Showing posts with label Gerson Therapy. Show all posts
Showing posts with label Gerson Therapy. Show all posts

Thursday, December 4, 2008

A New Possibility

I had a great appointment with my Surgeon, Dr. Cagir (that's him on the left), his Nurse Practitioner, Nan Walsh as well the hospitals ostomy Nurse. Dr. Cagir was pulled into emergency surgery 10 minutes before my appointment, so I met with Nan and Sue. Nan said my body is healed from the surgery and responding beautifully. That being said, my second concern was the possibility of being able to irrigate on a daily basis.

[Reminder: to irrigate is to take a warm water enema every 24 - 48 hours which flushes out the large intestine thus allowing the individual to go without a pouch [sweet!] and instead simply wear a large bandage.]

Nan did request that I speak to Cagir to confirm that irrigation is a possibility, yet she did read the surgery report which stated that I do have enough remaining large intestine to be a candidate for the possibility to irrigate. Yes, only the possibility. It can take one to two years of irrigation on a daily basis to train the large intestine to void once every 24 - 48 hours. And it doesn't stop there. I will then have to irrigate once a day for an hour in order to keep the large intestine trained. And I am fully committed to taking it on.

Sue then followed up with a visual of the necessary equipment used to irrigate and showed me how long and exactly how the process works. Very simple and very similar to the coffee enemas I did while on Gerson Therapy.

Considering I am a young man with lots of life to look forward to, a one to two year wait for the desired results, is a drop in the bucket if daily irrigation will provide me the freedom from wearing a pouch on a daily basis. Hell, I'd even wear a pouch for years if I had a damn near guarantee that it would stay empty until the next morning. And, of course, the large bandage would be ideal.

After my meeting with Nan and Sue, I caught Dr. Cagir on the way out of my appointment (and gave him a big hug - love the guy) and he said I will need to wait until 14-days after chemotherapy is over (in March of aught-9) before initiating daily irrigation. Regular chemotherapy treatments apparently causes consistent irregularity of the large intestine and irrigating would therefore be a waste of time.

He also thanked me for giving him a copy of my Letters to the Prison City CD and suggested I call it Prisons of Cagir. He's a nut. Today's meeting was great. I am very pleased with my new possibility.

Wednesday, November 19, 2008

Relapse vs. Mortality Statistics

At my meeting with Dr. Allerton yesterday, he reviewed with me the statistical probability of cancer relapse and cancer mortality. The analysis was based upon:
  1. Age: 38
  2. Gender: Male
  3. Comorbidity (Health Status - other than cancer diagnosis): Perfect
  4. Depth of Invasion: T4 - Maximum within the stage
  5. Positive Presence of Lymph Nodes: 1
  6. Examined Nodes (following surgical removal): >10
  7. Histologic Grade (Stage):  Grade 2
  8. Stage 3 (I was a stage, but treated as a Stage 3 due to minute cellular presence of cancer cells in one lymph node)
Calculation of risk of relapse within first 5 years 
without current post-surgery chemotherapy: 49%

Calculation of risk of relapse within first 5 years 
with current post-surgery FOLFURI chemotherapy treatment: 20%

Calculation of risk of mortality within the first five years 
without current post-surgery chemotherapy treatment: 42%

Calculation of risk of mortality within the first 5 years 
with current post-surgery FOLFURI chemotherapy treatment: 22%

I then asked Dr. Allerton if the software was able to account for there being no traceable cancer in the tissue removed with surgery and he said it was not. My specifics results are extremely uncommon in the world of oncology so there is no statistical equation for it. It's pretty much a random occurrence in their world.  (Gerson Therapy, BABY!!! Thank you everyone for your support. xoxo) However, he did provide say that considering the 100% disappearance of cancer from my system, the risk of relapse or mortality is even lower. I didn't ask him for a number, but I say it's down by another 50%, putting it at 10% relapse and 11% mortality.

I have to be honest - 10% ain't perfect, but it's pretty damn good when it comes to cancer. Yesterday was a good day.

Wednesday, November 12, 2008

The Beautiful Truth

Below is a link to a trailer for the new film on Gerson Therapy and the modern approach to healing cancer. The trailer is quite short, just click on the image below.

Tuesday, October 14, 2008

I'm Back

In case you're wondering, I haven't posted much lately because I wanted to keep the WELCOME entry visible to any new readers who found out about the blog via this recent series of articles that we were fortunate to have in three different newspapers.

Well, it seems the blog address only made it into one of the three papers, so there weren't very many visitors. And just imagine - all this time I could have been filling your ears with multiple entries describing how miserable I've been feeling.

Just kidding!

Don't get me wrong. I genuinely appreciate the articles in the paper. In fact I'm thrilled about them - informing people about the benefit, my CD, and how happy we are about my positive progression throughout this diagnosis. Not to mention the opportunity to acknowledge all the wonderful people who have contributed to us in so many ways. It's just that my intention with this blog is to reach as many people as I possibly can. Which I will continue to do.

