The End Of Cancer Has Begun



Laura Ziskin- By Laura Ziskin

This past September 5th, Stand Up to Cancer launched in a powerful way. Thanks to a landmark broadcast on three major networks, the passion, support and dedication of leading doctors and scientists, and generous contributions from the entertainment community, corporate sponsors and the general public, we raised more than $100 million for innovative cancer research projects. Now, to paraphrase Tony Kushner, it is time to let the great work begin:

In early October, Lisa Paulsen, Noreen Fraser and I (representing the Executive Leadership of SU2C) traveled to Philadelphia to attend a dinner on the eve of the inaugural meeting of the Stand Up To Cancer Scientific Advisory Committee. Dr. Raymond DuBois, president, and Dr. Margaret Foti, chief executive officer, of the American Association for Cancer Research (AACR), our scientific partner, hosted the dinner. Nineteen of the twenty Committee members, including the two representatives of the SU2C Advocate Advisory Council, attended the meeting. Nobel Laureate Dr. Phillip Sharp presided over the meeting, along with vice chairs, Dr. Brian Druker and Dr. Arnold Levine. For Lisa, Noreen and me, it was our first time meeting many of these extraordinary scientists who have generously agreed to donate their time and expertise to our mutual cause.

We already knew Dr. Sharp and Dr. Druker, of course, both of whom were featured in the Stand Up To Cancer broadcast. Dr. Sharp took me around before the dinner and gave me a personal introduction to a number of the other attendees, including Dr. Levine who was a key figure in the discovery of the p53 tumor suppressor gene; Richard Kolodner who has done seminal work in genetic recombination and DNA repair; Tak Mak who co-discovered the T-cell receptor, a key component of the immune system; Cecil Pickett from Biogen Idec, who is a world expert in drug development; Vicki L. Sato, whose expertise is in both drug development and business in the biotechnology and pharmaceuticals industries; and Samuel Wells, who, Dr. Sharp reminded me, is the only surgical oncologist on the Committee, and is a pioneer in treatments for thyroid and other endocrine cancers. It was a heady experience to have this much brain power together in one room. But what was really rewarding was to hear first-hand how genuinely excited and challenged they all were to be such an important part of this endeavor. To learn more about our Scientific Advisory Committee go to: http://www.standup2cancer.org/su2c/advisory.

In July, the AACR put out a broad call for ideas for cancer research "Dream Teams," reflecting the following general SU2C principles:

SU2C is committed to improving the outcomes for cancer patients by raising awareness of the importance of the problem and providing significant incremental resources to apply to its eradication. SU2C understands that its goals can only be achieved through the support of very high quality research and has formed a partnership with AACR to facilitate the distribution of research support in a fashion that both promotes the highest quality science and adheres to the specific priorities of SU2C:

  1. SU2C aspires to support proximal translational research. By this we mean both laboratory and clinical research bridging the gap between basic science and the bedside, clearly focused on the problem of human cancer, with a discernible potential to lead to the development of markedly better treatments or preventions for this disease as rapidly as possible. SU2C places the highest priority on initiatives with the greatest potential to translate within the funding period and that address the greatest unmet medical need.

  2. SU2C believes that open communication, collaboration and cooperation between the best scientists and clinicians is essential to moving the research agenda forward as rapidly as possible and is therefore critical for cancer patient welfare. SU2C therefore wishes to foster group efforts and discourage individual and institutional competition in its funding activities.

  3. SU2C wishes to promote goal-directed research. While it is understood that true innovation and major improvements in cancer prevention and treatment will begin with the best basic laboratory research, projects that are most consistent with SU2C objectives will unambiguously embody and specifically articulate a clear bedside objective.

  4. SU2C is committed to maximizing the efficiency with which scientists pursue the research objectives we support. We therefore wish to minimize the time spent in preparing proposals and awaiting funding and optimize the time spent on SU2C projects. Noreen, Lisa and I addressed the group at dinner and thanked them for their commitment. We also each encouraged them to think boldly in their upcoming meetings; to think out of the box; and to think about what will get better treatments to patients in the fastest way possible. It was gratifying when Dr. Sharp, Dr. Druker and Dr. Levine each took the podium to address the group. Dr. Levine spoke about how far we have come since Nixon's war on cancer. How in those days we thought all cancers were caused by viruses. How we have subsequently learned about the effects of chemicals and carcinogens; about the role of aging in cancer; and most importantly about how genetic changes can cause cancer. Indeed, technology has given scientists so many new tools and they now understand the mechanisms of cancer so much better. Dr. Levine reinforced that cancer researchers are on the cusp of real breakthroughs.

Dr. Druker then told the story of a colon cancer patient who asked him when there would be better treatments. He told the patient things were moving forward and that new treatments were just down the road. The patient was not satisfied. When Dr. Druker went home and recounted this to his wife, she reminded him that you cannot ask a cancer patient to have "patience". We need answers now, and Dr. Druker and cancer researchers around the world are committed to finding them. Finally, Dr. Sharp said that the entire Committee understands that the SU2C leadership, and the public we continue to rally, have given them an incredibly difficult challenge, but that they were all really turned on by that challenge and dedicated to doing their very best to deliver results.

We left the dinner more excited than I think we had been throughout the entire year we had been working on SU2C. This was what we had been working and waiting for. The next morning these scientists would meet to discuss their charge from the SU2C and to evaluate the proposals that were submitted. This meeting marked the beginning of an important process to identify the most exciting team projects to be supported by SU2C funds. In the coming weeks and months, Dr. Sharp and the vice chairs of the Committee will be updating all of us on their progress. I will do my best to pass on their findings to all of those who have generously supported our cause. But for all of us who were in the room October 9th, I can tell you there was a feeling of enormous excitement that the end of cancer has begun.

102 Comment(s) on this post | View Comments | Post a Comment | |

Posted by Christy Langston | December 18, 2009 2:10 PM

I am so excited to hear about SU2C! My cousin was diagnosed with Cholangiocarcinoma in July of 2007. In 2008 the doctors said it was gone. Well it came back with a vengance! Just the other day they informed us that they are taking him off all his chemo treatments and there is nothing else they can do. We can't give up!! He has been very strong and has put up a fight for two years how do they expect him to give up. The doctors told him that China has a pill that will cure his type of cancer but it is $1300.00 for a 30 day supply. Have you heard of this? Do you know where we can get help financially to purchase the first month? Or do you have any suggestions for us to Stand Up to his Cancer? Again I am excited for your launch of SU2C.

Posted by Madeline Ryan | December 9, 2009 7:07 AM

My name is Madeline Ryan ( they call me Mati or Min)., I am a Cancer survivor. Yes, I'am one of the lucky ones:) I want to tell the world everyday, how lucky I'am and want to help or join Stan Up to Cancer and do what ever it takes to let the world know we can beat it....But, we do need help. However, I had a "Stem Cell Transplant" my own cells, three years ago....I'm still here & to tell my story. I had one year of Chemo, I had two slavge chemo and " BEAN" before my Transplant. I had Hogdkins Lymphoma, stage 2b I was 46 yrs. I had the works and if I had to do it again, just stay alive I would. But, I believe in Stem Cells, it works. I had it done at Moffitt Cancer center, in Tampa Fl. I was treated with Chemo at Jackson Memorial, Miami - Fl....Next week I will have two birthday. Dec 22, I'll be 49 and Dec 21., I will be three years.....God Bless me and God willing. I want to become part of the team. God Bless - always Mati Ryan

Posted by Preeniefrobby | January 12, 2009 10:34 PM

I think you are thinking like sukrat, but I think you should cover the other side of the topic in the post too...

