Cea 3.8 and pet scan clear, post 3447 is my most important by far. "HOPE AT LAST"
https://docs.google.com/file/d/1u1yfZFuumGcHCs0vVBvvMzkPk7S0qSzWLFxRFPnMeveq3pfNwQ9DfPij4_Fr/edit the german medical report detailed, the english is not great, but the results more than make up.
I am filled with gratitude to everyone who has helped me.
To blake, kerry, rodger, lisa, cheryl and jennie and so many others. May they all rest peacefully, as we that are left live peacefully.
I have battled my stage 4 recurrence with lots of therapies and had lots of jokes and ridicule at my attempts.
Well chasing windmills has worked for me and it may work for you.
I have unbelievable news, my terminal illness per the many oncologists, my incurable illness per the doctors well is not on the pet scan any more based on what i understand.
I will post the scan reports and full images tomorrow.
my cea is 3.8 down from 81 six months ago, the normal level is 2.8 on the test.
if you followed my posts and german therapies well you know what has helped me.
I have called about 40 friends, doctors and supporters tonight and thanked them.
tomorrow is see hipec surgeon 8am and oncologist 12noon.
i got the cea and scan result 5pm today from my alternative doctor who said my result is the best cure he has scene in 20 years. we hug and i kissed on the cheek.
I had dinner with the family tonight. i am investing the remainer of the life insurance and retirement savings in the company whose drug i think was instrumental in helping me beat my colorectal cancer.
I am going back to germany to hopefully work at the clinic while continuing maintenance therapy for the next year. thats my dream. its early days, but i am sharing my results for what they are, like i have previously.
I have climbed my mount everest, well i am a few few steps from the summit. its a grand view from where i am sitting. my wife and kids look great.
life is absolutley blooody wonderful!!!!!!!!!!!!!!
persistence and faith has helped me, I have had so much support here and everywhere.
I know what has worked for me, now as opposed to anecdotal stories on the net that many question, my story is real, speeling and grammar errors as well.
I have shared it openly day by day, blow by blow.
I have not had hardcore systemic chemo for my stage 4 illness, i have used the best alternative and integrative therapies and I am here to tell you that my incurable illness is looking vulnerable now, not me.
I am not out of the woods completley. But the woods are looking beautiful, the woods i am refering to are the black forest.
I publisher called today, again about my book, what a co-incidence.
I still have to email my german doctors, they don't know the knews.
Goodluck with whatever you try, my blog is a mess, but its pretty honest, its been added to on the spot.
I suspect my immune system has saved me, as well as faith , prayer, love, diet, exercise, yoga, qigong, supplements, accuptuncture, meditiation, sauna, enemas, juicing, eta eta eta.
thanks again for all the help and support, even your silence and challenging responses has helped.
those few who have been truly caring and supportive well, you know who you are and I will always be grateful.
this is the most joyful post, i have ever posted.
I firmly believe I have found a path to cure for myself for this "incurable illness". Of course I have along way to go. but todays results are the most conclusive proof of effectivess of alternative medicine I have found. Alternative as opposed to conventional.
I make no apology for suggesting evidence based medicine may not hold the cure for colorectal cancer, personalised individualised medicine does. It may hold true for other cancers.
My story is real, my name is peter trayhurn. I believe I have found a possible cure for colorectal cancer. Its a complicated path, but its worked for me.
I cannot wait to see what my onc and surgeon say tomorrow about todays the scan and blood results. I will be humble as always and listen to their opinion. After all I am paying for the consult. Now I may not follow their advice, but I will listen and be respectful. they have helped and cared for me as much as my alternative doctors, as much as the german doctors. All of them together have got me to where I am tonight.
To quote a top class country doctor who I met at the gym while weightlifting
"you are the healthiest person I have ever met with an incurable illness" that was last thursday, 5 days before these magnificent results.
Yes, this is a long road and an evil illness. I am back to germany 4th february to continue therapies and seek opinions re maintenance therapies.
tomorrow between the surgeon and oncologist i am sneaking off to get intravenous vitamin C.
