain tumor or brain cancer?
A: Treatment of brain or spinal cord tumors includes surgery, radiation, and chemotherapy, depending on the type, rate of growth and location of tumors. It usually begins with surgical resection to remove all or part of the tumor. Although complete removal of the tumor (gross total resection) is often the treatment of choice, partial removal of the tumor will occasionally relieve a child's symptoms.

For parents who find themselves facing this life-altering journey, help is available in many forms, and from several well-respected organizations. Whether the need involves education about this dreadful disease, finding sources for medical or financial assistance, or simply connecting with others in similar situations, the resources are available. Reaching out to one of these organizations can often make the difference in how this journey is traveled-by the parents, and by the patient.

This article was written by Joe Fay, Executive Director of the Children's Brain Tumor Foundation. For more information, or to make a donation, please visit http://www.cbtf.org/. Contact Joe Fay at jfay@cbtf.org or 800-228-4673. This article is free to be reprinted as long as the bio remains intact.

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