Posted by Miriam Palacio | December 5, 2008 1:59 PM

I wish that more research is done on early cancer
detection. My husband was complaining from stomach pain for several years before an agressive rare gall blader cancer was found which by then it was stage IV. He went through exploratory surgery where they found the cancer and a biliary obstruction which was cholangiocarcimoma. Two more long complicated surgeries, chemo, and radiation only added one more year with us. I am devastated by his quick
departure and I am asking that early detection of all rare cancers is also included in your research
as well as that doctors are upfront with the families of terminally ill cancer patients. None of the Drs involved in my husbad's case ever
alleged to the gravity of his condition, I was told that they always want to give hope, but in terminal cases, I believe most families would like to be forewarned. I am looking forward to finally some day, in the not too distant future, with scientists and fundraising like yours, cancer will be eradicated. I was at the Kodak Theatre for the TV show which brought many tears to my eyes. Thank you for your efforts and I hope that SU2C fundraising will become a yearly event. I was thrilled when donations reached
100, million. Great job!

Thank you for your hard work and God Bless everyone of you.

Miriam Palacio

Posted by Brenda | December 5, 2008 6:29 AM

I would like a response to the question, please, if any of the Dream Teams will be focusing on childhood cancer? Let's make SUC2 include everyone! Forest Whitaker on SUC2 talked about a young boy who just wanted to be six. Please just let us know that you will include childhood cancer in your research funding. Thank you for your assistance. I await your reply.

Posted by Casey Greenly | December 4, 2008 6:31 PM

Our son Isaac was diagnosed with ALL Leukemia on October 9, 2006 at the age of 3 1/2. Watching him and the other children battle cancer when they should be having a childhood is something I hope someday families will not have to see. No child should have to know what cancer, methotrexate, 6MP, accessing ports, dexamethasone, daunorubicin, vincristine, and my 5 year old can tell you all about the medicines and when his ANC is low he knows he can't go to school or play with friends. As parents we have to advocate for our children as ask that you please at the very least divide the funds equally. Currently childhood cancer receives less then 3% of research funds.............these are our children.........our babies and they need our help! Thank you for listening and we look forward to seeing how the funds are distributed. Thank you so much!

Posted by Jamie Cataldi | December 3, 2008 8:31 AM

Please EQUALLY distribute the funding!!!! Make sure that Pediatric cancer is not at the bottom of the list. There should be a dream Team designated toward each type of cancer!! Yes pediatric cancer is SAD, but even SADDER the fact that it is NOT equally funded!!! I STAND UP FOR THE CHILDREN !!! Jamie Cataldi

Posted by Rebecka | December 2, 2008 10:25 AM

My husband 4th stage of a rare and aggressive cancer.They think we may have some time. I hope rare cancers won't fall by the wayside.We also cannot bare to see children go through what he has been through. Children need to have a chance to grow up and live normal lives. I hope SU2C is also working with ACS and the NCI and the main research arms so that all research can be shared. That seems to be the problem sometimes. My prayers are with all of you going through this, and I pray for those doing research that they may be guided in their work.

Posted by Elizabeth | November 29, 2008 6:08 PM

My 17 year old daughter is in the 13th month of a 24 month protocol of treatment for pediatric lymphoblastic lymphoma. We nearly lost her in the midst of chemotherapy. She currently follows a protocol based on a trial that ended 2 years ago. There are currently no new trials available. Her treatment will follow old information until new side effects or deaths from that previous trial can be communicated properly and quickly to her pediatric oncologist. At that time her treatment for the next 12 months will be "tweaked". How crazy is this? I pray the scientists in this great think -tank put together by SU2C will help save our children. We need these great minds to act quickly and thank SU2C for getting the ball rolling.

Posted by Brenda | November 27, 2008 10:26 PM

I never thought about childhood cancer until it happened to our son. 46 kids each day are diagnosed with cancer. That is two classrooms. 1 in 330 kids will have cancer before they are 20. Yet no one talks about childhood cancer and it gets only 3% of the funding for research. Please help to change this. Our kids are our future. They can't speak, but we can and we will keep speaking until someone listens. Please remember the kids when you divide up the funding. Thank you for a great project. I am a mom who is seeking a cure for all cancers someday.

Posted by Jim Perry | November 27, 2008 6:29 PM

As you can see from the posts here, there are alot of children out there effected from cancer, just read the letters here. The reason those parents are screaming for more research funds, isnt to be selfish, its to attempt to get a more even division of the research dallars. Children do and have recieved alot less dallars then the other cancers. The problem is, you almost have to be a parent of a child with cancer, to find this out. PAC2 is a group of parents, medical professionals, and even major fundraising groups. All we want, is a fair and even distibution of funds.

Jim Perry F/O Dustin
http://www.caringbridge.org/visit/dustinperry
People against childgood cancer
http://curechildhoodcancer.ning.com/

Posted by Rachel H. | November 26, 2008 10:41 AM

The end of cancer sounds really nice. As a mom who has had to watch her second grader go through 30 treatments of radiation and 4 week long rounds of high dosage chemo each time followed by stem cell rescue, the later all inpatient. I would like to never see any person battle cancer again. Now my on has to live with the late effects; One of those being the chance of reoccurrence. We have two things that need to be addressed right now, better treatments and prevention research. We need larger research projects (not just the piecemeal that typically happens, but large nation wide research projects). I would like to see Stand Up to Cancer back up HR 7153 National Childhood Brain Tumor Prevention Network Act of 2008. There is a push to get it reintroduced into congress under a new number in January. I am having trouble understanding why we just want to treat cancer and not prevent it? I feel both are equally important and I don't see much being done to prevent any childhood cancers. I believe that we are capable of understanding this beast and someday eliminating it. But we have to start to care about prevention along with better treatment. Then we have really stood up to cancer.

Posted by Brandi Kessler | November 26, 2008 7:10 AM

We have never said that any life is more important than another. We want for there to be a cure for all types of cancer. We are simply asking for equality in funding. We are advocates for the children. Awareness and funding for childhood cancer is inadequate. The National Cancer Institute's budget was $4.6 billion. Of that, breast cancer received 12%, prostate cancer received 7%, and all 12 major groups of pediatric cancers combined received less than 3%. That is not equality. Our children deserve better than that.

Posted by Kathi | November 25, 2008 2:23 PM

KIDS CANCERS, EVERY SINGLE ONE OF THEM, NEED TO GET AN EQUAL SHARE OF FUNDS FOR RESEARCH. I don't see why that is too much to ask. Every single one of us would give our lives for our childs...why are we not saving our kids first? Please help them.

www.curechildhoodcancer.ning.com

Posted by Kara Cunningham | November 24, 2008 7:43 PM

For 1 ½ years, my young son Lane fought a very difficult battle, a battle that no one, especially a baby, should have experienced. Before he was nine months old, Lane was diagnosed with neuroblastoma. He endured 16 months of treatment and now shows NED (no evidence of disease). Lane is one of the lucky ones. Too many children lose their lives to cancer each day. Something needs to be done to reduce, or even eliminate, childhood cancer. Children shouldn’t have to fight for their lives, they should simply be able to enjoy a carefree, and cancer free, youth. Much more research is needed to help improve treatments and find cures for OUR CHILDREN. I urge you to fund pediatric cancer research. Our children, the future of this country, deserve this funding. Please support pediatric cancer research. Do it for my son and the many other children that are facing the hardest battle of their lives. You never know, it could potentially save the life of your child, grandchild, neighbor or friend.

Thanks in advance for your support! www.caringbridge.com/visit/lane

Posted by dari mcmanus | November 24, 2008 4:59 PM

noone is trying to be selfish here. what you are seeing is begging and pleading. do a little research and see how the funding is handed out. kids get next to nothing in compared with other adult cancers. we are simply not willing to accept that. not anymore.
our littest warriors cannot vote, nor can they lobby. what is sad, it that seems to matter. it matter alot.
i stand up cancer. i ask you to stand up for those whom are too little to stand up for themselves.
current cancer therapies DO NOT WORK THE SAME on little bodies. Just one example. Pediatric Brain Tumors are BIOLOGICALLY DIFFERENT from adult Brian Tumors. never mind the secondary cancers these kids deal with, when they get their MIRACLE CURE.
there is an argument to be made about how these kids dont have any appropriate treatment at all.
its not selfish, its aware.

Thank you again, StandUpToCancer. i came through with a whole bunch of donations. i have every to suggest where my money goes.
PLEASE stand up for the kids.

in HOPE for CHANGE!

