Leroy's War

Every question Leroy asked was important. When he sat with his doctors and discussed treatment, rarely did he accept their suggestions at face value. He had questions, and ultimately he'd say, "What else have you got?"

For some doctors, this didn't sit well. But as you'll see in today's blog from Hopkins radiologist Dr. Joe Herman, Leroy's questions will provide better answers for future patients.

Leroy was a very successful war correspondent. He would leave his family and friends for long periods of time and travel great distances to cover wars throughout the globe. Often he would risk his own life to bring the reality of war and hardship to those at home in the U.S. and abroad. While other reporters would stay on the fringes where it was "safe", Leroy would travel into the war zone where even armed soldiers would fear for their lives... He was determined to tell the real story about war.

In 2001, he was diagnosed with early stage rectal cancer. He underwent surgery to remove the tumor, and he went back to work. Then, in 2005, he developed blurry vision. CT scans showed that his cancer had come back and had now spread to his brain and lungs. He had surgery to remove the tumor in his brain, and was sent to me in January of 2006 for whole brain radiation therapy.

I distinctly remember meeting Leroy. He was a cancer patient, but he was still a journalist. Only this time, he was reporting from the trenches of his own war ... his war on cancer. Although I did not know it at the time, I now realize that we (the doctors, nurses, and other health care personnel) who cared for him may have been similar to the soldiers and civilians he would interview in the war zone.

I explained that he needed whole brain radiation. Why? he asked. While most patients would take my explanation at face value and accept the radiation, he persisted. What are the side effects? What happens if new lesions appear? Can I get more radiation in the future? What are my other options? His inquisitive journalistic nature persisted.

Only this time, it was Leroy's war, and he wanted to make sure he would be able to continue reporting as long as possible. He was concerned that whole brain radiation might decrease his memory and cognition. We discussed the potential risks and benefits of whole brain radiation, and after we addressed his questions, we decided to delay the treatment and start chemotherapy.

This experience and many more over the years have taught me the importance of educating patients and listening (very carefully) before making final treatment decisions.

Over the next few years, Leroy received chemotherapy and radiation therapy to many body sites from another physician in our department. I saw him in passing one day when he was waiting for his radiation, and said hello. Soon after, I was flipping through the channels and saw his Ted Koppel special on TV. Leroy was again reporting about his war. He was presenting the bitter truths about the war, his war, on cancer. His comments about his struggles were poignant and, to some, maybe controversial, but they were honest.

Dr. Meyer (his medical oncologist) asked me to see Leroy again for some palliative radiation to his spine. By this time, his disease had progressed. He was clearly losing the war. Like a strong soldier, he had suffered through many hardships, including chemotherapy, radiation, and radiofrequency ablation of lung nodules. He had had brain and spine surgery. He was often in pain and required medicine that caused confusion and constipation.

Despite this, in his trenches for the final time, he reported on his war. Thousands logged on to his blog daily to hear about his war on cancer, and were amazed by his perseverance and determination to survive despite his suffering. He fought cancer with the same pride as the soldiers he had reported on over the years. He was determined to win, despite the cost and suffering that it might cause him. He was an inspiration to others fighting the war on cancer, including me.

Leroy and his wife Laurie invited me over to their home for dinner about two months ago. I have to admit, I don't usually have dinner at my patients' homes. I am not sure why I don't, but for some reason, the doctor/patient relationship often doesn't leave the hospital.

I had grown quite close to Leroy and Laurie, like many of my patients, and was very intrigued by both of their life experiences. He was a war correspondent, and Laurie was a sports reporter in an era when women were not very welcome in the clubhouse. Both of them survived very hostile environments.

As I ate nachos (great salsa) and sipped wine, I listened to their stories and memories from over the years. I was so impressed by their relationship. How strong their bond remained, despite being away from each other for long periods of time. Laurie explained that sometimes the only way she knew he was still alive was if she saw him on television on the evening news. Leroy shared stories about risking his life in Iraq and the death and suffering he saw in Rwanda.

It was then that I realized we shared a common bond. We both met people daily where the space between life and death may be very short. Leroy met soldiers and civilians in war zones where they knew that life might be cut short by an attack. As an oncologist, I meet patients daily who have terminal cancer, and whose deaths may be imminent.

Knowing that the people in front of you may not have long to live changes you. It makes you appreciate every minute you have on this earth, and inspires you to make a difference. Although Leroy was losing the war on cancer, he was still determined to make a difference by sharing his story.

Leroy also shared with me how we (the doctors at Johns Hopkins) had succeeded, and how we had failed. While he was very happy overall with the care we provided, he specifically stressed, "It's very important to listen to the patient and explain what to expect with each treatment. For example, the radiation table is very hard and the room is very cold. It seems like a basic thing, but to us patients it is a big deal."

Lance Armstrong often says that you can beat cancer if you fight hard enough. Unfortunately, for some patients, no matter how hard they fight, the cancer is destined to win the war. This was the case for Leroy.

Although he has left us, he has left a legacy. His final report on war -- his war -- is one that has touched all of us. I know I am a better doctor for knowing him, and will continue fighting this war for him.

-- Laurie

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god bless you laurie. leroy is in a better place and we all miss him. we can honor his courage by supporting you and those we know who are fighting the beast. i visited my sister in law yesterday in the icu. she is suffering from terminal cervical cancer complicated by colon and kidney issues. sitting with my brother, a vietnam vet who served as a marine scout, i relived some of my experience with cancer two years ago and saw for maybe the first time the horrifying affects it can have on one's family. they have been through so much yet their bond is strong. i pray for her; that she will know peace and an end to this boundless, useless suffering.

Sent by jessie | 8:55 AM ET | 08-27-2008

To say Leroy was "losing" his battle while his cancer progressed and that he "lost" his battle by dying seems in conflict with all we know about how he handled his illness. The battle metaphor may be inspiring to many people when faced with cancer, but I believe it is a misguided metaphor when used after someone like Leroy dies.

I've explained this further in an article for clinicians:
http://www.oncology-times.com/pt/pt-core/template-journal/oncotimes/media/WendyHarpham-MisguidedMetaphor-OT-July252007.pdf

With hope, Wendy

Sent by Wendy S. Harpham, MD | 9:25 AM ET | 08-27-2008

Thank you Ms. Brynes and Dr. Herman for continuing the wise and open-hearted sharing these past two days. Yes! to breaks from talking about cancer -- especially in chemo rooms! - and yes! to full narrative explorations of a patient's life and goals before suggesting therapy. Knowing what THEY prize, what THEY still dream of doing in the time they have left, what constitutes quality of life to THEM, how THEY view the cost of potential side effects, and what THEIR ethos and life story means, will help you offer the options in the context of their experience. There are few greater gifts to a person whose time may be foreshortened that the kind of true listening. Thank you each for being in the field you are in, and for prizing the sacred ground of every day spent with people in such an intense part of their lives. Especially, thank you for recognizing the particularity of their individual journeys, and for managing to be so fully present with each person. May your tribe be rewarded. May your tribe increase. May we all be met with such care, and with the desire you show to welcome challenge and new learning from the patients on the front lines.

