Sunday, May 13, 2012

Survial rates after treatment.

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Hello WSmith,

I agree, the stats on positive outcomes for stage iv, need to be championed. My husband after 3 rounds of chemo, took his CT scan and we were told the mass in his right rib is gone. The docs looked surprised , they are trained to deal with the immediates and are not fortune tellers. His primary tumour is in his esophagus and has greatly decreased in size as well. We are living strong...enjoy every day.. do not create your bucket list quite yet....

Stay strong, surround your self with postive thoughts and positive people and ignore the nay sayers... there is a lot  of goodness for stage iv cancer patients.. we just are kept in the dark... mmm???? wonder why?

Best ,



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Friday, May 11, 2012

non small cell stage 1-b lung cancer

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Goodness sakes, that is a GOOD diagnosis, very low stage, and according to my oncologist, stage 1 non small cell lung cancer is curable.  Not just treatable and survivable, but CURABLE.  Possitive attitude is huge, and knowledge takes away fear.  There are so many who are not as fortunate as you.  Most lung cancers are found in late stages, since symptoms don't present themselves until then.  When found in early stages such as yours, it is usually found while doctors are checking for something else.  Count your blessings, and give thanks to God it's been found so early.  I was diagnosed stage 3a, on May 26th of 2010.  I had my upper right lung removed on August 12, 2010, had chemo, and now have been cancer free since then.  I also, count my blessings every day, and give thanks to the Good Lord for blessings of life, love, and doctors.

Take care, and keep your chin up, this is not a death sentence for you.  God Bless, Byrd



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I feel like I have been given a death sentence today.

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I was diagnosed with almost same dx. check out my caring bridge site.. Stage 4 lung cancer in October 2007 with 6 months to live,, Still here and doing well, mine was also inoperable.. Defentely NOT a death sentence. Read my storywww.caring bridge/visit/russellyoung

hope this helps you !!! will be in our prayers!!!

Russell



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Promising new drug for patients with myeloma

health day

Studies found lenalidomide lengthened time disease did not worsen, but risk of second cancers was doubled(Wednesday, 9 may HealthDay News) - three new studies confirm that drug lenalidomide can significantly increase time than multiple myeloma patients did experience any worsening of their disease, is after a transplant of stem cells or to chemotherapy.

However, what is not clearly studies is or not the improvement in survival time "without progress" will result in a longer overall survival.

"They are very promising, early studies," said the author of an accompanying editorial, Dr. Ashraf Badros, Professor in the Department of medicine at the University of Maryland School of Medicine in Baltimore. "I think that these studies will generate much discussion."

Potential areas of debate, he said, include or non-progression-free survival is sufficient if it is not a benefit in overall survival. He said that progression-free survival may well justify this treatment if the quality of life improved considerably. However, none of the studies reviewed measures of quality of life. Another important factor is cost; This drug is estimated at about $163 381 per year to treat a patient, according to the editorial of the Badros costs.

Studies and writing are published in the issue of the New England Journal of Medicine on May 10.

Multiple myeloma is a cancer that affects plasma cells in the blood. Each year, approximately 22,000 Americans receive a diagnosis of multiple myeloma, according to the American Cancer Society. The current rate of survival at 5 years for multiple myeloma is only 40 percent. However, recent advances will likely increase the survival rate for people who are diagnosed to move forward, according to the cancer society.

Lenalidomide (Revlimid) modifies the immune response and direct toxic effects on tumors, according to background information in one of these studies.

Among younger people, the standard treatment is usually a stem cell transplantation to replace the many cancer cells from plasma. However, many older patients are ineligible for this treatment.

The first study looked at treatment lenalidomide in people who were not candidates for transplantation of stem cells, and it included slightly more than 450 people more than 65 years old, who was recently diagnosed with multiple myeloma. A group received initial chemotherapy which included lenalidomide also followed by treatment of maintenance by lenalidomide, while the second group has just received the initial chemotherapy, including lenalidomide. The latter group received standard chemotherapy without lenalidomide.

