going home to sydney after almost a year, in remission, its my 47th birthday as well
everyday is special, but birthdays after our oncologists useby date are xtra special!
so clear scans, cea 14 base 5, ca199 19 base 47, crp 0.1, frinogin and all blood normal except white bloods 3.1 when they should be 4, but they are up from 2.0 3 weeks ago. stopping 500mg xeloda and eating raw liver worked. thanks tans.
i am fundrasing in australia to raise 4 million aud, to setup a dendtritic cell lab , i have the doctors consent as long as i get my governments approval. coming home after my 47th birthday, one i was not supposed to have, might allow me some success. of course i will have a soft spot for early stage 4 colorectals where immunotherapies have the most potential.
http://petertrayhurn.blogspot.de/2013/08/dear-australian-priministerplease-help.html
taking the family camping for a few months and living a very quiet life. my gcmaf yogurt cultures are arrving in the usa, the longer i live the people want gcmaf probiotic yogurt. its not certified or approved, its for free, and costs 5 us dollars a week to make. i am sending this yogurt around the world, it works i think, even ren is going to have another try.
be happy and joyful and have hope in whatever therapy you choose, you all know that i am passionate about wholistic and experimental therapies and conventional. the secret to our survival, my survival is getting the balance right.
the german cancer business works, but its focused on money. i used up my 500,000 in the last year, i have been camping for free in the german summer, eating raw eggs and organic liver. a simple enjoyable, nature filled existence has helped me achieve my healing potential.
last post for another few months, going off line to camp and dive. of course the diving is on a rebreather at 2 atmospheres, this works with ketogenic and 2dg.
ren gave me a months worth of 2dg for my birthday, what a friend, i have left a bag of avastin in the fridge if he wants it.
pm me if your interested in lifestyle and experimental.
its always been about our health, its always been about our immune system. now more than ever, with everyday single 70 trillion cells in my body do i know this to be true.
I am back in duderstadt early november, renting a 10 bedroom house and running my non profit lifestyle based, ketogenic communal home, I already had my first taker yesterday, the first person i told, she has a beautiful smile and a couragous sole. the first years results or 20 early stage 4 cancers using the best lifestyle and dendtritic cells therapies and all the medical resources is essential.
there is the worlds best alternative cancer conference at baden baden, on the blog, meet me their if your interested.
hugs,
Pete
ps i have apologised for my radical beliefs and the upset they cause, alas they are so different to most here i post very little because i hope and joy are essential to healing. 5% chemo based survival for stage 4 says it all, i am aiming at 100% cure and with god as my assistant i will achieve it, and help those interested as well.
Comments
-
Happy birthday Pete!
Congrats on your results and on reaching another annual milestone-happy day. I'll be 47 this year too, I hope. 1966 was the year of the fire horse in Chinese astrology btw.
good luck with the clinic. If the therapy works, it will catch on.
all the best and thanks for posting. I'm sure yor blog and posts have a lot if lurkers who are benefittfrom your your "radical" posts. More than you know
karin
0 -
Happy happy, birthday, dearest Pete!
It sounds like you are living the way you want to live, and no one should judge you for that!!!!
I am sad that, in my joy that you are going home, I have not had the opportunity to meet you face to face! We are tethered here in so Cal until at least July 2014 because of my beau's heart transplant. With the threat of rejection diminishing every day, a year post surgery is when they will set him free!
And the first thing I will do then is book tickets to Europe!
BIG hugs, dearheart....safe travels....Tot Zeins.....Hartelijke gefeliciteerd met je verjaardag!
Knuffels, Kaatje
0 -
Happy Happy Birthday
Wishing you a very happy birthday. Hope you have a wonderful time camping and spending it with your family. Can't get any more wonderful than camping and seeing all God's nature around you. Congratulations on all your successes and hoping you continue to heal.
Kim
0 -
Happy Birthday Pete!
Birthdays are landmarks so, Happy Birthday Pete!
I am glad your treatments went well! It is always encouraging to hear good news. Have fun with the family camping! That is one of our favorite things to do. We love walking in the mountainns and enjoying life.
Best Always from the Mountains in the AZ! mike
0 -
On your blog...
you included this bit:
"after a year of the walking post experiment on csn I should know about what colorectal patients do and do not do! most do not do enough, and they don't wont to be told about their lazy is contributing to their death, that's what amazed me about lifestyle, but that's the truth!"
