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LDN & Prostate Cancer

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I don't know if anyone on this site deals with any cancers at all. I

wish we had more tools at our disposal to promote the benefits of

this treatment, so I'm posting again. (I'm still hoping for more

detailed testimonials about fibromyalgia that I asked for a few weeks

ago--I've received one.)

I build medical foundations for launching clinical research into LDN

for treating serious diseases, and my daughter has one (see previous

posts). That means developing pathways to collect scientifically

respectable clinical case studies for later presentation to a

reputable researcher in the target disease.

I've collected dozens of medical research abstracts on various

subjects, that serve to educate docs and researchers on the potential

of LDN for treating serious diseases, both cancers and immune

disorders. I don't have time to try to give someone the information

that could change their prognosis if they're not interested. It's

already happened too many times, so to not dwell in frustration too

often, I withdraw my energy until I run into another possible way to

help--like the water searching its way thru obstacles in the I-Ching.

My latest chink in the obstacles to revamping medical treatment by

adding LDN is this: in 10 minutes during my yearly urology

appointment, I convinced my alternative-pitching urologist,

Cantwell (Daytona Beach FL--if you know someone in that area in

danger of PC), that LDN would be worth a try on patients with nascent

prostate cancer who want to watch and wait before jumping into

standard treatment, and handed him about 30p of abstracts,

correspondence & website info, so there may be a way for the promise

of LDN to make headway on that cancer treatment.

I firmly believe that there are enough of us with LDN experience to

design, finance, and get doctors to monitor careful case studies that

would provide medically respectable evidence that LDN could be a

godsend for many many diseases. But we need to be better organized

than we are now.

My model for how to do this was accepted by the clinical trials

activism subcommittee at last June's LDN conference, and NOT ONE

person from that committee or anywhere else has contacted me about

working together to make that happen. (MS has a raft of organizers,

no other disease has ANY.) So perhaps I am that committee. Who wants

to organize and help?

Write me off list nphbrown@... and copy to the list, so

this can grow.

Norman Brown, Ph.D.

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Hi Norman,

What exactly in a nutshell is it that you are asking for here? I think you

are saying that you would like medical research abstracts from those with

other ailments than MS that are utilizing LDN. First of all it is very cool

that you are doing this. A more scientific approach or significant research

and studies that back LDN as a viable treatment would be extremely helpful

in advancing it use. And if anything like that is available it would be

great if someone on our chat site has that info would see your post and

share it. But I think it is important to note that most of us are " users "

of LDN and are not necessarily science minded or have this info available.

I think the biggest key on this site is antidotal evidence and sharing all

of our experiences. In fact as far as a person with no science or study

back ground I have found this far far more useful. It is like our own

science study if you think about it. We are not isolating the events or

creating hypothesis we are a whole group with many problems associated with

what ever our ailments are and as a whole group in each ailment we are

finding out " overall " what works and what does not with a LDN and that

disease. We are finding out that everybody is different and that there are

many reactions to LDN, and that there are many solutions that work for

different people. This as a user has been so much more valuable than a

scientific study in which a doctor prescribes the med and does not have all

of these different scenarios in which to share with you to look at when

things go wrong or things could be enhanced. In my opinion, every patient

in the future (for every drug) would benefit highly from having such a

resource available with other users of that drug signing in and sharing

their experiences.

I will look and see what earlier chats I have saved in regards cancer and

other ailments. I hope I have anything that you are looking for. As far as

putting things together to help with your project, that would be great if

anyone has the time and recourses, but I think many of us have just don't

have the resources or the time to do that. I had gathered some links and

some attachments from the chat site and put them together in a sort of

" welcome e-mail " for those with MS and asked the group if there was anyone

with other ailments that would mind putting their valuable info in a similar

" welcome e-mail " for cancer, Lupus, Parkinson's, Fibro etc. but I have had

no one able to do that yet. It is all time consuming. Just responding to

chats, sending out welcome e-mails to new people and trying to find saved

chats on different things to those in need has cost me so much time and some

of my own business dollars. But I can't help but want to help those in

need. Besides that others had taken the time to help myself and my husband

out with LDN and it completely changed my husbands life. I must help others

in anyway that I can.