Anyway, I am happy to inform you that I have been taking regular walks with with Daniela and Beau (and Max our dog, too) and enjoying this absolutely gorgeous Autumn weather. It seems like a nice thing - going for beautiful Autumn walks. Actually, it's absolutely incredible. I was put on bed rest essentially the day I got to BajaNutricare: May 14, 2007. And when I ended my Gerson treatment and began traditional treatment, I was in too much pain to be anywhere but on the couch. And then there was surgery recovery. It's still a new thing to be going for walks. I LOVE IT.

Not to mention the turning of the leaves which is such a treat every year. Each years Autumn always comes as a surprise to me. Not like I'm surprised that it happens, but when I see the pinks and brilliant golds, I always wonder, "Were they that beautiful last year?" Just amazing.

So, I have had a cold which started on Sunday October 5th and was finally gone in time for the benefit. As a result, I also got to see our 10 year olds soccer game on Sunday [Tie: 3 to 3] and go shopping with Daniela & Beau which hasn't happened in...two years? It was definitely worth missing a little football for that. And now my cold is back. In my ears, nose & throat along with a side order of body ache. So, I emailed Dr. A (my chemo doctor) a request to post-pone my chemotherapy treatment until I'm feeling better. Shortly after, I received a call from his office letting me know my appointments for this week have been rescheduled for next week - same Bat-Time, same Bat-Channel.

I am quite relived. It was not a good feeling knowing I had an appointment for more chemotherapy while I'm feeling lousier than I have in the last few 10 days. That stuff takes a toll on the body and I'm in no condition for more right now. So, it's all rest, fluids, fluids, fluids and food. Man do I get hungry when I have a cold. And with a healthy serving of Tabasco Sauce on my evening snack,



thank you Kevin & Claire for a fantastic wedding favor

my sinuses are not as nearly stuffed up as they were a few hours ago.

Friday, September 12, 2008

My Chemotherapy Tretament Has Been Scheduled

My chemotherapy treatment has been determined and is scheduled to begin on Wednesday September 17, 2008. Dr. A asked when I wanted to start chemo. I told him never. He smiled and I said, "How about as soon as possible. The sooner I start, the sooner it's over. Not to mention I want to be certain the cancer is gone for good."

The regimen will consist of twelve treatments administered every two weeks for a total of 6-months. 6-months is not what I was hoping for, but it's what the doctor recommends so that's the plan. The treatment is a 3-day process consisting of a 2-hour infusion for day one and a 2-hour infusion on day two. At the end of each day's treatment, I will be sent home with a pump directly connected to my port infusing 5-FU. On the third day I will go in to have the port removed and I will be done for another 11 days. On the fourth day, I will receive an at home subcutaneous shot called Neulasta to stimulate the production of blood cells lost as a result of the chemotherapy.

The treatment will be a slightly different cocktail than the last two because the previous cocktail caused neuropathy in my hands and forearms - the sensation can be permanent and we want to avoid that as a potential outcome. Instead I should expect some nausea and serious lethargy. When it comes to the side effects, I continue to remind myself that as a result of following Gerson Therapy with chemotherapy & radiation, there is no trace of cancer in my body or the tissue that was surgically removed. And that kind of result - at least in the experience of my surgeon and oncologist - is unheard of. That combined with the beautiful faces of my wife and children is likely all the encouragement I will need.

Monday, September 8, 2008

giving thanks...


hello blogworld! daniela here...for this first monday entry, i first wish to thank a large handful of people who made this whole journey for the past 18 months a possibility, and a successful one, at that. it has taken the help of so many people to make this path a feasable one...i will apologize in advance if i have forgotten anyone...this journey is the sum of the efforts of many,many beings...some visible, some i'm certain of the spirit world, and others belonging to the realm of the Divine...with the lines between all three realms being fuzzy, as many of you we saw on a weekly basis clearly have hidden wings...

fran & my dad: for your limitless love, kindness, empathy & support. you have been at cause for the greatly reduced stress on all of us, especially for the kiddos. the additional miracles bestowed upon us by many others would not have had the space to show up in, had it not been for your ability to deeply empathize with us & to then step into action... because our income went from "ok" to a few dollars above "zilch", we were able to stay in our home. may your profound generosity be returned to you both in infinite ways...

bert's mom & step-dad: for faith in a tough path...for weekly journeys to b-dale..for financially making the benefit-miracle happen, even with the risk of the miracle possibly not happening...(even though it did!!!)...for your caring, sweetness...for your help with carrots, greens, washing, drying, rolling...(is it coming back to you now???xoxox)...for your infinite love, your care, and help...for a dishwasher!!!! for a food processor!!!! you made our lives easier...for the airy fairy swing, which provided beau fun while i made more juices!!! you are loved & deeply appreciated...

little peanut: for rolling with a whole heck-of-a-lot, with smiles, hugs, and sweetness. i love you sooooo much...

viv & kevin: for making it possible to have live in help when we needed it, right after bert returned from mexico. for your words of encouragement, for your late night talks with bert when he was the mad-insomniac (i could always tell when he'd talked to you because his spirits were uplifted), and for all the hassle & inconvenience that goes along with schlepping yourselves all across the country to come see us, multiple times...thankl you for getting 'in our world' on so many occasions, and really making a difference...xoxo

kiff: for all that goes along with making trips out here happen...for being the most amazing brother he could ever have...you are so loved...