After an average 30-month follow-up period, the researchers found that the first group had an average of progression-free survival of 31 months, compared to only 14 months for the second group, only 13 months for the final group. This study was not designed to evaluate overall survival.

"This approach is approximately double the duration of remission of 15 to 30 months old therapies," said author Dr. Antonio Palumbo, of the study of the Department of Hematology at the University of Turin in Italy.

Palumbo, stated that the cost has always to be considered in the treatment. He said that there are some costs associated with lenalidomide because economies it is an oral medication, which must be administered intravenously. In addition, if it prevents complications, such as bone fractures, it can help prevent them disability and hospital costs.

The second study, conducted by researchers from the Roswell Park Institute in New York, included 468 persons less than 71 years who received transplants of stem cells. From 100 days after their transplants, half of the Group was given daily lenalidomide and half received either a placebo. Once the progression of the disease, study participants said what treatment they received, and if they were to a placebo, they were allowed to begin to lenalidomide.

At the time, the results were decoded, only 20% of people lenalidomide progression of the disease compared with 44% of those receiving placebo.

The third study, reported by French researchers, was also considered in the maintenance treatment of lenalidomide in those who have had a stem cell transplant. This study included 614 people aged under 65. The group taking lenalidomide was progression-free survival an average of 41 months, compared to 23 months in the placebo group. Four years after the start of the study, the average overall survival was similar in the two groups, according to the study.

Secondary effect the most important and what has been an increase in the risk of a second cancer. In the three studies, the rate of cancers of the second was more than doubled in people taking lenalidomide. Low white blood cells were also commonly related to lenalidomide therapy.

Badros said that all cancer treatments have secondary, and that for the most part, lenalidomide did appear to have unexpected effects, except for the increase in the rate of cancers of the second. This finding, he said, deserves further study.

More information

Learn more about multiple myeloma of the American Cancer Society.

SOURCES: Ashraf Badros, M.B., Ch.B., Professor, Department of medicine, University of Maryland School of medicine and the University of Maryland Medical Center, Baltimore; Antonio Palumbo, MD, Department of Hematology, University of Turin, Italy; May 10, 2012, New England Journal of Medicine

Copyright © 2012 HealthDay. All rights reserved.



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The infection causes Cancers from 1 to 6 in the world: study

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Stomach, liver and cervical malignancies top the list(Wednesday, 9 may HealthDay News) - one in six cancers in the world is caused by infections preventable or curable, a new study finds.

Infections cause approximately 2 million cases of cancer, a year and 80% of these cases occur in the less developed regions of the world, according to the study, published online may 8 in The Lancet Oncology. The death by cancer of 7.5 million worldwide in 2008, approximately $ 1.5 million were due to potentially preventable or curable infections.

"Infection with certain viruses, bacteria and parasites is one of the largest and most preventable cause of cancer in the world," authors Catherine of Martel and Martyn Plummer, principal of the International Agency for research on Cancer in Lyon, France, said in a press release of the journal. "Application of present methods of public health for the prevention of infections, such as vaccination, practical safe injection of antimicrobial treatment - could have a substantial effect on the future burden of cancer throughout the world."

Researchers examined data on 27 cancers in 184 countries and has calculated that about 16% of all cancers in 2008 have been linked to infection. Cancers related to the infection rate was 23% in the developing countries and 7% in developed countries.

Rates of infection-related cancers varies from 3% in Australia and New Zealand to 33 per cent in sub-Saharan Africa.

"Many cancers related to the infection is preventable, particularly those associated with the virus of human papillomavirus (HPV), Helicobacter pylori and hepatitis b and hepatitis c virus," said researchers.

In 2008, these four major infections caused together 1.9 million cancers, mainly of the stomach, the liver and the cervix. Cervical cancer is about half of cancers related to the infection in women and hepatic and gastric cancer accounted for more than 80 per cent of cancers related to the infection in men.

The results of the study "show the potential of preventive and therapeutic programs in less developed countries to significantly reduce the global burden of cancer and the wide disparities between regions and countries," Danaei Gudarz, of the Harvard School of Public Health, Boston, wrote in an accompanying editorial.