I'll see what I can find for you.

Aletha

[low dose naltrexone] LDN & Prostate Cancer

>I don't know if anyone on this site deals with any cancers at all. I

> wish we had more tools at our disposal to promote the benefits of

> this treatment, so I'm posting again. (I'm still hoping for more

> detailed testimonials about fibromyalgia that I asked for a few weeks

> ago--I've received one.)

>

> I build medical foundations for launching clinical research into LDN

> for treating serious diseases, and my daughter has one (see previous

> posts). That means developing pathways to collect scientifically

> respectable clinical case studies for later presentation to a

> reputable researcher in the target disease.

>

> I've collected dozens of medical research abstracts on various

> subjects, that serve to educate docs and researchers on the potential

> of LDN for treating serious diseases, both cancers and immune

> disorders. I don't have time to try to give someone the information

> that could change their prognosis if they're not interested. It's

> already happened too many times, so to not dwell in frustration too

> often, I withdraw my energy until I run into another possible way to

> help--like the water searching its way thru obstacles in the I-Ching.

>

> My latest chink in the obstacles to revamping medical treatment by

> adding LDN is this: in 10 minutes during my yearly urology

> appointment, I convinced my alternative-pitching urologist,

> Cantwell (Daytona Beach FL--if you know someone in that area in

> danger of PC), that LDN would be worth a try on patients with nascent

> prostate cancer who want to watch and wait before jumping into

> standard treatment, and handed him about 30p of abstracts,

> correspondence & website info, so there may be a way for the promise

> of LDN to make headway on that cancer treatment.

>

> I firmly believe that there are enough of us with LDN experience to

> design, finance, and get doctors to monitor careful case studies that

> would provide medically respectable evidence that LDN could be a

> godsend for many many diseases. But we need to be better organized

> than we are now.

>

> My model for how to do this was accepted by the clinical trials

> activism subcommittee at last June's LDN conference, and NOT ONE

> person from that committee or anywhere else has contacted me about

> working together to make that happen. (MS has a raft of organizers,

> no other disease has ANY.) So perhaps I am that committee. Who wants

> to organize and help?

>

> Write me off list nphbrown@... and copy to the list, so

> this can grow.

>

> Norman Brown, Ph.D.

>

>

>

>

>

>

>

>

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  • 2 months later...
Guest guest

Hi Folks!

I am a newby trawling the list for info re: the subject line.

My history is briefy Dx'd 10 years ago age 49 with a very poor

prognosis. Surgery followed by salvage radiotherapy with a rising PSA

followed by repeated bouts of Zoladex (castration therapy) to keep PSA

under control. In the end I gave up Zoladex because it was making me

sick. Some of my friends have died from 'unexpected' heart failure

when on Zoladex and I am pretty sure that is the way I would go if I

kept up the conventional treatment.

For the last three years I have been OFF treatments and maximising my

testosterone level. A recent MRI scan confirmed no recurrence in the

prostatic bed, but since I do have a PSA it must be coming from

somewhere, and I want to get rid of thre source of that PSA. I have

not had a bone scan recently because of the high dose radiation

associated with the procedure. [ A bone scintigraphy scan is ~ 1000 >

than a single chest x-ray, even a CAT scan is > 100 a single x-ray. I

figure with all the x-ray therapy I have had in the past I can do

without more and will just rely on MRI.]

My take on the " LDA for 'untreated' prostate cancer only " which I

read on the LDA website, is that castration therapy disables the LDN

effect. [ Similar to castration therapy disabling vitamin D therapy.]

I infer that anyone with a near-normal testosterone level will respond

to LDN. Presumably having had various kinds of chemotherapy with other

cancers does not interfere with LDN ? Am I on the right track here or

is there something I have missed ?

Thanks for being here.

Sammy.

