Kissing Away the Boo Boos: Helping Kids Fight Cancer

Mothers will always try to protect their children from everything they possibly can. We keep them away from sick people and make sure they have enough layers on to keep them warm in winter. Being a mom is a challenge, sometimes we lose, and sometimes we win.

Children who are frightened or injured will cry out for mommy. Mommy will administer tender loving care, a kiss and a band aid; the child will instantly feel better. There are those times when a kiss and a band aid simply do not cover the situation.

We hear more and more about children with cancer these days. These children and their parents are discovering that life is about to change for them forever. Cancer treatments are very apt to include surgery along with chemotherapy or radiation. This is terribly hard on a child, and possibly just as hard on the parents who stand by helplessly. Mothers are used to taking control of their kids' wellbeing through sickness and health, we fall apart when hugs and kisses won't make it all better, our child is in pain and there is nothing we can do about it.

Fortunately there are doctors working around the clock to find new ways to cure cancer. A tremendous amount of money is being sent from all over the world so doctors and researchers can devote all their time and energy into finding new ways to make a difference in the treatment of cancer. Thankfully there have been huge medical advances in the last several years.

Most years there are big corporations joining in the cause for cancer awareness by seeking donations from their customers to help cancer research. Companies like Wal-Mart and McDonald's ask their customers to donate an extra dollar or so at the check out counter to help fund research. Many customers who are able to donate do so. Obviously, one must always contribute to their own family's support before helping others, but if each customer gave just a dollar, a huge difference could be made in discovering better cancer treatments and even a vaccine that would stop the disease before it started.

Most of us never imagine that it could be our child who suddenly gets sick and is diagnosed with cancer. We figure that since we have no history of cancer in our family surely our children won't have to worry about that. No parent ever expects their child will get sick, especially not with cancer. But those parents and children who suddenly find their world upside down cannot stress enough how important cancer research is.

It doesn't matter who we are, we are all in agreement that no child anywhere deserves to suffer, particularly something as painful and stress-inducing as cancer. It is fortunate for us that millions of dollars are donated annually to find ways to mitigate the disease if not end it entirely. There are some rare forms of cancer that sadly have no chance of a cure as yet. Even among the cancers where treatment plans are available, a patient is deemed to be cured if they have been in remission for five years. Five years does not seem like a big deal when a child is involved.

As parents, the thing that we want most for our children is for them to live long and happy lives. While we cannot kiss their boo boos to make it all better, we can donate to cancer research in the hopes that one day doctors will be able to discover a permanent cure for cancer because every kid deserves the chance to live their live to the fullest.

If you enjoyed the above piece, it is easy to go look at additional related posts at Sy Schlager or this Sy Schlager Article.

Cancer Alternatives Cures - Introduction: Towards a Freedom of Choice

This quick guide on therapies for cancer treatment is to be understood in a purely informative nature. The aim of those who wrote it is not so much to steer the patient to start a therapy rather than another, but to inform him of the existence of possible "different" than the official ones already known.

In this sense, the information, which is the first step towards knowledge, could lead the patient or his family, to think freely and wider, the better chance of cure. Move towards a freedom of choice is a difficult path that can never be separated from knowledge.

We will speak more of the situations with poor prognosis, cases where the disease is advanced and the chances of healing are minimal, because it is assumed that in the most fortunate cases there is less need to reflect and to evaluate the possibility of taking different treatments.

This account can not be considered exhaustive at all about the different therapeutic options existing for the treatment of cancer, but does represent a strong effort of reflection on them.

In this perspective, this report can be considered certainly not an end point, but rather a starting point, a first step towards a brave awareness about this disease and what the patient or his family can "groped" beyond what they already know. In this sense, start to assume a more aware and active behaviour against the disease, could be of great help in precisely those situations with unfavorable prognosis, when despair is that we no longer know what to do.

The sense of impotence is not only devastating for the patient but also for all the people closest to him. So, overnight, they are in a "tunnel" without knowing why they have entered a way without a glimpse of an exit. But sometimes it can happen to feel the need to do something, and then think of alternatives is absolutely necessary, just to keep alive the hope.