Sent by Sarah | 9:25 AM ET | 08-27-2008

another great reflection on Leroy's character. The legacy he created became larger than the individual components of it, and reached out to include us. Thanks again, Laurie, for sharing w. us. from Sherri in Texas

Sent by Sherri Eggleston | 9:28 AM ET | 08-27-2008

Thanks to the doctors who write here and to those who are willing to let their patients know that they really do see us as individuals; individuals they may not share nachos and wine with, but about whom they do care.

Peggy

Sent by Peggy | 9:31 AM ET | 08-27-2008

Wow. This by far was the best post from one of his doctors and nurses thus far. It really spoke of Leroy and the battle he fought.

Sent by Tara | 9:33 AM ET | 08-27-2008

Thank you Laurie and Dr. Herman for sharing this important insight about Leroy, who set so many great examples for people struggling with a cancer diagnosis. Being a strong advocate for himself and his care was just one of those examples. For those who don't possess the naturally inquisitive skills of a seasoned journalist such as Leroy, the Cancer Survival Toolbox - a free audio set of CDs that is also available for free through itunes - has helped thousands of people develop these communication skills, specifically for the purpose of advocating for themselves while they navigate their cancer experience. The Toolbox has been provided free of charge for the last 10 years by the National Coalition for Cancer Survivorship, and anyone can access it at http://www.canceradvocacy.org/toolbox/.

(You don't have to post this next comment, but we are also the organization that created the "cancer sucks" buttons and wristbands that Laurie mentioned yesterday.)

We hope you find a way to make this information available to your readers, even if it's not through a direct post of these comments. So many people have benefitted from this free tool, and this blog is one way to let others know it's available.

Thank you

Sent by Susan Silver | 9:35 AM ET | 08-27-2008

Dr. Joe Herman and Laurie, These thoughts from you and others are so appreciated. I am a question-asker too and my oncologist is a pretty good listener! I am a believer that knowledge conquers fear as well. Thanks again!

Sent by Susie R. from Ohio | 9:35 AM ET | 08-27-2008

Jessie...love to you and your family..keep fighting the good fight.
Doc, thanks for the Leroy moments, we all miss him so much.
I admire Laurie for her incredible fortitude. She is remarkable.Stay strong sista girl.You are loved.

Liz Z ( about to be hit again by another Hurricane here on the Mississippi Gulf Coast!!)

Sent by liz Zimmerman | 9:35 AM ET | 08-27-2008

It's both wonderful and important to hear this kind of sensitive report from an oncologist. Doctors usually seem very clear about maintaining boundaries. This entry should be part of every med student's reading.

Sent by GD | 9:42 AM ET | 08-27-2008

Today is chemo day for my husband and like every other Wednesday we go through the same ritual. He, like Leroy, is a strong soldier fighting for his life. It is so very sad to know that this is one battle he cannot win. After two and a half years I still cannot accept the inevitable. Thank you Laurie for continuing this blog for us caretakers. It's so hard to think of having to let go of someone you love. But, I see now that life does go on........there is no choice.........you do survive......I'm just not ready to let go yet..........

Sent by sasha | 9:43 AM ET | 08-27-2008

Thank you Dr. Herman. Our son didn't have the privilege of having a compassionate radiologist. Theodore had many questions and the doctor was usually too busy to answer them or even listen to the questions. It was pretty frustrating. Theodore was 25 years old. His cancer was invading his spinal cord and he was in a wheelchair when he came to the hospital for the results of the tests they had done. The first thing that needed to be done was radiology to reduce the tumor by his spine. He didn't have any time to think about or absorb what was going to happen to him. It was a very scary time for him and we didn't have any better answers. The techs were all very nice to him but Dr. Eden was quite stand offish. Theodore, like Leroy, didn't want to just accept what they wanted to do to him. But I believe since he was young his questions were poo pooed. Makes me ticked just thinking about it.

Leroy was right. Taking the time to listen to the patient and explain the procedures and what comes with it is very helpful to the patient. Cancer is a very scary disease and the patient so looks to the medical staff to trust and to be treated like a human being. Thank you Dr. for recognizing that.

Laurie, wishing you a day of peace.

I was wondering if the special,Living with Cancer,will ever be aired again or if the DVD is available? I never got to see it and would like the opportunity. Thank you.

God bless you Laurie and fellow bloggers.

Take care,

Judy

Sent by Judy Voller | 9:52 AM ET | 08-27-2008

Thank you (again) Laurie, for collecting these essays from Leroy's doctors and nurses. It is so interesting to see cancer from the doctor's point of view; I have often wondered what it is like to spend your days with people who are looking at death in the face. Thanks to Dr. Herman, Dr. Meyer, and Pierse Byrnes for giving us a view of cancer from their side.

Sent by Gretchen Hoag | 10:04 AM ET | 08-27-2008

We really should organize Leroy's Army.

I can think of no better way to honor Leroy then to start an organization to help people live with cancer.
I see something that collects all of the available information from all of the other cancer charities/organizations and places it all within easy reach of those who need it.
This blog has become a beacon, drawing patients and care givers together. This would the natural continuation of that idea.

Well that is what I think.

NPR can you help us with this? I will volunteer, but this is a bigger job the one person could handle.

Sent by Brian "Brit" Goss from Long Island, NY | 10:19 AM ET | 08-27-2008

Thank you Dr. Herman for sharing your experience with Leroy and Laurie. They truly are an amazing couple for sharing their life with us. Also thank you for stating that one cannot "try hard enough" and beat cancer. A positive attitude is essential but not cancer curing. It's irritating when people say we control the cure or the cause.

Sent by Lisa | 10:19 AM ET | 08-27-2008

My dad served with valour as a medic in the 77th infantry division in the South Pacific theatre during WWII. As a medic he was regularly the last to leave the front lines and eventually put most of his buddies in body bags. Of course this experience profoundly shaped his life and ultimate dedication to medicine. Patient care: caring -- compassionately for patients -- became his 37 year legacy at Cornell University Medical Center in New York City. Because of this love and compassion for people and teaching (which came from all the death he saw in the war)the medical college named a lecture after him: "The Graham G. Hawks Annual Lecture Series" ( I am a "Junior"). My dad would have loved Leroy and served him faithfully to the end. My dad encouraged all patients to be like Leroy and he lectured medical students about the importance of being "Servant Leaders to their patients", being by their side whenever they had a question or were afraid and lead them down the path their illness took them. My dad often bemoaned the sad state of poor patient care by physicians now a days. He would, as I am, been deeply touched and reassured by your essay Dr. Herman. Thank you so much for its length because it is complete and beautiful.