buck & juliana: for your faith, support, and help...you are both 2 amazing people, and we are so blessed by having you in our lives...

sheila: for limitless motherly love, support, and sweetness...

david mcilroy: for help when we desperately needed it...thank you to you & julie...for your support even though this path seemed nuts!!

ingrid & erich hess: for your assistance when we needed it, and your deep love and prayers.

manfred odendahl: for your love & gifts which made a difference

steve & adrienne hopkins: for all of your positive support, encouragement, and generosity

chris stadlemair: for being an extraordinary human being. going to mexico and helping to save my sweeties life. thank you will never quite cut it...

jackie gartenmann: for tons of laughter at times when it felt like the boat was sinkin', fast!!! for one juice after another...for living with us & still liking us afterwards!!

kate lunde: for being nothing short of a bona fide angel...you got us through one of the hardest months during this whole journey. forever grateful to you...

maryam: for your earnest efforts and huge heart

meghan vanloon: for pulling bert through some tremendously painful moments. you were a lifesaver.

neil weinberg: for donating your lunchtime to come out to B-dale & help bert with pain management

sally ramirez-warren: for your Divine love & generosity...for your angelic voice....your radiant smile...bless you, sally

tim smith: for being a beacon of light when we came upon several crossroads...immense gratitude to you...for recommending paul bruntion's, the wisdom of the overself...for helping to make sense of it all...blessings to you...

michelle newhart: wow...hard to figure out where to begin...first, for being the cause for the success our benefit...you made that all happen...for your tremendous generosity of time every monday & thursday night, coming out here to make juices, prep veggies, and clean...for your love, friendship, and inner radiance. you are simply one of the most amazing people i have ever had the honor of knowing...thank you, michelle.

sue cosentini: for your wit, humor, love & generosity...for driving out here at 2am to keep the generator going...for being an amazing friend...for an awesome garage sale!!!! you are one unstoppable woman!!!

anke wessels: for your enthusiastic support, generosity, and authentic tears of joy when we met our goal at the benefit.

tess lawlor: for being the genuine calm in the middle of a category 5 hurricane, those first days bert came home from mexico. i'll never forget looking you in the eyes, and all you saw was my sheer terror at trying to figure out how to turn our home into a gerson factory. you joyfully and calmly created a miracle in our home...for creating the most delicious alkaline carrot cake...food of the gods. for your bags of alkaline cookies...for your all out deliciousness!!!! xoxo

john suter: for shopping every saturday for us. for donating valuable chunks of every time every weekend. for managing huge produce orders, and always having a smile at delivery time, and encouraging words. for your generous 'discounts' at reimbursement time....you were such a huge contribution...

patty & jerry; for your dependability and many, many hours of time spent here at the house washing carrots, greens and playing with beau. you are an angel...for helping plan this next benefit!! jerry, for all your driving to & from sayre...and for all your good "VIBES"...xoxoxo you are both huge heros to us.

sparx & jen: for support, love, and friendship. your talks with bert really pulled him thru some tough, dark moments. for your generous contributions...for our kitchen table...for bert's recliner....multiple rides to sayre, coming from auburn...visits...you are both just amazing...

ann harch: for generosity, support, supplements, and love...for hour long talks about health, reiki, macro, and oodles of laughter. you are such a kind spirit....a blessing to be friends with you.

carol crossley: for your belief in our path, for your generosity, and love, which could be felt very strongly here, despite an ocean between us!!! for EFT!!!!!!!!!! we love you...

don blazely: for such thoughtfulness regarding our family, and the CCR tribute show. i'll never forget the day you called outta nowhere...you were truly an answer to my prayers. we are deeply grateful to you.

emily hunter & the sweet land farm in t-burg: for long drives from tburg to bdale with oodles of the most gorgeous produce EVER, you were lifesavers, and truly generous...thank you so much...

dustin & michelle stuhr: for being such a dear soul to bert...for the americana jubiliee...for caring so lovingly for leo...thank you thank you thank you

jen bubel: for a new friendship that i know will be forever...for your love of our family, and your sweetness...for your generosity...for putting huge smiles on our children's faces...we love you deeply.

cuqui: for being my anam cara

ion birch: for patiently, and generously helping me on a 'greens' day... xoxo

carl, our neighbor & mailman: for snow shoveling many times before i was up at 5:30...many, many thanks!!!

the kingsleys: for your generous skill & contribution to the benefit!!!

kristin campagnola & jodi peters: for all your assistance, after i left IMS....for hosting the benefit...for never ending support and kindness...

andrea riddle: for deep insight, empathy & compassion...thank you...

tony pain: for making something unobtainable become a workable possibility...thank you...

marne & ben: for limitless smiles, check-ins, and being our compost godsends!!! for picking up 5 gallons of compost every day for over a year.....bless you both!!

marne & ira: for being a champion for bert...for bringing avi & michael into our lives...for your faith, trust, and love, we are forever grateful

mitch bobrow: for your wisdom & grace...thank you...

marli stahler: for being Divine sunshine on days that, at times, felt as if no rays could possibly penetrate thru thick clouds...

adrienne mcnair: for practically living with us at one point, when we needed so much help. for your beautiful smile, cheerfulness, and kindness. your multiple rides to sayre...you were a lifesaver. thank you....

