Thursday, March 7, 2013

I need them barred from Practicing Law and or Medicine to protect the Public and US Veterans.




To communicate accurately what the problem is, I am writing this with a computer and spell checker, because though I fully comprehend each word, and I have eidetic memory, I am dysedetic dysgraphic dysphonetic dyslexic, that was diagnosed by School board appointed Doctors in Jackson Michigan in 1966, so that is why I cannot spell or pronounce most of these words correctly. The Fairview and VA Doctors do not have any of my Medical Records from before 2006, and do not know my complete Medical History, and have been misdiagnosing me.



Even if it is not Porphyria, because my Medical Records show that I get all the same blood levels thrown off as they do, and I have the same adverse reactions to Infections and Foods and Drugs as they do, and those adverse reactions according to the Medical Journals, could kill me, and the Court here because of Social Workers’ and Doctors’ perjury committed in Court, falsely claiming that I have no adverse Medical Condition in my Medical Records that would prevent them form force treating me, who will not run the right tests when needed, and they raised my Iron and AST and ALT and ANA Levels causing upper and lower digestive tract bleeding that the Doctors refused to look for, and will not run the right tests when needed, almost killing me, I need them blocked from practicing Law and or Medicine to protect the Public, and I need them arrested, because they put me next to the VA against my will, and they have no real doctors here, and will not run the right tests when needed, and cannot get me Medications that do not have Inert Ingredients that raise my ANA Level, and they just cause one adverse reaction after another that could kill me, so I need them barred from practicing Medicine to protect US Veterans.



I need that bulge that Dr Tran’s Nurse eye witnessed, and that he would not treat saying that is a Gastroenterology problem, reported to a Doctor that will run the right Tests and treat it, it could be a hemorrhage or an infection of some kind. That Bulge expands at times increasing in size, and contracts decreasing in size at times, and because my Food is not digesting, I have a lot of Ketone in my Urine that the Urologist did not test for, and seeing that my Home Test Levels were way off, he did not even run a Urine Test to rule that out, and said that my Home Urine Test strips were not accurate, but they matched on their previous Lab Test days. None of these Doctors run the right Tests when needed, and they are causing me Medical Harm.


Though I have no Medical Records to prove it, because I have eidetic memory, I know that Dr Tran and my sister were wrong, I know that I saw Urology in Fridley in 2009. Before I saw him, I called the offices, and they said that I saw him, but the records were not on the Computer, and would be put on the Computer so that I could view the test results in Mychart, but it was not done, but I wrote a letter to him, before seeing him. After the Kansas City VA in 2005 caused my Iron Levels to skyrocket because they would not listen to me and get my Diet, and forced Psychiatric Drugs on me because they falsely called me delusional about a Neurologist who told me in 1990 to stop taking those drugs because they were making me more dysfunctional, and then the New York Hospitals caused my Iron Levels to skyrocket as I had adverse reactions to all of their Foods and Drugs for many Months, the Court and Medical Community in New York forced me to be in this state against my will, under escort, in 2006, without any of my Previous Medical Records, and because the VA here would not listen to me and was misdiagnosing me when I was in Anoka until early 2008, I began going to Allina Unity Hospital asking for a second opinion as to the rashes from Cornstarch, and asking why Corn Syrups caused me to have Hypoglycemia, and why I have so many Infections, when I moved to Blain. In December 2008 and January 2009 I had an acute attack that was wrongly diagnosed as just a Gall Stone, and Dr Crystal Dexter was set up as the follow up Doctor, during three infections in a row, she set me up with the Nurse Practitioner Mark Boldt at Minnesota Gastroenterology for the Hepatitis, and with the Urologist in Fridley for the Blood in my Urine, and the Dr Bryant at Fairview riverside Hospital for the high ANA Level, and the Fairview Doctors in Elk River would not listen to me, and elevated my ANA Level, and they cut off the liver treatment that was working and caused my ANA Level to elevate, and caused my Iron Levels to skyrocket, in Riverside Hospital, because I had none of my Medical Records that showed the high Iron or high ANA Level readings, to stop them. I stopped the Allina and Annandale Hospitals from doing that the second time, though they did cause my iron level to elevate, because I had some of my previous High ANA and Iron Level readings with me. Even if it is not Porphyria, because I get all the same blood levels thrown off as they do, I have the same adverse reactions to Foods and Drugs as they do, and those adverse reactions according to the Medical Journals, could kill me.


