http://www.beatrcc.com/kidneycancerforum/ A forum for KC patients, caregivers, professionals... en-US Sat, 31 Jul 2010 04:05:29 +0000 http://bbpress.org/?v=1.0.2 q http://www.beatrcc.com/kidneycancerforum/search.php http://www.beatrcc.com/kidneycancerforum/topic/alternative-cure-for-cancer#post-18 Thu, 18 Mar 2010 05:47:43 +0000 callpau 18@http://www.beatrcc.com/kidneycancerforum/ <p>hello .. my name is paul from baltimore maryland.. i am a living witness to the cure for cancer through natural medicine.my dad and mom both died of cancer and its something ive had to live with for so long last year i was diagnosed with kidney cancer and it has caused me so much pain..ive spent thousands of dollars and at a point , i couldnt afford the medication. so someone told me about a man who can cure it in africa through herbal and natural means.. i didnt believe it but i just had to give it a try... and behold in just 4 months of using the therapy, i went for another test and they told me the cells are already dying and in just a few months away, i will be completely ok... i still cant believe it..... incase anyone needs him, his email address is <a href="mailto:lekanysf01@yahoo.co.uk">lekanysf01@yahoo.co.uk</a>....hope he helps you out as well. </p> http://www.beatrcc.com/kidneycancerforum/topic/kidney-cancer-metasticized-to-brain#post-15 Sun, 22 Nov 2009 03:53:11 +0000 Jacob G 15@http://www.beatrcc.com/kidneycancerforum/ <p>Hi there,<br /> My Mom just found out she has a lesion at the back left side of her brain. Does anyone have anything they can share regarding kidney cancer in the brain? Thank you!<br /> Gail<br /> ---------------------------------------------------------------------------<br /> Question asked in Yahoo kidney cancer support group </p> http://www.beatrcc.com/kidneycancerforum/topic/can-i-drink-alcohol-if-i-have-only-one-kidney#post-14 Sat, 21 Nov 2009 05:50:43 +0000 kenny1983uk 14@http://www.beatrcc.com/kidneycancerforum/ <p>Many ppl have asked about if they can drink alcohol id they have only one kidney left. the standard answer is: <strong>"Drinking alcohol in moderation. This is no more than 2 standard drinks per day for men and 1 for women plus 2 alcohol free days per week." </strong></p> <p>and also check out this post: <a href="http://www.beatrcc.com/2009/10/top-10-most-asked-questions-about-kidney-cancer-part-3">Can I live a normal life if I have only one kidney?</a> </p> http://www.beatrcc.com/kidneycancerforum/topic/second-opinion-is-always-necessary#post-13 Wed, 07 Oct 2009 04:39:54 +0000 lisa 13@http://www.beatrcc.com/kidneycancerforum/ <p><strong>Why</strong><br /> First, you can get a different perspective on your options. Some doctors are more conservative and others more aggressive. There may be good arguments for several different options; getting a second option can be a good way to hear some of them.</p> <p>Another doctor might come up with a completely different and promising option - one that your first doctor didn't think of, or didn't know about. It happens - no doctor can know everything or make the right decision all the time.</p> <p>A second opinion can also serve a general quality check - to make sure you're really getting the most up to date, most effective treatment.</p> <p><strong>When</strong><br /> Here is a list of some reasons why you might want a second opinion. This should help focus your thinking, but there is no cookbook answer for when you need a second opinion. So you'll need to consider your situation and think about whether you might benefit.</p> <p>If You Have Been Given No Hope<br /> Many patients are told there's no hope and that no further treatment can be of benefit. In this case, there's certainly nothing to lose by getting a second opinion, but there is a chance, however small, for a huge gain, since if your doctor is in error, a second opinion could save your life. Sometimes tumors deemed inoperable by one surgeon are found to be operable by another. Sometimes close examination of the case could change the diagnosis from one kind of cancer to another, more treatable type. Sometimes another doctor will know of a promising treatment that the first one didn't know about. All of these things have happened. You don't know until you check.</p> <p>If There is Something "Borderline" About Your Case<br /> If your tumor is almost operable, but not quite, or conversely almost inoperable but not quite, you might want a second opinion. You might either save yourself unnecessary surgery or you might save your life. Similarly if your tumor is on the borderline of requiring adjuvant chemotherapy you might want a second opinion.</p> <p>If You Live in a Rural Area<br /> If you live in a rural area and get treatment as a small hospital, it may pay to get a consult from a major hospital. I'm not saying you can't get good treatment from a small rural hospital, but I have heard some real horror stories.