sigrid kulkowitz: for your fantastic music cd's for bert! for just showing up when we needed it the most. for giving us the opportunity to really get to know & love you! we miss you!!!

jenna robarge: an answer to our prayers...showing up daily, even at 6:30 am to wash chard & beet greens...scrub carrots...learn to make juices, all at a time when you were getting ready to move across the country!!! we will never forget such extraordinary generosity....we miss you, jenna....

deborah simms & george: for being angels who also showed up at a time when extra help was needed!!! thank you for loving beau so sweetly. thank you for driving out to the hospital when i broke my toe!! thank you for cleaning out the shed!!! bless you both....

chad novelli & jonathan panzer: your generosity & kindness via the many trips to and from sayre...

kati andressen: for your great sense of humor!! for your angelic voice that hypnotized beau...for washing oodles of greens & carrots...for helping us thru the "broken toe days"...we love you!

mary anderssen: for being a real-deal angel...for helping with maxi-poo....for opening your home to our little guy...you are all a second family to him. we are in deep gratitude to you & rich. namaste...

ally burch: for your grounded energy, that was contagious. for all your love, and belief in what we were doing...xoxoxo

adrian lucas: for having such peaceful, calming energy...for drawing bert's blood monthly, and schlepping it over to the lab for analysis

christian prysgaki: for helping bert with massage, especially when he was in terrible pain.

kevin kinsella: for being nothing short of true 'family' to bert...

rob & kelli: also for being true family to bert, and for kelli's delicious dal, and for being extraordinary friends

mr & mrs verity: for finding a fantastic sandbox for beau to play in, which gave him hours of enjoyment!! thank you...

lindy cummings: for your sweetness, grace, and peacefulness in our home

marion deats (rain): for being front & center of the cheering team!! for your empathy, thoughtfulness and kindness...we thank you so much...xoxo

catherine martinez: for your wisdom, humor, and genuine friendship...i love you

jane schantz: for your peaceful centeredness, your knowledge of homeopathy, your support in sayre, and friendship, i love you! thank you...

karen schantz: for just showing up when help was sooo needed,and for giving beau fun, love & smiles!

avi baumgold: for all your sweetness with beau...you were a miracle at a much needed time...

michael margolin: for your shopping, your generosity, and enthusiasm...thank you so much...

sim redmond band, pasa fino, hank roberts: thank you for contributing your time, and artistic gifts at our benefit. you helped make that massive miracle possible...

john ryan : for taking on the huge task of getting a stage to the scene of our benefit...thank you so much!

wegmans: for bagging up our groceries (5 bags worth!!) , in advance, on wednesdays...for being so helpful thru very tough times...thank you

greenstar: providing us with a juicer while we awaited the arrival of the Norwalk juicer...for getting granny smiths when no one else could!!!

charlotte gerson & dr cervantez: for carrying on a legacy...for saving robert's life...may you be blessed...

dr cagir, dr allerton & nan walsh: for your dedication, care, and skill...for saving robert's life...may you all be blessed...

the following people i thank because you all helped with contributions at a time when it was looking terribly grim...you helped without hesitation, and very generously...may kindness return to you as well...

susan scott
mario cerame

karen maslinak

laurie smith

larry ulfik

ed smith

phil fergueson

pat & julie walsh

rick emmanuel:
for support, empathy, and thingking of our kiddos...xoxox

linda stout: generous & supportive reporting...namaste...


...it's amazing that having cancer does not have to mean "going down a road alone" . we were, and still are, blessed beyond my wildest dreams to be supported by this whole global community...ask and ye shall receive...in abundance.

in deep gratitude,
daniela


Friday, August 8, 2008

One Heck of a Day!!!

First of all I want you to know I came home from the hospital at the end of the day on Thursday. However, it was one heck of a long day...

The day started with a CT scan and a blood draw for lab work as scheduled. Then Daniela & I took Beau to a playground where we played with Beau then had a little lunch since my next appointment wasn’t until 1:20 PM with Dr. Allerton (my chemotherapy doctor). At the meeting with Dr. Allerton, we discussed the different chemotherapy options which he said said he would not start up for another four to six weeks. After that was discussed he told us he was amazed the cancer was gone. He kept saying different things like “I’m amazed - I don't think you understand how rare this is- We don’t see things like this – None of us thought this was going to happen. A T4 tumor usually involves some major difficulties...” he repeated these sentences a number of times and when he finally let up I said, “Feel free to say anything like that as long as you like – as long as it’s true.” He smiled and I let him know I believe it’s a result of the Gerson Therapy and explained my theory that due to such low toxicity in my body, the chemo & radiation were far more effective.

Once we wrapped up in the exam room, he walked us to one of the administrative desks to set up my next appointment. What followed next amazed me. Now you need to understand that Dr. Allerton clearly has a great sense of humor, but as far as the emotions go, he keeps things quite professional. Given he’s that kind of guy, I went to shake his hand and say thank you and instead he said, “Let me give you hug. This is amazing.” Coming from him. A guy who sees the worst of it every day and knows the odds, it felt pretty darn good to get that hug from him. I feel like I’ve won the Triple Crown.

