DIAGNOSIS! Can you read or your eyes are so fucked up?
....
As for the other question I did a colonoscopisis and they got samples from my gut yes. But you know better.
I see a pattern here.
A psychiatrist could confirm this.
You need one.
...
The only reason you did not end up (yet) killing people with an automated riffle is maybe the family that raised you & your belief in God.
Well we can see who goes to extremes and thus needs a psychiatrist.
Can you fucking read:
All the classic symptoms of M.S....
- Numbness sometimes from knee down, other times just hot/cold/numb feet. Sometimes very swollen feet and ankles (edema?).
- Welts on the back of the head, when touched the pain goes deep. More than just a surface pimple. Sometimes same soreness without a welt at surface.
- Sometimes felt the skull was numb or feeling of a wet towel draped over it.
- In the past have tinnatus and difficulty swallowing.
- I had at times weakness on my left leg and even my left arm.
- Drastic reduction in my vision. Blurry vision, reduced acuity.
- Uncontrolled muscle twitching/spasms.
- chronic fatigue syndrome and brain fog
- excessive (volume & frequency) and sometimes uncontrollable urination
- lately losing my voice
https://en.wikipedia.org/wiki/Multiple_sclerosis#Signs_and_symptomsA person with MS can have almost any neurological symptom or sign, with autonomic, visual, motor, and sensory problems being the most common.[1] The specific symptoms are determined by the locations of the lesions within the nervous system, and may include loss of sensitivity or changes in sensation such as tingling, pins and needles or numbness, muscle weakness, very pronounced reflexes, muscle spasms, or difficulty in moving; difficulties with coordination and balance (ataxia); problems with speech or swallowing, visual problems (nystagmus, optic neuritis or double vision), feeling tired, acute or chronic pain, and bladder and bowel difficulties, among others.[1] Difficulties thinking and emotional problems such as depression or unstable mood are also common.
I told you already that my case history is that from the time I arrived in Mindanao in 1994, I had dysentery and amoebas nearly ever week in the 1990s, then a series of gut infections over the years from 2006 forward, culminating in two severe gut infections clustered closely at the end of 2011 and Spring 2012, which precipitated being rushed in an ambulance to ER in May 2012 for an exploded acute peptic ulcer which was leaking acid into my abdomen thus causing my internal organs to tear and bloating my mid torso. I was in ICU and they were not sure if they would need to do surgery. That was the most pain I had ever experienced in my entire life.
That gut dysbiosis was surely caused by repetitive uses of antibiotics to treat those routine gut infections. Since the doctors found h.pylori in my stool, they again prescribed more antibiotics to the tune 6000 mg per day for 21 days (because the first 7 days I had to change to remove the Clarithromycin which screwed up my sense of smell so bad that I would puke even from the smell of a car exhaust). From that I got a severe fungal infection in my pelvic area which I assume was my bladder or colon. My doctor was nonchalant, said I looked stressed when I described the fungal infection symptoms, and never did he recommend stool tests nor a colonoscopy (it was about then that I completely gave up on him!). I had a lot of pain throughout my abdomen area for months I presume because I was scarred from the affair, which included for example taking PPIs which are known to be a factor correlated with chronic gut dysbiosis.
In November 2012, I proceded to the best hospital in Cebu (thinking it is more modern and more foreigners than Davao) and asked them to give me all the diagnostics they could. For example, the blood work showed my lymphocytes sky high. For example they confirmed I was negative for Syphilis, Clamydia, HIV, and other STDs they could test for (HPV not being one they could test for and one I had acquired in 2006 and unknown if ever fully cleared). The remainder of the tests had to be sent out to a lab in Manila, so they took my email address, phone number, and address so they could forward the results to me. They gave me their phone number for follow up. I never did receive any communication. I called but no one can help me. Typical for the Philippines, you totally waste your money because even if you do get a result, you can't even be sure you can trust the result you get. So what is the point of paying for diagnostics when you are not even sure the information you are getting is reliable???
Come on Mr. Know It All? Pray enlighten me fool.
