Cancer

My opinion on Doctors in general. Some are vey good at diagnosing, while others you wonder how they get dressed by themselves. My journey started in 2020. When I had a routine MRI. I was called the next day. After the X-Ray Doc & my Doc reviewed my MRI. My Doc said, "I have good news & some bad news. "We think you might have bone cancer?" So I went through more tests. Then I was sent to another hospital for more testing. At that hospital I seen an Oncologist. So more testing with him. Those tests were reviewed by that X-Ray Doc & my Oncologist. So after 13-14? tests later. ALL 4 Doctors could NOT say for a FACT. Whether I had bone cancer or not?

Moving on to 2022. I underwent a lot more testing. Between all 4 of those doctors. Then after a long wait....I was told I had stage 4 Lymphatic cancer. So I opted to take "Chemo infusions". 9 days after the 4th infusion. Is when my body was wracked with maximum pain. I could barely walk & I was in total agony. I've taken some stout painful blows in life. But nothing compared to that chemo agony. So I quit chemo. I did some on line research for alternate cancer treatments. I came across a cancer story about a Mr. "Joe Tippins". Who was dying of fast spreading small cell lung cancer. He was given 3-4 months to live. So he had every cancer treatment known to man. YET.... he was still dying. However, one day he took his pet to he Vet. His Vet told him about "Fenbendazole". That has been used on animals to cure cancer(s). He was put in contact. With a lady Oncologist. Who did not see patients. but only worked in a lab. Seeking a cure for cancer. She ended up using Fenbendazole on her lab mice. Who were injected with various types of cancers. Fenbendazole, an anti-parasitic med. Cured those lab mice of their cancers. Mr. Tippins took Fenbendazole. Along with a few other "health medicines". He was shortly thereafter cured of his deadly cancer.

So I took Fenbendazole, alone with no other med or health medicine. Roughly 1 month later after I was tested. My cancer was gone. Completely gone.

As a side note; When I was a county paramedic. On various calls. I had to deal with "idiot" Doctors. Had I treated those serious injured & ill patients as they ordered. They would of not made it alive to the ER. So I ignored their orders. And went on our established "protocol's". And I delivered those critically injured & ill. Patients to the ER alive.

Frankly, imho. If you ever get seriously sick or injured. Get at least 2 opinions, if not 4 or more. Because there are a few doctors out there. Who are so vain & ignorant. About what they THINK they know. When in reality, they are in FACT clueless.
 
Well since this post has kinda taken a turn. LoL

A few years ago I started getting this horrible pain in the right side of my stomach. At first I thought it may have been constipation because I hadn't been using the bathroom like I normally do and it was during the winter so I hadn't been drinking enough fluids either. Well, I took several things to remedy that. The paid would get a little better, but not go away. Then one night I was on my knees in pain. My father tried to take me to the ER, but I was stubborn and finally went to sleep. The next morning the pain was about 3/4 gone so I went on with life. This happened a 2nd time and I finally had enough. I went to my family DR and they said right away that it was my gallbladder. Ordered an ultrasound which showed that I did have a few stones, but not many. Referred me to a surgeon. He looked over everything and decided it was my gallbladder and so he took it out. Pain got better for a few months then right back. Went back to surgeon, which was a waste of time. Went back to family DR, waste of time. So I kept on with life for a year. The pain would come and go. One night Weekender and I was hunting it was hurting so bad I could barely walk and get into his truck. I took a motrin 800 and the pain eased off. After that I started going back to the DR's again. Seen a gastrologist, got more CT's and Ultrasounds done of my stomach. Kept being told that it would get better because I didn't have anything there to hurt anymore. Finally about a year plus after getting my gallbladder out I went to see a new general physician and he came up with a new theory. He thought that it would probably a pinched nerve or a muscle. After MRI's and this and that later, sure enough it turned out to be a nerve that was being pinched, but wasn't hurting at the pinch point, instead it was hurting way over in my belly.

What I took from this whole thing was that next time a surgeon wants to cut on me and remove an organ there will definitely be a 2nd and possibly 3rd opinion.
 
I have a few friends in the healthcare field. Some are registered nurses, and they have all at one point or another told me that if surgery or extreme treatment is ever proposed by a doctor as the only option, to PLEASE seek more opinions before agreeing to it.

There’s a lot of greed and random assumptions thrown around in the medical field. Do you due diligence and be in control of your own health.
 
Short time back I had hernia surgery, all went well til the following Fri. 103F, white count off the charts and 2 days of penicillin. Told if it comes back, another hosp visit. Previous visit - 2 yrs ago, they didn't find anything (unconscious for about 10 min). Recent pre-op visit, I found they classified it as a stroke. I didn't know.
Older bro passed from throat cancer 2 yrs ago. Was on chemo during covid, chemo was stopped due to covid. Spent max days in ICU, then home to die.
 
We are our own best medical advocates.
Thanks to youtube coverage of medical conferences ,etc- we can listen in on the experts - trying best to understand their med-speak.
I'm on a PCa journey and need therapy for localized PCa, and my Medicare DISadvantage insurance program has denied my choices of therapy twice.
Ironic part of this is original medicare covered both therapies, but insurance used waffle words to deny.
A further issue is each denial is costing months of delay.
Obviously insurance is in it for the profit not the patients.
Several big insurance co admit to trying to shed certain customers to be more profitable, sad !
 
We are our own best medical advocates.
Thanks to youtube coverage of medical conferences ,etc- we can listen in on the experts - trying best to understand their med-speak.
I'm on a PCa journey and need therapy for localized PCa, and my Medicare DISadvantage insurance program has denied my choices of therapy twice.
Ironic part of this is original medicare covered both therapies, but insurance used waffle words to deny.
A further issue is each denial is costing months of delay.
Obviously insurance is in it for the profit not the patients.
Several big insurance co admit to trying to shed certain customers to be more profitable, sad !

Sadly everything in the US is about profit now. I send you my wishes and prayers.
 
Kirby you and I don't get along, and probably don't particularly like each other. Wouldn't be friends in person. But know this, I sincerely and genuinely hope you stay healthy and cancer-free. I hope that you have loved ones near to give you the support and care that you need. Take care and best wishes from the Ozarks.
Best wishes to you GC.
 
I know of 2 that swear by it !
Both were stage 4 and there hear years later
 

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