I don't know what component of my excessive regime worked, I don't ever really care. in its synery its worked. I probably was removab and the vaccine and gcmaf. it probably was not the seacumuber smoothies. the sheep brains well who knows.
hugs,
Pete
PS I am off to the sauna to meditate and contemplate gratitude.
If at first you don't succeed, try try again.
PPS my blog
http://petertrayhurn.blogspot.com/2013/01/cea-38-and-pet-scan-clear-post-3447-is.html
Comments
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thanks chelseaChelsea71 said:Wonderful. You so deserve
Wonderful. You so deserve this outcome. You've tried so hard and have inspired so many others along the way. Congratulations Peter.
Chelseathats kind, to inspire others, now thats the greatest achievement of my life by a long way.
A cure for colorectal cancer, for cancer its a dream.
But dreams come true, we walked on the moon, we got the light, who knows what we can achieve ?
If faith counts for anything, well we posted about faith and the immune system a few weeks ago. thanks tony for that one.
If all my stage 4 friends don't have a bit a sparkle when they look in the mirror tomorrow, well i just don't know. I am looking in the mirror, into my eyes, i am smiling a big smile.
I am here, I am going to try and stay here. At least for a few more days, those days will be filled with hope. Whats helped me, may not help anyone else, but at least its an example of a path thats worked for one, it may work for others.
as i said previously, my magic bullet, is a machine gun, with lots and lots of little magic bullets.
the most important is faith and persistence.
thanks again chelsea. doctor vogel "google him" said he would offer me the best quality and quantity of life. he does not say cure, i don't. If I live day by day with no expectation of the future, i place no unrealistic pressure for cure on my doctors. to be painfree, and well enough to live and love is sufficient. anymore is greedy in my buddist approach to life.
to smile and breathe peaceful is ample, its also healing and then i will not take each day for granted or the people i met. sorry to ramble but I am pretty emotional and I have not hit the booze yet. I have promised myself a bottle of baileys next year on holidays. i got this illness on the run and I am not going to let it off the hook.
hugs,
Pete
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thanks jenjen2012 said:Congrats Pete on your
Congrats Pete on your wonderful news! Many wishes for good health to you!good health to you and us all. I am off to sleep peaceful healing dreams. was it removab ? was is it the vaccine ?
was it god ? maybe the answer will come to me in my dreams. you know I started dca for 2 weeks on the 25th december and metformin.
I have tried so many therapies, actually unravelling whats helped is going to be tricky. Sweet dreams everyone from the land downunder.
hugs,
Pete
PS I was going to get bolus 5fu and avastin tomorrow, my onc can keep it on the shelf. the alternative solution was saved by a day. thats just to dam close, i think that must make this an alternative miracle. serious i got the script from my german onc to get systemic avastin and xeloda, but the onc's here prefer bolus 5fu. to save my **** without systemic chemo was always an impossible dream, until 5.30pm today.
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I got a tear or two myselfjanie1 said:PEEETE!!!!!
That is such great news, I am sitting here crying my eyes out. I was laying in bed last night, thinking wouldn't it be great if your tests results came out really, really well. Even better than was hoping. And I think this exceeds expectations.
-J-
dream sweety dream,
if i am wrong i am sorry, but tonight I can dream.
anyone who wants to piddle on this parade well you will be flagged away, sorry but this positive little post will stay that way.
its possible J, it really really is.
don't stop the tears, its been years coming. to many friends gone, lets not think of the pain.
think of this as the best xmas present the colorectal forum has had so far, its just a little late.
do you remember I had a german pet on the 14dec and I still don't have the results, its cost me $2400 euro, i am so happy I am just going to ask for a freebie in another 6 months. this would have been nice for xmas day. but better late than never.
as one on my kindest supporters, a heart felt thanks. baby a little hope stretches along long long way.
according to my research the immune system of the entire colorectal community, at least on csn just got a dam big lift. thats got to be.
say 10,000 stage 4 get this get news, well we boost their NK cells by 10,000 each, just by faith. thats lots of tumour eating NKs. I am just dreaming.