Following the meeting with Allerton we went to Dr. Cagir’s office to discuss the results of the CT scan. The CT scan showed the fluid was still present and the recommendation was to drain the fluid from the suture area and send me home with an antibiotic prescription. Naturally, I asked what the process entailed and it was explained to me that a needle would be pushed through my behind and into the cavity where the fluid was building up so it could be drained. Once drained, it would be determined if the fluid was infected. If infected, a drainage catheter would be installed and I would be sent home on an antibiotic with catheter to be removed in a week or two. If not, I would simply be sent home on oral antibiotics.

Well, the fluid was drained and I was sent home on an oral antibiotic. HOWEVER...

When that doctor told me he was going to stick a needle through my behind and into...some cavity...my mind was spinning like a top. I could barely think straight. You’re going to stick a needle all the way through my butt? Okay. I won’t pretend. I don’t exactly have a whole lot of butt to go through. But my butt’s my butt. And I would prefer to NOT stick needles THROUGH IT. HOLY CHRISTMAS. I said, “Doc. I want this to work well for all of us. And the idea of a big ole needle getting pushed through my butt.... I am FREAKING OUT. If I flinch while you’re doing it. Man-oh-man.”

Yeah folks. Forget humility. Forget pride. This guy was going to impale me with just a little numbing agent to ease the pain. Yes I said impale me because in my world that’s exactly what he was going to do. I must have confirmed with him and his staff at least 53 times that they were going to sedate me. And I must have been white as a ghost because they sedated me - heavily. Hell, I woke up on the couch on Friday morning and Daniela had to remind me what happened the day before.

Needle through my butt and into the “blah-blah-blah” cavity. No, no, no, no, no. Say it ain’t so!

[note from wifey: bringing bert home last nite was memorable. the nurse who wheeled bert out to the curb left us with the instructions to relax, take it easy, do nothing strenuous...so bert immediately says he wants to go for a walk when he gets home & is that ok? she said "what kind of walk" (she was suspicious, clearly, so wisely inquired further). he then says, "i like to go about a mile or so".

now, keep in mind, he's on MAJOR painkillers, and just woke up from almost total sedation. downright loopy, actually, and now declares he wants to go bloody HIKING when we get home??? we've only been at the hospital for about 10 looooong hours, had minor surgery, and next we're up for HIKING??? i shot the nurse a look that begged " please god, not hiking..." so she says he can only go for a short walk with someone...

so, we proceed out to the car, with bert telling me he's going for his walk anyway, and does not need assistance. i had images of me out in the fields up by our house trying to find bert, only to discover him laying in some field, claiming he can now communicate with crickets...

we began to head home, and he's fully outta his mind. just yammering up a storm, about nothing that mae too much sense. next he wants pizza. we stop at Sopranos Italian market, and i said i'd go in for him. he says, " i can do it myself, i'm not sick you know!" so i said fine, go ahead...he comes out with a large bag...i'm trying to figure out what's up with the bag?
"hon, what did you get?"
(big grin...) "apple pie!!!"
"how much hon?"
"the WHOLE PIE!!!"

when we got home, he remembered the walk...i had to lure him onto the couch for a minute, thinking the mystical powers of the couch would beckon him to sleep. thank goodness for mystical-couch-powers...worked like a charm....zzzzzzzzzzzz]

and to cap it all of, bert opened the fridge this morning, like a little kid at christmas morning, and says to me, "WHO GOT PIE???????????????"

Tuesday, July 29, 2008

Gerson Flashback???

It seems I took the weekend off from blog posting. By Sunday night my hope was to post something on Monday afternoon (yesterday), but at 4 AM on Monday morning I woke up to intense abdominal spasms. By 4:30 AM I took a Vicoden and sort of fell back asleep. I eventually woke up around 8 AM and spent all morning and early into the afternoon reeling from the pain. If I was on my back, the next spasm would have me on my knees and leaning over the back of the couch or on my knees and bending down with my head on the cushions - the way a newborn baby sometimes sleeps. Eventually, I would wake up in one of the said positions from another spasm and either turn over and lay on my back or my side in hopes that I would fall asleep before the next spasm came. I felt like a slow moving rotisserie chicken, minus the heat of course.

And the toughest part about it was that my brother, who I haven't seen in over a year, was in town for only 24-hrs. He arrived Sunday at 2 PM and we had lunch with our folks and then he left around 4 PM on Monday to have dinner with them and then see my Mom's performance at the Merry-Go-Round Theater in Auburn. Not how I hoped our visit would go. Our relationship has grown so much since our adolescent years where being right about...whatever...was more important to me than the little bit of compassion it takes to have a great relationship with one heck of a great guy. The best part was when I attempted to eat some cereal to help my stomach tolerate a dose of Cipro (antibiotic) - prescribed for what seems to be a UTI resulting from the catheter I was blessed with for most of my hospital stay. I got about a half a bowl of cereal in my belly before my stomach decided it would be happier empty. Yeah. I have to say that vomiting just short of two weeks post-abdominal surgery with staples in my abdomen isn't exactly a recipe for a good time. I rarely consider the feeling of someone taking their hand and gripping onto my abdominal staples and pulling as a fun. Then again, I've been considered a bit odd now and again - maybe it's just me.