In this contribution, rather than provide answers, deliberately trying to create questions, to question the certainties that seem to be acquired, conscious of the fact that the absolute truth on cancer unfortunately has not been found yet. The different therapeutic options to be discussed will not be deliberately treated comprehensively and completely, to leave to each patient or family, the right space for personal investigation. It is only through a series of reflections and subjective evaluations on the different treatment options that each patient will be able to decide their course of treatment.

The author has found an alternative source of Cancer cure. You can read further info by clicking here

Learning More About Mouth Cancer Symptoms

Mouth cancer, which is also known as oral cancer, commonly involves the tongue, lips, gums, palate as well as the mouth cavity's membrane lining. This cancer is developed as the result of malignant cell growth. Mouth cancer can affect men and women especially those who have reached the age of 40. The risk of suffering from this disease will increase if the individuals chew smokeless tobacco. Besides, severe periodontal disease and family history of oral cancer can also put someone at higher risk of oral cancer. Learning the symptoms is a good initial step to know if you are infected by this disease. By identifying mouth cancer symptoms, you still have time to prevent more complications such as speech problems or the spread to lymph nodes. In addition, learning the symptoms may give you the chance to get early treatment. Here are the symptoms that you can learn:

1. Sores or lump inside the mouth, on the gums or on your lip. These sores are symptoms of oral cancer when they don't heal, there is a change in its size and bleed easily. Thickening skin or lump in the cheek can also be the symptom of this cancer. Notify your doctor when you experience these symptoms so that he can check if you are suffering from this cancer.

2. Red or white patches in the mouth, gums or tongue. The size and appearance of these patches can change and they can be the sign of this cancer.

3. Numbness and teeth problems. A sign of mouth cancer can be painful teeth. If your teeth become painful or they are loose, be wary of this condition. Oral cancer can also cause the jaw to swell. Thus if you wear denture and your jaw swells, you will feel that it doesn't fit properly anymore. Another sign of this cancer is any numbness in the mouth.

4. Bad breath and voice changes. Commonly, someone who is suffering from this cancer has bad breath and voice changes. The breath usually doesn't go away with brushing or mouth wash usage. You should also notice any voice changes as it can be the sign of oral cancer.

These are some common symptoms of mouth cancer but if you experience one of these symptoms, it doesn't mean that you are infected by the disease. You may only have an infection that can be cured with antibiotics. If you are suspicious about the symptoms that you experience, take a note of them. Make a list and show it to your doctor on your next visit.

To find out more information about mouth cancer symptoms please visit http://symptomsof-disease.com/2011/10/prevention-of-the-mouth-cancer-symptoms/ You will find some useful information and tips.

Liver Cancer Tell Tale Signs and Symptoms

Liver is one of the important parts of our body that secrets bile juice and helps in the digestion of the food we eat. When cells in the liver start growing at an abnormal rate causing problems in the normal functioning of the liver then it should be suspected as liver cancer. It is very difficult to identify liver cancer at an early stage as it shows no signs and symptoms. Often the symptoms shown are also misleading and felt as some other health problem.

Scientific research shows that the causes of liver cancer are obesity, hepatitis B or C infection, extreme alcohol use and forming of Aflatoxin B1 from a mold called Aspergillus in our body. This mold enters our body through food. Coming to types of liver cancer the most common type is Hepato cellular cancer also called as Carcinoma. The other types are Cholangio carcinoma, Hepato blastoma and Angio sarcoma.

As told no particular symptoms are shown in the early stages of this cancer. But as the cancer develops then we can see some symptoms like pain in the abdomen. The pain is because of swelling of liver due to cancer cells. The other common symptom is Jaundice. Jaundice causes yellowing of skin or whitening of eyes. In the early stages we can see discoloration of skin.

Usually upset of abdomen is also observed in the cancer of the liver patients. This makes the patient lose the urge for food which leads to abnormal weight loss. Patients may feel unusually nauseous and may begin to vomit. As the disease progress one may observe fluids forming in the abdomen. Most of the times patients suffer with fever because of which patient may get headache, chills or sweating. Other common symptom is white and chalky stools.