Posted by Renee Rodkey | November 24, 2008 4:01 PM

Would love to see more of the money raised on our future..........THAT'S IS CORRECT - OUR CHILDREN. Having lost my precious 12yr old daughter to a brain tumor, that is what made me call in and support your efforts - NOW IT IS TIME FOR YOU TO SUPPORT OUR EFFORTS.
Renee Rodkey
proud mommy of Abbey
06-14-94 ~ 12-02-06

Posted by Amy Bucher | November 24, 2008 11:34 AM

Wow. I've met so many parents and families affected by Childhood Cancer. "Selfish" is NEVER, EVER a term I would use to describe them. The caregivers give 100% of their time to their children who need them so very desperately. They also look out for the other families, even if they are grieving their own loss. These are the people who shave their heads; they, and the children, sell lemonade in a desperate attempt to provide funding where there is none to spare. When we advocate for increased funding for Childhood Cancer research, it is not because we are being selfish. Heck, my daughter is already gone; there's nothing to be gained for our family any more, unless, of course, another child among us is diagnosed. What if your child is next?

We recognize that the research funding needs to be shared among all cancers. We also recognize that for far too long, childhood Cancers have been "orphaned," either underfunded or not funded at all. Drugs that should be available today sit on shelves because pharmaceutical companies do not consider making them available to the children who need them "profitable." This is FACT. Are we being selfish when we provide voices for the weak, vulnerable, most innocent members of our population?

I'm not sure about that.

Is a person who throws around a term like "selfish" without knowing the stories behind those voices being cruel, disrespectful, and immature? You bet.

Again, thank you for your efforts. We are sure you will do your best to "spread the wealth." We want to be sure that the children are not forgotten (even though their images will certainly be used to get more donations) in the process.

God bless your efforts,
Amy Bucher
mom of ^^Arden^^

Posted by Lara Bancroft | November 24, 2008 8:53 AM

SU2C has an amazing opportunity to help make a difference where other organizations have not yet. The research and statistics are clear - pediatric cancer is an area that lacks funding but deserves the focus. The average years lost is way too high. And children are our future. These kiddos deserve better and we need to stop losing so many of them. Please remember the kids and their years lost when allocating the funds. Thank you!

Posted by L. Rehrauer | November 23, 2008 8:03 PM

Please think about the children when making decisions on the equitable distribution of your efforts. You have the power to change history, to wrong a right, to look into the faces of the children stricken with cancer and tell them that there is hope. There is money to fund research that will find the answers to make their pain go away. To make sure that yet another mother doesn't hear the sickening diagnosis that her baby, her reason for living, has a "rare" childhood cancer. That there isn't another funeral. Please be a voice for the children. Please stand up with us "People Against Childhood Cancer" and fund childhood cancer research. Do the right thing. You have the power. Our children need you to remember them front and center when you are considering your distribution of research funds. Thank you.

Posted by Kelly Parent | November 23, 2008 7:21 PM

Why should SU2C support Childhood Cancer research for cures and survivor programs?
1) some pedi cancers remain largely untreatable: Overall, 3/4 kids diagnosed with cancer will survive, but 1/4 will die. This statistic skyrockets with certain cancers such as brain tumors, neuroblastoma and certain sarcomas. A majority of these children will die.
2) It is difficult to detect pedi-cancer in early stages: Attempts to detect childhood cancers at an earlier stage, when the disease would react more favorably to treatment, have largely failed. Young patients often have a more advanced stage of cancer when first diagnosed. (Approximately 20% of adults with cancer show evidence the disease has spread, yet almost 80% of children show that the cancer has spread to distant sites at the time of diagnosis).
3) THe causes of pedi-cancer remain largely unknown: The cause of most childhood cancers are unknown and at present, cannot be prevented. (Most adult cancers result from lifestyle factors such as smoking, diet, occupation, and other exposure to cancer-causing agents). Scientists are beginning to make genetic and cellular breakthroughs that will also help adult oncology patients and adults and children with a multitude of other diseases. BUt they need money.
4) childhood cancer survivors are developing many problems caused by the cures: 2/3 of these survivors are experiencing late effects of treatment, that are serious or life threatening. Additionally, our society health system is not supportive of adult survivors of pedi cancer--many of which have cognitive deficits caused by the curative treatments leading to under-education, under-employment and under-insured adults.
PLease help our scientists fine a a cure and better cures for our children.

Posted by Jackie Hegarty | November 23, 2008 7:11 PM

My dad was diagnosed with Pancreatic cancer in March of this year. They said the cancer was endocrinated in the tumor and it was operable. He was operated in late April to remove but the operation was unsuccesful. From the operation though he developed an infection and became septic. I live in Australia and the doctors told my family I needed to come home. Well being in ICU and on a ventilator for nearly 3 weeks he recovered and left the hospital after nearly 5 weeks of being in there. At that time he was OK so I flew back to Australia. He gained some strength so was advised to have another operation to remove the tumor so second operation was successful in August. The doctors said that most of the cancer was removed but not all of it and needed to gain some strength before they started chemo. Well after a cat scan that was done 2 weeks ago they found that their were lesions on his liver and abdomen and he has 2 to 3 months to live. Of course the family is devasted because he has fought so much. He is not ready to give up and neither our we but unfortuantely with no cure where do we stand. Thats why its very hard for cancer patients to wait as well as their faimly. Thank you for trying to find a cure so lets all pray that a cure is found sooner than later for all cancer patients especially my dad!

Posted by Sherry Monahan | November 23, 2008 6:44 PM

Everyone who is touched by cancer knows the fear and chaos it creates. Your reality is completely changed - forever. Twenty months ago, our daughter was diagnosed with ALL leukemia. She spent her fifth birthday starting her daily chemotherapy that will last until next May for a total of 2 years 3 months. Cancer is not rare when it happens to you. Cancer represents a sobering paradigm shift for anyone. It is a daily reality of cancer: the daily meds, scheduled procedures and the knowledge of possible relapse percentage as well as side effects. For pediatric cancer patients, the kids are given old adult protocols that were not developed for children. Those kids that are able to get into a clinical trial are considered lucky. There are too many trials being canceled due to lack of funding.
In my daughter's case, she has a serious but "rare" side effect with lesions on the white matter of her brain due to the CNS methotrexate she receives every 90 days. There are no alternative drugs for her to take. We won't know the extent of the damage for years to come. Yet, she is one of the lucky ones. Every month we see new faces in the clinic. How can pediatric cancer be considered rare when one in 330 kids is affected - and pediatric cancer is the number one disease killer for kids? These kids desperately need our help. Pediatric cancer gets such a disproportionate amount of the funding from the government (NHI.) As parents, we are realizing that we have to stand up for our kids. Please stand up with us.
God Bless,
Sherry Monahan
http://www.caringbridge.org/visit/fionamonahan

Posted by Rosanna Mangini | November 23, 2008 3:23 PM

My beautiful fifteen month old daughter died just three days before last Christmas from Infant leukemia. She loved her life, she loved living, she never stopped smiling, blowing kisses, and clapping until she spiked a fever that ultimately ended her life due to complications from leukemia.

From the age of three months, she was subjected to aggressive chemotherapy when most babies are home. The hospital became her home.

I wish I could have taken her illness, I've had a life, hers hadn't really even begun. The doctors always told us that they wish they knew more, in 2008 they still weren't completely sure of the best way to attack this cancer.

One may ask why? The lack of research and funding is a big one. Please help our children, they shouldn't have to have tailored down adult treatments, they are our future. Let's support all cancers, but in the "all" don't forget our children who are too often getting only scraps of research funding.

My story could easily be yours,

Zanna

Posted by Dawn Emerson | November 23, 2008 8:44 AM

I have never been more proud of those who have come together for a cause as to standup2cancer. I cried with joy and hope that we will find a cure. My mother died in 1992 from Overian cancer and she was young. I continue to Pray for a cure and for all who are sick. I thank God for all of who care and who gave and who Pray!! Thank you and Please keep us posted and have a Blessed Holiday!

