@Avenger and others.
I finally got a doctor to write a script for the Mayo Clinic D-lactate urine test but I don't know if I should put myself through eating a bunch of carbs that could kill me by putting me in acidosis. I was on the carnivore diet and taking herbals for three months and it basically saved my life. But I eventually had to go off of it because complications arose. For the past couple months I've been getting progressively worse after having to eat carbohydrates. Right at the moment I've basically been only eating meat and drinking apple juice to get my sugar in. Simple sugars seem to not aggravate the condition as much as it gets absorbed quickly enough that my gut doesn't ferment it. But I still get issues with it that are significant.
Should I go through with the test? I want to eat enough to show the d lactate being excreted in the urine but not too much that it could do significant damage. I'm very fragile at the moment. Whenever I eat carbs I get severe neuro/cognitive issues, autonomic issues, acidosis, fatigue, and go into a coma like state among other symptoms. Each time I get worse and worse to the point that if I do it one more time I fear it may kill me. If I go through with it I feel like I'm going to have to be hospitalized to correct the acidosis and correct my gut issues. But I have little faith in the doctors as they are incompetent with issues like this and I've been in acidosis at the ER so many times without them investigating or doing anything. I'm very under weight and don't know what diet I should go on. My stomach, gut and gallbladder all work at like 5%. To the person wondering about CCI/AAI I'm 95% convinced this is caused by vagus nerve damage and brainstem dysfunction or at least in my case. It all controls how your stomach, gallbladder, liver, pancreas, and gut works. I believe the vagus also modulates the gut bacteria and microbiome. Any damage or dysfunction can cause many issues related to those organs. I developed ME/CFS after forceful chiropractic manipulations along with getting sick. I have upper cervical ligament damage and lower cervical instability confirmed by Digital motion X-Ray, CT, and MRI. I've been diagnosed with CCI, AAI, and subaxial instability by Dr. Gilete.
Anyways I'm running out of options on what to do here. I think I might have to try antibiotics just to do something because I'm running out of ideas. Don't know what antibiotics would be the best. Also going on an elemental diet I think.
ME/CFS and Covid-19 long haul probably due to Viral changes within the Microbiome (Virus can enhance some species of Bacteria and advantage them to kill other species) Virus need to find host Bacteria or die and the Gut is a main target;
Hi Jwarrior77,
I thought that you might all like this report;
New post on CFS Remission
Long Haul Covid – Welcome to the ME/CFS world!
by lassesen
Long haul COVID is sometime referred to as Post-Virus Syndrome. I prefer the more general, Post-Infection Syndrome. Most people with a CFS/ME diagnosis fall under that classification and causation.
Forget about Disability etc
A few people may get it, those with positive test results for something wrong, for example a SPECT scan of the brain. In general, long haul covid show no atypical results from standard medical tests. This has been the situation for ME/CFS for decades. Some people may get it granted for up to one year... and then will get turned down on renewal.
How will the insurance company respond?
From ME/CFS experience, it will be suggested that it is either psychosomatic, or work-phobic , or someone using it as an excuse not to work, or psychologically crippled from COVID stress. There is nothing wrong with the patient according to medical tests. Hence, it is psychological or attitude. Benefit denied.
Probable Cause ... microbiome dysfunction
Microbiome dysfunction, even when shown, would be viewed as an experimental or research diagnosis and thus, not applicable for disability. This gets much worst because almost no physician knows now to effectively deal with a microbiome dysfunction apart from a Fecal Matter Transplant (which may require multiple attempts using different donors -- they still have not figured out compatibility and compensation vectors for FMT). FMT in the US is restricted to a very small number of conditions, and long haul covid is unlikely to be included for decades.
Technically, sufficient information appears to be available on PubMed (National Library of Medicine). It is not consolidated into a cookbook formula but spread across over 3000 separate articles. Clinical MDs do not have time to consume this, and applying it would be contrary to existing standards of care. Their supervisors will veto it (been there, seen that!)
Bottom Line
The cure for Long Haul Covid is likely the same cure as ME/CFS. From existing studies, we know that a percentage will spontaneous recover every 6 months, with the percentage decreasing over time. Some will never recover. A few will, like ME/CFS. continue to get worst.
lassesen | March 2, 2021 at 3:11 pm | Categories: Chronic Fatigue Syndrome | URL: https://wp.me/p2Sdu4-b2b
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