Even though it is not possible to diagnose cancer of the liver in the early stages it is better to go to a doctor and undergo required tests when any of the above symptoms are observed. The chances of cure are high when liver cancer is in early stage than in advanced stage. In advanced stage the option is liver transplantation. With liver transplantation you are put on a waiting list until a compatible liver is found.

Best rout to take would be to go to the doctor when you are feeling bad. That way they can do the necessary test to see what the problem is and how best to treat it.

Next, read about Liver Cancer Signs. To read more about this subject go to Liver Signs and Symptoms blog.

Article Source: http://EzineArticles.com/6605223

The Official Goal of Therapy in Advanced Stages of the Disease: Increase Survival

For any type of cancer there are 4 stages (in ascending order of severity) that assess the extent of the disease. Knowing the stage of disease is important to provide the most appropriate care for the sick, as well as to formulate a likely prognosis.

Stages one and two are considered early. The tumor is limited and the prognosis, especially if there is no lymph node involvement, is often positive. Stages III and IV are considered advanced and the prognosis is usually poor. The disease has spread to other organs and usually turns out to be more aggressive and resistant to treatment. The tumor, at this point, having made metastases, must be attacked in a systemic way.

As a result of this surgery is often not valid clinical indication and therapy is usually represented by the most appropriate chemotherapy for the initial treatment (1 st line) and molecular targeted drugs for the next treatment (2nd line), possibly more cycles of radiotherapy.

In advanced disease, these therapies, while having systemic action, like acting on the whole body, no longer aims to heal, but they are designed to increase survival by limiting the possible symptoms of the disease and the patient's pain (objective cure / palliative). With a few exceptions represented by tumors with low-grade malignancies (eg testicular cancer), the finding with advanced neoplasia III or stage IV for which you can only groped to slow down the development, is living with the situation more dramatic for a patient with cancer (and its expensive).

It's a terrible psychological situation: it feels condemned to death. They are negative thoughts like, "maybe I'll die in a few months", "maybe the disease progresses I will try to short to unbearable pain", "what will the lives of my loved ones be without me", and other conflicting thoughts which a natural instinct for survival leads in any case to entertain hopes of "maybe if I can survive for some years, then I can count on a new cure", "maybe I can get into some new experimental protocol", "maybe there is a Unofficial miraculous cure ".

My mother died of cancer that is the reason why this information is very dear to my heart.

Maybe you also know people of you have dear ones that have left you due to this serious illness.

Still there is always hope. Research is evolving each an every day. Be confident and have faith. Alternatives cures for cancer may be the way.

The author has found an alternative cure for cancer. You can read about it here.

Article Source: http://EzineArticles.com/6604235

Pediatric Brain Tumors and Brain Cancer - Funding Is Key for Research and Support

Every day, across America, people are talking about the progress being made in medical research, or the support provided to patients and families affected by a devastating disease or illness. One thing that often gets lost in these conversations is the issue of money. Research can only move forward if there's funding to support it. Nonprofit organizations and other support groups operate primarily from donations; and even fundraising activities require a budget of some sort. None of these can happen without money.

And, somewhere out there, right now, a group of parents is having that very conversation about the deadliest of all childhood cancers-pediatric brain tumors and brain cancer. What's the latest in research? What kind of support is out there for the kids and families? Why isn't more being done, and faster? It is the mission of the nonprofit organizations that support this worthwhile cause to provide answers to these questions, and they understand that the answers come through proper funding.

Research

Research on the causes and cures of pediatric brain tumors and brain cancer is ongoing, but often progresses at a slower rate than desired. There have, however, been some recent successes in this area of research, including the creation of a tissue consortium, and the publishing of a major study of medulloblastoma, a type of brain tumor typically found in children. ("The Genetic Landscape of the Childhood Cancer Medulloblastoma"; Science, published online Dec. 16, 2010.)

Support

Through a variety of programs and services, most nonprofit organizations work to meet the needs of these young patients and their families. Services such as support groups and various family events, as well as assistance with a variety of issues relating to care, treatment, and financial aid give these families the sense that they are not alone on this difficult journey.

Awareness and Education

Anyone who owns or operates a business understands the necessity of marketing. Awareness of the product or services offered is critical to the success of that business. Of course, successful marketing requires a sufficient source of funds to "get the word out."