</p> <p>If You Are an HMO Member<br /> Although HMOs can and do offer fine care in many cases, there is a fundamental conflict of interest between an HMO and its members. The more money the HMO spends on you, the less it makes, so there is an incentive to give less expensive care, and an incentive not to refer outside the network. As a consequence, HMO members may not be told of clinical trials, or other promising new treatments. They may also be discouraged from trying expensive treatments that have only a small chance of success - even if that chance is real.</p> <p>Actually it's worse then that. Some HMOs actually prohibit their doctors from telling their patients about options that aren't available through the HMO. According to an article in Oncology Times (5/96 P22), "virtually all" HMOs have a "gag rule" in the contract between them and their doctors that discourages them from, "fully informing patients about options not included in their coverage." The AMA calls this practice "unethical" which it surely is. The contract between an HMO and its doctors is not a public document, so there's not even an easy way to tell if your HMO doctor is operating under a Gag Rule. While I think public outcry has probably reduced the number of HMOs which have Gag Rules, the very fact that Gag Rules were once common, and may still exist, is very strong evidence that HMOs are not always motivated to inform patients of the best possible treatment.</p> <p>Given this, I think don't think any HMO patient can assume that they are getting the best treatment, or that they have been informed of all of their options. Therefore, I think that any HMO member should have their treatment plan reviewed by an outside oncologist. You'll probably have to pay for the opinion yourself, but it's worth the expense. I recommend getting the opinion at a major cancer center or university hospital.</p> <p>If Your Doctor Wants You to be in His Clinical Trial<br /> If your doctor wants you to take part in a clinical trial that he is participating in as an investigator, then I think you ought to get a second opinion before signing up. One of the toughest things about running clinical trials is finding patients to participate. So the doctor has an interest in having you sign-up that goes beyond his interest in getting you the best treatment. Sometimes there is a financial incentive or other pressure to accrue patients. Don't get me wrong. I'm not saying that all doctors who want to sign you up for their trial are just doing it to have another body. Many if not most, physicians enter patients who they feel would benefit from the trial.</p> <p>Many trials are "multi-center", that is they are done in many hospitals across the country participate in the trial. If the trial you are being proposed for is like that, the experiment probably wasn't your doctor's idea to begin with. But it is natural for a doctor to be excited about a new treatment especially if it was his idea. An objective second opinion is in order!</p> <p>Clinical trials vary tremendously in their promise. A trial that was in essence randomly selected (Because your doctor just happens to be participating) may well not be the most promising one out there. For this reason, I also think you ought to research all of your options in clinical trials rather than automatically accepting the one your doctor happens to be offering. For much more, see CancerGuide's Clinical Trials Section.</p> <p><strong>Who</strong><br /> Independent Doctors<br /> You want your second opinion to be independent - so you should choose a doctor who doesn't have a close relationship with your doctor. Doctors who practice together are likely to think similarly, and might tend defer to the opinions of their colleagues. What you want is a fresh perspective. I'd go so far as to recommend finding a doctor who practices at a different hospital. A research hospital or major cancer center is usually a good place to get a second opinion since they should be up on the latest in treatment and diagnosis.</p> <p>Tumor Boards<br /> There is a special kind of second opinion that, while not independent, is worth considering because it's a great way to get a wide range of opinions all at once. This is the "tumor board" or tumor conference. Most hospitals have a tumor board which is a regular meeting of a group of doctors to consider the best treatment for specific cases presented by members of the group. Typically, doctors from several specialties such as surgery, radiation oncology, and medical oncology will attend. If your doctor doesn't seem to have a clear recommendation for you, consider asking if he could present your case to the tumor board.</p> <p>The R.A. Bloch Cancer Foundation has been instrumental in setting up a program of "multidisciplinary second opinions" which works much like a tumor board, but the patient is actually present when their case is discussed. This is intended for patients who have been diagnosed with a new cancer or a recurrence within the last three weeks. Their information on Multidisciplinary Second Opinions includes a listing of participating centers.