Posted by Dr. rer. nat. Peter Keller | November 23, 2008 1:08 AM

I completely agree with Laura Ziskin that effective treatments of malign tumors can be developed. I proposed several times a new synergetic approach, the combination of
1) Angiogenese Inhibitors
2) Immunostimulantia
3) physical methode of local hyperthermia by focussing micro-wave radiation
The canceroangiogenese has been discovered by Dr. med. Wolfgang Wohlgemuth, a coworker of Professor Ferdinand Sauerbruch Charite Berlin. Many evenings we discussed his theory of induced blood vessel growth into the tumor. Later the biomolecular basis of angiogenese was investigated by the US american researcher Folkman PhD. using animal cornea experiments. Since then effective angiogenese inhibitors are available. The cancerostase effect was clinical tested a decade ago.
The immunotherapy should me more effective if the angiogenese is simultaneously inhibited. The tumor cells are weakened and the growth is stopped. I proposed this idea to NIH, INSERM and the german DKFZ. I got an answer of Dr. Bronsema from the DKFZ that this is a sensefull and probably effective new approach.
The local hyperthermia using superposition of computer tomography to localise the tumor and 3D-infra-red imaging system to direct the micro-wave radiation focussing in the tumor region is save. The methode proposed by Professor Manfred von Ardenne, a physicist not a medical doctor, a whole body hyperthermia is very dangerous and led to a fatal accident. He than had to stop his research. But the new modern methode using micro-waves focussing in the tumor region is absolutely save. It is known that tumor cells are much more temperature sensitive than healthy somatic cells.
I hope that clinical testing of this synergetic approach will show tumor necrosis in many cases.

Posted by sandy | November 22, 2008 10:42 PM

This is a long time coming a unity of all cancers. My mom my best friend has been battling NHL-IV since July 26th,2004. I will never forget those words Cancer. She has fought a tough battle and the cancer kept sneakiing up. My mom is now tired and at peace and only has a short time left. Although she fights with heart and soul and Faith in love and hope. She is a true inspiration to me and many. I am so humble and inspired by this unity. Stand strong and fight the fight. Sandy a caring loving daughter fighting the fight for all Cancer patients.

Posted by Deaner | November 22, 2008 3:49 PM

I am currently a recovering breast cancer patient. Although it has been 3 years I really do not feel that until a cure or at least a treatment that can stop the advance of cancer is found that I will be a survivor. In the 2 years I fought the disease I lost my mother, brother, aunt, cousin and best friend to this disease. Almost everyday I hear of someone just receiving the news that will change their life forever. I am so glad that you are doing this for all of the people who are either fighting the disease, lost the battle,those who yet know that they will have to fight it themselves as well as the ones who love and support them. I went to Duke University and spoke with Dr. Kimberly Blackwell who I will say is the greatest doctor I have ever met and with the help of my dedicated Oncologist Dr Larson and Robin Cox I am writing this to you today. Thank you for your updates and know that your efforts are greatly appreciated everyday. THANK YOU ALL.

Posted by Tracy | November 22, 2008 7:49 AM

I am so disheartened that some people think the research should only be focused on one group of people. How selfish! Every cancer patient is a human being with friends and family who love them dearly. They desire to live as much as anyone else. No one person's life is more important to another...child or adult.

I work in the oncology field and see the devastation of this disease every single day. The toll it takes on the patients AND the families and loved ones. Now, my own sister, at age 29, has been striken by this horrible disease. Stomach cancer...a rare cancer which is typically not diagnosed until late stage. Her cancer was unable to be resected. She now undergoes chemotherapy. Never did I imagine such a thing happening to our family.

Please, divide up the funds and research amoung ALL cancer patients and ALL cancer types.

Posted by Renee White | November 22, 2008 7:43 AM

I have been battling primary peritoneal cancer and the chemo combination of taxol/carboplatinum which had been working no longer does. Peritoneal requires the same treatment as ovarian cancer and yet there seems to be no new medication for this disease. Does anyone know of a newer protocole?

Posted by Loren Loveness | November 21, 2008 8:40 PM

I lost my wife, Elsie to ovarian cancer last April. We had the standard cancer treatments (cut poison & burn). We researched every option possible, and yes, she participated in a "trial". We were so disappointed with the options offered in this Country and felt let down by "conventional medicine". When SU2C came on board, I was so impressed that I gave a donation the next morning. I feel you have the right approach to curing ALL cancers. I hope you can convince the drug companies, Universities, and the Federal government to work together instead of every one trying to find the magic bullet on their own for the almighty $$$$$. May you find the cure with God speed!

Posted by Cheryl Nygren | November 21, 2008 3:33 PM

November is lung cancer awareness month. My mother was diagnosed with NSCL cancer Nov 2007
She passed away July 20th. I pray that you find a cure or more treatment options. She already had mets to the spine when diagnosed. Thankyou for putting on this fundraiser for cancer research.

Posted by James Perry | November 21, 2008 12:53 PM

My 5 yr old son, Dustin, is being treated as we speak for Medulloblastom, a form of pediatric brain tumor. The cancer treatments for childhood cancers are mostly just down sized treatments for adults, and they shouldnt b. Their bodies are not the same as adults. More research needs to be done specifically for children. Alot more then the 2% average.
My son is at this moment fighting problems that have been caused from the treatment, not the cancer and most lickly will not be able to continue his cancer treatment. There are very few options out there, even though 465 kids a day are dx with a form of childhood cancer and 7 a day will die from it. Please get some of these funds to the researchers for childhood cancers. I belong to a group called People Against Childhood Cancer or PAC2 for short. we are over 2200 strong and growing dailey, trying to raise awareness and help raise funds to fight Childhood cancers.

You guys did a fantastic thing with raising these funds, please get some of them to children.
Jim
http://curechildhoodcancer.ning.com/
https://www.caringbridge.org/visit/dustinperry

Posted by Janis Burke | November 21, 2008 11:24 AM

I was diagnoised with Ovarian Cancer in January of 2008. I had surgery at that time and have been doing well. I thank God for my surgeon Dr. Charles Dunton and the entire staff at Lankanau Hospital in Wynnwood Pennsylvania for my recovery. I feel certain that we will find a cure for many cancers with people like yourself in this world. God bless you. Janis Burke

Posted by Debra Cornman | November 20, 2008 10:45 PM

I know that there is progress. I hope there will be more. I had a Aunt die this year from breast cancer, she stuggled for two years. Know My husbands wife is fighting against this evil cancer. I'm greatful for all that has been done.

with lots of love & deepest gratitude
Debra Cornman

Posted by S. Showers | November 20, 2008 5:45 PM

I appreciate those who feel desperate for funding of pediatric cancers in particular, but trust me, it's also important that we fund the cancers that are killing the mothers and fathers of small children. I lost my mother at 10 years old and it's not something you get over or that I would want another mother to live through. So let's fund all cancers and get to the basics instead of focusing on just one age group.

Posted by Amy Bucher | November 20, 2008 5:01 PM

I sincerely hope that there will be a "dream team" formed for each of the forms of Childhood Cancer, the NUMBER 1 disease killer of children (my 3 1/2 year old daughter among them.)

* Acute Lymphoblastic Leukemia (ALL)
* Acute Myelogenous Leukemia (AML)
* Brain tumors/Medulloblastoma
* Neuroblastoma
* Osteosarcoma
* Ewings Sarcoma
* Soft Tissue Sarcomas:
* Rhabdomyosarcoma
* PEDIATRIC Hodgkin disease or Hodgkin's lymphoma
* PEDIATRIC Non-Hodgkin Lymphoma
* Hepatoblastoma
* Hepatocellular carcinoma
* Wilms tumor, a.k.a. nephroblastoma
* Clear Cell Sarcoma
* Retinoblastoma
* Germ Cell Tumors

Save the children first. Give them hope - FIRST. Their lives represent our future. Their lost years represent our failure.