In that sense, nonprofit organizations are no different than any other business. In order to promote awareness of pediatric brain tumors and brain cancer, there must be a solid marketing plan in place. How else will the average person learn that every day, across this country...

• Nine families will learn their child has a brain or spinal cord tumor;
• Three families will mourn the loss of their child to a brain or spinal cord tumor; and
• Six families will transition to survivorship.

Funding for the ongoing research and essential services provided by the nonprofit groups comes primarily from a mix of events, direct response, online fundraising, and major and planned gift solicitation. For the most part, events constitute the predominant source of funds to back these activities.

With adequate funding, progress can continue that will improve the treatment, quality of life and long-term outcomes for children with brain and spinal cord tumors.

How does the old saying go? "No gift is too small; no kind gesture goes unnoticed." Contact a nonprofit organization today to find out how you can help in the fight against pediatric brain tumors and brain cancers.

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.

Pediatric Brain Tumors and Brain Cancer Alter the Definition of Normal

For most of us, today will begin like any other day. We'll sip our coffee, skim the morning paper, drop the kids off at school, and perform the normal rituals that make up our daily lives. The good, the bad, and yes, even the somewhat ugly; we'll tackle it all with confidence and a sense of comfort, knowing that tomorrow, as routine as it may be, we'll get to do it all over again.

But, for several families across America, today will be different. Today will be life-changing.

Today...

• Nine families will learn their child has a brain or spinal cord tumor;
• Three families will mourn the loss of their child to this dreadful disease; and
• Six families will transition to survivorship.

Each year, an estimated 3,400 children in the United States are diagnosed with a brain tumor or brain cancer. Approximately one-third of these children will survive no more than five years, making this the deadliest of all childhood cancers. For the families of these kids, there will never be another "normal" day. Their days will now be filled with medical appointments, treatment options, and learning how to operate within a new definition of "normal."

Thankfully, hope springs eternal. The survival rate for children with brain tumors and brain cancer has increased significantly over the past twenty years. Advancements in research have resulted in better treatment methods, improvements in the quality of life and the long-term outlook for these young patients. However, survival does bring with it an all-new set of unique challenges. Treatments can cause damaging late effects on survivors; effects that range from cognitive impairment, to physical challenges, to social isolation.

Collaborations between nonprofit organizations, research foundations and leading medical institutions have proven to be instrumental in the fight against these childhood cancers. By joining forces, these groups are able to connect the best of the best to keep research moving forward, raise public awareness, and provide support to the patients and families who need it.

Several non-profit organizations have been established over the years to provide help to families who find themselves on this new and very difficult life path. Most of these groups offer resources for education, assistance with medical and financial services, and much-needed emotional support through a variety of family outreach programs and special events.

These nonprofit organizations work tirelessly in their battle to make pediatric brain tumors and brain cancers a disease of the past. They are continually searching for research partners, corporate sponsors, and private foundations to help support ongoing research. Individual donations are also critical to the success of these organizations. While much work is being done, and progress is being made, the need to raise awareness, fund research, and provide support is ongoing.

A quick Internet search and a few simple clicks of the mouse will land you on the website of one of these dedicated, nonprofit organizations. Once there, you'll likely find an abundance of valuable information, along with resources and opportunities to help. Why not spend a little time today learning more about this devastating disease? Perhaps, make a donation, or even sign on as a volunteer. Not only can you help to redefine "normal" for these kids and their families; you might just alter your own idea of "normal" as well.

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.

The Brain Tumor Symptoms

The symptoms of brain tumor vary from patient to patient, and most of these symptoms can also be found in people without brain tumors. So the only way to know if you really have a brain tumor or not is to consult your doctor and get a brain scan.

Headache is the symptom that is common with 46% of patients with tumors. They described this headache in a different way and no reason is a sure sign of a brain tumor for many. Perhaps most people have headaches at some point in their lives, so it is not sure sign of brain tumors. You should talk to your doctor if your headaches are different than you've ever had, with nausea / vomiting, aggravated by bending or effort to go to the bathroom.

