look for mould your gcmaf suppositories, I alerted my gcmaf friends, see photo, email them, copy me if you want. love and health, pete
ps lets not die from cancer or mould, see photo, 3 out of 10 boxes stuffed, doing 2 supps a day AM PM
Is this the worlds most brilliant, brave, courageous oncologist?
I lovelly red sunset, everything in life is a precious gift! the sunset, the oncologist, my friends.
there is unlimited joy in our greatest challenges, the trick is finding it.
this blog almost makes sense, that's another miracle. see there must be a god, he loves you unconditionally in my concept of god, its bliss to realise this, that bliss, makes the critics discussed here my most blessed gift. and yes of course I must be nuts, and I don't even have the thc drops anymore.
Go to love the cave man
http://www.cavemandoctor.com/2015/06/03/are-cancer-cells-trying-to-hijack-your-vitamin-d/http://abstracts.asco.org/156/AbstView_156_149805.html
comment for caveman
great article, I wanted to add that research I follow and scientists I love, find the vdr needs d3, gcmaf and oleic acid to correctly activate the inn ante immune. you do a great job writing and presenting.
alas this ommission will rob many cancer patients of life saving immune responses.
the key which I explained today on my blog, very poorly may say, but is that for colorectal a robust innanate response is the difference between life and death, I and I know.
google bamlet and hamlet and gcmaf and millions of lives can be saved
http://csn.cancer.org/node/210911
I shared, I cared and learned so much, I save my energy from this point on for my ongoing miracle. I have no regrets, I always had and have the best intentions.
LIFE SAVING TIP, SUPER HIGH D3 CONFERS ACROSS THE MCRC SURVIVAL BOOSTS, DESPITE TCELL LACK OF ANTIGENICITY, IE 93..% NOT MSIHI, SO THE IMMUNE STRATEGIES, MUST FOCUS INNATE. SO AHCC, GCMAF YOGURT, SUPPOSITORIES. MAYBE OTHER TLR AGONISTS.
ITS NOT ROCKET SCIENCE, MIXED LOVE AND DESPERATION , AIN'T LET ME DOWN YET.
DOING 30K A DAY, NO POINT FFING AROUND.
THIS SIMPLE POWERFUL CONCEPT SHOULD WORK WITH OTHER NONANTIGENIC CANCERS IE PIP CUP
IMPLIES IPI MAYBE WASTED EXCEPT FOR NDV TAGGED CELL, AND THOSE DIEING ONCO AND ALTERNATIVE THERAPIES IE PDT, INFUSIONS
will he a man before I come home ?
been attacked somewhere, see discussion on my beloved colon chat. maybe there are no safe haven from ignorance.
http://www.colonchat.net/forum/viewtopic.php?f=1&t=2517
http://www.colonchat.net/forum/viewtopic.php?f=1&t=2517
http://www.colonchat.net/forum/viewtopic.php?f=1&t=2523&p=6250#p6250
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News on CRC 'and' immunotherapy: A Cry for Perspective
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News on CRC 'and' immunotherapy: A Cry for Perspective
by frances » Sat May 30, 2015 9:37 pm
http://www.oncologytube.com/v/1034975/d ... cer-asco15
I just read a heart rending account on an old, dreary as blue dishwater colon cancer forum by a caregiver who tried to be the perfect caregiver only to confront her patient's impending demise. Why, she beseeched, was this happening when "I" had done everything right as a caregiver?
One of the things that was a problem, too, was the news this caregiver was seeing about "IMMUNOTHERAPY."
Surprise, surprise.
Today we have out of ASCO, "news" on some results in a tiny sub strata of patients with CRC and one of the PD-1 immunotherapy drugs that has shown major success in other cancers - that we at Colon Chat do hardly find to be "news." We have long been aware of the use of exclusively MSI-Instable, specifically MSI HI patients - in these studies. We knew they could not even recruit enough subjects for these studies bc the number of such patients is so SCARCE!!
We are talking about 8-16 percent (!!!) of all CRC patients who fall into this category.
