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Re: Brain Mets information request


JoAnne Shott
 

Thanks for your reply Rod.

I believe where I went wrong is that I followed the protocol perhaps 75% from the beginning- although I never?ate any forbidden foods. ?However, although I followed this pattern for 3 years I did not wait until the tumors were completely gone before relaxing the protocol a bit more. ?So, after seeing my lung mets?double in size recently I have?recommitted?to following the Protocol to the letter until the tumors are gone. ?Interestingly- and I hate?to bring this up - I have read reports of cancer aggressively returning?following Covid vaccines. ?I suppose we will never know if there is a link, but my tumors were completely stable until recently after vaccine and boosters. ?Oh, well.

Doebucky




On Monday, May 16, 2022, 1:59 PM, jpac via groups.io <jpaconnolly@...> wrote:

Thank you Rod I will try artemisia too - I am sitting here doing my oxygen at the moment which has made a difference this week. I have 3 sessions of cyberknife- radiotherapy next week.?

I had forgotten how nice the FO/CC was - so no idea why I let it lapse in 2021.

regards

John



On 16 May 2022, at 18:35, Rod Holmgren via groups.io <s4sindus@...> wrote:

?
Hi, Doebucky. I was quite committed for about a year, following the diet as best I could and all. I healed physically but I was miserable. I suck at being vegan. So I determined that Budwig would have to coexist with the occasional slice of pizza or taco, etc. As long as I didn't go too far I was able to keep cancer at bay and still enjoy life. A few times over the past years for one reason or another I did go too far and symptoms would return. I would then buckle down for a few months and again get healthy. I have tried many things over the years to compensate for my diet. I have recently been experimenting with artemisia annua herb and it has shown promise but I have discovered that there is a great deal of variation in the strength (or amount of artemisinin) from lot to lot with the herb. But that is another story.

I am fairly sure I will be doing a partial protocol, FO/CC in the morning, for the rest of my life. I eat raw cruciferous for evening meal every other day and the other days I alternate vegan and more "traditional" foods. I juice every day at lunch time; apple or pineapple, carrot, celery, beet, tomato, ginger, kale. But I haven't eaten a salad in years. I had a salad with a dressing made from equal parts flax oil, pumpkinseed oil, olive oil and apple cider vinegar for years but I began to gain weight so I eventually stopped and just have juice and a little hard cheese.

I believe in the protocol and if you can maintain the diet restrictions it should heal you. I have always lived by my own rules and this battle is no different. There is more to life than just being alive.

All the best, Rod in MN/USA
On Friday, May 13, 2022, 10:32:58 AM CDT, JoAnne Shott <doebucky@...> wrote:


Rod,

Question from Doebucky (Cervical cancer with lung Mets since 2015). ?Since the time?your cancer cleared up after one year are you continuing with the full protocol or a modified protocol!

Thank you,
Doebucky




On Friday, May 13, 2022, 11:09 AM, Rod Holmgren via groups.io <s4sindus@...> wrote:

Good day, John. Have you continued with the Budwig flax oil and cottage cheese as well as diet continuously even after NED in 2021? I had brain mets when I started BP back in 2015 because of lung cancer and all seemed to clear up within about a year.

Rod in MN/USA
On Friday, May 13, 2022, 03:29:29 AM CDT, jpac via groups.io <jpaconnolly@...> wrote:


Dear Friends

I had Oesophageal Cancer in 2019 -

NED 2021 doing Budwig + HBOT Oxygen +
Mistletoe and Essiac since 2029 but ¡­¡­

Feb 2022 told I have Brain Mets after a seizure playing golf my speech went spent 10 days in hospital loads of tests told I had brain mets 5 lesions and it happened again Apr 9th even longer

biopsy Apr 30 one lesion removed it is Brain Mets ?

anyone come across this before as ECBC is rather rare and they said I had lung mets May 2021 which proved to be sarcoidosis (had it in 1990)

I did read the Pfizer adverse effects reports March? 2022 which states brain mets and sarcoidosis but its done and nothing I can do about the 3 Pfizer in my system

so I am curious about prognosis of brain mets and ways to overcome - I am having cyberknife radiotherapy for the other 4 lesions on May 23rd

anyone with info on brain mets and tips for dealing with it for myself and from a wife and adult children perspective much appreciated

John





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