</p> <p>A Different Specialist<br /> Many types of cancers are treated by several different types of specialists. For instance, prostate cancer is treated by urologists, who are surgeons, by radiation oncologists, and by oncologists who use drug treatment. After doing some basic research on your type of cancer, you will probably know what specialists treat it. It often makes a lot of sense to see one of the other types of specialist to get a different perspective. For instance, a surgeon may be convinced that "he got it all" and that you need no more treatment. At the same time, an oncologist may have more detailed knowledge of studies that show benefit from adjuvant treatments such as chemotherapy or radiation. Similarly, a surgeon may have a better idea than an oncologist of whether a tumor is operable or not. Very often, one specialist will call in another for a consultation, so you may not have to do anything to get this second opinion. But I have heard from patients who didn't get a needed consultation, and who missed out on potentially life saving treatment.</p> <p>A World Class Expert<br /> In some cases, what you need is world class expert - a surgeon who does operations most others don't - an oncologist who is in the forefront of research in a new and promising area that applies to you. Or an expert in a rare cancer.</p> <p>In many cases, expertise is quite narrow - Dr. X is skilled at removing a particular type of brain tumor. Dr. Y is an expert in biological therapy for melanoma. It's not as simple as just finding someone who's got a reputation as a good doctor. I know of no foolproof way to find the expert you need (If you do, please let me know!). Doctors often do know who the experts are, and your doctor may be able to give you a referral. You can also research the medical literature to see who's published papers relating to your particular problem. Often, this will be quite effective.<br /> reference:http://www.cancerguide.org/second_opinion.html </p> http://www.beatrcc.com/kidneycancerforum/topic/photos-of-asia-pet-fair#post-9 Sun, 27 Sep 2009 08:25:59 +0000 kenny1983uk 9@http://www.beatrcc.com/kidneycancerforum/ <p>Hi folks, I went to asia pet fair yesterday, that was pretty nice. &lt;img src=&quot;http://www.beatrcc.com/kidneycancerforum/my-plugins/bb-smilies/default/icon_razz.gif&quot; title=&quot;:P&quot; class=&quot;bb_smilies&quot; /&gt; I took lots for photos, <a href="http://www.beatrcc.com/album?album=2&amp;gallery=6">click to see</a>, the one with sport suit in the first 2 photo is my chocolate. more pics are coming soon.( they are too big, have to edit them before uplading) &lt;img src=&quot;http://www.beatrcc.com/kidneycancerforum/my-plugins/bb-smilies/default/icon_sad.gif&quot; title=&quot;:(&quot; class=&quot;bb_smilies&quot; /&gt; </p> http://www.beatrcc.com/kidneycancerforum/topic/stages-and-survival-rates#post-11 Tue, 06 Oct 2009 08:22:07 +0000 kenny1983uk 11@http://www.beatrcc.com/kidneycancerforum/ <p>Renal cell carcinomas often start as small tumours. They may be few symptoms. About one quarter of RCCs will have spread to other organs by the time they are recognized. The most common sites for renal cancers to spread are the lungs, bones and lymph nodes near the kidneys.</p> <p>At the time someone is diagnosed with kidney cancer, the specialist will determine the "stage" of their disease. There are four stages. Depending on the stage of the disease (ie how big the tumour is, or whether it has spread), the best decision about treatment and the likely outcomes can be discussed. </p> <p>Stage 1: the cancer is confined to only one kidney and is not more than 7cm. These patients have the best long-term survival and are most likely to be cured with surgery. The five year survival rate is almost 90%.</p> <p>Stage 2: the cancer is more than 7cm, but does not extends outside the surrounding layer of the kidney (known as the capsule). These patients also have a high rate of survival and surgery is a good treatment option. The five year survival rate is more than 75%.</p> <p>Stage 3: the cancer may be of any size, but it extends outside the capsule of the kidney and into blood vessels. In these patients, the specialist will give advice about appropriate treatment. These patients have a 5 year survival rate of close to 65%.</p> <p>Stage 4: the cancer of the kidney in these patients may be of any size. However these patients have the lowest rate of long-term survival because the tumour has spread outside the kidney to other organs. Less than 10% of these patients survive 5 years.