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"Meredith W." wrote:

My step-dad's brain tumor has grown back according to the MRI, we have
been at the BP for a little over 2 mos. This is so discouraging.

They said he has about 3+ mos to live and they wont be good ones with
no radiation or chemo. Ya know the brain is very different from other
organs...When their is regrowth or swelling it can kill. So
we are trying to figure out whats best. We know radiation only delays
and seals the deal in most cases, so we want to keep going with BP but
there is so little time for it to work...Any thoughts?

Meredith: My nephew was a doctor, he had brain cancer. He opted for
radiation and chemo, at the end his brain was destroyed, cooked, so he
only had mush. That was the description the medical team told my sister
and they told her not to worry because he was no feeling any pain. I
know that for brain swelling Dr Jacob has used DMSO and has saved
patients with that procedure. He is retired now but has trained other Dr
on how to use his procedure. If you are interested, call Jacob Lab at
1-866-375-2262. Also leatrile or Vitamin B 17 may help, their protocol
is fresh veggies and juices, My best wishes to you and step dad. Ursula

Hi Janet

The answer is yes. I've been told there's a link (whatever that means)
between epstein-barr virus (mono) and the lymphoma I have - follicular
center cell NHL. In high school, i had two long bouts with mono and my
neck lymph nodes were like golf balls - much, much larger than they are
now. i dont think i had the lymphoma in high school though. Many
conditions can bring on swollen "glands" such as the flu and other
infections. The only way to know whats in the node is a biopsy. In
many lymphomas, recent research has shown that the "microenvinonment"
within in each node can and does vary. Hence, biopsies dont always
provide useful info of whats going on in the whole body, just whats
going on in that particular lymph node. me personally, i've declined
biopsies and bone marrow extractions.

regards, steve

you wrote:
Can you have an enlarged lymph node and have no cancer there anymore ?

Janet

When do you eat the second serving of FOCC - towards evening or at lunch? You mention when you eat the full 6 FO to 12 CC amount in a day, the nodes are not enlarged. Do they stay un-palpable until you cut back to 3 FO and 6 CC ?

thanks, steve

Hi Dawn,

Any updates on your sister's dog? My brother-in-law's dog had a
hind leg removed a few months ago (due to cancer) and I just
introduced them to FOCC last night; the dog ate the half cup of FOCC
I prepared (he says the dog doesn't have any appetite at all). I
was just wondering if your sister started giving it to her dog and
how he's doing so I can let my brother-in-law know too.

Thanks.
Veronica

"Dawn wrote:

I have been a lurker here for some time and picked up much of your

wonderful information. I now have a dear friend who has a Jack
Russell ( she is the sister of mine) who has an aggressive tumour in
her mouth. It was operated on a month ago and has already started to
grow back and they can see it growing daily and are very upset of
course. I was speaking to her today and suggested she try the budwig
protocol, but she has to start from scratch knowing nothing about it
so I have suggested she joins this list. However, do people know if
this has been used on dogs, and is it easy to get them to eat it of
course. Anyone with any ideas please, would be most welcome.
regards Dawn in SW France