God bless your efforts,

Amy Bucher
New London Twp, PA
mom of ^^Arden^^ (forever 3, dx. stage IV, high risk Neuroblastoma 10_11_07, died 08_30_08)

www.caringbridge.org/visit/ardenquinn

www.curechildhoodcancer.ning.com

Posted by Michael Konieczki | November 20, 2008 3:29 PM

I posted under "son of a cancer death". I can't believe you posted such a negative posting. I am impressed. Please contact me I want to be involved in Stand up to Cancer. I want to be involved in a positive way.

mkczki@cox.net

Posted by Carole Young | November 20, 2008 3:13 PM

Please encourage the FDA to release the new test Ovasure that gives good results in testing for ovaian cancer. We who currently fighting this sneaky disease have only the CA=125 which is not paid for by the insurance companies. After we are diagnosed the test is paid for but other women need to have this test yearly. The test has many false positives but currently it is the only test we have. Too many of had to wait to be at stage 3 before we even began our treatment now it is hurry up and wait.

Thanks for listening and please get more research going, Carole

Posted by Catherine Andrews | November 20, 2008 2:21 PM

My husband and I are both cancer survivors and certainly would not be here if it wasn't for the wonderful treatments we received. However, I would like to see more research on causes, especially looking at the environment along with genetic factors. When we find the causes, then hopefully prevention can follow before cancer cells have an opportunity to grow.

Posted by myron kurtzman | November 20, 2008 1:05 PM

I would like to help by telling about my cancer. I am a man I had a rare form of cancer for men. Most men and women do not know that men can get breast cancer. I had breast cancer (mastectomh,chemo, radiation and presently on my 3rd year of tomoxifin).

To the best of my knowledge there is presently no reseach with respect to male breast cancer. Our treatment follows the treatmennt that female breat cancer patients receive. There are drugs that are replacing tomoxifin for postmenopausal women. Am I as a man post or premenopausal? Present research,as I understand, do not address the question as to whether male cancer survivorx can take the new drugs.

Posted by Brigid Reilly | November 20, 2008 11:20 AM

It is amazing what you have accomplished and I cannot wait to see and hear the results of all of this. My two cents about spending the money is to make sure that children are getting there fair share.

My niece was diagnosed with Osetosarcoma at 3 years old and is now thank God cancer free. However, being exposed to the world of childhood cancer is heart breaking. Even when children are able to beat cancer, the treatments can do horrible things to them and their development.

In on way you say thank God this child is only deaf, has a weak heart and will always need special help in school. In another, has to be a better way.

I think research into treatments that help children without harming them so much is of the utmost importance.

Posted by Brandi Kessler | November 20, 2008 10:38 AM

It should go toward Childhood Cancer
Gunner was a happy, healthy and athletic 7 year old when he was diagnosed. He left us on October 23, 2008.
Childhood cancer is considered "rare". 7 children are fighting right now, but will loose that battle by the end of the day. Another 7 tomorrow and 7 more the next day…tell those families “it is rare”.
It is the #1 killer disease of our children today, more than from asthma, diabetes, cystic fibrosis, congenital anomalies, and pediatric AIDS combined. Each year 35-40,000 are in treatment. Childhood cancer has a huge societal impact - 180,000 potential years of life are lost to it EVERY year! Does that sound RARE?
And yet, awareness and funding for childhood cancer is woefully inadequate. The National Cancer Institute's budget was $4.6 billion. Of that, breast cancer received 12%, prostate cancer received 7%, and all 12 major groups of pediatric cancers combined received less than 3%. And, while the American Cancer Society and others parade bald kids around, it's for sympathy only, the funding they give towards childhood cancer is the same, 3%.
Two major fundraisers for childhood cancer research are St. Baldrick's Foundation and Alex's Lemonade Stand. To save the lives of the children, they rely on parents to shave their heads or sell lemonade to raise money for childhood cancer research. It is a national tragedy. Yet it's our approach for dealing with the #1 killer disease of our children today!
And Yes research into adult cancers is transferred to our kids. The result… Right now the treatments are “down-sized” adult doses. 60% of survivors develop secondary cancers, infertility, major organ damage, developmental problems or other issues. Awareness and research has lead to treatments for several form of adult cancer. We are saving fathers and mothers…now lets save their children.
I fight back. I am a member of People Against Childhood Cancer (PAC2). Our mission is to raise awareness of childhood cancer. Join the fight at http://curechildhoodcancer.ning.com. It could be your kid. They need us to advocate for them.

Posted by Renee Wertjes | November 20, 2008 10:14 AM

November is Lung Cancer Awareness Month. We need to get the word out. It doesn't get the attention it deserves. Anyone can get lung cancer not just smokers. No one deserves to die of this terrible decease. Lets get the word out to the public.

Posted by Joanna Reschman | November 20, 2008 7:31 AM

I agree with Dr.Druker's wife. You cannot expect cancer patients to have patience, especially those who've been diagnosed with ovarian cancer at the age of 67 and are told their tumor is gynormous! This was my mom's situation who after experiencing a colostomy bag, 6 chemo sessions and still lingering nueropathy will concur. We are grateful and thankful that her recent biopsy results proved cancer free. I am hopeful that SU2Cancer will find a way for early ovarian detection and chemo drugs that one can more easily endure instead of wanting to surrender and has less painful side effects. When you experience it yourself or thru your loved one, you will then understand. This is a bond that all cancer patients understand without uttering one single word. A picture tells a thousand words.

Posted by Mary Ann | November 20, 2008 6:58 AM

I am thrilled to find out how much money was raised to help cure this dreadful disease once and for all! It is a long road - with many different types of cancer, but it looks like we are on our way. I just wish my mom could have lived long enough to be a part of the cure.

She lost her battle with kidney cancer 10yrs. ago.

Perhaps she, and all the other angels above, are looking down at us in joy that we are working TOGETHER to fight it. Isn't that what life's all about?
M.A.

Posted by Deborah Urry | November 20, 2008 6:58 AM

I am so very excited about SU2C and the amazing work that is being done. My family has been ravaged by cancers of many types over the generations and I am now a stage 3 melanoma FIGHTER. I have learned that there have been less developments in the treatment of melanoma that any other cancer in the last 20 - 30 years. PLEASE work to erradicate this horrible, sneaky, life-threatening disease.
THANKS to all of you who are working so hard to make cancer a thing of the past!

Posted by BETH NORWICK | November 20, 2008 5:46 AM

I HOPE MORE GOES TOWARDS CHILDHOOD CANCER.
WE NEED TO INVEST IN THE FUTURES OF OUR CHILDREN.

BETH NORWICK
MOM OF JARRETT WITH CHILDHOOD CANCER.

Posted by Adina Horowitz | November 20, 2008 4:17 AM

I would just for once like them to consider giving more than just 2% to childhood cancer research. Too many of our children are suffering from this "rare" disease. If it's so "rare" then why is it that 46 children every school day will be diagnosed w/this "rare" disease? PLEASE seriously consider donating more than 2% to childhood cancer. Our children are our future what kind of future can they have if they can't even get proper treatments for them.

Thank you for listening.

Posted by Joan Gaideski | November 20, 2008 3:08 AM

This article is a hard read. I am still unsure of what is being done. As a metastatic breast cancer survivor, I am very anxious and interested in any progress with this SU2C team. Please keep me posted. Thanks.

Posted by Beth | November 19, 2008 9:41 PM

I am encouraged, but also deeply saddened by this post. A person whom I've never met face to face, but love dearly,(having spent hours on the phone with), is leaving us all soon. Chemo and radiation did not work, it owns every part of her now, except her brain,the one that is attched to emotion, pain, and thought of a future. When we spoke just short months ago, we tried to make light of it...there is nothing light about it, and I knew it then. She is a sister-in -law that I never knew existed, a valued friend,and this thing will take her before I can know her. Linda, thankyou godspeed

Posted by myla kent | November 19, 2008 9:26 PM

Dear Laura,

My name is Myla and while I'm not crazy about tooting my own horn, I'm tooting it only so that you can see that I have a great desire to help.

I am a semi-pro photographer and webdesigner (I've been Meryl Streep's webmaster since 1997) here in Seattle (my work has been featured in National Geographic, Seattle Magazine, and at the giftshop of the Louvre).

Dr. Slamon was my Mom's doctor -- and without making this comment an entire book, my story is here: http://www.mylakent.com/8b/ (first draft of the website).