"Since effective vaccines and relatively inexpensive for HPV and [B] are available, increasing the coverage should be a priority for health systems in high-burden countries," Danaei added.

More information

The U.S. National Cancer Institute offers an overview of cancer prevention.

SOURCE: Lancet Oncology, press release, may 8, 2012

Copyright © 2012 HealthDay. All rights reserved.



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Scientists map genome of Melanoma

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Findings include genetic link to breast cancer, researchers say(Wednesday, 9 may HealthDay News), researchers have completed the first sequencing of the genome of melanoma, an aggressive and often deadly form of skin cancer.

Understand the landscape of genomics which contributes to the development of melanoma can provide the new overview of the tumor biology and therapeutic resistance, the authors of the study say. They believe that discoveries can stimulate the development of new treatments for melanoma, which are likely to kill more than 9 000 people in the United States this year, according to cancer experts.

In a study published online on May 9 in the journal Nature, the scientists describe 25 sequencing human metastatic melanoma - cancers that have spread - and find a common denominator between melanoma and breast cancer, and the rate of mutation in melanoma varies with the level of ultraviolet light.

The authors found PREX2, a gene associated with breast cancer, about 14% of tumors of melanoma. "This is a moment of light bulbs in research," said Dr. Lynda Chin, Chairman of the Department of genomic medicine of the University of Texas MD Anderson Cancer Center in Houston author of the study. Potentially, this could change "the paradigm of the way in which we understand what is happening in cancer", she added.

Research has shown that PREX2 begins to lead the cancerous activity in genetic mutations, modify or disable cellular functions. Also other mutations have been identified for the first time in studied tumors.

The next challenge will be to understand how the PREX2 gene is a melanoma tumor grow, said Chin. "PREX2 is a large gene, and we're not sure what aspects are essential for the development of cancer." We have the "what", but now we have the "why" and the "how". »

Their study also helps to lay the groundwork for a new definition of cancer which includes the genetic tumor constitution, but also the site of the specific organ.

These features will also lead the development of future cancer treatment, said Chin. "this adds another layer of how we approach the cancer.". "Tell, tell me first, the genetic composition of the tumour and tell me then, origin of the tumour," she said.

Cancers are now described by a system based solely on the location of a tumor and its microscopic anatomy. Chin, said the research shows how genetic information adds a new element that can help to understand and classify tumors with greater precision.

The authors have also learned that the mutation rate is higher in persons with chronic sun exposure. This is another evidence that the development of the disease is related to ultraviolet light.

United States, melanoma has increased over the past three decades. It is one of the most common cancers in young people, and more than 76 000 new cases will be diagnosed through all age groups this year, according to the American Cancer Society.

While the study has discovered new important information, Chin warned that the Melanoma genome is very complex. For example, researchers have seen what she described as a large number of "structural rearrangement" on the genome. It is unclear what this means.

"It's like a bomb s gone off and all in the wrong order," she said. "And we are not sure how to put all together."

Dr. Darrell Rigel, Clinical Professor of Dermatology at the New York University Medical Center, said that it was interesting that the researchers found a breast cancer gene in melanoma tumor. "Regroup us melanoma as a type of cancer now, but in five to ten years, we are likely to see too many types of cancer," said.

Rigel also said that he was encouraged that researchers have found another potential target for drug therapy.

More information

Learn more about melanoma to the American Cancer Society.

SOURCES: Lynda Chin, M.D., Chairman, Department of genomic medicine, University of Texas MD Anderson Cancer Center, Houston; Darrell Rigel, M.D., Clinical Professor, dermatology, New York University Medical Center; 9 May 2012, Nature, online

Copyright © 2012 HealthDay. All rights reserved.



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Tarceva

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Sorry, I could not read the content fromt this page.

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Colon Cancer gaps for black, white, mainly because of the screening

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Survival differences could be narrowed with more equal care access, computer model suggests(Wednesday, 9 may HealthDay News) - differences in screening and account for much of the disparity colorectal (colon) cancer incidence and rates of mortality between white and black Americans, a new study said.