Seizures: This was the second most common symptom reported, with 33% of patients reporting a seizure before the diagnosis was made. Seizures can be caused by other things, such high fever, as epilepsy, stroke, trauma and other disorders. This is a symptom that should never be ignored, whatever the cause. In a person who has never had a seizure before, it usually indicates something serious and you should get a brain scan.

A crisis is a sudden and involuntary change in behavior, muscle control, consciousness, and / or sensation. Symptoms can vary from attack and sudden loss of consciousness total agitation of the violent shaking or slight shaking of a limb. A person can experience blurred vision, slurred speech or staring into space and doing other odd behaviors, while having a seizure. About 10% of United States population will experience a single seizure in their lives.

Nausea and Vomiting: As with headaches, these are non-specific - meaning that most people who have nausea and vomiting do not have a brain tumor. Twenty-two percent of our respondents said nausea / vomiting as a symptom.

Nausea and / or vomiting are more likely to look for a brain tumor which is accompanied by other symptoms mentioned here.

Vision problems or hearing: Twenty-five percent reported vision problems first. It is not easy if you have a problem with your hearing or sight, to be extracted. I have often heard that the eye doctor is the first to make diagnoses. When you look in your eyes, sometimes you can see the signs more. Intracranial pressure, because it must be studied.

Problems with the weakness of the arms, legs and facial muscles, and strange sensations in the head or hands: Twenty-five percent reported weakness in the arms or legs. Sixteen percent expressed feelings of weird and strange sensations in there head. This can lead to an altered gait, falling objects, falls, or asymmetric facial expression. These can be symptoms of a stroke. Sudden onset of symptoms is an emergency - you should go to medical emergencies. If you notice a gradual change over time, you should know.

Support Programs Are Vital To Families Of Children With Brain Tumors And Brain Cancer

When a child is diagnosed with a brain tumor or brain cancer, the initial impact that news has on the family is simply overwhelming. This is a crucial time for the patient, parents and families, as well as friends. Time is often of the essence; quick decisions and fast actions are typically required, and, in a split second, lives are changed forever.

Thus begins a journey down a very long and difficult road. Where do parents go for information? Who do they turn to for support? How will they know what's best for their child? It's imperative that these families have resources available to them to assist them in making the critical decisions that they now face.

Thankfully, there are a number of exceptional family support and outreach programs sponsored by nonprofit organizations focusing on children's brain tumors and brain cancer. These programs provide valuable resources for education, assistance and support. While there are many reasons for parents of children with brain tumors to connect with a support group, three of the primary reasons are discussed below.

Education

One of the first questions asked by parents of children newly diagnosed with brain tumors and brain cancer is "What does this mean for my child?"

Family support and outreach programs can answer this and countless other questions by providing resources for general awareness of the disease, treatment options, and even facilities equipped to provide the best treatments available. Support programs can also help families stay abreast of the latest research that's being done with regard to treatments, survivorship, and long-term effects for the survivors of this deadly disease.

Assistance

Assistance for families taking this difficult journey can come in a variety of forms. It may involve locating the right doctors and facilities to care for their child, or perhaps, working through the maze of insurance forms and red tape. Researching options for financial aid, or finding local resources for supplies or services that might be needed for the child's care and recovery are also ways in which these support groups can offer help to these families.

In addition to the assistance provided to individual families, these nonprofit organizations work tirelessly on promoting and servicing the overall mission - finding better treatments for kids suffering from brain tumors and brain cancer, and improving the quality of life for survivors.

Support

Above all else, the parents and loved ones of these kids need emotional support. They need to belong to a community of people who are traveling the same, long road that they find themselves on. They need to know that they are not alone in their journey.

The emotional support that is given so freely in these family outreach programs cannot be found anywhere outside these unique groups of fathers, mothers, sisters and brothers. Who can better understand the grief a mother feels when she learns that her instincts about her child's health were right? Or the sorrow that consumes a father when he finally allows himself to cry, alone in the shower? And who better to share the joy when a family transitions to survivorship?

These family support groups offer not only support for parents and extended families, but for the patients, as well. Understanding the toll that this dreadful journey takes on all, most support groups sponsor a variety of conferences, camps, and other events throughout the year as a respite to the families. These events provide opportunities to connect with others in this unique community, while also gaining insight into educational and vocational opportunities.