We are not getting excited about something a world class oncologist or two has told us directly has no hope of working in the rest of the 92 percent of CRC patients -- or pushing misinformation to desperate, brow beating caregivers at the end of their rope. We are NOT misleading patients with mCRC - like one or two self-appointed net addicted information junky 'experts' on said dull, misinformational forum.
I am not just saying this out of the "blue" today. I have seen seriously smart people take literal advice from one of the spammers on said forum and act on it clinically. When that spammer has no clinical experience or qualifications or experience as a patient or medic and literally has given what I consider
dangerous clinical advice on said forum - at least on three occasions that I have witnessed. Said spammer enjoys a serious following. And is the first to condemn our Pete Lost at Sea for allegedly misleading patients - on the basis that he now charges for his services. He's been open about that and we are not part of that - that is his legitimate right to do, if he wants to be a consultant for German treatments. Just on his own domain and webspace - which he has done. His posts on here are just sharing his information. People can weigh that information for themselves and he has NEVER given clinical advice here. I would be all over that in a flash. Calling him a charlatan on an open forum is probably illegal - like a lot of what they post - and is the pot calling the kettle a very dark blue in the case of the main offender aka spammer. I for one, am not going to sit back and watch misleading clinical advice - about for example laser lung surgery in wait for it... Germany ... continue.
We are and always will be maintaining a clear perspective. And promoting accuracy and the best of science via our stellar contacts in oncology and the CRC community and our deep experience and history with the literature and in the clinic.
Have a good day.
Frances
frances 772 Sun Feb 03, 2013 10:05 am
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Re: News on CRC 'and' immunotherapy: A Cry for Perspective
by pete43lost_at_sea » Thu Jun 04, 2015 1:22 am
been off the air,
I agree with francis,
tried to make some money,
failed.
I sleep in my car, I beg for all my treatments.
I am not msi hi
I had no tils.
my miracle not been emulated anywhere.
When I swim in this beautiful german lake tomorrow and plan my program next 4 week, I imagine all my Critics being pushed into the same colorectal lake I was 3 years ago with lung, liver and peritoeal mets everywhere.
all clear per scans, markers falling as of today.
I pray god saves all who fall into the quick sand of metastatic colorectal.
I know why I am alive, I have shared it all.
we all have our journey s, I thank god for mine, especially the critics.
I have no time or interest to waste energy, they have no clue.
like the colorectal scientists francis replies on, yes I am arrogant in the extreme, just stating a fact, I chat to these EXPERTS,
what they said was next to useless, and I told them.
the deaths continue, and I live a healthy good life, chemo free for next 4 weeks.
I desperately looked for help to explain 3 new peritoneal in last 3 months with dc ipilumimab nivolumimab, removab.
I am a decade ahead of these scientists,
I pray ill be in compete ongoing remission while these smart, greedy, scientists and doctor chase after rat tails.
they won't catch me, I'll swim like a fish tomorrow
no offence meant to the science types, what I have access to in alternatives these scientists and doctors cannot even spell, let alone integrate into an effective colorectal program, like I have been blessed to find.
I protect myself, my doctors and friends and the critics can swim towards whatever treatment they have faith in.
I push nothing, on no one, I voice my opinion based on my results and success.
not seem anything coming from any of the other forums that's helpful.
I wish peace for us all, but having an opinion is a blessing for the living, thanks why I pray first for my critics, as they have no clue, where as I do.
tonight I say,
dear god,
heal the critics of ignorance, help them to find effective therapies, also heal my friends and I.
love and peace and no poop,
pete
ps I put up with enough poop on other forums.
if you want to live read
petertrayhurn.blogspot.com
together we can smash this illness out of existence
join the immunotherapy revolution
pete43lost_at_sea 383 Fri Feb 08, 2013 3:34 pm
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he already is a brave young man.
he is 9.
he has more love and strength then all my critics put together.
maybe god is my safe haven!
ps i have the biggest dc vaccine lump ever one week post dc vaccine delivery, a small but significant miracle, along with clear ct, mri, ultrasound and marker fall to 325 from 495 in a week.
so herzog was fantastic today, the bloods he did yesterday, faxed asap to dr kopic, great service team herzog.
i recommend all my doctors, of course, would you goto someone who does not love you and work for your miracle. maybe those at rest did that.
we have our journeys, mine continues