Differences in screening are responsible for 42 percent of the difference in the incidence of cancer and 19 per cent of the disparity in mortality rates, according to the study.

The study also concluded that the differences in survival linked to the stage of the cancer at diagnosis (which probably reflects differences in treatment) account for a 36 per cent additional differences between blacks and whites in colorectal cancer mortality rates.

The results suggest that equal access to care could significantly reduce these disparities, according to the study published online April 18 in the journal Cancer Epidemiology, biomarkers and prevention.

Researchers led by Iris Lansdorp-Vogelaar, then a visiting scholar at the American Cancer Society, used a computer model to apply rates of screening and survival of colorectal cancer given white of black Americans more of 50 years. They then compared the actual incidence rate and black to determine the extent to which racial disparities in cancer colorectal mortality rates are due to the differences in survival screening or specific step.

Application to blacks, the screening of white pattern would be the gap in the incidence rates of colorectal cancer in people over 50 years of approximately 28 to 16 cases per 100,000 and the gap in mortality rates of 27 to 22 deaths per 100,000, according to a press release American Cancer Society.

Researchers have also found that if blacks had the relative survival of where white, the disparity in rates of mortality of colorectal cancer decreases to about 17 deaths per 100,000.

In total, the differences in screening and survival represented 54% of the disparity in the rates of mortality of colorectal cancer between white and black. Researchers said that the rest of the disparity between the most likely is due to lifestyle factors that increase the risk (such as consumption of alcohol, smoking, consumption of meat and obesity) and decrease the risks (such as physical activity and hormonal replacement in women after menopause).

More information

The U.S. National Cancer Institute has more on colorectal cancer.

SOURCE: American Cancer Society, press release, 3 may 2012

Copyright © 2012 HealthDay. All rights reserved.



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Latest news on my mom

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We went for my mom's appointment to day and was told that she has Adenocarcinomas.  There is a tumor that has wrapped her Bronchical tube and the tumor is beginning to make it difficult for her to catch her breath.  I am not sure what the prognosis is and what we are looking at, but I did not get a very good feeling today when we spoke with the doctor.  i knew in my heart that she was sick and I knew that she had the Big C, but I just did not want to attempted it was true.  Today was very hard and it really hit home.



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times running please help

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Hi Bill,

I recommend looking into Reliv Advanced Nutrition. It is #2 on the American Anti Cancer Institutes top ten list for cancer fighters/prevention. Reliv nutrition is an exclusive carrier of Lunasin, which STOPS cancer cells from reproducing. The nutrition is also synergistic, bioavailable and of the very highest quality and standards. This website will verify this:http://relivingrecipes.com/2011/09/12/american-anti-cancer-institute-recommends-reliv-products/

Here is another place where people get together and share thier cancer success stories on how this nutrition helped them to overcaome thier cancer(s):http://healthwellnessandincreasedenergy.com/cancer.html

When fed extreme nutrition, our bodies can do miraculous things.

I wish I would have known about this when my father was still alive dealing with his cancer. My family and I also take the nutrition and get great health benefits and results.

My prayers are with you, your sister, your family and everyone else in these discussion forums. If you'd like to know more, you are welcome to contact me.

In hopes for a better and healthier tomorrow,

Christena



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Please pray for a miracle for our daughter!

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My 27 year old daughter, mother of my 5 month old grandson and center of my life, has recently been diagnosed with what one medical team is most likely "poorly differentiated adenocarcinoma" with the lung as its primary origin and another oncologist as " a highly unusual, very aggressive advanced carcinoma of unkown primary." With observable symptoms of blood clots at 4 weeks post partum, cancer was not investigated until late January when she presented with enlarged lymph nodes in her neck. She has a mass in her chest, carcinoma in lymph nodes in her abdomen, chest, arm pits, and neck, SVC syndrome as the tumor in her chest grows into this vein, and one 6 mm tumor in her brain. One oncologist today told me that given the best response to her treatment (10 days of radiation followed with chemo treatments of Taxol, Carboplatin, & VP 16), she may have 1-2 years. If she has a weak response to the treatment, she may only have weeks or a few months. I had her path specimens, reports, and images sent to the Cleveland Clinic and will take her there to learn their opinion within the week. My husband is a 12 year survivor of a severe traumatic brain injury when his medical team told me he would not live. We are people of faith and I am trying to stay positive and hang onto hope. Please help her by praying for a miracle.



