Cancer Information

50 years ago asbestos was hailed by many as a miracle product, they said nearly anything could be made from this mineral. It is used as additive to reinforce mortar and plastics. Asbestos fibers can also be separated into fine threads that do not conduct electricity and are unaffected by heat or chemicals.

In the 1970’s, following the discoveries of the health dangers of asbestos dust inhalation, the U.S Consumer Product Safety Commission prohibited the use of asbestos in several products that could liberate asbestos fibers into the environment during use.

Asbestos can cause dangerous diseases that call Mesothelioma cancer. These fibers lodge themselves in the lining of the lung and infected mesothelium tissue. Asbestos can trigger tumors growth between 30 to 40 years after they are inhaled.

When asbestos fibers enter the body, by either breathing in the tiny asbestos fibers or by swallowing them, they can cause healthy cells to mutate into cancer. Asbestos may also cause coughing, lung damage, and shortness of breath in the short period for inhaled this.

According to one survey, one out of seven general public who came into contact with asbestos may develop any of the poles a part types of asbestos-related cancer, including mesothelioma.

Today it is understood that anyone working with or near asbestos has an increased risk of developing mesothelioma, so there are strictly controlled limits of exposure in the work place. But since the dormancy period of mesothelioma can often be 30 or 40 years, there are millions of workers who are at risk because of their exposure in the decades before the safety controls were put in place.

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There are two types of lymphomas: Non-Hodgkin’s Lymphoma (NHL) and Hodgkin’s Lymphoma. Among the two, there are more cases of Non-Hodgkin’s Lymphoma among those that suffer from cancer in their lymphoid systems; it encompasses over 29 types of lymphomas. In the United States, the cases of reported Non-Hodgkin’s are at least seven times as common as cases of Hodgkin’s Lymphoma.

Characteristics

This type of lymphoma is characterized by a malignant growth of B or T cells in the lymphoid system of a person. There are over twenty-nine types under this category, classified according to the type of cells that multiply and the rate by which they do so. The symptoms that people with this disease exhibit are the same as the general symptoms that people with lymphoma exhibit, including a higher incidence of infections and enlarged lymph nodes. However, just like other lymphomas, some symptoms can be very hard to detect.

Diagnosis and Treatment

Once NHL is suspected, physicians make the person undergo a series of tests that are aimed at confirming if it is indeed NHL, and if so, more tests are done to determine the type of cell growth by examining the cancer cells. With NHL, it is very important to arrive at an exact diagnosis so that the most appropriate treatment can be employed to beat the cancer.

The most often-used mode of treatment is chemotherapy, which involves administering powerful drugs that target cancer cells. This treatment is often used if the cancer is found in different areas. On the other hand, if the cancer is localized, the treatment that is employed is radiation therapy, where radiation is used to target cancer cells in a certain area. In some cases, radiation therapy and chemotherapy are combined to treat some cases of NHL. In more advanced cases, the treatment that is used is a bone marrow transplant, which is aimed at bolstering the body’s immune system, which the cancer has severely compromised. Some of the most recent treatments that have been developed include immunotherapy, using vaccines and monoclonal antibody therapy.

Non-Hodgkin’s Lymphoma (NHL), is the most common type of lymphoma. Given this, a great deal of research has been done to better understand this disease and to find ways of treating it. Fortunately, this research has provided vital information that can help the people who have cancer as well as those who are treating it.

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The prostate gland is part of the male reproductive system. Cancer that grows in the prostate gland is called prostate cancer. Prostate cancer is the second leading cause of cancer deaths among men in the U.S.

Men, who are younger than 40, are rarely ever diagnosed with prostate cancer. Men have traditionally been less likely to seek medical attention than women, especially for minor problems, which often serve as warning signs for more serious underlying illness. The most common cancer in American men, excluding skin cancer, is prostate cancer.

If cancer is caught in its earliest stages, most men will not experience any symptoms. One of the most common symptoms is the inability to urinate. And having one or more cancer symptoms does not necessarily mean that you have prostate cancer.

