Hello.. I mentioned your site on another forum. I am sure some more people will follow. People are curious to see the results of your most recent prostatitis patient recovery or hopefully symptom relief as the months go by.
i have had prostatitis for 3 years now. and have been all over the united states looking for a cure. im much better since i have been getting injections from doctor duke bahn. but im always looking for a cure . this condition is terrible both physical and mental.
its a journey i want to end and never go on again . im open for suggestions. thanks for being here for us poor guys.
Thank you for the invitation, Dr, Krongrad.I will follow your suggestion as soon as a learn the tricks in maneuvering within this site.
Hope we can learn from each other here.
Over the past 18 years, I have been all around the world trying to find a cure for my chronic prostatitis. I have just returned from having treatment at 2 specialist clinics in China, where they use intraprostatic injections of a special de-clogging formula, along with broad spectrum antibiotics: neither treatment worked. In fact, my condition is now worse. I now have severe testicle pain after the injections, along with severe lower back pain. I am presently considering having the prostate removed, but my urologists here in the UK strongly advises against it.
I have contacted you before with questions about the LRP for prostatitis etc. I am currently undergoing a treatment which has so far given me a great deal of relief, but remain interested in the LRP if I relapse after finishing the treatment.
You may be aware anyway but I contacted your UK equivalent Chris Eden and he says he has done 3 LRP's on CPPS sufferers all with good results. He did not go into detail about each case but I could only presume he meant they were all pain free with their continence/sexual functions intact.
I just wondered if you have regular contact with Chris Eden and compare notes etc, and if you knew anything of his Prostatitis patients?
What's the cost of laparoscopic radical prostatectomy including the hospital and anasthelogist or just a approx total on everthing? And how do you get your insurance to pay for it if you have prostatitis?
The out-of-pocket cost to the patient varies by insurance policy. Having said that, for patients paying without insurance, the "retail" cost varies depending upon which facility we use. I can offer two facilities in Miami and one and perhaps soon two abroad that will be less costly.
To investigate something like this we need to go through two steps:
1) review of the medical situation
2) review of the insurance policy
This is best handled in direct coordination with our medical concierge, Hope, and our finance coordinator, Ruth, who can be reached at (305)936-0474 and/or hope@laprp.com and ruth@laprp.com
Thank you for your response..I guess there's no ballPark price on this surgery because there are so many variables involved.. What do you think about this procedure or do you already do this..
http://www.prostate-report.org/__prostate_surgery_need_not_mean_loss_of_potency.php Can this be done with laparoscopic radical prostatectomy???
What percentages do you see of sexual function coming back when the cancer is not in the nerve bundles after laparoscopic radical prostatectomy???
After laparoscopic radical prostatectomy do you see your patients the same for the most part as they were before getting the surgery except no more fluid on ejaculation. Like when you have your appendix out your back to normal.
When I watched the Arthur 'Bud' Burnett, MD, video it kind of freaked me out. Just sounds like not much of a chance of being whole again (Sexually) because so many things can go wrong like no more erections, no more libido, penis deformity and color deformity.
Sorry for all the questions. I just think it’s nice to hear from a Doctor that has done so many of these operations so maybe we can see what the chances of being sexually active again and what penis deformity's if any after laparoscopic radical prostatectomy when your in shape don’t smoke or drink no other health problems??? You know like 30% 50% 80% or better yet 99% ..
Hi Soso. I have not used Cavermap but don't really see the point. We can see the nerves just fine and there is no evidence that it adds anything.
The likelihood of return of function coming back varies with age, baseline function, illness (diabetes), smoking history, obesity, mood ... it's a complicated formula. Here is the story of one young man who regained his erections. I would expect that for a 39-y old, but not a 79-y old.
Thats great to hear you can see those nerves I wasn't sure about that.. when I looked at it being done on the net everything looks the same to me..LOL . Thank you for your time and showing me the testimony. That's great!!
I understand what you're saying, Dr Krongrad: which is, what worked for Pete the Plumber, may not work for me. I appreciate your candour.
Also, I get the impression that you think I should lower my expectations in respect to LRP--especially post surgery. I would just like to say that after reading Dr Eden's reply to my latest question regarding his sixth chronic prostatitis patient, my expectations can't get much lower.
Anyway, I have decided to do an internet blog on your forum regarding my upcoming LRP surgery; starting from entering hospital to leaving it--followed by periodical bulletins regarding my progress (or lack of) while recuperating.
I feel if I am going to be a sacrificial lamb, I want the whole world to know about it. If you have any objections to the blog, please say so.
I would welcome any questions. The idea of the blog is to educate the patient considering such a radical medical procedure, and to give first-hand knowledge of exactly what he will have to go through--the highs and the lows.
I feel I must warn you, though, Dr Krongrad, that I put up a daily blog on another prostatitis forum about my failed treatment in China, which attracted 32,000 hits. That was last year. Since then, the prostatitis forum has been forced to close down, because the doctor who treated me was discovered to be a fraud.
I'm sure nothing so dramatic will happen twice over.
dr krongrad.. will any side effects from the surgery be collected and displayed after each surgery.. I think men will want to see that data along with the cure in order to make a informed decision. thanks
I was just wandering if the 31 year old cancer patient you operated on was lucky enough to have bi-lateral nerve sparing or not, and if so have you heard how is he doing with regards to erectile function & continence?
Fantastic news Dr Krongrad. Just what we all want to hear. Especially as I am 37 LOL...!!! I am becoming more and more tempted to do this just as soon as my partner & I try IVF and god willing succeed.
It might be interesting to note in the trial how many sufferers have had this problem start due to past hemorrhoid treatments (Injections, banding, hemorrhoidectomy etc.) . I know mine and many other's prostatitis was caused by similar rectal treatments.