Why edit your opinion of us lazy folks at CSN out of this version, Pete?
0 -
And sorry to be a jerk here, folks...annalexandria said:On your blog...
you included this bit:
"after a year of the walking post experiment on csn I should know about what colorectal patients do and do not do! most do not do enough, and they don't wont to be told about their lazy is contributing to their death, that's what amazed me about lifestyle, but that's the truth!"
Why edit your opinion of us lazy folks at CSN out of this version, Pete?
the rest of y'all are niceer than I am and I probably should just follow your lead. But Pete's frequent and very specific bad-mouthing of this forum really gets on my nerves.
0 -
Where do I sign up! Germanyannalexandria said:And sorry to be a jerk here, folks...
the rest of y'all are niceer than I am and I probably should just follow your lead. But Pete's frequent and very specific bad-mouthing of this forum really gets on my nerves.
Where do I sign up! Germany bound!
0 -
No Annannalexandria said:On your blog...
you included this bit:
"after a year of the walking post experiment on csn I should know about what colorectal patients do and do not do! most do not do enough, and they don't wont to be told about their lazy is contributing to their death, that's what amazed me about lifestyle, but that's the truth!"
Why edit your opinion of us lazy folks at CSN out of this version, Pete?
You are not alone, when he wrote that bit about being "like the miricle gas chamber survivor alive on a mountain of corpses"....I was done with him. He constantly belittles those that are on CSN in his blog and then in his egotistic way is like the survivor of the Holocaust, because he got German therapies, sorry you don't get to go there Pete, can't say what I feel about it on CSN. That language is not approved.
Winter Marie
0 -
Ann and Winter:herdizziness said:No Ann
You are not alone, when he wrote that bit about being "like the miricle gas chamber survivor alive on a mountain of corpses"....I was done with him. He constantly belittles those that are on CSN in his blog and then in his egotistic way is like the survivor of the Holocaust, because he got German therapies, sorry you don't get to go there Pete, can't say what I feel about it on CSN. That language is not approved.
Winter Marie
You two are so very correct. I often found the blog disturbing and simply stopped reading it. Thank you ladies for veryifying my thoughts on the subject.
Tina
0 -
Yes, I agree on all points.geotina said:Ann and Winter:
You two are so very correct. I often found the blog disturbing and simply stopped reading it. Thank you ladies for veryifying my thoughts on the subject.
Tina
Yes, I agree on all points. His blog is filled with extremely insulting statements on traditional chemo patients. The blog disgusts me, and he has some friggin nerve to continue to post to us "sheep" (Pete's word, not mine) on this board.
0 -
Dear Nana-Nana b said:Where do I sign up! Germany
Where do I sign up! Germany bound!
I would read Pete's blog very carefully before letting his posts influence your decision-making process. I would also correspond directly with these German doctors, and ask for actual numbers on how many patients reach even short-term remission with these treatments (I'm not sure those numbers even exist...they don't seem to track them, which seems odd to those of us who are used to the "American" way of providing evidence for the efficacy of treatment with large, longitudinal studies, unless it's a clinical trial, of course). And as Pete himself would no doubt happily tell you, he is the "miracle" patient, who has had results never before seen in the world of cancer treatment (although even with a careful reading of his blog, it's hard to tell what those results actually are at this point).
At any rate, I'm sure you don't need or want my two-cents, but I think it's important for newcomers to this board (who don't know Pete's history here) to hear all sides of this debate.
AA
0 -
Hi Annannalexandria said:Dear Nana-
I would read Pete's blog very carefully before letting his posts influence your decision-making process. I would also correspond directly with these German doctors, and ask for actual numbers on how many patients reach even short-term remission with these treatments (I'm not sure those numbers even exist...they don't seem to track them, which seems odd to those of us who are used to the "American" way of providing evidence for the efficacy of treatment with large, longitudinal studies, unless it's a clinical trial, of course). And as Pete himself would no doubt happily tell you, he is the "miracle" patient, who has had results never before seen in the world of cancer treatment (although even with a careful reading of his blog, it's hard to tell what those results actually are at this point).
At any rate, I'm sure you don't need or want my two-cents, but I think it's important for newcomers to this board (who don't know Pete's history here) to hear all sides of this debate.
AA
I've read Pete's blog a while ago too and found it quite disturbing. Either a person is done with us or they're not. You shouldn't bad mouth us Pete then expect us to still cheer you on.