There are a number of symptoms to be aware of. One symptom is the need to urinate frequently, especially at night. And if you have one or more prostate cancer symptoms, you should see a qualified doctor as soon as possible.

A chest x-ray may be done to see if there is a spread of cancer. The prostate-specific antigen (PSA) test measures the PSA enzyme in your blood for abnormalities. The decision about whether to pursue a PSA test should be based on a discussion between you and your doctor.

A prostate biopsy usually confirms the diagnosis. A PSA test with a high level can also be from a non-cancerous enlargement of the prostate gland. CT scans may be done to see if the cancer has spread.

Prostate cancer that has spread (metastasized) may be treated conventionally with drugs to reduce testosterone levels, surgery to remove the testes, chemotherapy or nothing at all. Whether radiation is as good as removing the prostate is debatable and the decision about which to choose, if any, can be difficult. Since prostate tumors require testosterone to grow, reducing the testosterone level is used to prevent further growth and spread of the cancer.

Surgery, called a radical prostatectomy, removes the entire prostate gland and some of the surrounding tissues. The conventional treatment of prostate cancer is often controversial. Surgery, radiation, hormonal therapy and chemotherapy all have significant side effects; know fully what they are before you proceed with any treatment.

Hormone manipulation is mainly used as a treatment to relieve symptoms in men whose cancer has spread. Surgery, radiation therapy, and hormonal therapy can interfere with libido on a temporary or permanent basis. Treatment options can vary based on the stage of the tumor.

In patients whose health makes the risk of surgery unacceptably high, radiation therapy is often the chosen conventional alternative. Some drugs with numerous side effects are being used to treat advanced prostate cancer, blocking the production of testosterone, called chemical castration; it has the same result as surgical removal of the testes. Other medications used for hormonal therapy, with side effects, include androgen-blocking agents, which prevent testosterone from attaching to prostate cells.

Radiation therapy is used primarily to treat prostate cancers classified as stages A, B, or C. In the early stages, surgery and radiation may be used to remove or attempt to kill the cancer cells or shrink the tumor.

In the end, only you with the help of your doctors, knowing your individual situation, can know the best treatment program for you. Once diagnosed you may want to join a support group where you can share experiences and problems with others. It’s important to get as informed as much as possible and read all the newest books, ebooks and research available.

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Have you have chest X-Rays? Well they can lead to Breast Cancer, or rather they can greatly increase the risks they say. A recent report in the UK says the women who are genetically susceptible to breast cancer can greatly increase their risks by getting chest X-rays.

The report States the Following; A chest X-ray could increase the risk of getting breast cancer; More than 1 in 500 with the susceptible gene face a dramatic rise in threat; Women with the BRCA1 and 2 mutation should opt for MRI scans. At least one medical cancer professor states that although this study appears to have proper data showing this there are limitations to the study because those women who are more apt to be in the hospital for another reason might have other issues involved as well.

Nevertheless the study shows the tens of thousands of women have increased their chances for breast cancer thru chest X-rays in the past. There is more information here and in much greater detail than this article shows.

This disease is caused by an abnormal growth of cells. If someone in your family has breast cancer, there may be a chance that you will have it as well. Women twenty-five and up have a higher risk of developing this disease. There is no way of preventing cancer. Women need to go to the doctor regularly for check ups. They must learn to recognize the symptoms and know the causes and treatments available for breast cancer.

We do not know exactly what causes breast cancer, but there are several risks that we need to be aware of that may cause cancerous cells. You need to investigate your family’s history with breast cancer: early menstruation, and late menopause, and breast exposure to radiation are factors may affect your health.

If you begin to notice abnormalities on your breast, you need to get checked. Know your body so you can give yourself self-examinations. A sign of breast cancer is a lump in the breast or armpit area. Sometimes these lumps are the beginning of breast cancer, but may or may not be cancerous yet. These lumps may be removed by a simple operation. Other symptoms that may be detected during the self examination are the following: thickening in the breast or arm pit area, a change in the size, shape or color of the nipples, dimples or redness of the skin on the breast, or changes in the size or shape of the breast.