>

> Hi Norman,

>

> What exactly in a nutshell is it that you are asking for here? I

think you

> are saying that you would like medical research abstracts from those

with

> other ailments than MS that are utilizing LDN. First of all it is

very cool

> that you are doing this. A more scientific approach or significant

research

> and studies that back LDN as a viable treatment would be extremely

helpful

> in advancing it use. And if anything like that is available it

would be

> great if someone on our chat site has that info would see your post and

> share it. But I think it is important to note that most of us are

" users "

> of LDN and are not necessarily science minded or have this info

available.

>

> I think the biggest key on this site is antidotal evidence and

sharing all

> of our experiences. In fact as far as a person with no science or

study

> back ground I have found this far far more useful. It is like our own

> science study if you think about it. We are not isolating the

events or

> creating hypothesis we are a whole group with many problems

associated with

> what ever our ailments are and as a whole group in each ailment we are

> finding out " overall " what works and what does not with a LDN and that

> disease. We are finding out that everybody is different and that

there are

> many reactions to LDN, and that there are many solutions that work for

> different people. This as a user has been so much more valuable than a

> scientific study in which a doctor prescribes the med and does not

have all

> of these different scenarios in which to share with you to look at when

> things go wrong or things could be enhanced. In my opinion, every

patient

> in the future (for every drug) would benefit highly from having such a

> resource available with other users of that drug signing in and sharing

> their experiences.

>

> I will look and see what earlier chats I have saved in regards

cancer and

> other ailments. I hope I have anything that you are looking for.

As far as

> putting things together to help with your project, that would be

great if

> anyone has the time and recourses, but I think many of us have just

don't

> have the resources or the time to do that. I had gathered some

links and

> some attachments from the chat site and put them together in a sort of

> " welcome e-mail " for those with MS and asked the group if there was

anyone

> with other ailments that would mind putting their valuable info in a

similar

> " welcome e-mail " for cancer, Lupus, Parkinson's, Fibro etc. but I

have had

> no one able to do that yet. It is all time consuming. Just

responding to

> chats, sending out welcome e-mails to new people and trying to find

saved

> chats on different things to those in need has cost me so much time

and some

> of my own business dollars. But I can't help but want to help those in

> need. Besides that others had taken the time to help myself and my

husband

> out with LDN and it completely changed my husbands life. I must

help others

> in anyway that I can.

>

> I'll see what I can find for you.

>

> Aletha

>

>

>

> [low dose naltrexone] LDN & Prostate Cancer

>

>

> >I don't know if anyone on this site deals with any cancers at all. I

> > wish we had more tools at our disposal to promote the benefits of

> > this treatment, so I'm posting again. (I'm still hoping for more

> > detailed testimonials about fibromyalgia that I asked for a few weeks

> > ago--I've received one.)

> >

> > I build medical foundations for launching clinical research into LDN

> > for treating serious diseases, and my daughter has one (see previous

> > posts). That means developing pathways to collect scientifically

> > respectable clinical case studies for later presentation to a

> > reputable researcher in the target disease.

> >

> > I've collected dozens of medical research abstracts on various

> > subjects, that serve to educate docs and researchers on the potential

> > of LDN for treating serious diseases, both cancers and immune

> > disorders. I don't have time to try to give someone the information

> > that could change their prognosis if they're not interested. It's

> > already happened too many times, so to not dwell in frustration too

> > often, I withdraw my energy until I run into another possible way to

> > help--like the water searching its way thru obstacles in the I-Ching.

> >

> > My latest chink in the obstacles to revamping medical treatment by

> > adding LDN is this: in 10 minutes during my yearly urology

> > appointment, I convinced my alternative-pitching urologist,

> > Cantwell (Daytona Beach FL--if you know someone in that area in

> > danger of PC), that LDN would be worth a try on patients with nascent

> > prostate cancer who want to watch and wait before jumping into

> > standard treatment, and handed him about 30p of abstracts,

> > correspondence & website info, so there may be a way for the promise

> > of LDN to make headway on that cancer treatment.