Anyway, by mid-afternoon, Daniela decided to call my surgeon's office for their input. She had talked to me about it earlier, but since I had no fever, chills, etc., etc., I asked her to just give me some time. Well, once I threw-up we both agreed it was a symptom worthy of a phone call. After a short conversation with the Nurse Practitioner in Dr. Cagir's office, we agreed it was a little less than a "blockage" moving it's way through my intestines (not uncommon post-intestinal surgery) or possibly intestinal spasming. During our second conversation with the NP, she and I agreed I was dealing with intestinal spasming. It seems my diet was a little too rich when the family was here.

PAUSE - This is like a Gerson Therapy flashback: intense abdominal pain for long hours. Man. I had hoped those days were over. Even Daniela felt like we'd gone back in time to the days of the Gerson detox flareups.

By 6 PM, I was on strictly clear liquids and the spasming had seriously diminished, but it was still there a little. So, at 6:30 PM, I took some Milk-of-Magnesia and got everything moved out a little more quickly. The spasming naturally increased as I had anticipated, but I took another Vicoden and after about half-an-hour and a few very difficult spasms, I found myself peacefully relaxing on the couch watching the Red Sox (loosing unfortunately). The point was to move through whatever was triggering my intestines and get it out of there ASAP.

By the way, you may be wondering how sports ever found its way into this blog. Well after 13-years of living without cable or antennae, we decided to take advantage of the local cable company's internet/telephone/cable deal - same price as what we were paying for internet and phone - you know how it goes. With all my "rest" and pain management, hockey playoffs into basketball playoffs into Summertime baseball has been the progression. As long as I stay away from television drama, I can control my addiction to the "boob-tube," which explains to you why I chose to be without it for the last 13-years. Some people find they can't stop drinking alcohol once they start. I have the same difficulty with drama TV. Some may say I'm "still using" even if I watch TV,
but there's nothing like a good ball game to keep me clean.

When I woke up today, I was a bit hesitant to move too quickly - concerned about another bout of abdominal spasms. Fortunately, I was free of such problems. On Monday night, the Milk-of-Mag moved the last of whatever was causing the spasming right out of my system. A
nd I ate very conservatively today. I'm going to ease food back into my body.

Oh. And most importantly, Dr. Cagir requested I have a CT Scan on Thursday, along with my previously scheduled appointment to have these staples removed, just to be sure all is well. I'm told I will feel much better once these metal hooks are out of my belly. I'll let you know.

Saturday, July 12, 2008

Surgery Recovery

I left out that surgery recovery will be six-weeks. They want me up walking around the day OF surgery if I have it in me - made possible by an epidural - but apparently there will be no heavy lifting or a slew of other things (for which I'll likely get the full list on Wednesday afternoon). There goes joining the local Australian Powerlifting Team any time soon!!!

Which reminds me, I have gained 24 lbs. since I stopped Gerson Therapy last March. It still amazes me that a fellow patient actually gained weight on Gerson Therapy while I on the other hand was slowly disappearing. Well, once I gain another 16 lbs, I'll be back up to a reasonable weight - as long as it's muscle I gain.

Sunday, July 6, 2008

Just Around the Corner

I felt great today and I have to tell you it's strange to feel great. What I'm used to is either having one hell of Gerson Therapy detox flare-up or the horrendous side effects from the chemotherapy & radiation. I am without any of that. Oh, it's great and I love it. I'm not saying it's not. But it's definitely a new experience when I compare it to the last year or so.

On Wednesday July 9th I go in for a pre-surgery CT scan followed by blood work and a visit with Dr. A - my chemo Doc. That should be pretty uneventful as long as my counts are good. I am imagine they will be. Like I said - I'm feeling great.

On Thursday July 10th, Daniela & I will meet with Dr. Cagir - my surgeon - and discuss the plan for my surgery on July 16th. We'll also meet with a Nurse Practitioner (whose name I don't recall at the moment) who will provide me with all the information I need about managing the colostomy.

After that, I will relax for four days. On the fifth day - July 15th - we will celebrate Daniela's birthday!!!!!!!!!! And in addition to the WILD PARTY we're sure to have, I will begin my pre-surgery prep. I will only drink clear fluids for the entire day along with enough laxatives to keep an elephant home from work!!!

Oh YEAH - good times. Hopefully I will be able to make it through all 15 seconds of "Happy Birthday" without having to excuse myself from the room in order to complete my hundred-n-forty-seventh trip to the bathroom. I suppose I could leave the door open and sing a little louder. Then again, maybe we should just celebrate her birthday on the 14th this year. She might like that a little better.

Monday, May 28, 2007

Reflection

I have traveled to many places in the United States and a few spots across the Atlantic and I have never felt homesick. Today I am homesick. I sat on the beach within feet of the Mexican border fence just watching the people on the side of the United States and thinking about how far away those few feet really are. It's amazing to look at my home and not be able to to simply take a few steps and be there. There were children on the Mexican side of the beach walking through the holes in the fence to the United States. Then they turned around and ran back to Mexico. The border patrol was watching them and an American woman walking on the U.S. side. A fence...hmm. Wow. Reality check.