The treatments needed in case you have this disease will depend on how serious and developed the breast cancer is. The simplest treatment is the lumpectomy that consists of removing the cancerous lump. During this process they also remove some of the lymph nodes in the arm. Another treatment which is a more serious one is known as mastectomy. In this process, the doctor needs to remove the whole patient’s breast because the lump has become very large and cancerous and the patient runs the risk that the cancer will spread all over the chest muscle. In some occasions, the chest muscles that are around the breast and the lymph nodes of the arm are removed. This is called a radical mastectomy. If the doctor finds cancer cells on the lymph nodes, this means that the cancer has spread throughout other parts of the body. When this occurs, the patient will require a more aggressive treatment. There are three common forms of treatment for breast cancer: radiation, chemotherapy, and hormone therapy.

In conclusion, breast cancer is very common in women of all ages. For doctors, it is important that the patient knows her body and knows how to conduct self-examinations, and be aware of any changes in her breast area. Women need to take extra precautions if they have any history of breast cancer in their family. Make sure you examine yourself regularly to prevent any surprises. Remember that the lumps may or may not be cancerous, but to make sure you should go to the doctor and have a mammogram done before it is too late.

New research shows that chemotherapy may be responsible for the shrinkage of key brain areas, but that the effect is only temporary.

The short-term changes could explain the impairment of thinking, memory, and focus that many cancer patients complain of after treatment, according to a Japanese research team.

The changes are marked by a temporary dimunition of certain brain areas that control concentration and focus, problem-solving, execution, and memory. This shrinkage can bring on a general cognitive malaise often referred to as “chemo-brain.”

However, these reductions in the brain were no longer evident three or four years after chemotherapy, the Japanese team reported Monday in the online edition of Cancer.

“These findings can provide new insights for future research to improve the quality of life of cancer patients,” concluded a team led by Dr. Masatoshi Inagaki of the Research Center for Innovative Oncology, part of the National Cancer Center Hospital East in Chiba, Japan.

The current study both supports and contradicts prior research into chemo-brain.

For example, a study released last month by researchers at the University of California, Los Angeles, suggested that the adverse affects experienced by chemo patients are largely due to blood-flow changes in the brain that can endure for a decade or more.

The UCLA findings also suggested that anywhere from 25 percent to 80 percent of breast cancer patients who undergo chemotherapy are subject to chemo-brain.

The condition is poorly understood and is often accompanied by a range of other chemo side-effects, such as gastrointestinal disturbances and weakened immune systems.

However, it is widely known that chemotherapy has greatly improved cancer survival rates in recent years.

So, to better understand the treatment’s negative implications, the Japanese team analyzed three years of MRI scans from breast cancer survivors who received follow-up care at the Chiba hospital. The women were between 18 and 55 years of age and none had experienced recurrent breast cancer or had a history of any other type of cancer. Furthermore, none of the patients was still undergoing chemo at the start of the study, and none had had any cases of dementia in their family history.

Over 100 patients underwent an initial MRI brain scan one year after cancer surgery. About half of this group had also undergone chemotherapy.

According to the researchers, patients who had received chemotherapy had smaller brain volumes in areas that control cognitive function, compared to those who had not been exposed to chemo and it’s radiation.

However, imaging taken at the 3-year mark from 130 patients showed no remaining brain size differences whatsoever.

The authors stressed that cancer, on its own, did not explain the reductions in brain volume. Cancer patients often displayed brain volumes that were similar to healthy controls, they said.

Instead, the short-term changes seemed likely linked to chemo and not to malignant disease, they said.

Inagaki’s group cautioned that their finding is just an observed association and does not confirm a cause-and-effect relationship between chemotherapy and brain changes. They called for additional MRI imaging to further investigate the issue.

Dr. Claudine Isaacs, an associate professor of medicine and the director of the Clinical Breast Cancer Program at Georgetown University in Washington, D.C., described the findings as “encouraging.”