> >

> > I firmly believe that there are enough of us with LDN experience to

> > design, finance, and get doctors to monitor careful case studies that

> > would provide medically respectable evidence that LDN could be a

> > godsend for many many diseases. But we need to be better organized

> > than we are now.

> >

> > My model for how to do this was accepted by the clinical trials

> > activism subcommittee at last June's LDN conference, and NOT ONE

> > person from that committee or anywhere else has contacted me about

> > working together to make that happen. (MS has a raft of organizers,

> > no other disease has ANY.) So perhaps I am that committee. Who wants

> > to organize and help?

> >

> > Write me off list nphbrown@... and copy to the list, so

> > this can grow.

> >

> > Norman Brown, Ph.D.

> >

> >

> >

> >

> >

> >

> >

> >

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Guest guest

That is a very nice web site Bruce. Generally informative and a good Google search engine incorporated, but I did not find the info I was looking for as per the limitations for use with prostate cancer.

While I am on the subject of limitations, are there any restrictions for use if say you have a cold? [Or is 'having a cold' an oxymoron with LDN users?]

I read the bit about restricting LDN if opoids are in use (even codeine by the look of it). I wonder, do MS sufferers who use cannabis to control pain have difficulty with LDN ? How about mild narco-hallucinogens like nutmeg ? Is LDN contraindicated with ibuprofen or aspirin ?

Sammy

[low dose naltrexone] LDN & Prostate Cancer> > > >I don't know if anyone on this site deals with any cancers at all. I> > wish we had more tools at our disposal to promote the benefits of> > this treatment, so I'm posting again. (I'm still hoping for more> > detailed testimonials about fibromyalgia that I asked for a few weeks> > ago--I've received one.)> >> > I build medical foundations for launching clinical research into LDN> > for treating serious diseases, and my daughter has one (see previous> > posts). That means developing pathways to collect scientifically> > respectable clinical case studies for later presentation to a> > reputable researcher in the target disease.> >> > I've collected dozens of medical research abstracts on various> > subjects, that serve to educate docs and researchers on the potential> > of LDN for treating serious diseases, both cancers and immune> > disorders. I don't have time to try to give someone the information> > that could change their prognosis if they're not interested. It's> > already happened too many times, so to not dwell in frustration too> > often, I withdraw my energy until I run into another possible way to> > help--like the water searching its way thru obstacles in the I-Ching.> >> > My latest chink in the obstacles to revamping medical treatment by> > adding LDN is this: in 10 minutes during my yearly urology> > appointment, I convinced my alternative-pitching urologist, > > Cantwell (Daytona Beach FL--if you know someone in that area in> > danger of PC), that LDN would be worth a try on patients with nascent> > prostate cancer who want to watch and wait before jumping into> > standard treatment, and handed him about 30p of abstracts,> > correspondence & website info, so there may be a way for the promise> > of LDN to make headway on that cancer treatment.> >> > I firmly believe that there are enough of us with LDN experience to> > design, finance, and get doctors to monitor careful case studies that> > would provide medically respectable evidence that LDN could be a> > godsend for many many diseases. But we need to be better organized> > than we are now.> >> > My model for how to do this was accepted by the clinical trials> > activism subcommittee at last June's LDN conference, and NOT ONE> > person from that committee or anywhere else has contacted me about> > working together to make that happen. (MS has a raft of organizers,> > no other disease has ANY.) So perhaps I am that committee. Who wants> > to organize and help?> >> > Write me off list nphbrown@... and copy to the list, so> > this can grow.> >> > Norman Brown, Ph.D.> >> >> >> >> >> >> >> >

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  • 4 years later...
Guest guest

Prostate cancer is one of the cancers listed on the LDN Homepage that

LDN is useful for (provided it has not had "prior treatment"...by that

I believe the treatment referred to is hormonal treatment).

http://www.ldninfo.org/index.htm#What_diseases_has_it_been_useful_for

Anita Meyers wrote:

Has anyone ever heard of LDN helping prostate cancer? A friend has

recently been diagnosed with it and the cancer is beyond surgery.

Thanks, Anita

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