Remember, the people you meet on your way up are often the same ones you meet on the way down
0 -
I continue to read Pete's blog,PhillieG said:Hi Ann
I've read Pete's blog a while ago too and found it quite disturbing. Either a person is done with us or they're not. You shouldn't bad mouth us Pete then expect us to still cheer you on.
Remember, the people you meet on your way up are often the same ones you meet on the way down
in part because some of his stuff is actually of interest to me. If my cancer comes back, I won't be a candidate for chemo (unless something new has come up in the meantime). It's too bad he can't present his information without all the insults (and incomprehensible spelling and grammar...if you're reading this, Pete, pls have someone edit your stuff! It would be so much more useful if you did.).
0 -
I know pete personally and togeotina said:Ann and Winter:
You two are so very correct. I often found the blog disturbing and simply stopped reading it. Thank you ladies for veryifying my thoughts on the subject.
Tina
I know pete personally and to his defence he is a great guy who wears his heart on his sleve. He is very passionate about what he is doing and what he has achieved, maybe to a fault, and he wants to save everyone with cancer and change the medical establishment in the process. His attempts tend to fall on deaf ears and I think he finds that very frustrating. His comments are a little harsh at times and that is probably his frustration showing. I know he means well and is trying to kick others into taking action which may save their lives, but I guess often those attempts backfire.
The german therapies are expensive and not for everyone, but core elements can be done even in the US and do not need to break the bank. If I sum it up, the core treatments are.
1. Holistic approach to lifestyle. No stress, meditation, qigong, good organic nutrition and optimizing the body's overall wellbeing which a good homeopath can manage anywhere. And yes carb free keto diet.
2. Immunotherapies. These are harder, but one does not need to travel to germany as Dr. Chan in the US can do the same therapies. Cost wise this can still be prohibitive, but many Australians in particular that I come across in germany have no means to be here, but fundraise to be able to get the treatments. Where there is a will there is a way.
3. TACE - very effective and though prof. Vogl is the world's foremost authority and works out of Frankfurt, TACE is offered by many hospitals everywhere.
4. Lastly there's Removab, and as far I know only Hallwang offer this unfortunately. Although I am doing removab as well, I think one may be able to achieve good results without it.
The greatest hurdle is finding the will to take charge of one's treatments and relying less on traditional oncologists, as most are only good for dosing chemo anyway.
0 -
renw said:
I know pete personally and to
I know pete personally and to his defence he is a great guy who wears his heart on his sleve. He is very passionate about what he is doing and what he has achieved, maybe to a fault, and he wants to save everyone with cancer and change the medical establishment in the process. His attempts tend to fall on deaf ears and I think he finds that very frustrating. His comments are a little harsh at times and that is probably his frustration showing. I know he means well and is trying to kick others into taking action which may save their lives, but I guess often those attempts backfire.
The german therapies are expensive and not for everyone, but core elements can be done even in the US and do not need to break the bank. If I sum it up, the core treatments are.
1. Holistic approach to lifestyle. No stress, meditation, qigong, good organic nutrition and optimizing the body's overall wellbeing which a good homeopath can manage anywhere. And yes carb free keto diet.
2. Immunotherapies. These are harder, but one does not need to travel to germany as Dr. Chan in the US can do the same therapies. Cost wise this can still be prohibitive, but many Australians in particular that I come across in germany have no means to be here, but fundraise to be able to get the treatments. Where there is a will there is a way.
3. TACE - very effective and though prof. Vogl is the world's foremost authority and works out of Frankfurt, TACE is offered by many hospitals everywhere.
4. Lastly there's Removab, and as far I know only Hallwang offer this unfortunately. Although I am doing removab as well, I think one may be able to achieve good results without it.
The greatest hurdle is finding the will to take charge of one's treatments and relying less on traditional oncologists, as most are only good for dosing chemo anyway.
I don't question Pete's intentions but he could reread (or read) his posts before he hits submit. I also feel that he confuses what seems to be helping him with having found the cure for cancer. It's a major difference that needs to be distinguished.
I'm sure Pete's helped many by trying different approaches and sharing them with everyone. He certainly does not have to do that. Many of the approaches he talks about make a lot of sense and have merit for sure.
At the same time, he knows that many in his audience read both sites so I can't understand why he expresses himself so differently on the sites. I know that I've been less than thrilled to read his opinions at times.