“The problem with chemo-brain is that it is often hard to tell what it is related to, because there are so many factors involved — chemotherapy, the medication that goes with it, the fatigue, and everything else that goes along with a diagnosis of cancer,” she said. “They all play in together.”

“Although this study is relatively quite small, it is a good attempt to look at ways — with MRI, functional PET scans — of trying to get a better handle on a real phenomenon in a structural kind of way,” Isaacs added.

“But we need to be careful,” she cautioned, “because we still don’t have the perfect study yet. So we really can’t tell patients exactly what the parameters are at this point.”

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January 31st First appointment with specialist, Dr G.

He seems a youngish guy – 40 something – I’ve been told he has an excellent reputation. He gets right to the point. They are going to take about 13 needles full of tissue from the gland itself. Under a general anaesthetic the “entry options” are either via the penis (ow) via the bum (sterility issues) or the preferred- the area between the balls and the anus. That sounds much better to me too. It’s a day clinic thing – into the Private Hospital early in the morning and out early afternoon. The procedure is booked for March 13th and I’m sent to have another blood test on my way out the door.

Feb 21st

I receive a phone call from Pam (Dr G’s assistant). She tells me they have a vacancy first thing Monday morning next (Feb 26th) and want to do the biopsy procedure then. That suits me- let’s get it over with. I’m still thinking- this is a total waste of time.

Good mate Silvio, kindly volunteers to be my driver for the day, taking me into the hospital and collecting me afterwards. When I had a knee job done 2 years ago he did the same thing. I feel awkward about disrupting his schedule yet again (for nothing).

Monday Feb 26th

Silvio sleeps at my place the night before so we are ready for the early start, to be at the Hospital by 6.45 as instructed. All goes to plan and I’m told I’m going to be the “first cab off the rank” that day. As usual, fill the obligatory forms, pay some money to the hospital and am then taken to the admission part. Have to put on the usual light green garb with the split up the back – complete with the paper cap and get into bed. It seems I have to keep answering the same questions over and over- no I haven’t eaten or drunk anything since late last night and yes I did give myself an enema early this morning. The Anaesthetist comes around – she seems to be a nice middle aged lady and seems to have a sense of humour – especially when she asks about my smoking habits and I tell her I do but I don’t inhale. They give me a pre med injection and put in a needle thing into my left hand. It all feels pretty cool actually- I’m slightly enjoying the tipsy feeling when they wheel me for what seems like a short while. I vaguely recall we arrive somewhere and that’s it- whammo- I wake up in a room somewhere else with a garbed lady asking me if I would like a cup of tea and something to eat. The “something to eat” is some really nice sandwiches.

Once dressed I’m told Silvio has been called to collect me and Dr G will see me before I leave.

We wait a while as Dr G has been caught up- he arrives apologetic – the usual stuff, all went well and phone us tomorrow afternoon for the results. We leave and I’m still apologising to Silvio for wasting his time. I’m not in any pain but just a mild ache is about as much as I can feel. I’m already putting my thoughts back onto my work projects and imagining walking into my Doctors clinic “soon” to say “well that’s all clear- now what?”

Tuesday Feb 27th.

I’m working from home this morning – remind myself not to forget to ring Dr G after lunch to get the all clear and keep on working.

10.15 am the phone goes- it is Pam from Dr G’s. In an instant my life changes as she says, “Dr G would like to see you at 2 o’clock this afternoon – and please bring a friend with you”. She goes on to add, “It’s just that he’s got some important things to say and two sets of ears are always better than one”. Yeah right! I think. I’ve already got the picture. I get off the phone – my mind is in a whirl. Everything I thought before- every reality has changed. I don’t even know how to react.

Immediately I think, well I’ve got “it” but how far has it spread? I try to console myself with the thought that he only examined the prostate didn’t he?- so if it has spread further he wouldn’t know anyhow – would he? Those thoughts only make it worse. Why the friend bit? It must be really bad. No one is around so I say “shit and fuck” loudly several times over hoping somehow it might help but it doesn’t.