<br /> reference: <a href="http://www.virtualcancercentre.com" rel="nofollow">http://www.virtualcancercentre.com</a><br /> <a href="http://www.beatrcc.com/2009/07/kidney-cancer-survival-rates">Kidney Cancer Survival Rates</a> </p> http://www.beatrcc.com/kidneycancerforum/topic/berry-fruits-good-for-kidney-cancer-patients#post-2 Tue, 15 Sep 2009 21:09:51 +0000 kenny1983uk 2@http://www.beatrcc.com/kidneycancerforum/ <p>A doctor told me that all the fruits with a word " &lt;img src=&quot;http://www.beatrcc.com/kidneycancerforum/my-plugins/bb-smilies/default/icon_arrow.gif&quot; title=&quot;:arrow:&quot; class=&quot;bb_smilies&quot; /&gt; BERRY" in their names are good for kidney cancer patients, such as strawberry, waxberry, blueberry, etc. not sure if it's good for patients of other kinds of cancer. </p> <p>And also Kiwi fruit, good for patients during chemo-treatment period. </p> http://www.beatrcc.com/kidneycancerforum/topic/what-is-the-survival-rate-of-a-person-diagnosed-with-stage-iv-kidney-cancer#post-5 Tue, 15 Sep 2009 21:37:09 +0000 landry 5@http://www.beatrcc.com/kidneycancerforum/ <p>My wife was just diagnosed with kidney cancer, she is 53. I was told that it had already spread to her lung (5 tumors) She has already had the kidney removed and we were told that it was in the tissue also. </p> http://www.beatrcc.com/kidneycancerforum/topic/what-should-you-ask-your-doctor-about-kidney-cancer#post-4 Tue, 15 Sep 2009 21:23:16 +0000 lisa 4@http://www.beatrcc.com/kidneycancerforum/ <p>It is important to have frank, open discussions with your cancer care team. They want to answer all of your questions, no matter how trivial they might seem. For instance, consider asking these questions: </p> <p>What kind of kidney cancer do I have?<br /> Do you think my cancer has spread beyond the primary site?<br /> What is the stage of my cancer and what does that mean in my case?<br /> What treatment choices do I have?<br /> What do you recommend and why?<br /> Based on what you've learned about my cancer, what is my long-term prognosis (outlook)?<br /> What risks or side effects are there to the treatments you suggest?<br /> What are the chances of recurrence of my cancer with these treatment plans?<br /> What should I do to be ready for treatment?<br /> How soon should I be treated?<br /> What type of follow-up will I need after treatment?<br /> Are there any clinical trials I should think about?<br /> Along with these sample questions, be sure to write down some of your own. For example, you might want to know how long it might take you to recover so that you can plan your work schedule. Or you may want to ask about second opinions or about clinical trials for which you may qualify. </p> <p>reference:ACS cancer.org </p> http://www.beatrcc.com/kidneycancerforum/topic/curative-treatments-and-palliative-treatments-for-rcc-treatment#post-3 Tue, 15 Sep 2009 21:16:27 +0000 kenny1983uk 3@http://www.beatrcc.com/kidneycancerforum/ <p>• Surgical treatment (for early RCC)<br /> • Palliative therapies or experimental protocols (for advanced RCC)</p> <p>Curative treatments: Radical nephrectomy (removal of kidney, adrenal gland, perirenal fat, and Gerota's fascia) is standard treatment for localized RCC and provides a reasonable chance for cure. Results with open or laparoscopic procedures are comparable. Nephron-sparing surgery (partial nephrectomy) is possible and appropriate for many patients, even in patients with a normal contralateral kidney if the tumor is &lt; 4 cm. Nonsurgical destruction of renal tumors via freezing (cryosurgery) or thermal energy (radiofrequency ablation) is being done in highly selected patients, but long-term data about efficacy and indications are not yet available.<br /> For tumors involving the renal vein and vena cava, surgery may be curative if no nodal or distant metastases exist.<br /> If both kidneys are affected, partial nephrectomy of one or both kidneys is usually preferable to bilateral radical nephrectomy if technically feasible.<br /> Radiation therapy is no longer combined with nephrectomy.</p> <p>Palliative treatments: Palliation can include nephrectomy, tumor embolization, and possibly external beam radiation therapy. Resection of metastases offers palliation and, if limited in number, prolongs life in some patients, particularly those with a long interval between initial treatment (nephrectomy) and development of metastases. Although metastatic RCC is traditionally characterized as radioresistant, radiation therapy can be palliative when metastatic in bone.<br /> For some patients, drug therapy reduces tumor size and prolongs life. About 10 to 20% of patients respond to interferon alfa-2b or IL-2, although the response is long-lasting in &lt; 5%. Three new targeted therapies have shown efficacy for advanced tumors: sunitinib and sorafenib (tyrosine kinase inhibitors) and temsirolimus, which inhibits the mammalian target of rapamycin (mTOR). Other treatments are experimental. They include stem cell transplantation, other interleukins, antiangiogenesis therapy (eg, bevacizumab,thalidomide), and vaccine therapy. Traditional chemotherapeutic drugs, alone or combined, and progestins are ineffective. Cytoreductive nephrectomy before systemic therapy, or as a delayed surgical procedure to remove the primary tumor after response in the metastases, is commonly performed in patients healthy enough to undergo it.</p> <p>Last full review/revision December 2007 by David A. Swanson, MD<br /> Content last modified December 2007 </p>