My last words with my Father before he died of cancer 11 years ago began with him saying: "Well "G" I guess we are not going to "win this war". I said, "No dad we will not win this war but you have won the battle. I love you". We need to get it right - Leroy may have not won the "war" but he won the "battle". With Love - Graham from Sag Harbor.

Sent by Graham G. Hawks | 10:21 AM ET | 08-27-2008

My hat is off to Dr. Herman for writing so powerfully today about the role a patient can take in his or her own treatment. The standard of treatment is constantly changing. What wasn't a standard last year may be a standard today. In an ideal world, the most successful treatments would be adopted by all medical professionals immediately. But we don't live in an ideal world and the time to adoption is not instantaneous. As a patient, take the time to research your condition and then come prepared when you meet with your doctor to ask the tough questions, push the envelope, and understand your options. Good doctors will listen to you, provide honest feedback on your queries, and most important, respect your wishes. In Cancer World there are not always clear cut results and directions. It's no different than many other decisions one has to make; moving forward with imperfect or the lack of full information. Much of what happens in Cancer World is outside of one's control, but that leaves a portion which is within one's control. As a patient, it's your life and you have the obligation to yourself to take the initiative and exercise that which you can control.

Dr. Herman -- Thank you so much for today's wisdom, perspective and the time you spent to write about it here.

Regards,

Ed Steger
www.hncancer.blogspot.com

Sent by Ed Steger | 10:25 AM ET | 08-27-2008

Thank you Dr. Herman for your blog today. Yes, Leroy has taught us all many life lessons. I'm glad to know that he touched your life, not medically but emotionally, so that you can be a better physician to each patient.

Sorry to say that one thing often missing from doctors is the human side of treating cancer patients. I know of situations where an apparently very caring and compassionate doctor often tells cancer patients to "go home and get your affairs in order" when he has no trial to enroll them in. He has lots of drugs at his disposal to try and the patient is willing to endure the hardship but is not given the chance. Please tell me: if the patient is willing to try, to fight, to endure, why is it that the doctors are often not willing to do the same?

One of the many enigma's in the cancer world is that we both have the same cancer...we both try the same drug or treatment regime...it works for you but not for me!!! So that being the case and if the patient is willing to fight, who knows, perhaps the drug or treatment will work when everything else has failed. (I know that there is a limit to this supposition). Enough of my rant....

I am fortunate to have oncologist who will get "into the trenches" with me and remain there until I decide its enough. Thank you Dr. Herman. You sound like the type of doctor I would like to have on my team.

Blessings and prayers to Laurie.

Sent by Al Cato | 10:30 AM ET | 08-27-2008

For Judy, I think sometimes that doctors in their haste to do something to preserve a patient's functions forget that the patient doesn't understand the need. In a spinal cancer, there is a very limited amount of time before the initial paralysis becomes permanent. It's often just a matter of hours and they must move quickly. It's one of the few instances in radiation therapy where there is only one option and that is to begin treatment immediately. After the initial therapy sessions, then there should be more time to explain and discuss other options.

Sent by Chris | 10:37 AM ET | 08-27-2008

Thank you for taking the time to share such an informative and beautiful tribute. Leroy was undoubtedly a very special person. Janie

Sent by Janie | 10:38 AM ET | 08-27-2008

This forum and Leroy continue to touch me in ways I can almost not describe. Despite this being the information age, I think as patients we often still feel as if our doctors are gods and we can not question their treatment decisions, no matter the side effects or toxicity. But this post reminded me that we control our lives and our destiny. It's very reassuring to hear a doctor voice the same types of thoughts.

Sent by Lauren | 10:42 AM ET | 08-27-2008

Laurie, we all are still here lifting...

Thank you so much for inviteing Dr. Herman, Dr. Meyer, and Pierce Byrner to address this blog community. Today Dr. Herman's post showed the personal connection. Such a very important one. I am so glad that Leroy had these fine people to share and help him through what had to be a very frightening time. This blog community also has helped many others to not be so alone in their fight with cancer.

I say Thank You to the many fine Dr's. and Nurses and Medical Staff that help everyone dealing with this horrible disease. It can not be easy but so many of you deal with it and your patients so well.

Laurie, I will keep you in my prayers. We all will continue to keep lifting. And I hope there also is some comfort from the postings of these fine Health Care Providers, and this blog family. Try to have a better day today than yesterday, (that one day at a time trek).

Sent by dorothy in oregon | 10:47 AM ET | 08-27-2008

Leroy was blessed to have a doctor like you. As I begin my journey of goodbyes I always have to remember the docs that took just that little extra minute to make sure i was okay.

laurie, i miss leroy.. i think of you so often.

with love

Sent by Laurie in NJ | 10:50 AM ET | 08-27-2008

Thank you for sharing your experiences with Leroy, Dr. Herman. We're hearing from the best on this blog. I only hope those who would benefit the most, i.e., members of the medical field who struggle making connections with their patients, are reading and learning. And Laurie, thank you for giving Leroy's medical team the opportunity to speak to us about him. He truly was exceptional, wasn't he?

Sent by Sharon | 10:51 AM ET | 08-27-2008

Wendy Harpham -Amen to your comments. The battle metaphor is so widely used - just read the obituaries and you will see "lost his battle with" or "after a valiant battle with." It does not even have to be cancer, it can be any disease. I personally reject the battle image, but I think "whatever floats your boat" applies too, and some people need that image to keep going.

And Dr. Herman - I agree it is so important for doctors to be compassionate and good listeners. However, doctors are only humans too, and some of them are simply robotic in their interaction with patients. I had one like that, but I won her over by constantly joking with her, giving her compliments, making her laugh. Finally she broke down her reserve and we could communicate. I learned she was really very kind. It should not have to be that way, but I sometimes think if we knew what people have gone through and where they are coming from we could better understand why some of them are seemingly cold and distant. Including doctors.

Sent by Wendy | 10:55 AM ET | 08-27-2008

Dr. Herman, Laurie and all,
What a wonderful insight today. You just brought to life what so many of us as "lifegivers" live through as well. Yesterday, Dee, VT was asking what she should do in regards to her treatment choices.
Dee, after reading this I hope this helps you to find the answers you need. As Neil's "lifegiver", I would like to add that every moment we shared together creating memories for him, for myself, and for his daughter were moments that brought us all a little more joy and laughter.
I remember celebrating his daughter's birthday month. She was not with him for her birthdays often and he was so happy to have had that moment with her. It was such a fun day. I also remember celebrating his half birthday when she was with us. What a fun time we had and I hope she still enjoys remembering.
None of the treatment choices for cancer are easy. But as his partner and lifegiver, I have no regrets helping Neil with his battle. I will always cherish our time together. As far as Neil and the choices he made, I know he felt he made the right choice too. A friend of his once told him that a cure could be found while he was fighting. Those words helped him to make that decision. He wanted to keep fighting as long as he could. He wanted to believe that he too, could win the battle. Even though he is no longer with me, I want to believe, now, he did.
I miss him so much and some days I can hardly breath but I know I will be forever blessed by his memory!
Thank you for being here for me. I truly do not know how I could have survived these last nine months without ya'll! Leroy's words will always be etched in my heart.
1-2-3 Lifting all of you in prayer!