I know I have to ring Silvio but I also know it’s his recording day in the studio and he won’t be able to be the one to accompany me and I know that will upset him. I ring him- he is likewise stunned- I’m relatively calm on the outside but inside I’m churning. I have another person in mind whom I can phone – long time friend and work colleague, Luke. I ring him and ask if he’s free- he is. I congratulate him telling him he has just won a lottery etc and is about to go through a “new experience”

We turn up at 2pm- Dr G is delayed a while. Finally get in there and he says “I’m not going to beat about the bush, you have prostate cancer”. After this morning’s phone call it’s no surprise but just hearing it still kinda stuns me. I’m pretty calm – how am I meant to react?

He starts to explain- 13 needles of tissue = 3 positive – 2 from the same tumour category 5 (as bad as you can get) and one lesser, smaller category 4, mainly on the right side of the prostate. “By the way”, he mentions “I never told you before the procedure but your last PSA test you did came back reading 8.7 (a rise of 2 points in a month).

He goes on to explain that the best course of action is to either remove or neutralise the gland. I’m too big (fat) to operate normally- it would be too difficult. He gets me on the couch again to prod around and confirms his thoughts. Robotic surgery might be a good option- or else Brachytherapy.

Before anything else- next step is to do CT scans and bone scans to make sure the cancer hasn’t spread. He’s confident it hasn’t because I’m “thankfully” so early stages. If it hasn’t spread he says I’ve got a 95% chance of beating it and being cancer free in five years- that’s a pretty good bet I reckon!

He adds that once it has been confirmed “no secondaries” they will put me onto Hormone therapy- which will shrink the prostate and stop the cancer from spreading while further assessments are done to decide which treatment is appropriate for me- to be done some months ahead.

Doc is generous with his time and continues to answer all questions matter of factly. The stuff he tells us about the side effects such as impotence and incontinence almost seem surreal at this time- my mind is still concentrating on the survival aspect so I barely take it all in, just noting “things are going to become very different” in a lot of ways.

I wryly note that many of the questions are now coming from Luke who has been clearly “overtaken” by the experience. When we leave he can only say, “Shit Dan! When I woke up this morning I had no idea I would go through something like this today- how do you feel?” I admit if I really think about it I want to stand on a mountain top and scream. I didn’t tell him the reason I say this is because I’m mainly thinking of all the disruption to my life and I’m not really sure “how” to react anyhow. I’ve been around too long to get into the puerile “why me?” routine. I like to think I’m a realist and have known for many years that life is really “why not me!”

Anything can happen to any one of us at any time – I can only be grateful that it’s not something worse and will take the “good bits” that I can, out of the things to come.

Luke is younger than me by about 8 years– I’m already thinking, this is good – my experience will help spread the word to another man – who needs to know.

Not sure now what to tell people. Have decided to only tell people really close that I have to tell, until I have been cleared of “secondaries” because that in itself will determine “the gravity” of my story. I am hoping to be able to put out something that while it is negative- also has a huge positive side.

I get home and ring to arrange the CT scans and bone scan- schedule CT scan Thursday and bone Scan Friday.

Thursday March 1st

p> CT scan day. I turn up and have to drink three raspberry flavoured weird tasting drinks over the preceding hour. I am then taken through and put onto “the machine”. It all goes routinely- the staff seem cheerful and I take heart later when they don’t ask me to stay back for more (which can be a sign that there is something there). Friday March 2nd

Bone Scan Day. Very similar to the day before on a slightly bigger scale. The drink is taken three hours before they put you on the scanner – plus there is a small injection then you lie on the table and “move in and out of the machine”. I am quietly amused the way they set you up then leave the room to carry out the procedure from an adjacent lead-lined room.

The “operator” tells me she is amazed at the number of people she sees coming through there but adds – “from now on you will be treated and monitored so count yourself lucky” – I do – but please, God – let there not be any secondaries!

I ring Pam at Dr G’s who tells me she will get the results on Saturday morning and put them in front of Dr G- she will then call me.

Saturday March 3rd.