I started this project because I would like to help, but I really would feel better about having your support. I would like to donate my photography (and have a bunch of photographer friends who will do the same) to help raise $$ for SU2C.

Please do get in touch and let me know how I can help.

All my best,
Myla

Posted by Carole A. Cohen | November 19, 2008 9:20 PM

I am thrilled at the amount of money that was
collected for "Stand Up To Cancer". I hope and
pray the total amount will go to research and a
cure. I've heard some news about a vaccine, and
this would be wonderful. The information that
you emailed me was enlightening and sounds exciting.

Posted by Angella Allen | November 19, 2008 7:51 PM

Thank you for the constant progress reports & God Speed...

Posted by Charles Barton | November 19, 2008 6:36 PM

My wife has pancreatic cancer.Nobody seems to give her a chance to recover.Are there any updates on treatments or cures. Thank you

Posted by Son of a cancer death | November 19, 2008 6:11 PM

If you have the pharmaceutical companies involved with you will never find a cure. They don't want one. There is more money to be made with no cure.

The NCI doesn't want a cure either. I know of one cure that beat out to forms chemo and it couldn't get out of the first phase for further testing.

If you post this I will give you my info.I would like to talk to you.

Posted by Valerie Lopez | November 19, 2008 6:01 PM

I hope SU2C will include funds to support Pancreatic Cancer research which is greatly underfunded. My sister died August 20, 2008 from this dreadful disease. We were all hopeful, little did we know she did not have a chance. Treatment really has not changed in 30 years. Part of me and my family died that day also. We need to find a cure and give others the chance she did not get. Sincerely, Valerie Lopez Jupiter, Fl.

Posted by Margaret Goga | November 19, 2008 5:56 PM

I am so glad someone realized cancer patients can't wait. Every month, I see the ovarian cancer ladies in the support group lose a little more of themselves to this disease. They can't wait. Some of them are on their fourth or fifth different chemo, none of which has been new within the past 8 years since taxol. We need something new; we need hope; we need help. Won't you please help us?

Posted by Midge Rosenberger | November 19, 2008 5:47 PM

A lot of us are looking with renewed hope to this endeavor. Please stay true to your goals. The suffering from cancer is a scourge upon our society today. Good luck and God bless.

Posted by Heather Waymire | November 19, 2008 5:04 PM

When the Titanic was sinking- who was saved first? The children. When a house is burning, who are the firemen looking for? Children. How outraged would America be if 90 year old men were elbowing ten year olds out of the way for a life raft, leaving the child to a much greater chance of death? But why does that anger us? Seriously, how many children would be lost if they were all left to die on the Titanic, or every child in a burning was left to perish? In the grand scheme of things, that would be an extremely rare event.

If this scenerio leaves a bad taste, why is it that our children are left to perish in a burning house- cancer? They receive a miniscule amount of funding from most major funding sources- including The American Cancer Society and the Government. If you look at the amount of money spent per years of life lost, it is pathetic. Do we really care so little for our children?

The next time you see a house burning on the 6:00 news imagine this commentary: The firemen are doing everything they can to keep the fire from spreading to the neighbors. This tragedy is unfortunate, but there is no funding for the firemen to go in a rescue that child you see in the window. Hug your kids, and be thankful that it is not them in that window. The fireman is well trained in calming down the screaming parents, please think of them in your prayers.

Please join our fight. www.curechildhoodcancer.ning.com

Visit my child in the burning house-
www.caringbridge.org/visit/eliaswaymire

Heather

Posted by Carolyn Doherty | November 19, 2008 5:03 PM

It is very rewarding to finally see so much talent in one organization which has the potential to finally solve the mystery of cancer. As a cancer patient, I implore you to move quickly toward a cure for present and future patients. I know it can be done. Thank you.

Posted by Monica Biscardi | November 19, 2008 4:30 PM

El c�ncer me dio una fuerza especial que jam�s cre� que ten�a, hoy llevo 2 a�os desde que me lo diagnosticaron tuve 4 tumores, 2 en cada mama, me hicieron mastectom�a bilateral e histerectom�a, 5 cirug�as fue muy duro pero hoy rescato la fortaleza pero adem�s ayudo espiritualmente a quienes conozco que padecen la enfermedad trato de transmitirles mi fuerza y valor, el c�ncer no perdona no debemos tenerle compasi�n con el tratamiento aunque sea dif�cil llevarlo adelante, el tiempo vale oro debemos atacarlo r�pidamente pero sin olvidar que forma parte de nosotros porque no se contagia es una falla de nuestro sistema inmunol�gico

Posted by Sue Kuchman | November 19, 2008 4:30 PM

Hopefully, the research will go beyond finding "new drugs" to researching causes and eliminating them, ie, are there chemicals in our foods causing types of cancer. Will they actually recommend certain food additives are bad for us and force the FDA to remove them from our food (ie, is sugar cane as bad as aspertame). Will they stand up to the big companies and save us

Posted by Daniel McNabb | November 19, 2008 4:07 PM

After reading this I feel like there might be some hope after all. The old system just doesn't seem to get enough done, plus the problem of research funding on the decline. This seems like the way to go to get something done!
Thank you Laura for doing this. Even though my wife passed away 3 months ago from Sarcoma Cancer I pray for anyone who might be facing this now or in the future.

Daniel

Posted by fred fegel | November 19, 2008 3:49 PM

is there a cure for necrosis on the brainstem ??
my 6 year old son has been burned from radiation..
we both have necrosis. my son has it on his brainstem and i have it on my leg, after my sarcoma was removed.

Posted by Pamela Ricci | November 19, 2008 3:41 PM

Where do I begin? After recently seeing the statistics of funding distributed to breast and prostate cancer, I am sick to believe that I live in a country that dedicates so much money toward these types of cancer, yet a pittence to childhood cancer. These tiny victims are unable to fight for the funding, unable to hire lobbyists and so they are forced to raise small sums by selling things like lemonade, etc. Their parents are grief stricken and just trying to function on a daily basis. If those of you determining where these funds will be distributed have never been touched by childhood cancer, get down on your knees and thank god. Our family has been touched, actually trounced as we experienced the death of my 14 year old nephew. Imagine looking at a child you love suffering with cancer and saying "well I'm sorry, this is so rare we just can't put alot of money into solving this". So there you have it, if the whole country could only know, but it is too sad, so no one really wants to focus on this. Do the right thing!!!! Make the funding more equitable.

Posted by Patty Antolic | November 19, 2008 3:37 PM

It only takes a few people to start something so important that affects so many lives. Now that you all did the starting, we can all do what we can to help. I truly believe that this can be done and done now!!!!!

Thank you

Posted by Vince Hanscom | November 19, 2008 3:20 PM

I am excited that SU2C is moving forward with real goals and results oriented research to find a cure for Cancer, not a new treatment but a cure! I am convinced a cure or prevention is well within our grasp if we can but create a focus. The world is a global community and research results should be communicated instantly with other researchers. Thank you SU2C for your leadership!

Posted by Rebecca Wright | November 19, 2008 2:53 PM

I certainly think this is a noble and worthy cause. I would just ask that some special consideration be given to funding PEDIATRIC cancer research and treatment. Our kids are the "red-headed step-children" of the cancer world, and the majority of the funds for THEIR treatment have to be raised by already-too-stressed parents and families.

I challenge anyone to stand beside me and look into my four-year-old grandson's eyes and have an answer for him when he asks, "Can you just make this all go away?"

I told him that I was doing everything I could to do just that. But we need HELP.

Posted by Kathy Shade | November 19, 2008 2:51 PM

Thank you for the update! I am so excited about the idea of putting a dream team of scientists together to work collaboratively rather than competitively that I just wish I was in the field and able to take part! While I am sympathetic to those who are trying to build a professional identity and are reluctant to share ideas before they have a chance to do their own research, I also think that at some point we need to just get ego out of the way, get those ideas on the table and let everyone get to work. I feel very hopeful that once this ball starts rolling, results will come in faster than imagined and soon other fields of research will follow the lead of your organization. Best wishes and Godspeed!