Right now my legs ache, my back aches, my head hurts, my stomach hurts, I miss my family, I miss my job & being at work with all my residents, I miss my friends and neighbors, and going on walks with the dogs, and I'm sick of eating the same damn thing every day - vegetables. I'm constantly craving meat and cheese with the cheese melting all over the place with a nice side of bacon. Mmmm, and a milkshake. And a coke and roast beef sub from Wegman's with too much mayonnaise. And a cheeseburger. Man, oh man. And, there's no way on God's green earth that I would eat anything but what's on the Gerson diet. Restraint is not the problem, but the cravings are a bitch.

And I can not wait to hear people speaking English everywhere I go. Don't get me wrong. I love being around people speaking Spanish and experiencing this country AND, the language thing is a constant reminder that I am not at home. I am more than ready to be at home and I am definitely counting the days.

Sunday, May 27, 2007

Update/Reflection

The pain in my knee is GONE. My legs still ache today and they did a bit yesterday as well. Yesterday was a nightmare. Emotionally I was way, way down. I was cranky, grumpy, impatient, angry and exhausted. Yeah, a real joy to be around. They told us to expect it. Then at 10 PM, like the flick of a switch, I felt great. Unbelievable. I turned to Chris and asked him how his day went. Up until that point, I couldn't see past my own nose...

Today I am experiencing body-ache, like a lousy cold without the ear, nose & throat symptoms. Also very little energy. Two hours ago I felt fine. I stepped out into the courtyard and stood in the fountain for a little refresher. I looked up and the kitchen staff were looking at me saying "Roberto es LOCO!" The pool is not warm enough. I will ask them to turn up the heat one day before I go.

The kitchen staff are the best - Chris and I agree on that. They are the angels of this place. I finished a song for a woman named Lola and sang it to her last night. It was a lot of fun. We will definitely miss them. Not to mention they're masters at cooking the Gerson meals. We'd sneak one home with us, but their children would have to come and the house is just too small (and I suppose immigration might have a small problem with that).

Marguerita just delivered my gruel to me and asked to see the family photos. They love to see our pictures of our families and Marguerita always asks how the babies are.

Monday, May 21, 2007

Reflection

One factor I have mentioned very little is the companion. Chris Stadelmaier is my Gerson Companion - all Gerson patients must have a companion for the duration of the stay here at the institute. Chris's girlfriend Jackie is at home without him when his presence there would make a difference to her - Thank you , Jackie. Chris's mother whom he is very close to and sees regularly is at home without him - Thank you, Mama Chris. Chris is in business for himself and all of that is on hold while he is here with me. Chris eats an almost exclusively raw diet which he has had to adapt while he is here since very little of what he eats is available at the Gerson Clinic. He has put his life on pause so that I can heal my body a purely natural way and live to see my children grow with my incredible wife as we grow old together.

It is a huge undertaking to be a Gerson Companion. Chris has little time for himself and the time he has is not of his choosing. He finds time for himslef when my needs have been met and at this point the doctors have me on only about 60% of the standard treatment. Because the tumor is in the rectum, they are starting me slowly. A rectal tumor is vulnerable -it's exposed, so things need to start slow. Chris will be taking on more in the near future. It's not that I couldn't do all of it on my own, but healing does not happen with Gerson therapy unless the patient is resting CONSTANTLY. So, I am required to rest throughout the day. Some days I am too tired or sick (from the detox) to go to the dining room, so he brings me my meals. He makes sure I have remembered to take my supplements, which I forget when I am out of it or sick (again as a result of the detox). Chris prepares the enemas and he cleans the bucket and tube when I am done using them. And when the enema, let's say, doesn't go so well, he cleans it up without a word. To say I am humbled by his generosity and kindness barely touches the surface. I have yet to find the words to express my gratitude.

To comprehend my gratitude, close your eyes and imagine tears running off my face faster than I can wipe them away. I am deeply moved by who you are, Chris. I will be present to love and gratitude for you for all of my life time.

Love Bert

Saturday, May 19, 2007

Reflection

During the morning I felt great. I wrote a song for one of the staff - she requested it - although her request was in Espanol and she had to ask me a couple of times before I understood her. I am at the point where I am just beginning to understand a ridiculously small amount of Spanish. I catch a verb and a pronoun and start to pull together what's being said. There's no chance I can repeat it...yet! So I threw together a sweet little tune about what a nice job she does and her beautiful smile - all in Espanol. That was a challenge! It's kind of hard to remember the words when I've never used them in my life. I will sing it for her tomorrow.

I never thought I would be looking forward to coffee enemas!!! They provide SO MUCH relief when I'm going through a flare-up. "Who'd a thunk that?" (quote from Dave Wheeler...Pittsburg '92) addressing Brotha D. Sorry. That last entry will make no sense to you if you weren't at Deer Creek with us in '92. On that note, God Bless the Grateful Dead Family. We love you Jerry!!!

Oh yeah, coffee enermas. Who would think I would be so looking forward to them. Before Gerson Therapy, ALIEVE would of done the trick just fine. No more. Now I do coffee enemas to get rid of headaches. And the worst part is that laughing makes them very difficult to retain. And trust me, there's a laughing going on during the process. I won't share any of the things we say on this blog during these enemas. Your mother might be reading this!!!