Sent by Laurie Hirth | 10:56 AM ET | 08-27-2008

Although I read Leroy's blog every day, seldom do I save it or feel the need to respond. Today was different. I read the blog just after returning with my husband to his room in the hospital, where he is now for the second time in three weeks. We had just been wheeled back from radiology where he had undergone a bone scan, his second in the past six weeks. After the scan, I was standing by the stretcher holding his hand, waiting for an assistant to help us transport back to his room, and he looked over at me and asked me if he was going to make it. To be honest, I have my doubts, but no way I was going to tell him that. So I told him what I knew to be the truth: his doctor said he would go home from this hospital stay. And then his drugs took over and he went back to sleep, holding onto the hope that I had given him.

That is what Leroy and Laurie have given us all in this blog. And as Dr. Herman states in this particular segment, it doesn't matter that Leroy is no longer here to fight. The point is that he tried, he asked hard questions, he wanted straight answers, and even when things looked bleak, he still wanted to fight. Two nights ago I asked my husband if he was ready to give up the fight. He has been in tremendous pain, he can no longer do many things that made his life worthwhile, and I thought, perhaps I should let him know that whatever he is ready to do, I will support. He looked at me for a moment, then shook his head no. "I still want to fight," he said.

I hope he always feels that way. Its not purely selfish motive on my part, although I love him so much and would be so sad without him in my life, anyway I can get him. I don't want him to suffer. But....there is something about the courage he has, in those five words, about the strength of his spirit in a body that is threatening to betray him, that I hope he never loses.

He still wants to fight. And as long as he still wants to fight, I will stand here and hold his hand.

Sent by Tina Thomas Batchelor, Zebulon, NC | 10:59 AM ET | 08-27-2008

Wow. I read this blog every day and I am always in awe with the message. Today is no exception. It is very well written and I too am a better person because of Leroy and this blog.

Thanks to Leroy, Laurie, the doctors, and everyone else associated with this site. Please know that you have had a positive impact on many, many people.

From the bottom of my heart, THANKS. It helps to understand the brutal truth.

Pam

Sent by Pam | 11:09 AM ET | 08-27-2008

Dear Dr. Herman and Laurie,
Thank you for sharing some of what went on in the trenches with Leroy. I know a lot of people don't like saying you are fighting a war, but I have yet to see anything that describes the situation better. I have had cancer five times since 1961. I have had good doctors and not so good doctors. I am thankful for what they have done for me. I am so glad that Leory had you on his team.
Charlotte in Rural Ridge, PA

Sent by Charlotte Kewish | 11:11 AM ET | 08-27-2008

That Leroy was telling the doctors and all professionals who helped him that it was "very important that they listen to the patients" and really stressing that is very moving because I remember reading his comments maybe a year or so ago about the issues we all have with these helping people, and I recall reading so many people's comments as they then wrote in, about not feeling listened to by their doctors. To know that Leroy took these concerns directly to the professionals is very powerful and very very moving. What a man.

Sent by Nancy | 11:14 AM ET | 08-27-2008

Thank you so much, Laurie and everyone at NPR, for sharing this reflection moments. They are incredibly moving, and educating, and to say that they touch honesty and keep that door open to everyone involved with cancer as a patient, caregiver or health professional is not saying enough of how valuable they are.

Strong thought for you, as always, Laurie.

Sent by Pat Steer | 11:15 AM ET | 08-27-2008

Good Morning Laurie and Dr. Herman! Dr. Herman, your writing was a wonderful read, taking me closer into the lives of our very special friends, Leroy and Laurie, and gave some insight into the cancer world--though I already have more knowledge about it than I would have ever wanted. Still, almost 4 weeks after my Dad's death, the subject is still almost mystic in a way. Thank you for taking the time to write to us, an interested and captive audience. Laurie, love to you today...Linda

Sent by Linda Lee | 11:22 AM ET | 08-27-2008

Thank you for sharing these statements from the world of cancer care givers.

When I go to the oncologist, there is a slight air of detachment -- and I know this has to be for their own sake -- that I forget they are people too as much as I THINK they forget I am a person. Most often, I don't think they even remember me, and nary give a thought if there isn't a lab report about me in front of them.

But, it seems, these people do comtemplate from time to time the bigger picture, and humanity of it all, even with their intense, stressful, academic and scientific lives. In particular, Dr. Herman's statement that "We both met people daily where the space between life and death may be very short." -- yes, that is true, the recognition and honoring of that space touched me greatly. Sometimes, that is what is uppermost in a patients mind, before they tackle the practical aspects of managing their cancer.

Thank you for bringing all of this input to us.

I hope you are doing as well as you can, Laurie.

Sent by Pika | 11:42 AM ET | 08-27-2008

Tina Thomas Batchelor (10:59 AM ET): what a beautiful post. I'm glad you took the time to write it. Wishing you and your husband a good fight right now and then some time on leave from this battle.

Sent by keri | 11:47 AM ET | 08-27-2008

The posts from the last three days remind me why people fall in love with their doctors and nurses.

Sent by N. Holmes | 11:51 AM ET | 08-27-2008

Something unexpected happened recently. After much prodding from a friend, I went on a blind date over the weekend. I finally figured out that life was still going on without me, moving on doesn't mean forgetting, and nobody's handing out medals for martyrdom, so I accepted the date.

We hit it off immediately and have a second date next week. I couldn't have gotten to this place in healing without all of you over the last couple of years...thank you.

Laurie, I'm keeping you in my thoughts.

Sent by Bruce | 11:55 AM ET | 08-27-2008

Laurie, I am a Marine, have served abroad, and have seen some ugly things. Death lives with you, but its not the same; sure there might be a bullet out there with your name on it, but with certain types of Cancer, there are already toe tags made.

I have been fighting hard and will continue to do so, but you know, in the back of your mind,cancer has the upper hand. that is just the way of it.

Laurie, This interaction is great, I hope very much, you all continue.

Thoughts to all, Stan

Sent by Stan Wozniak | 11:55 AM ET | 08-27-2008

Dear Tina,
Your courage, like your husband's, is beautiful and inspirational. I will keep you both in my thoughts and prayers.