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bone pain from chemo?

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On 5/17/2007 Dothedewmom wrote:

Hello all,

 I have posted several messages on here before and have always gotten some great advice. Now I turn to you all again. My mother has NSCLC stage 4  with several mets. Anyway she is taking Taxol/Avastin/Carboplatin for her chemo. The past week she has been having some terrible bone pain. She says sometimes it feels like her bones are breaking. I have read and reread the info on these chemos and none of them say anything about bone pain. I can not call her doctor because I am not on her medical release form so they will not give me any information and she doesn't want to call because she goes next Wednesday for another PET scan. She feels like she is a bother to her doctors. I tell her that if her insurance is paying these doctors $14,000 for each chemo treatment then she is surely not a bother. Anyway I just wanted to know if anyone else has dealt with the bone pain before. Her doctor's have already changed her pain medicine to Oxycotin. Sometimes it helps sometimes it doesn't. I hope someone can give us some advice. Thanks ahead of time and God bless all who are fighting this terrible disease.

The best information I've found for this is at cancercare.org. They will send you information on any topic to your home that you request. I have NSCLC and I'm in my 30s. It is can be quite painful, especially that particular regimine. I'm on my 4th round of chemotherapy. The one your loved one is going through was my first experience with chemo and those chemicals are very hard. She needs to tell her doctor, anything and everything, that is hurting or bothering her. She is paying for the service, and doctors, especially oncology doctors, do not like to hear that their patients are in pain. They want to control that pain and make the experience as less stressful and as easy as possible.

 When I switched to my 2nd round of chemo, I had some symptoms that I didn't tell my doctor about and it almost cost me my life. My cell counts got too low and I developed a staph infection. I was new to the experience so I didn't think it was anything out of the ordinary. I had to learn the hard way to make sure I vocalized to my oncologist what was going on with me. It is good to keep a "pain" diary when you have pain what kind on a 1 to 10 scale, how long it lasted and where.

Bone pain is the worst pain a person can experience going through cancer, I think, beside the neuropathy. The website below might help too. But the only thing that really works for me is the pain management plan I take for the pain in my bones. I used to take loritab but now I am on a small dose of morphine. It keeps my pain in check, and if I have a sharp spike in pain, I also have a small dose that gets me through that spike, so I am at least comfortable. My doctor has asked me several times, "How much pain medication is too much?" He said it is however much you need not to be in pain. Some of folks I now like to use Fentanyl patches too. There are a lot of slow releasing pain meds that will help her feel a lot better. However, with this you can easily get constipated, so eat lots of fiber and if you still can't go, I recommend Miralax. It used to be a prescription only drug, but has now gone OTC. Its tasteless and you can mix it in anything. I usually drink a glass of this everyday and it works for me.

http://www.cancercare.org/pdf/booklets/ccc_lung_bone_care.pd

http://www.healthtalk.com/lungcancer/programs/16_480/index.c



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I do not where to start

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I absolutely do understand your situation, ironically I am the early stage of where your wife is now.  I was diagnosed with thyroid cancer in 2003 was told it was a simple surgery and an ablation and that would be the end of it.  This many years 5 ablations and another surgery later and I am now diagnosed with lung cancer and they have just done mri of the brain and have the abdominal and pelvic scheduled for next week.  I also go back to Vanderbilt which is where i had my last surgery.

I have decided I am not going to have any more treatment as my quality of life is so bad now, I do not want to prolong it and make it more difficult for my family. I can stay by myself now and still do simple things and do not want to get to the stage that I cant at least be somewhat independent.  I ust pray that God will let me go before I become more of a burden to my family.

I am so sorry you are in the position you are in, this is exactly why I dont want to go through all that to just  prolong the inevitable.  I am 58 and have grown children and 5 grandchildren. The saddest part for me is that I will not be able to be here to see my grandchildren grow up.