Hi Lynne,
I read your post this AM and a quick flood of tears prevailed as I
quickly recalled this same time in my path with my sister.
I am very relieved to hear that Tim is with so much peace and is
turning it over to God, but also doing what good things he can to
maintain his quality of life. Those are all very important. Barbara's
path was similar, but with a dad and brother in medicine and a
husband in hospital administration, she was not about to venture off
the beaten path in treatment. ;~) There were too many days
spent "overcoming side effects" (in my opinion).
I am glad you are fortune enough to have such a friend to have the
strong will to write such a book, and to have access to it.
I think the Ruta 6 is something I would look into as well. Not sure
if it is homeopathic or naturopathic (not sure it matters), but from
what I remember, it was pretty effective, not expensive, and not
filled with side effects. There is a yahoo group on this, if you want
to see and hear more. I was a member, but have dropped now. I think
it was "ruta 6" but you may have to do a little searching to come up
with it.
I looked into Burzinski a little, but he was so far from Barbara and
Bruce's comfort that for my time, it was futile. That is no put down
on Burzinski, just wasn't for our situation. I do not have any first
hand there.
I am glad Tim has that peace. I hope you and Meredith will as well
(and all the family). While this is no time to give up, deciding to
live well each of his days is a gift that God is blessing him with
and it will be a blessing to you all, too. I think that was Barbara's
biggest gift. The cancer took her life, but her faith was so secure,
that even when she could no longer swallow (food or water), she was
so confident in the love of her Lord that she could be happy and
joyful and praise God. In the end, she was looking forward to being
home. I have no doubt that she is not dead, but is transformed into
eternity. It has never been so real to me as now.
I found my "research role" pretty futile in our family make-up, but I
have a sense of peace that I did "my best" to see if there were any
open doors. The role I did end up with was setting up a CaringBridge
site to keep family and friends posted with updates and to let them
have a place to leave their thoughts, prayers and well wishes. That
has also been a huge blessing. I think a journey shared has the
ability to allow others to learn to live better, although sometimes
it makes it tough in the day to day stuff of life. Everybody does
have their opinion.
God has been in my family's journey and we have been able to "Praise
Him in the Storm." That also became one of my favorite songs during
that time.
I will be more than happy to share much more off line, or lend a ear
as the journey can be hard. If you would like to read her site, I
will give you the link. Most of this will become off topic, but feel
free to email me at mitfost @ yahoo.com (the spaces are to allow it
to come through).
Your note and Meredith's have both made me realize once again
the "why" of these journeys. It is not always that the problem can
be "fixed," but it is to make it better for the next person that has
to deal with such a difficult path. We loose that ability when we
won't share the journey.
Thank you for letting me share.
Your family will continue to be in my prayers for healing (never give
up), for peace, and for eyes to see the blessings in the journey. May
each of you feel the very presence of our Lord surrounding you and
uplifting and guiding you through your journey. I have no doubt that
if this is your desire, it will become your truth as well. "God's
grace is sufficient."
Blessings.
Martha


--- "healwithhands@..." wrote:

Martha,
My name is Lynne and I am the sister of Meredith's step Dad, Tim.

I have been reading the posts faithfully since joining this group
sometime in June, but have only written in response to one of them so
far. Thank you for all of your thoughtful suggestions, information,
insights and encouraging words. A friend of a friend has written a
book entitled "Painless Cancer Cures and Preventions Your Doctor May
Not Be Aware Of", which she sent to me at the beginning of this
journey. (After Tim's 2nd surgery, June 12). She is a licensed R.N.
with also a B.B.A. majoring in Managed Care. Her work in the medical
field along with the loss of three family members to cancer exposed
her to the "horrendous and discouraging effects that her family
members and patients suffered from chemo and radiation " and
she "started to question the appropriateness of conventional cancer
treatment". As a result. she "began an intensive study of alternative
cancer therapies which culminated in this book". After receiving her
book and reading it, I wrote to her and asked her if she knew then
what she knows now, what would she do. She responded that she would
first go on Budwig Protocol and then she would take her loved one to
the Burzynski Clinic in Texas, along with other things. I've said all
of that to ask the question: does anyone out there in this group
know of anyone going to the Burzynski Clinic and if so, what can you
tell me about the experience?

Tim has an incredible attitude, trusting and believing that all of

what he is going through is all a part of God's plan, and is set on
making sure that whatever happens, it all give glory to God,
somehow. He is extremely compliant with the BP and doing his part
and watching what will happen next. He is at peace with excepting
whatever comes as God's will. It's a little more difficult for the
rest of us, though. So, thank you so very much for your caring heart,
support and prayers, as we know that is where the only true power
is.

Lynne Shannonhouse, sister of Tim Shrewsbury
1st surgery March, 2007 (thought it was just a blood clot)
2nd surgery June, 2007 diagnosed GBM stage IV, Glidial wafers

inserted into cavity, no chemo or radiation chosen, started BP

Congrats Eric!!! BRAVO!!! Keep up the good work. Regards,Janice

Ed:

That's FANTASTIC! -- And great news for me and for my husband personally as he is fighting the same disease.

Are you on hormones, at all? How long have you be diagnosed with PC? Your PSA seems very low for you to have bone mets so I am wondering if you have had any treatments at all prior to the BP.

My husband was diagnosed with PC in 2000 with a Gleason score of 8 and no visible mets. He had the Radical Prostectomy in July 2000 after which his level dropped to 0.9 ng/ml. He started the hormone treatment in October or November 2000 and was on them intermittently until June 2006 (at which time they began to fail). When he was on hormones his PSA went down to negligible levels (<0.1). He stopped the hormones and his PSA has now risen to 15 ng/ml as of two weeks ago. He began the FO/CC about the 2nd week in March 2007 but at the same time his oncologist was trying secondary hormone therapy in the form of Ketoconazole/Hydrocortisone that kept his PSA from going up for one month before it failed as well. As of two weeks ago he has stopped all meds. He has gradually been incorporating the various aspects of the BP into his daily diet.