Dr.Herman,

It isn't surprising that you developed a close personal relationship with Leroy, of course -- who could resist him? It sounds like many of his medical care providers learned from him and were profoundly changed by him, just as we all were. I wish those lessons could somehow be shared with other doctors. My oncologist is an excellent and caring physician, but she isn't too thrilled when I do my own research and ask too many questions or -- God forbid! -- disagree with her. And she has said she feels it is necessary to maintain an emotional distance from her patients in order to give them the best possible treatment.I can understand that point of view, of course. But even though I'm not a journalist, I can't just passively sit back and do as I'm told when dealing with something as scary as cancer!I strongly believe we must advocate for ourselves. Still, no one wants to be considered a "difficult" patient. Maybe I should bake some cookies for her -- or whip up some killer salsa?

Sent by Doris | 12:04 PM ET | 08-27-2008

Dear Dr. Herman and Laurie,

What a absolutely wonderful post. You brought us Leroy as some of us did not have an opportunity to know. I suppose you can see why we coined the phrase "Leroy's army." And an army we remain in spite of our fallen leader.

His legacy is grand and continuing on. Any and every question related to the diagnosis of cancer is hard, equally and at times the answers are even harder.

Thank you....

Sent by Sue Chap | 12:32 PM ET | 08-27-2008

Hi
Thanks for the post today. It was great to hear from the other side so to speak. I know most of the techs and doctors dealing with cancer and the treatments are kind and caring people, but I have come across a couple that were not and I left them in no doubt as to how I felt.

When my sister was first diagnosed with NHL she decided to fight for all she was worth. She was in hospice care where she had been put because after surgery they thought she might not make it. They had done a biopsy and we were all waiting for the results.

I was there the day the doc told her she had cancer and that she was moving from hospice care to our local hospital. You would have thought she had won the lottery she was so happy to finally know what she had and to be able to fight it.

Her fight started the very next morning when she was scheduled to go for her first scan. The tech was late coming to get her. She ripped him a new one when he arrived. She told him he was messing with her life and she would not put up with it. He was never late again. She took charge. When she died I went back to that first hospital to deliver some money for a sleeper sofa for the family room. The head nurse whom we had met on her admittance 10 months before (he made us tea and toast at 11pm at nite) told me that because of Kath the doctors on the cancer ward had changed the way they treated patients. She taught them that she was a person and had lots of questions and wanted straight answers and would take nothing less. She got them.
Miss you Kath every day.
Keep up the fight everyone and do not take any sh**t, peace to all.

Sent by fay, az | 12:35 PM ET | 08-27-2008

Dear Dr. Joe Herman,

Thank you. Wonderful insights.

You are a hero; dishing out hope with medication and dedication. Best wishes for your continued success in helping so many.

Sent by Susan A. Baker | 12:51 PM ET | 08-27-2008

Tina,
That was beautiful...I remember Neil's daughter said he was going to die and I got very upset with her. She was having a very difficult time with it all. I told her we are all going to die and that he was fighting with all he had. Eventually, it may take him but he wanted to fight and I was going to be right there beside him. I am so glad I was.
Bruce,
I am proud of you. Someday, when I am ready, I hope to start anew as well! I wish you much happiness.

Sent by Laurie Hirth | 1:07 PM ET | 08-27-2008

Dear Dr. Herman,
Your powerful post emphasizes so many important ideas and gives strength to Leroy's legacy.

While Leroy taught many people how to ask questions and helped them find the courage to do it, you reiterated that asking questions is a good thing for everyone.

While Leroy showed the world that Healthy Survivorship is not all upbeat and pretty, you validated that caring healthcare professionals can do a better job when patients are honest.

While Leroy inspired thousands of patients and their loved ones, you reminded everyone that physicians, nurses and other healthcare professionals are inspired by their patients.

Lastly, you reminded everyone that we can only AFFECT the outcome, not control the outcome. (And this is why I shy away from the battle metaphor in the setting of progressive disease.)

Thank you for sharing this personal reflection with us.

With hope, Wendy

Sent by Wendy S. Harpham, MD | 1:13 PM ET | 08-27-2008

Being a prostate cancer survivor, I have followed Leroy's blog for almost two years. His courage and gift to us of his blog has been immeasurable.
I was touched by and agree with the words of dissent by Wendy Harphan. The war on cancer and the battle metaphor is misguided.
I have used an alternative metaphor of cancer being part of me, trying to teach me a lesson.
I think it is better to live with cancer than so aggressively trying to kill it with so much violence to the patient. How many of us have been harmed or killed in the chemo-radiation war?
A healthy life style, meditiation, diet, exercise, low stress, journaling, positive thinking and living one day at a time has worked better for me. I have taken medications and underwent salvage radiation -- that I didn't think I would survive -- but I think my change in attitude and life style has done as much (More?) than traditional medical-military violence.
I grieve Leroy's death -- it was not a defeat. It was a transition, and what a great legacy he has left us.
John Krejci, Lincoln, NE

Sent by John Krejci | 1:18 PM ET | 08-27-2008

Dr. Herman, Thank you for sharing the Leroy you knew with us as well as how treating cancer patients affects you. I often wonder about that with doctors but they have such a tight schedule it seems there isn't even enough time to ask all the questions I have at times.

It was timely for me to read the story about Leroy asking a lot of questions about the whole brain radiation too. My doctor here has just reommended a treatment that *may* help with one of the long term side effects of radaition which I am suffering from and I did not ask him eniough questions about it. It's good to be reminded that doctors do respect patients who really ask a lot fo questions.

Laurie, you are in my thoughts and I hope you are taking care of yourself and hinoring your grief.

Sent by N.R. | 1:23 PM ET | 08-27-2008

Oh how I love hearing these stories....please keep up....my prayers are with you Laurie...

Sent by sue | 1:23 PM ET | 08-27-2008

Wow! What a beautiful post. We need more doctors like you.

Inna

Sent by Inna | 1:30 PM ET | 08-27-2008

Laurie, words can't express what this place means to me and how your words touch my heart, Dr. Herman.. I hope if I ever have the big "C" I can find someone as caring and compassionate as you..

But Leroy didn't lose.. He WON!! His cancer is GONE!! He is still with us.. He said he would be back on Monday and he was.. He just can't write anymore.. I feel his spirit as tears run down my face.. He can make me "FEEL" more than anyone I have ever "met".. BIG guy, gentle giant..

And bless you, Laurie.. Thank you SO MUCH for continuing this place to come and find comfort.. I hope YOU are taking care of yourself..

1 2 3 LIFT!!
FROG

Sent by Patsy Elmore from Knoxville, TN | 1:31 PM ET | 08-27-2008

What an amazing gathering of hearts and souls and minds here today -- Leroy is surely present. Thank you, Laurie; thank you, Dr. Herman; thank you, Leroy ... The vision of the three of you sharing nachos and wine and conversation is one that I can so easily see. What fine examples you set for us all.