Nothing happens. I wait for the phone to go but it doesn’t. I phone my friend Noelene, who is a font of information about Specialists and the way they operate (due to a professional association). She assures me no news is good news and reminds me they (specialists) always get caught up and disrupted so don’t worry. I feel anxious regardless as so much seems to depend on this phone call.

Sunday March 4th

I go over to my friend Bill’s place (as I do most Sundays) to have morning tea on the veranda. I am surprised by a phone call from Pam to tell me Doc still hasn’t seen my files because he has been diverted in coming into the surgery but she can confirm the tests are all negative so Doc will be in touch. Great news- Noelene was right -I’m very relieved.

Dan Jarrett - one man’s journey battling prostate cancer includes a diary, resources and blog. We look at things in layman’s terms and discuss matters such as sex openly covering things that the medics don’t tell you.
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You’ll find a variety of stores to be host to a vast selection of awareness jewelry. Some of the most popular items in the collection are those designed to increase breast cancer awareness. Items like bracelets, necklaces, cookies, lollipops are now available to show support. A Breast Cancer Awareness Pin is an excellent example. A sophisticated and elegant lapel pin featuring dozens of beautiful pink Swarovski crystals, the purchase of this item is an excellent way to show your support.

The Breast Cancer Loop is another very popular piece of awareness jewelry. The great thing about this product is its versatility. It can be used as a purse or briefcase charm as well as an ornament for the car, diaper bag or even Christmas tree. Featuring handsome pink and clear Swarovski crystals and a Bali silver awareness ribbon, this tiny bracelet is as practical as it is beautiful.

You will still find, however, the Breast Cancer Awareness Bracelet to be the most popular. Featuring sterling silver, pink Swarovski crystals and delicate pearls, bracelets are ideal for the individual who wants to keep the cause close to her heart. Many bracelets include ribbon charms in silver, pink or crystals.

So, whether you are wearing a bracelet to show your support this year or sending of some delicious snacks or treats to a family, friend or loved one, be sure to think pink and help spread the word.

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Prevention efforts seem to have failed. The doctor used the dreaded “C” word…cancer. Now what? We hear a lot of buzz about amazing cures and successes, “If you’ll just buy my book, take my pills or visit my center.” The very word, cancer, scares us so completely, we believe we’re going to die any minute. Sadly, it’s those fears the frauds are counting on. They want you to be so afraid you’ll try anything…even their product. Many of us are so frozen in fear, we ignore that fact that many forms of cancer are treatable…often, actual cures have been developed and adopted as standard treatment for cancer. Sometimes, the fears generated by frauds can cause us to choose back-alley, ineffective treatments instead of viable ones recommended by our doctors. If we just calm down and begin to study the situation, we can often relieve our fears and make rational decisions that will avoid the frauds and help our doctors help us heal.

Natural Cancer Cure…and other fraudulent claims: Frauds come in all shapes, sizes and prices. Perhaps the biggest price people pay is chasing after these things when sound treatments are available. You will rarely hear a reputable doctor use the word, “cure,” when referring to cancer. Immediately, then, a red flag should go up in your mind if someone is offering or claiming a cure. Other claims that should strike you as suspicious are ones that suggest standard cancer treatments, like radiation or chemotherapy kill people. Let’s get this straight right now…people die from some types of cancer. Some terminal cancer patients choose to receive experimental treatments in a last ditch effort to try and slow the disease. For frauds to use this to get you to distrust a doctor’s standard treatment, however limited the success rate, should be considered a crime. The only time you should consider experimental treatments or claims of those outside of the medical community is if you have a terminal condition and you’ve exhausted all accepted medical treatments. You’re a grown-up, now. You should get all the objective advice and information you can, about every treatment you’re considering, but people trying to sell you non-standard treatments are not objective…you need to do your own homework…and this is the most important homework assignment you may ever get .