Being very much aware of the needs of bereaved families, and families of survivors, as well, there are also support groups that are geared specifically to their needs. Some of these groups have mentors; parents who have stood in the same shoes, who work with families in a number of ways as they move through the difficult transitions.

Education. Assistance. Support. Connecting with the right support group is essential for parents and families facing this difficult journey. Parents, you are not alone. Help is out there, waiting for your call.

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.

Strength in Numbers: The Value of Collaboration in Pediatric Brain Cancer Research

Scientific research is the key component in the battle to cure pediatric brain tumors and brain cancer. Its success points directly to the value of collaborations among researchers, medical facilities, nonprofit organizations and even private philanthropies. These groups often come together with a common purpose, and join forces to work towards a single goal - finding a cure for this terrible childhood disease.

There are many such collaborative efforts taking place in the area of pediatric brain cancer, which is considered to be the deadliest of all childhood cancers. For instance, there is the newly established, Brain Tumor Tissue Consortium, involving the Children's Brain Tumor Foundation and researchers at several leading pediatric oncology hospitals nationwide. This consortium enables researchers to obtain samples of brain tumor tissue that can be used to evaluate treatments. The results can then be documented in a database that can be shared with pediatric cancer facilities across the country.

The result of another such partnership recently came by way of a landmark study of medulloblastoma*, a type of brain tumor typically found in children. (*"The Genetic Landscape of the Childhood Cancer Medulloblastoma," Science, published online, December 16, 2010). The large, multi-center study defines the genetic landscape of this cancer, and holds intriguing clues to gene changes on signaling pathways that may become fruitful targets for future therapies. This is a very significant and hopeful finding, and one that researchers, doctors and parents alike are celebrating.

There are a number of other, ongoing research programs that also center on establishing better treatment methods, reducing the adverse side effects of these treatments, and increasing the number of survivors. While progress is being made, it continues to be challenging for a number of reasons:

• There are many different kinds of children's brain and spinal cord tumors, which has stymied research as investigators face the challenges of collecting and analyzing tissue;
• Because the disease is rare and tissue samples of tumors are small, it takes time to test and validate new treatment options; and
• Funds for research and treatment options are limited, due to the relatively low rate of incidence, compared to other childhood cancers and diseases.

While the incidence rate of pediatric brain tumors and brain cancers may be relatively low, with approximately 3,400 children diagnosed each year, nearly one in three of these children will not survive more than five years. And, those who do survive will likely suffer damaging, long-term effects from the very treatments that saved them. However, due to the dedicated research that has taken place over the last twenty years, there have been noticeable decreases in the overall cancer death rates. The research taking place today will hopefully, someday help to minimize the side effects and allow these survivors to live longer, healthier lives.

We read about breakthroughs in medical research every day, and when we do, we applaud the researchers, and rejoice for those who might benefit from the results. We celebrate the success of the research programs, as we should; but it's important to understand the efforts behind the breakthroughs. It requires unwavering dedication from the researchers, doctors and other medical professionals, tremendous commitment from the nonprofit organizations that help promote the cause, and an extraordinary sense of charity from the financial supporters. Talk about a collaborative effort! There likely would be no breakthroughs; no success stories to celebrate were it not for the alliances formed by these remarkable groups of people.

To learn more about current research efforts in the area of pediatric brain cancer, make a donation, or find out how you might become a partner in one of these collaborative programs, contact one of the many nonprofit organizations or medical research facilities focused on bringing an end to this dreadful disease. Many together can accomplish more than one, alone.

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.

Knowledge Is Power For Parents Of Children With Brain Cancer Or Spinal Cord Tumors

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.

Article Source: http://EzineArticles.com/5968272

What Are The Symptoms And Stages Of a Brain Tumor?

From the latest research in the field of medicine it is evident that there are lots of patients who are suffering from the painful condition of brain tumor. It is a disease which has taken many lives and still many are struggling hard to survive from this detrimental syndrome. For the cure, many neurologists have been successful in fighting back this disease but still there is a lot more to do to face this challenge. And for this reason, the experts from cancer treatment and radiation therapy are coming forward to participate in the fight against cancer.