Essentially, his cancer has been considered aggressive as his PSA seemed to double every 3 months in the past when not on the hormones. The Keto/Hyrdo slowed it down, but now we are relying on BP alone. His oncologist wants him to consent to chemo, but he says he will refuse and give the BP a chance to work as long as he has no real symptoms. We go for another appointment today at 1:00pm to see the results of yet another CT scan of his pelvis, abdomen and chest show any worsening of what they saw this past February (which was a suspicious "spot" on one lung).

Any insight into your specific case would be more than appreciated.

He needs some encouragement-- although he has been a real trooper throughout.

Thanks in advance for sharing.

Cynthia

ed bielek <ebielek@...> wrote:
Hello to all,

I'm still fighting prostate cancer with bone
mets... been on the BP diet a little more than 2
months and just had my 3 month checkup. My PSA dropped
from 1.4 to .5 and I couldn't be more pleased.

Fighting on in Apollo, PA






---------------------------------
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Hi Eric, it's Lisa from NY. So happy to hear your
news. I just got back from vacation too, and also
strayed. My scan is mid Sept. We'll see. So hard
sometimes, to stay true, when no symptoms are present.
Anyway, positive thoughts to you with your scan.
Lisa
--- "Eric G. Wruck" <ewruck@...> wrote:

Hi guys:

Had more bloodwork done & for the first time since
my lymphoma relapse

____________________________________________________________________________________Ready for the edge of your seat?
Check out tonight's top picks on Yahoo! TV.

WOW! CONGRATULATIONS to Cony!

What a great testimony and the advice that you gave is not only true, but
priceless in its value toward wellness. I hope that everyone prints that
out and puts it so that it can be read often.

Georgeta what an example of faithful support and coaching you have been to
Cony. That can sometimes be a difficult part to play, but so very rewarding
especially when the outcome is healing.

Good health and well-being to both of you! Your post is an inspiration to
many!

Blessings,
Loretta


Georgeta wrote:
After reviewing the blood test results and the 24-hour urine test result,
doctor told us: no trace of cancer. This was the first time we heard these
words. You can imagine
the joy and the hope we felt.

To all members reading my messages, here is some advice from Cony and
I:
- have faith and do the protocol entirely
- try to give up cancer/pain medications; the faster the better
- watch your environment and make changes as needed to get rid of
chemicals, to filter your water etc.
- stay away from chemo and radiation. The more you do or did in past,
the harder will be to recover because the cells were so much damaged
from those treatments. Chemo and radiation also produce anemia and
weakens the immune system.
- be patient. You need to be patient and let the protocol work on you.

The time to recover differs from person to person. It's based on age
(because ability of the body to recover), will power, fear and worry
experienced, how well and complete the protocol is implemented, type of
cancer, stage of cancer, type of treatments had in past and also how
heavy a person was treated with conventional medicine. Moral support
and the help received (if any) are also to be considered. All these
factors play a role in how fast someone recovers. But with patience and
perseverance, recovery will come.

I too, have often wondered about lymph nodes and why they appear
larger or smaller. How does his relate to he cancer ? If they are
large does that mean that they are more cancerous ? Does it mean that
if the are much smaller that there is less cancer ? Can you have an
enlarged lymph node and have no cancer there anymore ? Like I said in
a previous post, if I only take the ratio 3-6 instead of 6-12, I
notice that my lymph nodes in my neck are much larger.
Take care,
Janet

Re: 3 Month Checkup - PSA score dropped

Well done, another wonderful testimony going in the right direction.

Keep fighting on in Apollo, PA

Michele

Cynthia,

Just yesterday there were 2 positive experiences posted of people overcoming
cancer through the Budwig Protocol. People who we have watched progress in
months, so it is real.

Just read through the testimonials again and then make a reinforced and
informed decision. I do that every now and again to get myself back on track.

Michele

Hi Michele:

I have non-hodgkins lymphoma. Only symptoms now are two swollen nodes
in the neck area. They too wax and wane. There are different
theories what's going on. Possibilities are:

1) Waxing - could be the node filling up with some source of
infection say from dental issues such as root canals, cavitations, or
possibly sinus infections. Or it could be the cancer multiplying.
2) Waning - could be the body/FOCC fighting off and taking care of
the cancer cells, or could be the stuff from the node is being moved
elsewhere in the lymphatic system (and hopefully out of the body).

The MOST important thing is SLEEP. As you've noticed, most of the
waning takes place during the night. That is when the body does most
of it's healing. Quality/deep sleep in a very dark room is probably
the single most important factor in fighting disease. The more hours
you can get before midnight the better (this has been substantiated
numerous times in research). The darker the room, the more melatonin
your body will produce which is also key to the immune system.