Do Your Cancer Research: Biopsy is usually the first bit of research done to verify a suspicion of cancer. That’s where the doctor collects cells for the lab to analyze. Ask your doctor for a paper copy of the test results. This will give you the exact name of the cancer, if the cancer is malignant (harmful), and other useful information. Based on this, your doctor will recommend other tests to determine the stage (extent of growth) or grade (speed of growth) and treatment options to consider. Take lots of notes and ask lots of questions! While continuing the test/treatment recommendations of your doctor, take this information to a second opinion appointment with another doctor, not associated with the first one. While doctors are highly educated, they are human. Doctors and their staffs make mistakes. Second opinions are so you can head off mistakes before they happen.

Awareness and understanding of standard treatment options, risk factors, success rates, unique terminology and second opinions will all help you be a better patient, active in the treatment of your disease. This is why, before the second opinion appointment, you need to research the information from your doctor. Search reputable sources on the Internet for everything you can find about your specific cancer. Yes, you’ll need a dictionary and medical encyclopedia. A great place to begin your research is the cancer.gov/” target=”_blank U.S. National Cancer Institute. It’s where I’ve found most of my reliable cancer information. Print all the information about the cancer, stages, grades, treatment options, success rates, survival rates and treatment centers. Highlight the parts that apply to you and write questions for your doctors. Take all the information with you to all your appointments with your doctors. Make sure to point out when their opinions differ and gauge their reactions. If their recommended treatments differ from what your research shows, ask them why. Some doctors will be humble, thank you, and offer to look into it further. Other doctors will need to be replaced, as was the case with my wife’s father.

My father-in-law’s doctor made a mistake, treating a very aggressive life-threatening cancer with cosmetic surgery. By following the steps I’ve listed in this article, I was able to convince the new doctors to follow-up with radiation to significantly reduce the probability of relapse. Since, with his cancer, relapse is almost always fatal, it was better to be safe, even if it cost the HMO a couple more bucks.

Some doctors and HMO’s get a little confused as to who makes your health care decisions..

Cancer Treatment Team Leadership: The Oncologist (cancer doctor), your primary doctor and often other specialists are essential leaders in the successful treatment of your cancer but you are in charge. They will present you with options, including diet, supplements, surgery, radiation therapy, chemotherapy and a vast amount of information for you to digest to make informed decisions. If you do your homework, you can control the fear, eliminate the frauds, reduce the mistakes and make the right decisions in your fight against cancer.

Glen Williams is founder and CEO of EHF, Inc. and Webmaster for e-health-fitness.com e-health-fitness.com. He has done extensive research on personal and family health and fitness issues and has been helping and advising people on health since 1987.

Peritoneal Mesothelioma is a cancer of the abdomen lining caused due to prolonged exposure to asbestos. Thousands of lawsuits are handled every year dealing with the issue of peritoneal mesothelioma and its effects. Symptoms of mesothelioma may not appear until 30 to 50 years after exposure to asbestos. Shortness of breath and pain in the chest due to an accumulation of fluid in the pleural space are often symptoms of pleural mesothelioma Other symptoms of peritoneal mesothelioma include loss of appetite, nausea, and abdominal swelling. Fluid commonly accumulates in the abdominal cavity causing the swelling and pain. The symptoms can become quite serous over time, as the swelling will exert great force on surrounding organs and lead to great pain.

If diagnosed at an early stage, than there are chances of survival, depending upon on how advanced the cancer is at the time of the diagnosis. Treatment with radiation or chemotherapy and early diagnosis can be of great help. In fact, these treatments can help a patient to survive for a long time. It is often true that if the cancer is found early and treated aggressively, almost half of the patients whose cancer is found early reach the two-year mark and about 20% survive five years. For peritoneal mesothelioma, patients are often informed that they won’t be able to live for more than one year. But peritoneal mesothelioma specialists, working in leading cancer centers throughout the world, often report better statistics than this, based upon the clinical trials that they are carrying out.

e-peritonealmesothelioma.com Peritoneal Mesothelioma provides detailed information on peritoneal mesothelioma, peritoneal mesothelioma treatment, peritoneal mesothelioma lawyers, peritoneal mesothelioma survival rates and more. Peritoneal Mesothelioma is affiliated with e-pleuralmesothelioma.com Malignant Pleural Mesothelioma.