To all who have posted so far today, I am learning, learning, learning, and am so grateful. What an eloquent, compassionate, insightful, courageous, loving group of human beings -- I am honored to continue to absorb these lessons each and every day.

For Laurie, in remembering Leroy:

"At bottom every man knows well enough that he is a unique being, only once on this earth; and by no extraordinary chance will such a marvelously picturesque piece of diversity in unity as he is, ever be put together a second time." ~Nietzsche

With love ~

Sent by Kim Forester | 1:35 PM ET | 08-27-2008

This post by Dr. Herman and all of the responses have been amazing today. I especially like brian's post for us to do something more. Let's all really think about this. Laurie, I think if you often and am just so grateful you were surrounded by one amazing medical team. Best wishes for some peace today.

Sent by JaeMoyer | 1:53 PM ET | 08-27-2008

Laurie-It is wonderful to see how Leroy's profession has continued to help physicians like the radiologist listen better to patients. What a gift you gave us this morning.

Sent by Martha C. | 2:09 PM ET | 08-27-2008

PS to Dr. Wendy Halpern (9:25 am)-- I've just added your wonderful website to my list of "favorites" and will share it with others, as well. Thank you.

Sent by Kim Forester | 2:25 PM ET | 08-27-2008

I wonder...WILL the heat be turned up to a comfortable level in those radiation rooms? WILL the tables be cushioned so patients do not have to endure further (and unnecessary) suffering? Changing the protocol for that, right there, in radiation rooms across the country would be a wonderful legacy (one of many) that originated from Leroy. It seems to me it should have been changed many years ago. My mother (who died in 2004) was plagued by the exact same things. She said nothing...just endured them. The things that CAN be changed to help cancer sufferer's SHOULD be. It's a no-brainer...so why hasn't it happened already?

Sent by Karen Laven | 2:29 PM ET | 08-27-2008

It means so much just to have your physician show some compassion. When I went through Interleukin 2, the oncologist tending me in the hospital picked up my hand one day upon making rounds, patted it and my family was warmed. He had to know that I was so sick. He showed "compassion and understanding" that only took a second of his time. It is great to hear from the physicians that take care of us during our life and death battles! Leroy and Laurie have done such a service to us. It is wonderful to be in touch with people who truly understand our fears. Our physicians are such a part of our life when we find ourselves in a cancer fight. Every time I read this blog I can't help but cry. I will never forget the wisdom learned and the comfort gained from Leroy and this dear cancer family.

Love to all,
Betty Lewis

Sent by Betty K. Lewis | 2:42 PM ET | 08-27-2008

Tina - your comments have me in tears - not tears of sadness, but in appreciation of what you and your husband are going through. My husband also fought the beast with every ounce of courage that he had. I, too, supported him, although I shed many tears in private. I needed to be strong for him and I hope I was. But he was incredible--he was angry, sad, but never did he say, "I give up". It is a harrowing journey that you both are on, and my heart goes out to you. Thank you for sharing your thoughts with us, and my prayers are with you. Marsha

Sent by marsha bacenko | 2:50 PM ET | 08-27-2008

Laurie, thank you for the sharing the doctor's perspectives recently as I always wondered what really went on behind the scenes, how the medical staff feels. Sending hugs your way.

Sent by annie | 3:00 PM ET | 08-27-2008

To Chris at 10:37am.
I may not have explained myself very well in our dealings with our son's radiologist. My reference to the doctor not being open to our son's questions and concerns were not from the initial treatment the day he came to the hospital. There was only one thing that could be done at that point and that was radiation immediately. We are greatful for that.

It was during his radiology treatments after the tumor by his spine was shrunk that he encountered the situation with his radiologist.

I am not bashing the medical profession. But Dr. Herman's story brought to mind what we went through with our radiologist.

I apologize if I offended you.

Judy

Sent by Judy Voller | 3:23 PM ET | 08-27-2008

I learned of Leroy's passing a few days ago while talking with my mother. Since then, I've found myself thinking about Leroy, his experiences, wisdom, and kindness.
I'm not even sure how I came to Leroy's blog, but I know it was in the Spring of 2007, shortly after my diagnosis of rectal cancer at 29 years old. Although I never contributed my thoughts or posted a comment, Leroy's words instantly became part of my daily routine and I found a great sense of comfort here, at a time when my world was anything but predictable. As I continued through 24 weeks of treatment and three surgeries, Leroy's words were always there for me and often helped me to articulate what I was feeling to my family and friends, and even to myself. I remember printing out "The Toughest Kids on the Block" and reading it to my friends and saying, "See this? This is how I feel!" While I'm sure they already somewhat knew that, Leroy's precise and beautiful way with words made me feel less alone at a time when I didn't know anyone my age who was going through a similar experience. When I'm having a tough day I still go back and read it, and I always smile.
After finishing treatment in November and receiving a NED report, I have begun to make the transition back to a world without (as many) doctor's appointments. While I admit that I no longer read Leroy's blog on a daily basis, I think that's ok, and is a part of the transition I am now making. But most importantly, he was there for me when I needed him most, and I know his words, his wisdom, his humility, will always be a part of my cancer journey. And for that, I feel compelled to say thank you, from the bottom of my heart, to Leroy, his family and friends.
He will be missed.

Sent by Sara Mair | 3:34 PM ET | 08-27-2008

I was struck by a comment made by GIs during the European campaign that they refused to get to know the raw recruits sent in, since their life expectancy was so low.

I think it's natural for medical personnel and others to avoid cancer patients because getting to know them means pain when they die.

We need better treatment so more of us survive.

BTW it's difficult to read breathless media reports of cancer 'progress' knowing that most of these 'breakthroughs' will not work and will be forgotten in a few months. It's also difficult to realize the progress that is real is coming too slow to save your life.

I belong to some CLL lists, and, while it's nice to read posts that say, 'I'm in remission and I feel great', it is bittersweet when you yourself cannot get into remission no matter how hard you try.

I agree that the toughest fighter in the world may have no chance against cancer. That's how I feel.

Sent by Scott S. | 3:43 PM ET | 08-27-2008

Doctors who take the time, whenever they are able, to really get to know their patients, are the best doctors. To be a cancer patient is so hard, but when our physicians put as at ease, allow us to ask questions and crack a few jokes, our anxiety levels go way down...and that makes all the difference in the world. Thanks, and hugs to you Laurie.

Sent by NancyGM | 3:51 PM ET | 08-27-2008

The comments by Wendy S. Harpham concerning the flawed metaphor of a cancer patient 'losing the battle with his cancer' is right on the money, post #2.

I couldn't agree with her more.

I do often consider this a battle and I feel as though I have lost a battle here or there when my counts go up, in spite of my exercising, my herbs, et cetera.