0 -
I'm glad that he's a better person in reality...renw said:I know pete personally and to
I know pete personally and to his defence he is a great guy who wears his heart on his sleve. He is very passionate about what he is doing and what he has achieved, maybe to a fault, and he wants to save everyone with cancer and change the medical establishment in the process. His attempts tend to fall on deaf ears and I think he finds that very frustrating. His comments are a little harsh at times and that is probably his frustration showing. I know he means well and is trying to kick others into taking action which may save their lives, but I guess often those attempts backfire.
The german therapies are expensive and not for everyone, but core elements can be done even in the US and do not need to break the bank. If I sum it up, the core treatments are.
1. Holistic approach to lifestyle. No stress, meditation, qigong, good organic nutrition and optimizing the body's overall wellbeing which a good homeopath can manage anywhere. And yes carb free keto diet.
2. Immunotherapies. These are harder, but one does not need to travel to germany as Dr. Chan in the US can do the same therapies. Cost wise this can still be prohibitive, but many Australians in particular that I come across in germany have no means to be here, but fundraise to be able to get the treatments. Where there is a will there is a way.
3. TACE - very effective and though prof. Vogl is the world's foremost authority and works out of Frankfurt, TACE is offered by many hospitals everywhere.
4. Lastly there's Removab, and as far I know only Hallwang offer this unfortunately. Although I am doing removab as well, I think one may be able to achieve good results without it.
The greatest hurdle is finding the will to take charge of one's treatments and relying less on traditional oncologists, as most are only good for dosing chemo anyway.
than he comes across in his writing, Ren. But then, I can only judge him based on his writings, in which has has repeatedly called people on the forum names and said horrible stuff about us in general. I also find his "frustration" kind of ridiculous, given that he has had a recurrence since starting these therapies, and may or may not be NED even now (he keeps mentioning a few cancer cells in his blog, so I don't know what his actual health status may be...and anyway, it's almost irrelevant, as what really matters is whether he is NED 6 months, or longer, down the road). And the docs there have apparently told him he is a "miracle" patient. So in short, I don't feel that his quest to bring these therapies to the whole world makes a whole lot of sense. And honestly, much of what he writes (about starting clinics, and being a doctor, and other statements very difficult to swallow) leave me uncertain as to what is reality and what is fantasy.
At any rate, Pete is welcome to do his thing on his own blog, of course, but he shouldn't expect to come here and get a warm welcome from everyone. I was a big support of Pete's originally, and I'm interested in the alt therapies, but he has a very problematic personality, imo.
PS several trials of removab (for a variety of cancers) are recruiting right now in the States, just fyi.
PSS It makes little sense to say "where there's a will, there's a way". That's just one of those sayings that actually makes very little sense when you think about it logically. But I'll be sure to mention it to my friend who is presently raising funds to pay for her dead daughter's cancer-related medical bills. She's got 10K already (some of us have given twice)...should be no prob to raise the other 40K.
0 -
annalexandria said:
I'm glad that he's a better person in reality...
than he comes across in his writing, Ren. But then, I can only judge him based on his writings, in which has has repeatedly called people on the forum names and said horrible stuff about us in general. I also find his "frustration" kind of ridiculous, given that he has had a recurrence since starting these therapies, and may or may not be NED even now (he keeps mentioning a few cancer cells in his blog, so I don't know what his actual health status may be...and anyway, it's almost irrelevant, as what really matters is whether he is NED 6 months, or longer, down the road). And the docs there have apparently told him he is a "miracle" patient. So in short, I don't feel that his quest to bring these therapies to the whole world makes a whole lot of sense. And honestly, much of what he writes (about starting clinics, and being a doctor, and other statements very difficult to swallow) leave me uncertain as to what is reality and what is fantasy.
At any rate, Pete is welcome to do his thing on his own blog, of course, but he shouldn't expect to come here and get a warm welcome from everyone. I was a big support of Pete's originally, and I'm interested in the alt therapies, but he has a very problematic personality, imo.
PS several trials of removab (for a variety of cancers) are recruiting right now in the States, just fyi.
PSS It makes little sense to say "where there's a will, there's a way". That's just one of those sayings that actually makes very little sense when you think about it logically. But I'll be sure to mention it to my friend who is presently raising funds to pay for her dead daughter's cancer-related medical bills. She's got 10K already (some of us have given twice)...should be no prob to raise the other 40K.