I pushed my alt doctors receptionist to tell me my cea score on the way to the consult this arvo, she said 3.8 and my last was 81. I thought she was misreading it, i thought she was reading the range. which actually is 2.8. funny how my mind could not accept what I was told over the phone. I prefered to beleive that silly receptionist could not read the report and that I still had disease.
I was thinking a cea of 100 would be cool, so yes my expectations were exceeded. to be honest I had no expectations. they are a trap with our curse.
hugs,
Pete
PS I am posting the cea and pet report on my blog within the next 5 minutes, the proofing is in the pudding. read it and smile and taste the pudding!
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Congrats
Congrats Pete.. These results are awesome. I am following your story very closely and always pray for you and your family.
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dont worry very worriedvery worried husband said:Congrats
Congrats Pete.. These results are awesome. I am following your story very closely and always pray for you and your family.
smile a little, heck smile alot. awesome is a another great adjective.
I am staying up late until this melatonin kicks in, I am enjoying the positive replies as my yankee friends wakeup to a very bright new day.
thanks for the prayers, out gods listens, we have hope. this is a recording.
hugs,
Pete
ps wife and I did yoga together tonight, not in bedroom, but in the qigong class with 40 others, at the end of the class i thank master yang my qigong teacher for his guidance, they all clapped. those who were close to me shook hands, i wanted to spread my joyful news, in the real world and the virtual. spread my news if you want. heck we get so few positive anecdotal stories we can have faith in. our world needs faith, especially in the cancer business.
false hope is for the pessimists, real hope is faith the optimistists. I was never going to die without faith, that way cancer never could win, it was beaten from the very first cell. kerry taught us that message. attitude, attitude, attitude.
ps do you reckon i can get back onto good morning america with this survival story, i think its 50/50 i will do a plug for forum 128. did you know i already been their and done that. but it would be fun to do it again.
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Thrilled to read this!
I believe in miracles, in whatever form they come. So thankful you got yours!
Patch
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thanks craigSundanceh said:Congrats on the positive
Congrats on the positive response to treatment:)
we all have a night of glory, maybe tonights mine. i just uploaded the scan pdf and the cea pdf. can you check they look legit.
thanks for all the encouragement and support. its good to be kept honest, don't stop. i need it.
hugs,
Pete
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thanks patchPatchAdams said:Thrilled to read this!
I believe in miracles, in whatever form they come. So thankful you got yours!
Patch
me too mate.
hugs,
Pete
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thanks kathiKathiM said:Congrats, dearest!
...I guess I missed my chance at coffee in Germany with you....but for a FANTASTIC reason!!!!!
I am dancing as hard as I can!!!!
Hugs, Kathi
I am back to germany on the 4th feb, i got a return ticket to use.
I am in the middle of therapies. not counting my chickens before they hatch.
hugs,
Pete
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Sweet news Petepete43lost_at_sea said:thanks kathi
I am back to germany on the 4th feb, i got a return ticket to use.
I am in the middle of therapies. not counting my chickens before they hatch.
hugs,
Pete
Brought a tear to my eye our son got out of hospital yesterday (5th brain surgery) and we are about to start our own adventure (again) we are going out on a limb, coz that is where the fruit is, the techniques we discussed today with the Prof. are 20 years ahead of the game, we didn't raise enough money for all the treatments we wanted but time is of the essense so blood tests tomorrow and next week they will harvest my cells to inject into him.
Don't rest on your laurels, keep hitting the bugger!
Take care.
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That is such great news.
That is such great news. Second only to my clean scan. Heres to continued success thinking outside of the box andpryer.0 -
Pete, Savor the good news.janderson1964 said:That is such great news.
That is such great news. Second only to my clean scan. Heres to continued success thinking outside of the box andpryer.Pete, Savor the good news. Your joy is palpable!
Blessings galore,
Cathleen Mary
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