Sent by Scott S. | 3:56 PM ET | 08-27-2008

What a lesson to learn! Question everything! Even the doctors learn from patients challenging questions.

Sasha - hang in there!

Laurie - we're still lifting. Do you feel it?

Liz Z - Hope the storm fizzles out.

Sent by Liz L. | 4:05 PM ET | 08-27-2008

Laurie,

Thank you for showing us the great team you had. Pat and I were very fortunate to have wonderful people surrounding us too. His radiologist was a little stand-offish but still part of a good team.

I'm glad to notice so many drs. writing in--Leroy's message is SO important for them. Another minute to bring a sense of humanity into the equation of treatment makes all the difference in the world.

Dr. Herman, thank you for your blog today.

Graham from Sag Harbor, Glad to see you back. I've missed you. Your father left an incredible legacy.

Prayers and lifting...

Sent by Kathy Barney from Michigan | 4:38 PM ET | 08-27-2008

Bruce, I am so happy for you. When grief takes us over, it's easy to be irritated at the life that is still going on around you...how dare they! Until one day you take a step or two toward that cycle of life and connections as a newbie. Wish you the best.
Sasha, I am holding you in my heart, I look for your post each day. Never stop being so authentic and real.
Love to all from Sherri in Texas

Sent by Sherri Eggleston | 4:42 PM ET | 08-27-2008

Thank you again Laurie and thank you to the medical staff who have contributed to Leroy's blog.

I would like to add my voice to those who have asked NPR to help keep the blog going. Please. I need this community. There are so many of us who do. My cancer is incurable and so far the creature hasn't shown its teeth, but it will. Leroy and the community are helping me to take stock of my life and, I hope, to become a better, braver, more loving person.

Like Judy Voller, I would also like to see the Living with Cancer Special. I live in Spain, so I wouldn't be able to see it if it were aired again. Perhaps it might become avilable on DVD as some point.

With love from
Catherine (Spain)

Sent by Catherine Doyle | 4:51 PM ET | 08-27-2008

Laurie,
Today's comments were great. And like another fellow blogger said, we should start a Leroy's Army to help all of the people in cancer world......that is a wonderful idea.

Sent by Teresa in WV | 4:53 PM ET | 08-27-2008

Thank you Laurie for sharing this.

Sent by Chandana | 4:53 PM ET | 08-27-2008

Thanks to this blog and the podcasts, I can hear Leroy's voice asking these questions. He should get a Pulitzer for this war correspondence.

Sent by Dianne (DC) | 5:13 PM ET | 08-27-2008

Thank you for the continuing blogs. My thoughts are with you Laurie every day.

Sent by E.L. | 5:15 PM ET | 08-27-2008

A wonderful memorial to Leroy. Thank you, Dr. Herman and Laurie.

Sent by Paulette | 5:19 PM ET | 08-27-2008

Dr. Herman, I really appreciated and enjoyed your post. Thank you!

Sent by Nichole in FL | 5:49 PM ET | 08-27-2008

Leroy must be somewhere with a big cheesy grin on his face after these three blogs. Laurie thanks for sharing them. Thanks to the Hopkins staff for writing them. Thanks to the blog community for commenting. I still miss Leroy terribly. I am one of the many people who started each and every morning with him. Monday mornings were something to look forward to because I got my Leroy and my inspiration from him and from all of you back! Today it feels a little like that is here again.

Sent by JLMoyer | 6:18 PM ET | 08-27-2008

OMG! Graham, you came back!!!! Missed you! Don't stay away, we are still here!

Sent by Sue Chap | 6:42 PM ET | 08-27-2008

Dear Laurie,
Thanks for continuing these posts. You continue to be in my thoughts.

When I had cancer, the battle metaphor never worked for me. Rather than fighting, in retrospect I spent alot of time initially mourning the loss of my perceived health and strength. One day I was healthy and the next day I had a life threatening disease. But after the shock and deep sadness, I just tried to get through it---the surgeries and chemo, the pain and the unknown. I found great comfort in going to a local Buddhist center and beginning a practice of meditation. What was I to battle? I saw my job as learning to accept my situation and doing everything I could to be healthy and heal. Finding my way down a path that I had not anticipated was my challenge and my desire.

As for oncologists I was and am very, very fortunate. At the beginning of seeing my oncologist at one point I asked how she could bear the work she had to do...telling people they had cancer and discussing treatment. She said, that if that was all her job was, it would indeed be very hard. But, she said, she also gets to see patients who recover and is able to develop long term relationships with them. "You and I will grow old together", she said. At the time it moved me to tears, of course at the time many things moved me to tears. I knew then as I know now that no one can predict the future, but her words that were compassionate and caring stay with me after 7 years.

Sent by judith | 6:55 PM ET | 08-27-2008

Laurie, I have been crying since I heard of Leroy's death, I felt he was my friend. I pray for you to have strength and courage every day. Thank you for continuing this blog for all of us who do not want to lose contact with you. My husband is also fighting this beast for the second time. I have gotten so much srength from Leroy and you. I am also Lifting!!!! Jan

Sent by jan kmet | 8:07 PM ET | 08-27-2008

Sherri and Laurie H, thank you. I've realized there is always going to be an enormous Terry-shaped hole in my heart nobody else can ever fill, and I have to live with that.

But the key words in the previous sentence are "I have to live."

I really didn't expect to even LIKE my date, let alone think of words like "gorgeous," "adorable," "compatible" or anything else. It's really tossed me off-balance...but I like the feeling.

I still have good and bad days, but I find it easier now to face the day knowing somebody out there thinks of me, knows what I've been through, and is interested in me anyway.

May this feeling come to all of us who have loved and lost in its own time. Even if this new thing doesn't last for me, I'm enjoying it in the here and now, and that's all we really have, I think. It's an unexpected blessing.

Sent by Bruce | 8:11 PM ET | 08-27-2008

Dear Dee from Vermont,
My husband was diagnosed with Stage IV lung cancer and chose chemotherapy. I read this week in the Science section of the New York Times that if you do choose chemo and after three rounds, it doesn't seem to be helping, your oncologist should discuss comfort care with you. Unfortunately, there is no simple answer to your question about your choices. The best part of having chemo is that you're living with hope. The worst part is the side effects. Do whatever you feel is best. There is no right or wrong answer.

Sent by Elaine | 8:19 PM ET | 08-27-2008

Today was scan day, now we wait for the results. I am so glad Leroy had such great people caring for him. I wish we all had the Wizards of Hopkins caring for us. Waiting for the results is the worst fear, we could use a wizard to help us wait.

Sent by Kathy | 8:26 PM ET | 08-27-2008

Doctors are of course good people and have only the best intentions for their patients.. however many of them can learn many lessons from th etruly compassionate and caring ones....