Regards
Nik
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The Prostatitis social network is intended for informational and educational purposes only. It is not engaged in rendering medical advice or professional services.
Any person who appears to knowingly solicit and/or render medical advice or promote a professional or commercial service on this site may be removed by the administrators without notice.
Information provided on this site should not be used for diagnosing or treating acute or chronic prostatitis or any other health problem or disease.
The Prostatitis social network is not a substitute for professional care. If you have or suspect you may have a health problem, please consult your health care provider.
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Comment Wall (111 comments)
mike
its a journey i want to end and never go on again . im open for suggestions. thanks for being here for us poor guys.
Hope we can learn from each other here.
What are the downfalls of taking the prostate out??
And what are the pro's of taking the prostate out if it's alway's inflamed?
After everything you've seen if you had prostatitis would you take your prostate out??
Thank you
soso
I have contacted you before with questions about the LRP for prostatitis etc. I am currently undergoing a treatment which has so far given me a great deal of relief, but remain interested in the LRP if I relapse after finishing the treatment.
You may be aware anyway but I contacted your UK equivalent Chris Eden and he says he has done 3 LRP's on CPPS sufferers all with good results. He did not go into detail about each case but I could only presume he meant they were all pain free with their continence/sexual functions intact.
I just wondered if you have regular contact with Chris Eden and compare notes etc, and if you knew anything of his Prostatitis patients?
Best Regards
Nik
Great news that Chris Eden is happy to collaborate with the study.
Best Regards
Nik
What's the cost of laparoscopic radical prostatectomy including the hospital and anasthelogist or just a approx total on everthing? And how do you get your insurance to pay for it if you have prostatitis?
Thanks for all your help.
The out-of-pocket cost to the patient varies by insurance policy. Having said that, for patients paying without insurance, the "retail" cost varies depending upon which facility we use. I can offer two facilities in Miami and one and perhaps soon two abroad that will be less costly.
To investigate something like this we need to go through two steps:
1) review of the medical situation
2) review of the insurance policy
This is best handled in direct coordination with our medical concierge, Hope, and our finance coordinator, Ruth, who can be reached at (305)936-0474 and/or hope@laprp.com and ruth@laprp.com
I hope this answers your question.
AK
Thank you for your response..I guess there's no ballPark price on this surgery because there are so many variables involved.. What do you think about this procedure or do you already do this..
http://www.prostate-report.org/__prostate_surgery_need_not_mean_loss_of_potency.php Can this be done with laparoscopic radical prostatectomy???
What percentages do you see of sexual function coming back when the cancer is not in the nerve bundles after laparoscopic radical prostatectomy???
After laparoscopic radical prostatectomy do you see your patients the same for the most part as they were before getting the surgery except no more fluid on ejaculation. Like when you have your appendix out your back to normal.
When I watched the Arthur 'Bud' Burnett, MD, video it kind of freaked me out. Just sounds like not much of a chance of being whole again (Sexually) because so many things can go wrong like no more erections, no more libido, penis deformity and color deformity.
http://www.laprp.com/article.php?aid=351&type=7&r=6&page=4
Sorry for all the questions. I just think it’s nice to hear from a Doctor that has done so many of these operations so maybe we can see what the chances of being sexually active again and what penis deformity's if any after laparoscopic radical prostatectomy when your in shape don’t smoke or drink no other health problems??? You know like 30% 50% 80% or better yet 99% ..
Thank you for all you insight.
The likelihood of return of function coming back varies with age, baseline function, illness (diabetes), smoking history, obesity, mood ... it's a complicated formula. Here is the story of one young man who regained his erections. I would expect that for a 39-y old, but not a 79-y old.
Thats great to hear you can see those nerves I wasn't sure about that.. when I looked at it being done on the net everything looks the same to me..LOL . Thank you for your time and showing me the testimony. That's great!!
Also, I get the impression that you think I should lower my expectations in respect to LRP--especially post surgery. I would just like to say that after reading Dr Eden's reply to my latest question regarding his sixth chronic prostatitis patient, my expectations can't get much lower.
Anyway, I have decided to do an internet blog on your forum regarding my upcoming LRP surgery; starting from entering hospital to leaving it--followed by periodical bulletins regarding my progress (or lack of) while recuperating.
I feel if I am going to be a sacrificial lamb, I want the whole world to know about it. If you have any objections to the blog, please say so.
I feel I must warn you, though, Dr Krongrad, that I put up a daily blog on another prostatitis forum about my failed treatment in China, which attracted 32,000 hits. That was last year. Since then, the prostatitis forum has been forced to close down, because the doctor who treated me was discovered to be a fraud.
I'm sure nothing so dramatic will happen twice over.
mike
I was just wandering if the 31 year old cancer patient you operated on was lucky enough to have bi-lateral nerve sparing or not, and if so have you heard how is he doing with regards to erectile function & continence?
Thanks
Nik
Thanks for the info.
I was wondering how many patients you have operated for prostatitis so far? Are they doing ok?
It might be interesting to note in the trial how many sufferers have had this problem start due to past hemorrhoid treatments (Injections, banding, hemorrhoidectomy etc.) . I know mine and many other's prostatitis was caused by similar rectal treatments.
Regards
Nik
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The Prostatitis social network is intended for informational and educational purposes only. It is not engaged in rendering medical advice or professional services.
Any person who appears to knowingly solicit and/or render medical advice or promote a professional or commercial service on this site may be removed by the administrators without notice.
Information provided on this site should not be used for diagnosing or treating acute or chronic prostatitis or any other health problem or disease.
The Prostatitis social network is not a substitute for professional care. If you have or suspect you may have a health problem, please consult your health care provider.
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