No, he's not NED (from hisNo, he's not NED (from his own statement on a blog) or in remission. Not to mention that he's been taking irinoteacan with Avastin and then Xeloda!! So who's to say that the reason his tumors haven't grown was due to taking CHEMO DRUGS and not all of those alternative million dollar meds??? Seriously, can anyone claim to be in "remission" from only one month off of chemo? And he has a current CEA of 14!
From one of his recent blogs:
"i did tace 7 combined ipt to the liver with mitomycin, irenotecan , avastin, infusions 2dg, dca, dmso and 15 iu insulin..."
"clear scans, cea 14 base 5, ca199 19 base 47, crp 0.1, frinogin and all blood normal except white bloods 3.1 when they should be 4, but they are up from 2.0 3 weeks ago. stopping 500mg xeloda and eating raw liver worked.
0 -
renw said:
I know pete personally and to
I know pete personally and to his defence he is a great guy who wears his heart on his sleve. He is very passionate about what he is doing and what he has achieved, maybe to a fault, and he wants to save everyone with cancer and change the medical establishment in the process. His attempts tend to fall on deaf ears and I think he finds that very frustrating. His comments are a little harsh at times and that is probably his frustration showing. I know he means well and is trying to kick others into taking action which may save their lives, but I guess often those attempts backfire.
The german therapies are expensive and not for everyone, but core elements can be done even in the US and do not need to break the bank. If I sum it up, the core treatments are.
1. Holistic approach to lifestyle. No stress, meditation, qigong, good organic nutrition and optimizing the body's overall wellbeing which a good homeopath can manage anywhere. And yes carb free keto diet.
2. Immunotherapies. These are harder, but one does not need to travel to germany as Dr. Chan in the US can do the same therapies. Cost wise this can still be prohibitive, but many Australians in particular that I come across in germany have no means to be here, but fundraise to be able to get the treatments. Where there is a will there is a way.
3. TACE - very effective and though prof. Vogl is the world's foremost authority and works out of Frankfurt, TACE is offered by many hospitals everywhere.
4. Lastly there's Removab, and as far I know only Hallwang offer this unfortunately. Although I am doing removab as well, I think one may be able to achieve good results without it.
The greatest hurdle is finding the will to take charge of one's treatments and relying less on traditional oncologists, as most are only good for dosing chemo anyway.
Ren, I much prefer your approach to sharing information. It is direct and to the point.
I, as do all here, hope that whatever treatments each is following works for them and gives them years and years of a good life. It is unfortunate, but what works for one does not necessarily work for all...YET.
While we may not all agree as to what treatments to follow and which to discard, I don't think it is asking too much to be supportive of others' choices...after all it is their life in the balance...and their life situations which must also be considered.
Sharing ones choices and successes and failures helps others in their decision making process and is a good thing. This can be done without mocking or slamming other choices and folks, which is what Pete failed to recognize. It is also ok for others to have a differing opinion based on their own information gathering. There will always be those who prefer to swim close to shore and others who will brave the open sea.
A number of us tried to get Pete to focus on his treatments and leave the harsh words out of it...unfortunately it didn't work, and blurred any validity to his information. It also didn't help that he was giving way to much financial and marital information in his rants.
Glad that you posted the basics of the treatments and sincerely hope that it all works for you.
Marie who loves kitties
0
Discussion Boards
- All Discussion Boards
- 6 CSN Information
- 6 Welcome to CSN
- 121.6K Cancer specific
- 2.8K Anal Cancer
- 446 Bladder Cancer
- 308 Bone Cancers
- 1.6K Brain Cancer
- 28.5K Breast Cancer
- 395 Childhood Cancers
- 27.9K Colorectal Cancer
- 4.6K Esophageal Cancer
- 1.2K Gynecological Cancers (other than ovarian and uterine)
- 13K Head and Neck Cancer
- 6.3K Kidney Cancer
- 671 Leukemia
- 791 Liver Cancer
- 4.1K Lung Cancer
- 5.1K Lymphoma (Hodgkin and Non-Hodgkin)
- 234 Multiple Myeloma
- 7.1K Ovarian Cancer
- 56 Pancreatic Cancer
- 487 Peritoneal Cancer
- 5.4K Prostate Cancer
- 1.2K Rare and Other Cancers
- 534 Sarcoma
- 719 Skin Cancer
- 646 Stomach Cancer
- 190 Testicular Cancer
- 1.5K Thyroid Cancer
- 5.9K Uterine/Endometrial Cancer
- 6.3K Lifestyle Discussion Boards