I do not want to burden my children with the inevitable problems I  will have ,  I really think I am just mad because this happened to me.  I have not been the absolute perfect person however I always worked, two jobs and raised my children.  i  was married for 22 years and divorced then remarried (big mistake)  as I have wound up supporting my husband financiially which makes my life now even more difficult as I do not have a support system. noone to really talk about anything other than im feeling ok when someone calls.

When I had to go on disabiity and quit working I had to step aside from a business I bought, nOW i have a lawsuit against me, I lost my home of twelve years to foreclosure and really wonder each morning why i must wake up for another day. 

I think your wife may feel like me, and just be mad for having been the one to go through this..or maybe she doesnt realize how she is treating you.  Sometimes I think we hurt those that are closest to us, whether we know it or not.

I like you feel so empty, and wonder if I am just being selfish.  Maybe we aare both just being normal.  I do pray that God give you the strength to deal with what you have to come.  That is how I get through each day.  I would like to know how you are doing. My thoughts and prayers will be with you each day.



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Many young adults at risk of Skin Cancer: CDC

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Sunbathing, indoor tanning all too common, study finds(Thursday, 10 may HealthDay News) - despite warnings on the dangers of excessive exposure to the Sun, young adults in the United States still get or use tanning beds, responsible for federal health, said Thursday.

Both activities increase the risk of skin cancer, the most common cancer among Americans, including potentially deadly melanoma.

"People need to realize that exposure to ultraviolet light, if it is the Sun or tanning beds, is dangerous, especially when you are young, and they need to limit their exposure," said Dr. Marcus Plescia, Director of the U.S. Centers for Disease Control and the Prevention of cancer prevention and control division.

"We are concerned that tanning is more and more common, and we fear that this will become a real epidemic if we are not careful." The problem is that you do not see cancers of the cultures up to 10-15 years later, "he says.

To protect this generation of generalized melanoma, said CDC public health efforts are needed to increase the use of shade and sunscreen in recreation areas.

The results appear in the two reports published in the issue of CDC Morbidity and Mortality Weekly Report on May 11.

In a study, the CDC researchers found that 50% of those 18 to 29 years old had at least sunburned in the last year, despite an increase in the use of sunscreen and other protective measures, such as sit in the shade and wear protective clothing. Among whites, 66 percent had tans.

In the other report, researchers found frequent tanning in young adults, with the highest rate among white women between 18 and 25. Much reported tanning almost 28 times on average in the past year, according to the report.

About 6% of American adults reported indoor tanning at least once in the previous year. Among white indoor tanners, 58% of women and 40% of men had used tanning beds 10 or more times in the past year, the researchers found.

"People need to understand that there is a risk the use of tanning beds," said Plescia.

Tanning before the age of 35 increases the risk of melanoma by 75 percent, noted the report. The fact that the rate of Melanoma is higher among young white women that white men can be explained by their more frequent use of the tanning, the authors suggested.

Plescia said that approximately 30 States limit the use of tanning beds by young people, but these regulations vary.

"Only two States, California and Vermont, prohibition room tanning for anyone under 18," he said.

The U.S. Food and Drug Administration is considering requiring labels on tanning beds to inform users about the risks of skin cancer, he said. But it does not ban tanning is realistic.

Dr. Daniel Siegel, President of the American Academy of Dermatology, said that the numbers were not unexpected. "I am not surprised," we find that many people of tanning. It's like smoking and other habits risky; "you are young and you think that you are immortal," said.

"It's a habit, people must change," said Siegel. "You must protect yourself from carcinogenic ultraviolet light that enjoy the Sun and tanning."

Melanoma is increasing at an alarming rate, Siegel added. "If you look at the lifetime risk, it is close to 1 to 50;" "It was 1 to 1 000 forty years ago," he said.

To reduce the risk of skin cancer, the CDC recommends that:

Stay in the shade, especially from 10 hours to 2 p.m.Wear clothing to protect exposed skin.Wear a hat to wide in the shadow of the face, head, ears and neck.Porter of the multidisciplinary sunglasses that block most ultraviolet a and ultraviolet B.Utiliser sunscreen with a sun protection factor 15 or more that blocks ultraviolet and ultraviolet B u.n. ' use a tanning.