My nodes are about the same size as yours. I'm so greatful they
havent gone up in net size, and look forward to the day when they
melt away like the ones in my groin did. And I hope the same for you.

Regards, Steve

Janet,

re the lymph node problem

I am probably being really dense here, but what do you mean ratio 3:6 and
6:12? I don't quite follow what you mean.

Michele

Re: Swollen neck nodes

Steve,

Thank you. That really makes sense.

Keep going in the right direction.

Michele

Hi Meridith,

this is my first post here but I have been reading posts for some time.
Just a word about homeopathy: its much better to go to a classical
homeopath who can take up to several hours to work out a single remedy
rather than taking several different remedies in a "suck it and see"
way. Any homeopathic remedy can help a person to cure their cancer, as
long as it is prescribed for the individual. My mother is on fo/cc and
Homeopathy and very slowly improving after 10 weeks despite being given
2-4 weeks to live. She has small-cell lung cancer with a secondary
behind one eye (not in the brain). Good luck and keep your spirits up.

Andrew

Hi Devon,

Thanks for this info. May I know under which category your book
classifies carrots and beet root?

Thanks :)

--- In FlaxSeedOil2@..., "soundingchimes"
<soundingchimes@...> wrote:

Hi all,

I have a great book called "Fresh Choices" by David Joachim and
Rochelle Davis which is part cookbook and part informative book on
sustainable agriculture. It tells which produce is best consumed
organic and which is okay to eat conventional with minimum pesticide.

I made this list for my own use. I hope that this helps some of you.

Cheers
Devon

Eat Conventional:
Bananas, plantains, pineapples, mangoes, papayas, kiwi, honeydew, U.S.
cantaloupe, Grapefruit, oranges (without peel), lemons (without peel),
limes (without peel), blueberries, blackberries, U.S. grapes,
tangerines, watermelon, plums, asparagus, avocados, broccoli,
cauliflower, cabbage, Brussels sprouts, eggplant, okra, onions, peas,
radishes, sweet corn (non GMO), chard, romaine lettuce,

Eat Organic:
Apples, pears, peaches, nectarines, cherries, red raspberries,
strawberries, apricots, spinach, peppers, celery, potatoes, tomatoes

Check for "non GMO"
Canola, Corn, Soy, Cotton,

Check for "rBGH free" or "rBST free"
in dairy products, choose organic when available.

Hi
My wife is diagnosed with MMMT of the ovary. She was operated on and had
chemo. We turned down radiation and instead she went on BP and has been
on the basic BP (less Essiac tea and Eldi oil) for 2 months now. We
don't know if BP will help in her illness.
Has anyone with MMMT tried BP? I have to know if BP works for my wife.

Thanks
David

Very encouraging to hear such news! Thank you for taking the time
to share, you're an inspiration for us and many more folks reading
these posts who are to come. I was wondering which herbal teas you
make and how do you make this wine/honey/aloe cocktail? Is it taken
from Johanna Budwig's book?

gugu022005 wrote:

Hi Everyone,
Last week we've been again at Mayo for another 3-month visit for my
husband Cony with Multiple Myeloma. MM, being such a devastating
disease, needs constant monitoring. After reviewing the blood test
results and the 24-hour urine test result, doctor told us: no trace

of cancer. This was the first time we heard these words. You can
imagine the joy and the hope we felt......... Georgeta and Cony

Hi Ursula,
I'm new to the group, and I've made my first kraut according to the fast 5 day method. I'm going to try your way now because of the quantity. Can you please guide me. When the kraut is ready - what then. Do I eat it, drink it, and how much. I deduct from the posts that you drink it. How much do I drink per day in ml (mililiters)?

Thanks John

flursula wrote:
Jan: the bubbles are very small if you look closely on the scum you
will see them. Here is the way I do my kraut:
-1 large cabbage cut in chunks
-put cabbage in the mixer with water, give a twirl to shred cabbage
-repeat process until you finish with the cabbage
-put this mixture in a large glass jar
-shred half of a peeled pineapple in the mixer and add to the jar
-add water to fill jar to the top
-add 2 tbls. of sea salt and stir.
I have used a cloth covering or a lid. It does not seem to make a difference in the brewing. I stir the mixture twice a day every day.
I taste it to taste the sourness. I have found out that it is ready to drink on the 6th to 7th day. The longer you keep it out, the more sour it gets. this make a large batch of juice which is fine for me because my husband and I drink it every day. I hope this help. Ursula