Brain tumor is a very harmful and dangerous disease. It only results in the patient's death if it is not controlled in its earlier stage. By reading this article you will know more about Brain tumor, its symptoms and its treatment process. This information will be helpful if you are suffering from the same condition.

Symptoms:

There are many symptoms of brain tumor which neurologist describe. Among them, the most common symptoms are Headaches, Nausea, Hearing troubles, Sight misperception, Vision problem and sometimes problems in the behavioral functioning.

Headaches:

Regular headaches are common in a brain tumor patient. These are regular and frequent and can take place at any instant. When the headaches are in the primary stage, they are preventable, but when the disease enters a severe stage, they are unstoppable and can even take the patient's life. Well it can be and cannot be a complete sign of a brain tumor. If the patient is receiving constant headaches then it can be a sign but consulting the experienced practitioner to find out if it is really a symptom of this condition or not.

Vomiting and Nausea:

These symptoms are sometimes rare and sometimes frequent in the patient. Vomiting and nausea can be a middle stage symptom of the brain tumor, but for confirmation the patient should consult the neurologist. With the latest research, the experts have declared that there are 22 patients out of hundred who had called Nausea as brain tumor's symptom.

Loss of hearing and vision:

According to the latest report, there are 25% patients who had loss of hearing and vision. But it is also not a true symptom for brain tumor. Sometimes, it depends upon the tendency of the patient as to what sort of symptoms he or she is carrying with the disease.

Stages:

Stage 1:

This is a very primary stage of brain tumor in which the cells are not fully shaped and they do not even start to multiply. The cure is easy in this stage as the cells can easily be separated from the brain through a surgery.

Stage 2:

This is a stage where the cell activates in a slow growth form. This stage requires instant surgery; otherwise there is chance for the disease to go into its third stage which is more dangerous and risky,

Stage 3:

This stage is proficient for the cells to split up. They starts growing more rapidly and it requires a serious attention if the patient is to be recovered.

Stage 4:

This stage is the extreme of all stages where the cure becomes very difficult because the tumor cells have populated the entire brain section. This stage is very difficult to cure but can be cured if an urgent surgery is carried out. Most of the brain tumor's patient die in this last stage as many times the surgery does not remove the disease. That is why many neurologists advice the patients to treat it the very first stage so that the disease stops spreading.

Stewart Wrighter has been searching the term cancer treatment New York in order to find the latest options because he is authoring an article on the subject for a major news magazine. He searched the term radiation therapy New York in order to find a treatment center.

Article Source: http://EzineArticles.com/5987345

Lymphoma Cancer Survival Rate - Is There a New Cure?

The lymphoma cancer survival rate depends greatly on many factors. Typically, the survival rate is given in percentages during time frames. That is not an accurate prognosis, and you shouldn't be looking at it. Research is constantly conducted in the field of lymphoma and currently there is a very effective new way to put the cancer in remission.

The survival rate depends on the type of lymphoma. On average, 50% of lymphoma patients get cure, either by chemotherapy, or by spontaneous remission. Since now we have the new natural treatment option, the future survival rate of lymphoma patients will depend largely on how many people learn about the new treatment option. Chemotherapy has many side effects, and is generally speaking ineffective for treating lymphoma cancer. The lymphoma is one of the slowest spreading cancers, but it is also the one with the most profound symptoms, which makes it extremely difficult to live with.

Statistics show that most patients get cured of lymphoma cancer during their 4th-7th year of being sick. Now we know that the reason for that is spontaneous remission. We also know that 'spontaneous' is synonymic for 'idiopathic'. That means that the person usually did something very specific to rid themselves of the cancer, they are just not aware of it. Lymphoma gets cured by the body, and it is the only mechanism in existence, that can cure cancer. External intrusive procedures do not work. In rare cases, surgery can be done to remove cancerous tumors, but that is not effective when it comes to lymphoma. Generally speaking, the information on cancer is very controversial, because medical companies are trying to promote their products, which rarely work and often require daily administration. That is an effective business model, but the end result is nonexistent and people keep living with the cancer.