33 years ago at the ripe old age of 20.... my doctor must have decided he needed to get my attention as he sat me down after my initial surgery and ultimate diagnosis and commenced to tell me he "knew of ONE patient with my pathology that LIVED"!!

Needless to say... he got my undivided attention............

He then went on to tell me I had a less than 10% chance of surviving 5 years and that my primary tumor was "the worst he had seen"

The funny thing is... within a couple hours of hearing all that... I never again even considered I would not survive..................

Sent by Ron Bye (NH) | 9:15 PM ET | 08-27-2008

Laurie:

I just wanted to say thank you for your stroke of genius in allowing the MY CANCER blog continue in this way, right now. For those of us who are in the trenches every day, as Leroy was, sometimes it is difficult to see past your own pain to that of your loved ones and caregivers, and especially to the doctors and nurses. Everyone suffers from this disease - spouses, children, parents, siblings and friends. But it is truly a gift to be able to hear from those who are the "suppliers" (if you will) in this fight. They provide us with the tools to fight this battle, whether they be in the form of drugs, radiation, information, or just a friendly face in the treatment room. They are important, but they are easy to miss in the nitty-gritty of it all.

Many of us have relationships with our oncologists that end at the office door. You are truly fortunate to have developed such ties with the people who were so important in Leroy's fight. Thank you for not forgetting them, just as they, and we, will not forget Leroy.

Sent by Nancy Nelson | 9:36 PM ET | 08-27-2008

What a wonderful commentary from the Doctor. What a wonderful patient Leroy was to fight for all cancer patients. Things do go beyond treatment,beyond the consequences of choices made medically. Leroy showed the doctors, basic things that often gets taken for granted. Hard tables, cold rooms, ill-fitting hospital robes and on the list goes. It seems Doctors only think of treatment....which is very important.
However what Leroy accomplished is a lesson for all in the medical profession. Other things matter, and sometimes no matter how hard you fight, one battle is lost, but the others continue the war.
Prayers,
Wanda Amorose

Sent by Wanda Amorose | 10:08 PM ET | 08-27-2008

I have so much respect and admiration for the professionals that assisted Leroy through his "war". Their perspective has been extremely valuable. Why can't we meet as human beings in this painful process. I do understand that to full engage, for the professionals, it's "burn-out city". But a human, and humanitarian face would be nice...from time to time. I applaud those that have contributed - you're very good writers, as well as physicians - did Leroy teach you that? Laurie, how are you doing?

Sent by Jessica | 10:13 PM ET | 08-27-2008

I'm sure that Leroy is proud of Laurie and Leroy's army. He has not lost any battle, and look at how many hearts he has touched.

Thank you Laurie for staying close to us.

Sent by Tina from Alton, IL | 10:14 PM ET | 08-27-2008

Thank you Dr. Herman that fighting cancer hard enough doesn't necessarily make life longer

Sent by Victoria Hendricks | 11:35 PM ET | 08-27-2008

Laurie: Thanks for keeping the blog going.

Hearing from the doctors and nurses is great. I know they are all human, but like other professions, some are people persons and some are not.

It is always unfortunate when you don't have a doc you can relate too, especially in life and death situation such as Cancer.

As much as I would like to dislike the Battle analogy, after some of the things that happened to Burge, war and battle are the only words I hear and not just against the Cancer. For every great professional in the medical field, we met one that was too busy, or too distracted, or just plain unprofessional. Many were overworked and little things fell through the cracks which was unacceptable when it comes to working with sick people...being left in a cold hallway for half and hour after xrays with a full bladder, or ostomy bag is the first that comes to mind...or the day they all went home for the evening and left him in a wheelchair in a waiting room. I don't know what people without advocates and caregivers survive the "cure".

Bruce: So happy for you. Just don't rush. You have lots of time. I worry about my oldest son as I feel he is still very vulnerable and sort of on the rebound from his father's death. Lonely is a terrible place, but so is jumping too soon. Keep shopping! You can always come back for a second or third look. :>)

Laure Hirth: I know where you are. The second years seems as hard if not harder in some ways. I'm lucky because I have "too much to do" keeping the farm running, my commissioner duties complete and my sons going, but every day, I feel the loss of Burge in different ways and the happier things are around me, the more I miss him.

Love to all, especially those who are hurting tonight.

Nikki

Sent by Nikki in Kansas | 12:23 AM ET | 08-28-2008

Thank you Dr. Herman & Laurie for your wonderful post.
Laurie take care of yourself. Here is a lift for you with all my strength 1 and 2 and 3.........
Peace be with you
Marelly

Sent by Marelly Young | 12:34 AM ET | 08-28-2008

Dr. Herman, thank you for sharing your story. Laurie, thank you for continuing to share your thoughts. Your voice adds to Leroy's to bring the story of this battle - of patients and their loved ones - into an open place. Your thoughts now speak to me in my own journey as a family member who lost a loved one. Thank you. My thoughts are with you each day.

Sent by Eleanor | 1:07 AM ET | 08-28-2008

Everyone who works with cancer patients must be warriors themselves. I can't imagine what it must be like to see your patients suffer and, sometimes, die.

Thank you Dr. Herman for your insights and thank you, Laurie, for continuing to give all of us your help and support even in this time of grief. I know Leroy would be proud.

Sent by Gyla Fowler | 9:41 AM ET | 08-28-2008

Laurie, Thank you for posting "What else have you got?" I will take this question with me wherever I go, and I hope that other readers will, too.

Each weekday for the last weeks I've opened the link to "My Cancer" with some trepidation that there might not be a post. Laurie, thank you for the gift to us of continuing to share these deeply touching memories.

Sent by Sheara | 9:44 AM ET | 08-28-2008

To: Judy,

Please know that no offense was taken. I just know that sometimes quick action supplants compassion in the medical profession. Know that you and your family are in my prayers.

Sent by Chris | 11:17 AM ET | 08-28-2008

Dear Laurie,
When the time is right, I hope that you will consider putting all of Leroy's daily blogs into book form. I am a cancer resource counselor and I would love to be able to recommend the book to cancer patients. It would be so helpful for them, as it has been for those of us who have followed the blog on a daily basis and it would be a wonderful memorial to Leroy that would last into the future. If you do decide to do this, please let us know.
Thank you. I wish you peace.
Victoria B. Murray, Los Angeles

Sent by Victoria B. Murray | 4:08 PM ET | 08-28-2008

Echoing earlier comments, it was the cancer that lost the battle and went with Leroy's body, but he's won the ultimate war and the spirit & legacy lives on and on! How wonderfully ironic is that?

Sent by Jen in NOLA (hopefully forever!) | 5:39 PM ET | 08-28-2008

Thank you Laurie for your courage and continuing the blog.

Eileen

Sent by Eileen P | 12:19 AM ET | 08-29-2008



   
   
   
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