Thursday, May 17, 2007

Reflection

Yesterday I went to the beach. Juan the maintenance man gave me a ride. He dropped me off and I sat for a while and was met by Chris Stadelmaier (my Gerson companion) and another guest and two other companions. It took about 15 minutes for me to be captured by the motion of the sea. There's a lot of letting go here at Baja Nutricare. Letting go of the desire for comfort food is the easy part. Letting go of my active lifestyle is a little tougher. Gerson Therapy requires REST REST REST. I feel a little stir crazy, not being able to walk, but I guess I'll get used to it.

So there I was at the beach - irritated, uncomfortable, wishing I hadn't gone. It seems it's all a part of this process. Letting go of how I've done things for most of my life. So, I thanked my feelings for sharing and looked back out onto the sea. Then it captured me and I would have stayed for hours given the opportunity. But considering it would have required me to do a coffee enema right there on the beach, I opted for a timely return to the privacy of my room. As we left, I hoped we would see more dolphins and far more play on their part. The few dolphins we saw were not launching out the water (apparently they were yesterday). Instead they occasionally surfaced and soon they were gone.

I am learning rudimentary Spanish (having "studied" it in college may be having a little impact - but not much!) Didn't do so well at the ole Espanol. We have fun with the staff though. Many of them know little to no English, so we teach each other.

Wednesday, May 16, 2007

Reflection

It's been just over 36-hrs and I'm beginning to find my place here at Baja Nutricare. Arriving was different than I had anticipated. I didn't feel excited when I arrived, I felt resentful. I was annoyed with the other patients and their companions as they relaxed in the courtyard, smiling and talking. I didn't know why, but I was bothered and I wanted to be alone and away from everyone. Once we got situated, I realized that the transition was just a lot for me in such a short time. I questioned if I had made the right choice - like jumping from a cliff into a swimming hole and then wondering, "Should I have just done that?" Of course I should have, but I needed to allow myself that level of honesty. In addition, I only recently watched "Dying to Have Known" (the video about Gerson Therapy) so the whole thing was still very much conceptual. And suddenly we are here, interacting with a proud staff and excited guests and companions.

The guests and the companions want to know, "Are you here as a companion or a patient?" "Is he your brother?" "When were you diagnosed?" "What were the symptoms?" Most folks just cut right to the chase. We're all here to do one thing: stop the cancer from growing and best case scenario, reduce the cancer to the point that a local removal is possible. Everyone here has had surgery except me. Currently there are five other patients here (with their companions of course) so that makes 12 of us in all.

All of us eat our meals together (except one patient and her daughter - they eat in their room). It's buffet style. Most folks happily show us the ropes. The staff already walked us through the process and most of the guests are eager to help. We actually seem to be bonding quite quickly, finding out, "How many juices did they start you on?" "How many ounces are your enemas?" "Are they allowing you any exercise?" [rest is essential when the body needs to heal at this level]

This morning I woke up with a strong desire to play the guitar - first in along time. I asked who might know where to get one. I was directed to Dr. Cervantes and he said he might find one. Later in the afternoon a guitar was brought to me! It's an acoustic nylon string guitar strung with steel strings and most of the strings are strung on the wrong pegs. It's hysterical and gratitude is all I feel - what a treat! I'll restring it tomorrow or maybe send one of the companions out for strings. They seem to go out regularly. The cooks are looking forward to hearing a song tomorrow evening. It will be fun.

Tuesday, May 8, 2007

Reflection

This first entry is introspective: where I have begun to look...

Today is May 7th and I'm getting very excited about all you wonderful folks who will be seeing me off at the benefit on the 12th. I'm just as excited about going to Baja Nutricare and beginning the process of detoxifying my body.

As I have been reflecting upon this experience day by day, I have been inquiring into what is available to me out of having these cancer cells growing in my body. After the initial shock, the anger, the incredible sorrow and the sense of powerlessness I felt, I was able to begin looking at the purpose of my body having cancer - something that puts such fear into so many of us. I stopped asking "why?" Naturally I have no idea. But, I am clear that I have been provided with cancer - not stricken with it.

Today it occurs as a wake-up call as well as an incredible opportunity for me to take on the health of my body and my mind (something that I usually sacrificed for the great taste of cheeseburgers and milkshakes). On that note, one thing I've come to realize is that some folks will enjoy cheeseburgers and milkshakes up into the final days of a very long life. I, on the other hand, and clearly others as well, do not have the privilege of such gastronomic pleasures. So be it.

I am also clear that nothing of this magnitude occurs in my life without me transforming who I am in some significant way or another. Already, I have made huge strides in humbling myself and asking for the support of others. In the beginning, it took everything I had just to tell a single person that we were having a benefit. And how the world occurs to me today vs. two months ago is very, very different. I have come to learn that people truly love having an opportunity to make a difference in the lives of others. How do I know that? SO MANY PEOPLE have gone out of their way to make this benefit happen by contributing in countless ways - people I have never met and probably never will. I do not live in the same world that I lived in two months ago and I'm clear the world hasn't changed a bit - I have.