More information

For more information on skin cancer, visit the Skin Cancer Foundation.

SOURCES: Marcus Plescia, MD, Director, division of prevention of cancer and control, U.S. Centers for Disease Control and Prevention; Daniel M. Siegel, MD, President, American Academy of Dermatology; 11 May 2012, U.S. Centers for Disease Control and Prevention, Morbidity and Mortality Weekly Report

Copyright © 2012 HealthDay. All rights reserved.



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blurred vision

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Ray

I would talk to a Neurosurgeon and get their opinion and if anything can be done that's not invasive. Brain radiation especially if it's full brain radiation can cause that kind of problem. Give it a chance to heal for a few weeks.

Everything including the optical nerves are tied into the brain.

Here are all my personal notes and it tells you how to find 5 star doctors. You might look into some of the new vaccines that have come out especially those being used on GBM.

http://liveforeverwithcancer.com/

Keep writting.

John



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lung cancer surgery

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Hi there, I am sorry you have lung cancer.  I had my upper right lobe removed.  Let me tell you it isn't a piece of cake, yet it wasn't as bad as I thought.  I had excellent care at the hospital, and my doctors made sure I was treated appropriately for pain.  I can honestly say that my pain management was handled correctly.  I believe I, myself, have more problems with pain now (6 mths post op) at the site where the drain tubes were.  That seems to be the worst of it.  As for using your arm, yes you will be able to use it.  At least I was.  I think I was on a limit as to how much weight I could life.  LOL  Which for me, meant my hubby did the vacuming, a job I hate anyway.  I am totally off all pains meds as of Thanksgiving, so don't rush to quit them.  My oncologist didn't even want me to get off them then either, but I wanted to drive again.  I had dilluadid's, and it wasn't so bad when I quit.  I didn't even have to take ibuprofin or anything else.  So, I don't know if this helps you, but like I said, it wasn't as bad as I thought it would be, yet it was still REALLY tough.



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Dry Mouth

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Have you tried the biotene products.  I have dry mouth due to radiation and I use the mouth rinse durring the day.  When I go to bed, I use the biotene liquid which is thicker and can be swollowed.  Maybe a good time to stick to mild foods.  Oatmeal, eggs, mac & cheese, cottage cheese.  If he is not getting the calories he needs, there are ensure shakes.  Hang in there.  It will get better.

Paula



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Lung Cancer

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Surgery is what lung cancer patients always want.  That is the best treatment to start with.  Sometimes it is not possible, like if in both lungs, wrapped to near the heart, or other place that makes it in-operable.  But, all in all, we want to have it taken out for the best chance at survival.



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final stage small cell lung cancer

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My mother  to the doctor because she started getting shoulder pain then starting coughing up blood. Doctor told her she had lung cancer sept.2011. she had a biop. done and they said it was stage 4 small cell lung cancer. They started her one chemo and radiation but But it was too late. Last day of radiation she told them she was getting really bad pain in her rib and hip so they did a bone scan and found it she had metastasis in her hip,thigh and rib and specks of cancer in her liver. Now shes on hospice and a ton of morphine. Pretty sure she in the end stages. She gets really confused so not sure if its the medication or in her brain.Lost alot of weight. on oxygen because one lung is full of fluid and collaped. and just this last week she had been puking at least 1 cup of blood a day. So sad cause she was the life of the party. Very sweet lady never like to see this happen to someone so kind.



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swelling belly

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Hello.  So sorry to hear about your dad.  His swollen belly is most likely a condition called ascites.  Fluid is building up around his organs and distending his belly.  It is a very incomfortable condition.  The doctors usually try diuretics and salt reduction first.  If that doesn't work,  they drain the belly with a stent.  My husband had a catheter installed and they taught me how to drain him at home when he became uncomfortable.  It is a side effect of having cancer.  (pancreatic, liver, lung, and colon usually)  Hope this helps.  Prayers.  Tina



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