The "New" Prostate Cancer InfoLink Social Network

A Service of Prostate Cancer International

Michael Burke, MD
  • Atlanta
  • United States
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Have you been diagnosed with prostate cancer?
no
What brings you to the New Prostate Cancer InfoLink social network?
I am a psychiatrist who has been working for 15 years with patients and families affected by prostate cancer.
Would you help us grow the network? Would you tell others about it?
Yes
About Me:
I am the Clinical Director of Psychiatric Oncology at the Winship Cancer Institute at Emory University. For 15 years I have provided care and education of the psychological and social issues that often accompany prostate cancer to patients and families. My research has also been focused on understanding quality of life issues in men with prostate cancer. I look forward to sharing with and learning from others on this network with the goal of helping to decrease the burden of this disease.
For general information regarding quality of life issues in cancer and emotional issues www.cancerquest.org is a good resource. Emotional issues and physical isses commonly experienced are covered in text and interviews.

http://www.cancerquest.org/index.cfm?page=3763&lang=english

http://www.cancerquest.org/index.cfm?page=3922&lang=english

http://whsc.emory.edu/soundscience/2009/burke.html

Comment Wall (11 comments)

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At 2:14pm on July 15, 2009, Arnon Krongrad, MD said…
Well, hey, stranger! How are you doing? How's Mo and the kids?
At 12:20am on October 17, 2008, Eric said…
Thanks
The thought of not being there for my wife and son is unbelievable. I have found myself online looking for information to the point of obsession. My whole life style has changed and every thing seems to have taken on a new perspective. I hope this is a normal and look forward to life becoming more stable again all though I'm not sure it ever will be .
At 10:27pm on October 16, 2008, E. Michael D. ("Mike") Scott said…
Thanks Dr. Burke. I appreciate your early response, and I am sure Eric will too.
At 11:01pm on August 14, 2008, Kathy Meade said…
I would appreciate it if you would join the discussion The "Minor Complication" That Dares Not Speak Its Name http://prostatecancerinfolink.ning.com/profiles/blog/show?id=2034917%3ABlogPost%3A22823

I would appreciate to hear your opinions.
At 10:11pm on July 12, 2008, Charles (Chuck) Maack said…
Hello,

Dr. Krongrad suggested I make contact with you as a medical professional who may on occasion provide information of interest to me and who may find interest in my research, study, and advocacy regarding prostate cancer. You can learn more about my prostate cancer and advocacy background by accessing
http://www.ustoowichita.org/leaders.cfm?content=bio&id=1. Subjects of interest that I have authored, compiled, or saved can be viewed at http://www.ustoowichita.org/observations.cfm. My personal email address is
maack1@cox.net

I would like to add you as a "friend" on "My Page."
At 6:16pm on June 25, 2008, Arnon Krongrad, MD said…
Mark Hotzman is asking if this site is biased by having only men who do badly (it is not; some have done well). He points out that his complaint may be rooted in a "dark moment." Please click here to see the progression. An opinion from you would be valued.
At 12:07pm on May 1, 2008, Arnon Krongrad, MD said…
That's great (about your getting active; not about the call). Have a look at what Steve Hess wrote about PSA anxiety, in the Surgery discussion on High Grade and Low Stage. There are also discussions on ADT-related depression in Hormone Suppression, and elsewhere.

The group is growing. We're gonna consider some pages in Hindi, with the help of Drs. Shukla and Khan. How do you say "anhedonia" in Hindi?
At 10:36pm on April 21, 2008, Darryl said…
Hi! Welcome...please take a moment to read and consider signing the Petition to Make Prostate Cancer a National Priority, at, http://www.prostatecancerpetition.org Thanks!
At 6:55pm on April 21, 2008, Burt said…
Hi. Im a peridonist who has long done clinical research. AK is a wonderful painless surgeon. I had mine 3.5 years ago. However one thing I learned is that we doctors (surgeons) never quite tell the whole negative side of anything. I knew sex would be a while, but I think most of us in our 60s think we will be back in the sac in 3 weeks. More like 3 years, and AK has addressed this in an article that it takes longer than they thought, even with magic Pills and Shots.
As a psychiatrist I will tell you from my own experience is that once you have the surg you become more sexually focused. Obviously 60 plus patients havent been playing honey mooners for a while but still do enjoy the ultimate extreme act of love. The drugs are frustrating because they create the anxiety of no knowing what days they will work and at what timiming point will they work. I have a feeling Levitra etc have a refractory effect, meaning that it seems like they work faster after a while and therefore the trick is to be ready or you pass the maximum effectiveness for the drug. I once told Arnon he probably didnt think he would have all these old (60's) men worrying about their sex lives when he went into this.
I find the key to not get depressed is to see the humorous side of all the ups and mostly downs, pardon the expression, following prostate surgery. Most of us do realize healthy life is primary anyway, and those of us in the professional field realize prostate cancer is not the life threatening horror of pancreatic cancer, so I kept reminding myself that I am much better off than a lot of other diseases would have left me.
Thanks for joinng the group.
Burt Becker, DDS
I once published an article on why periodontal patients drop out of dental care and used the HBP literature about why men stop taking BP drugs because of the ED effects. Anytime we give patients diffictult to follow patient regimes that have bad side effects compliance is a problem
At 9:44am on April 18, 2008, Kathy Meade said…
Dr. Burke,

I am very happy to see you in this group. Depression and prostate cancer I believe is greatly underaddressed. Heck depression in men is greatly under addressed. That said, it seems that I have been doing a great deal of discussion about the issue. I am part of a group of cancer advocates attempting to educate patients about the recent IOM report and encouraging them to use the resources that were part of the report.

There is a beginning discussion on depression and reaction to side effect on Wives and Partners. Could you read the material there and help us by contributing your thoughts please?

I would appreciate your personal opinions on the IOM report. Problems? Ways to disseminate, etc.

Thank you.
 
 

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