As I told you, when I was in the office of my doctor who treated me for the acute peptic ulcer, I met a younger foreigner who was continually on morphine because my doctor had done a surgery on him to remove part of his digestive tract and sew together what remains. I believe it is referred to as a "j pop". Any way, the young guy (30s?) was clearly in such pain and years hence from the surgery he will never be painless again. It reminded me of how I could still see in my right eye after the incident where my eye was gouged with a hard object, but the surgeon in the Philippines managed to 100% detach the retina and destroy the eye. I had to return to the USA to one of the best eye surgeons in the country (whom I paid in excess of $100,000 in cash) to save my eyeball and reattach some of the retina (but lost 95% of the vision). So I asked the young guy, why did he operate in the Philippines and not back in the USA. He said lack of funds. There is no way I would operate in the Philippines again. I would at least hop over to Singapore or Australia.
So do you think I am going to trust a filipino doctor to stick a scope up my anus into my colon?!! Hell no! Not easily. I did recently get the names of some Gastroenteritis doctors at the same small brand new private hospital where I recently got my eye checkup. I am going to make an appointment to talk to them and detect whether I have found someone who I trust. Which is not likely, because I know very well the attitude the filipino doctors. Also I've told you that some of the tests are not available in Davao, e.g. I checked numerous hospital labs and none had e.coli nor salmonella stool tests.
So now what are the odds that my condition given the case history is not related to my gut? And what are the odds that the symptoms I have described are not M.S.?
And why do you think just because I am suffering in poverty that makes me insane because I have to juggle my priorities in terms of what I can and can't do at this time. And thus my treatment options follow accordingly.
You have demonstrated over the past few days how much of an indolent asshole you can be. Good riddance.
Which describes exactly what I am doing with diet (which isn't ketogenesis nor fasting idiots):
Here we show that dietary
factors and lifestyle may exacerbate or ameliorate MS symptoms by modulating the inflammatory status of the disease both in
relapsing-remitting MS and in primary-progressive MS. This is achieved by controlling both the metabolic and inflammatory
pathways in the human cell and the composition of commensal gut microbiota. What increases inflammation are hypercaloric
Western-style diets, characterized by high salt, animal fat, red meat, sugar-sweetened drinks, fried food, low fiber, and lack of
physical exercise. The persistence of this type of diet upregulates the metabolism of human cells toward biosynthetic
pathways including those of proinflammatory molecules and also leads to a dysbiotic gut microbiota, alteration of intestinal
immunity, and low-grade systemic inflammation. Conversely, exercise and low-calorie diets based on the assumption of
vegetables, fruit, legumes, fish, prebiotics, and probiotics act on nuclear receptors and enzymes that upregulate oxidative
metabolism, downregulate the synthesis of proinflammatory molecules, and restore or maintain a healthy symbiotic gut
microbiota. Now that we know the molecular mechanisms by which dietary factors and exercise affect the inflammatory
status in MS, we can expect that a nutritional intervention with anti-inflammatory food and dietary supplements can alleviate
possible side effects of immune-modulatory drugs and the symptoms of chronic fatigue syndrome and thus favor patient
wellness.
Ketogenesis and fasting are perhaps effective for cancer, because you are trying to starve the cancer. But starving the body of nutrients is generally not a good idea for most health issues.
No matter what an official diagnosis would say, that wouldn't change one iota the diet treatment I am pursuing.
So what is your point?Instead I am pointing out to you that you may be harming yourself by prioritizing ketogenesis and not Kefir. My next priority is Kefir because as I documented up thread yesterday, Kefir is a more diverse probiotic than Komucha (and the Yakult I am drinking has too much glucose and only provides one bacterium). You are barking up the wrong tree with ketogenesis focus, wherein up thread I even cited for you that Terry Wahls finds no statistical advantage for ketogenic diets from her clinical trials. Also nuts and legumes are hard on the gut because of the anti-nutrients, so I asked WTF were you doing eating nuts and coffee for breakfast. And yet you call me insane
The much more likely area of causation is microflora yet you are too lazy to go make some Kefir and then you call me insane
Dude you are one fine example of calling the kettle black.