Posted by Doris Smith | November 19, 2008 2:45 PM

As one of the donors, I would like to know specifically how much money was donated. To say more than 100 million was donated does not give me the information I would like to have. Please give us more informative information as to what research is being done and the progress.

Posted by Doris Sternberg | November 19, 2008 2:40 PM

Please-- Awareness for pediatric brain cancer--
So many of our babies and children are dying of this horrific disease called cancer. They have all lost their childhood and some their lives. They suffer through chemo, radiation, seizures. In a nano seconed lives have all changed forever. Very little research has been done, we need the spotlight on Pediatric Brain Tumors. I am a loving grandmother with a 3 yr old grandson with brain cancer. Thank You, Doris

Posted by Carol kaplan | November 19, 2008 2:25 PM

Do you do anything to help cancer victims?
When I was diagnosed with lymphoma in Jan 2007, the very next day my family abandoned me. I have an amazing cancer story to tell. From being left in a wheelchair after my physician husband broke my back to being diagnosed with cancer 3 years later. Then being abandoned by my only child and her husband and having my grandchildren ripped away from me, a heartbreak I can't begin to describe. I was naturally depressed when my husband left me but I lost 20 lbs. I went to the doctor who told me I has fine JUST depressed. My dog who got me walking again from my spinal injury began sniffing my tummy and pawing me and crying. after he did this for about 2 weeks I realized he was trying to tell me something was wrong. I got a PET scan and there was the cancer tumors he had been sniffing.

Of course cancer wiped me out financially and the IRS recently seized my bank accounts leaving me penniless. It goes on and on about what can happen to a woman left alone to fend for herself in our current system. If you could get my story on CNN or any other network if might bring in needed donations to help me save my life. I failed chemo and have been given 4-6 months to live unless they do something radical such as a bone marrow transplant. I cannot do this unless I can get help.
Please help me.

Posted by Joanne | November 19, 2008 2:22 PM

If all of the above can successfully become a reality, it will really be a dream come true for all of those who suffer from cancer, especially those for whom there is no treatment and they feel so alone out there. I do not believe that rare cancers, ie sarcomas, gain the attention needed. Much needs to be done to educate surgeons so that these cases are referred to cancer treatment centers with sarcoma programs so proper treatment is initiated in a timely fashion.
I know as I am one of these patients.

My prayers go with all of you in this endeavor.

Posted by Dave & Linda Green | November 19, 2008 2:17 PM

We are also excited about the progress being made in cancer research. Our son, 36 at the time, 38 now; was diagnosed with esophageal cancer; which has metastasized to his lungs via blood (lymph nodes were all clean as was the tumor contained in the esophagus); and then to a big toe (which was removed in 2008). There seems to be very little research being conducted strickly on 'esophageal cancer' and we would wish to hear more about the research presently going on.

Thanks for all you do.
Dave & Linda Green

Posted by Sweet Lily's Dad | November 19, 2008 2:04 PM

I applaud you all for the tremendous work being done here.It is my sincere hope that our children with cancer will benefit, especially since children's cancer gets less than 3% of ALL cancer research funding. As the father of a 4 year old girl with an inoperable brain tumor,( low-grade glioma ) which gets NO funding, my life's mission is now to save my daughter, and the thousands of children like her. Please consider the kids, they are our future after all.

www.caringbridge.org/visit/sweetlily

Sincerely,
Sweet Lily's Dad

Posted by arlene | November 19, 2008 1:57 PM

Are you connecting in any way with "the Army of Woman" research regarding Breast Cancer....???

Posted by Jeanne Rotert | November 19, 2008 1:52 PM

Thanks for your work in this. May you be blessed in your endeavors.

Posted by Kim | November 19, 2008 1:33 PM

I just wanted to say thank you so, so much for what you're doing for the fight against cancer - all cancer. My heart still breaks after the loss of a family member to cancer last year, but it helps to know that one day, hopefully not too long from now, no one will have to go through what so many of us are going through now. You all truly are changing the world, and I'm behind you 100%.

Posted by Cory | November 19, 2008 1:22 PM

Is there a priority list of the type of cancers that the team has been charged to work on?

Posted by Roberta | November 19, 2008 1:21 PM

I was so happy to see the special on TV and I didn't mind giving at all, especially since I am a Breast Cancer Survivor - 10yrs. I pray everyday that we can find a cure or prevention for this scary disease. And soon, so our daughters and granddaughters won't have to worry.

Posted by Merl Volk | November 19, 2008 1:15 PM

I lost my dad to pancreatic cancer this past Feb., so I am very interested in what advances are being made in some of the lethal cancers(pancreatic, lung and brain) such as cause, genetics, earlier detection and treatment. When I contribute funds, I want the money to go to these areas of research. These cancers kill people way too quickly and some are very difficult to diagnose early.

Posted by Daniel J. Goldstone | November 19, 2008 1:15 PM

In May 2005 I was diagonsed with advanced prostate cancer. There is no cure for advanced prostate cancer just treatments that reduce your quality of life. Nine months after radiation treatments my cancer returned. I was forced to think out of the box and discovered a holistic approach which reversed my cancer and I am getting healthier each day. Its a shame that the pharmacuticals control the research and won't look at herbs, vitamins and teas to treat this disease. The only way to get the word out was to write a book about it called Advanced Prostate Cancer and Me. My web site is www.alternativeprosatecancer.com I hope and pray that your organization is open to all treatments.
Daniel Goldstone

Posted by Rick Czap | November 19, 2008 1:06 PM

Laura, thanks for writing this and letting the world know what is happening with the SU2C fundraising campaign and the dream team of researchers. Real breakthroughs must happen now and I hope that as your part of this discussion you can continue to remind the scientific community that people are suffering and we need their urgent help to make matters better. Good luck, many are behind you.

Posted by Adam Calvert | November 19, 2008 12:58 PM

My grandmother is having a second round of chemo for uterine cancer. She was diag. and had surgery and chemo and was in remission a year. Its back and I hope that we can end this terrible disease. I love her so much and I will help out at benefits and do whatever it takes to help. If anyone wants me to help raise money for cancer I will do it . I am not a big star but my grandmother is . So if you need me I will do what I can to help. contact me at myspace.com/adamcalvert. thank you

Posted by Kauakea Winston | November 19, 2008 12:54 PM

Please do research Dr. RObert O Young's PH Miracle theory. His work " The PH Miracle for Cancer" has some profound information about diet and cancer. If Otto Warburg, who won the nobel peace prize, is correct, the cancer tumor is fermented glucose. The body tries to contain this within a tumor. See Dr. Young's websiote www.Phmiracleliving.com for more. The blood is holding the key.

Posted by Mary DellaVecchia | November 19, 2008 12:48 PM

I would like to know how this meeting and seminar was funded? Did any of the money raised in the SUTC broadcast pay for the following meetings? Also, as to Breast Cancer, what was the general informaiton regarding the reliability of the Braca 1 and Braca 2 gene testings? I only just read that these testings may not be accurate. I can not tell you the red tape I had to go through to get my testing paid for.

Posted by Sandra Weaver | November 19, 2008 12:45 PM

It is indeed exciting to think that there may be progress in the treatment of brain cancer which has seen, in the last 30 years, the median length of survival increased by only four months - to 14.6 months. Brain cancer is one of the most intractable of cancers, and if we can make progress with it, many other cancers will benefit. Johns Hopkins brain surgeon, Alfredo Quinones-Hinojosa is cited in AARP's recent bulletin as convinced that adult stem cells trigger brain cancer. Hopefully exploring this theory will unlock the mystery of brain and other cancers as well.

Posted by Ray Farris | November 19, 2008 12:44 PM

I have watched a number of people die from cancer over the years. Most recent my beloved Dad. It is my daily Prey that no one has to ever hear "you have cancer" and the unbelievable phrase "there is nothing we can do" again. God Bless and I will continue to offer my Preys and support to SU2C.

Posted by Vicky Freund | November 19, 2008 12:42 PM

I watched when the SU2C program aired and called to make a "pay it forward" donation in hopes that there will be a cure for cancer.