One of the most useful things is looking at stories of people who suffered from lymphoma, but got cured without apparent reason. When you look at countless such cases, certain patterns emerge and that can be used as the base of a new cure. That is exactly what researchers recently did, and its the reason why the melanoma cancer survival rate depends mostly on how informed people are of the new cures that can be used.

The Power of Red Reishi and Cancer

Get to Know the Immortality Herb

The red reishi mushroom botanical herb is a trustworthy herbal tonic. This mushroom has history that can be traced back to 2000 years ago. Chinese physicians have used this red reishi mushroom botanical herb to condition a person's health. According to the history of the early Chinese dynasties, this mushroom can be found at the Mount Penglai. This mushroom has been a symbol of peace and prosperity in the nation. It is also attributed for the longevity of emperor. Ancient Chinese people consider it a source of immortality. But the herb is difficult to find and acquire.

Reishi is a Japanese term that aptly means immortality plant. In China it has been known as Lingzhi. Ling is Chinese word for spirit or effective and zhi refers to plant that has source of strength. When put together, the red reishi mushroom botanical herb is considered a source of spiritual potency and strength. This mushroom has been given the botanical name, Ganoderma Lucidum. It generally tastes bitter and is red in color.

But there are other types of reishi mushrooms that have their own benefits:

• Blue reishi, which is known to improve eyesight and liver performance
• Yellow reishi for curing spleen problems
• White reishi for protecting the kidney from any irregularities
• Black reishi, which gets rid of lung disorders
• Purple reishi mushroom to boost eyesight, refine complexion, and release the tension in the joints

The red reishi mushroom botanical herb is the most recognizable and most widely used. This herb has been known to aid and protect the internal organs and also improve one's memory. This red reishi mushroom has been tapped to cure cancer and AIDS. Studies show that the mushroom is composed of substances that could make it the ultimate solution to modern health problems that have caused the death of many. Soon, there could be a cure to these deadly diseases and there is new hope for longer, more fulfilling life. This fungus is toxic-free and has no side effects. It should be safe to use, but that does not mean that you should not regulate your intakes. The ancient Chinese people may have placed their faith on the mushroom, but modern medicine is still yet to give the green signal on its effects.

So, how much red reishi mushroom botanical herbs do you need? Experts would prescribe a hundred milligrams to eliminate infection, increase your resistance, and relieve your joint pains. Others may suggest a thousand milligrams or the equivalent of three capsules a day. This is actually not wrong but bear in mind that it still depends on someone's body system. It will be best to consult with your doctor if you are planning on taking it as your supplement. Do not self-medicate if you do not want to gamble your health away. The reishi could be the hidden elixir of life, but the only way to keep you healthy is to be careful about what you take in to address your health problems.

Hotchkins Lymphoma - Is There Hope? Yes!

The hotchkins lymphoma disease is a dangerous type of cancer, which spreads very slowly. The symptoms of the hotchkins lymphoma are very uncomfortable and make it very difficult to live with this type of cancer. Fortunately, this type of lymphoma can be reversed with a very high success rate, provided that you follow the right principles and educate yourself.

When it comes to this type of cancer, doctors often follow routine protocol and make more harm than good to patients. There is a lot of new research in this field, which makes it easier and easier to cure the cancer. As we all know, there is currently no 'official' cure for cancer. That means that there is no 'magic pill', which works every time, not that cancer can't be cured. That may sound controversial, and it is. By far, the most effective way to deal with hotchkins lymphoma is to enable your own body to get rid of the disease on its own. That is accomplished by supplying it with the proper tools for the job, so that your body can identify which cells are cancerous and which are not.

Cancer cells are constantly produced in the body, and it has no problem dealing with them. In a certain percentage of people, however, the cancer cells become 'different', and the body can no longer identify them as harmful. That process can be reversed, and that's the most promising new cure for cancer. If you have lymphoma you probably know that you have a long time left. That does a lot of harm to many people, because as a result they just become comfortable and keep waiting for a 'magic pill' to be developed. That is not going to happen, and there are many effective cancer cures already. It is very important that hotchkins lymphoma patients educate themselves when it comes to the disease. There are many people who claim to have found a cure, but they have actually accomplished nothing. But there are also effective ways to enable your body to fight the cancer, and you should be focusing on them.