My husband and I are currently battling in-operable lung cancer. He was diagnosed July 2007 and I was diagnosed 8 months later in March 2008. Needless to say we were both devasted by the news. We are both in our early 50's, have one son and a 2 1/2 year old grandson. The odds of survival for lung cancer are slim, but we continue to be optimistic, do the treatments and try to live each day to it's fullest. Our son and grandson are the ones that keep us going. I pray everyday that researchers will find a cure for this horrible disease that affects so many people and their families.

Thank you for the updates.

Posted by Lori | November 19, 2008 12:42 PM

I am anxious to hear every update! They are right, these people need help now. Please continue your efforts, we are counting on you!

Posted by AJs Dad | November 19, 2008 12:41 PM

Thanks for the update Laura.


I know that there are literally hundreds of thousands of parents waiting to see how the distribution of the research funds works out. You see, they have been impacted by something that is considered "rare", childhood cancer. I am sure that the SU2C researchers recognize that the down-sized adult treatments currently used on our children have long term effects (e.g. - major organ damage, infertility, secondary cancers and developmental problems) in 60% of the kids treated.


I am sure that recognizing these problems, funding will be equitably distributed based on potential life-years lost, as well as incidence and cure rates. You see, the kids lose the most number of potential life-years, and we think THAT should be a consideration in distribution of funds. I am certain the Gold Ribbon Panel knows better than I. But if they would like some anecdotal evidence on how the treatments for children are working, they can contact me and I can tell them all about my son AJ, a victim of childhood cancer. Or, they can contact any of thousands of parents, family and kids impacted by childhood cancer at People Against Childhood Cancer (PAC2) at http://curechildhoodcancer.ning.com.


Truly, we hope that SU2C and society will stop considering childhood cancer as being RARE. Consider the futures lost. Consider instead how it impacts the youngest, most innocent in our society. They cannot vote. They can't lobby. They do not organize. And most parents are either too grief-stricken or involved in the day-to-day battle to become loud advocates.


But that is changing. We are fighting back. To raise awareness. To raise funds and influence funding decisions. Visit PAC2 and read some of the stories there. Read how we interpret the statistics. Read how we believe America should consider its children first and foremost in this battle. Read how childhood cancer, as you know, is NOT just another adult cancer that can be treated like we treat breast cancer and prostate cancer and colon cancer. These cancers are unique to children, and this country's lack of awareness of the #1 killer disease of its children and the lack of funding for childhood cancer research is literally a national tragedy.


Our kids are expected to sell lemonade and the parents shave their heads bald to raise funds? While it sounds like a comedy, again, I submit it is a tragedy.


Looking forward to future updates on the research grants, I am, forever,


AJs Dad

Posted by Sharon Hewitt | November 19, 2008 12:30 PM

A cancer free world is what I hope I will see in my lifetime. We need a cure now. I have 2 sons, who 2 years ago, were both diagnosed with cancer, within 8 days of each other. They were only 22 and 25.They are now cancer free. My husband was just diagosed with cancer 2 weeks ago. He has asaphagas cancer, stage 4. I watched SU2C and prayed, not only for my family, but also for all those that have been diagnosed with cancer. Thank you.

Posted by Lori Runyan | November 19, 2008 12:27 PM

After my Daughters 6 weeks of chemotherapy and 6 weeks of radiation she had her final treatment on November 6, the next day she got married !!! After all her and her new husband had been through this past year it seems like a new beggining, and with the research teams that SU2C has created there's hope that other women and their daughters won't have to go through the living hell we did, and the horror that it might come back someday. I cried watching the SU2C show and for a long time after, every e-mail update I receive makes me cry again, not for sadness, but joy, knowing that finally there's a group of people who just might find a cure, and with that a miracle!

Posted by Lisa Kurtz | November 19, 2008 12:16 PM

It is nice to be able to see where my donation has gone and that cancer will slowly be reigned in by these wonderfully talented, intelligent and energetic people. I hope that alternative medicine is among the proposals and working with the likes of Dr. Andrew Weil and his line of medical thinking. Combining new technology and drugs with elements of nature and alternative medicine can be the solution that makes the most sense. Looking at the food served in hospitals and using diet, herbs, Chinese medicine etc. is a must. This can also combat the environmental causes of cancer.

Posted by Caregiver | November 19, 2008 12:01 PM

Please, please, please do not spend too much time talking before the real work of finding a cure begins. Seven months ago my husband was given six months to a year to live after a diagnosis of Stage IV stomach cancer. Thankfully he is still with me, but we need a cure NOW. Not only for him, but for all of those suffering from this dreadful disease.

Posted by Pam | November 19, 2008 11:51 AM

God Bless each and every one of you for this selfless endeavor. I am proud to be able to contribute to and stay informed of the progress made in this unprecedented determination to end cancer forever.

Posted by Margie Ambrosanio | November 19, 2008 11:45 AM

How can I get involved? To help and serve someway, or to be a person for trials? I was diagnosed with adenoid cystic carcinoma of the trachea 11 years ago,treated with surgery and radiation. I thought I was in the clear for good only to get a second diagnosis 2 years ago in the lungs. Treated again with surgery and radiation. I am now on a very strict macrobiotic diet, and so far so good. I know that there will be a cure for this disease soon and i will do anything to participate!

Thank you,
Margie Ambrosanio

Posted by Justin Rubin | November 19, 2008 11:44 AM

Thank you, again, for all this tremendous work. When I made my film "No Next" I was trying to come up with one statistic, one number that, along with the story of my brother and sister both dying from the same brain tumor 20 years to the day, would shake people to the core. A number that would make them realize how much work remains to be done. If this doesn't do it, then I don't know what will. When Greg died in 1984, the 5 year survival rate for GBM ( the brain tumor that he and Carolyn both had) was 1.8%. Twenty years later, when Carolyn died in 2004, the 5 year survival rate was 1.8%. No movement in 20 years. Unacceptable. Stand Up To Cancer is dedicated to pushing the needle in ways that are significant and meaningful. God forbid this were to reoccur in my family, with one of my children, or one of my other sisters, or me, I want us to have a chance, a real chance of beating it. With the help of Stand Up To Cancer, and place like the Preston Robert Tisch Brain Tumor Center at Duke University and the many other wonderful research and treatment centers working together, I believe the dream of "No Next" can become a reality.
I thank everyone involved in this amazing operation.
Peace and strength.
Justin Rubin
www.nonext.org

Posted by Mark | November 19, 2008 11:44 AM

Thank you for the update!!As a stage IV Melanoma survivor( I have had 6 cycles of IL2 and it has WORKED!!!No active melanoma in my body)This is a process that was long over due. This does bring hope to every person & family being touched by Cancer. Continued success

Posted by Donna Bruneau-Lester | November 19, 2008 11:43 AM

I am excited about the SU2C team because of the way in which cancer will be treated not only as a physical ailment, but also the psychological side of a patient. I just lost a sister in March to Lung/Brain cancer and have lost another to Ovarian cancer. My brother lived after his diagnosis of lung cancer/treatment, but no one ever treated the psychological side of living through this disease. When he found out my sister was dying on March 4th, he seemed to give up on life and died of heart trouble on March 13th. We lost my sister on March 21st, and through all this my mother has just been diagnosed with Alzheimer's yesterday (Nov. 18th). I haven't even had time to catch my breath since the deaths and dealing with my mom, and my biggest fear is I too will become sick trying to be all to everyone. It was the hardest thing in the world to hold her hand and have her take her last breath, one I will never forget. I'm a small contributer to your cause because both deaths have left my financially burdened. I hope to some day be able to give more, if not $$$, then maybe support to someone else in need. it is the belief in person(s) like yourself that give others hope. Thank You and good luck in your efforts to eradicate this terrible disease, God Bless Each and Everyone of You!!!!

Posted by Margie Ambrosanio | November 19, 2008 11:40 AM

I am so grateful for the work you have done to eradicate cancer for good. I love the updates you send on the progress you are making. I know that this committee will be the answer for me and so many others!

With my deepest gratitude,
Margie Ambrosanio

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