I have a pre Hepatitis C history of high Iron Serum and Fe Saturation and Ferritin, that was originally diagnosed as Hemochromatosis, and it seems to cause a lack of Oxygen and Repertory and or Metabolic Acidosis at times, and a lack of Oxidized Glucose at times, though my Hemoglobin elevates at those times, (possibly do to low Blood Copper,) and that caused my Clubbed Fingernails since childhood, and it caused Ascending Cholangitis and Gut Infections at times since childhood, and I could find no Doctor that could give me a Diet recommendation to keep my Iron Levels normal, so though then I did not know what was in the Foods that blocked Iron Absorption, I knew that they worked, and I developed one, so I am on a diet that excludes most Iron Absorption Enhances, and includes high levels of the Iron Absorption Inhibitors Calcium, Oxalates, Polyphenols, Tannins, Phenolic Compounds, and Phytate, and Copper, that keeps my Iron and Copper Levels normal, but does not get rid of the underlying disorder. Besides a history of a swollen Prostate or Chronic Prostatitis since the late 1970s and early 1980s in the US Army, that seems to cause intermittent UTIs at times, I have other Medical Conditions that can and do result in Intermittent UTIs, and often even since I was a child, most of my Infections were accompanied with Throat or Sinus or Meningitis Infections, and I often had face rashes and seizures while taking any Medications with Inert Ingredients in them, but the oldest Medical records that I can get to document part of that, is where I went to a VA and asked them to help me find out why I had gotten so many Infections, and they gave me Medications that caused seizures and the Anticonvulsants and Psychiatric Drugs that made it worse, and they ran the wrong Test when they were suppose to be testing for Meningitis, running a West Nile Virus Test instead, and letting me out of the Hospital, only to wake up in another Hospital in Jackson Michigan with Meningitis, is from 1985 to 1990, from the Ann Arbor Michigan VA. That is complicated by the fact that I get no elevation in white blood cells, no matter how infected that I am, and I get little or no temperature, ever since having a severe multiple infection, Urinary Tract, Throat, and Meningitis, with a 107 Temperature in the early 1990s in Los Vegas. I produce no IgE Antibodies, but have a long History of high ANA Levels with Face Rashes, that are triggered by Cornstarch and Beta-glucans in Foods and Medications, because I have a variant form of Lysozyme in my Mucosa and White Blood Cells, so my diet excludes Beta-glucans to keep my ANA Level normal, because Beta-glucans in Foods or Medication or Polysaccharide Encapsulated Bacteria, also cause me to have Thrombocytopenia. And all of that began before getting Hepatitis in Washington State in the late 1990s. And though I could find no Doctor that could give me a Medication and or Diet recommendation to make my long history of high ANA Levels, normal, I found out in the late 1990s and 2000, basically what foods raise my ANA Level, and began developing a Diet from then on, to keep it normal, and I went to the Kanas City VA asking them to help find out why I got so many Infections, and asking them why some foods caused me to have rashes, and why Corn Syrups gave me Hypoglycemia, and they ran Diabetic Tests, and because they were Negative, they began falsely calling me delusional about adverse reactions to Corn Syrups and Cornstarch, but put me on a Celiac Diet when Hospitalized. It was then in the early 2000s, that I found out that many in my Family are Celiac, when I was being treated and tested at the Kansas City VA until 2005. Though I produce no Celiac Antibodies because I cannot eat those foods, I may produce Celiac Antibodies against Gluten, like many in my Family, if I could tolerate eating Gluten Grains long enough, but I cannot because of the Beta-glucans in them, they will raise my ANA Level long before causing Celiac Antibodies, and I cannot tolerate Fructan or Inulin Fiber, so my Diet excludes all of those things. I have a history of foods and sugars causing a hyperglycemic spike, followed by a hypoglycemic crash that leaves blood and or glucose and or protein in my urine at those times, especial Fructose the worst, and then Dextrose, but Sugar Alcohols cause the worst Gut and Kidney pains, and Tomatoes cause Hypoglycemia, so my Diet excludes all of those things. Iodine causes me to have Hyponatremia and Hypochloremia, so my Diet excludes it. I have a history of Phosphate Nephropathy, caused by Phosphate Food and Drug additives, and since then, too much Phospholipids in Foods cause secondary Renal Hypertension, so my Diet excludes Phosphate additives, and at the times when my Kidneys are irritated resulting in Hypertension, Phospholipid consumption is limited to small quantities spread out through that day till my Kidneys heal. I have a history of Hypovitaminosis D, and too much Phospholipid Vitamin D Milk causes secondary Renal Hypertension, so Cod Live Oil is being added to my Diet. I have a history of Hyponatremia and Hypochloremia caused by the things that trigger the Physiological and Neurological malfunction episodes at times, and Hyponatremia with Hyperchloremia caused by Diarrhea at times, and Hypocalcaemia at times, and Hypokalemia at times. Then that is complicated by Cirrhosis of the Liver from Hepatitis C strains 1 and 3. I have a history of acute episodes that manifest clinically to appear like Acute Intermittent Porphyria, but I think it is not caused by a genetic defect in the UROD gene itself, but a UROD deficiency which is observed only in hepatic cells, and nowhere else in the body, and alcohol abuse which I do not have because I have adverse reactions to alcohol and the yeast in them, which that and other Beta-glucans trigger my episodes, and or a Hepatitis C Infection like I have, seems to conspire to result in the clinical manifestation of Porphyria cutanea tarda, called PCT. The acute episodes manifest with elevated Glucose and Hemoglobin Levels, and then Liver Function and Bilirubin, and high Hypertension and often Hyponatremia and Hypochloremia at times, constipation and diarrhea at different times in the phases of the episodes, and Hyponatremia with Hyperchloremia at times, and Hypocalcaemia at times, and Hypokalemia at times, and Repertory and Metabolic Acidosis at times, and seizures at times,and Hyperammonemia and or Hepatic Encephalopathy at times, and Eustachian Tube Dysfunction at times, extreme Abdominal pains and cramps, and Foot and Leg and Back and Neck and Jaw cramps at times, and pins and needles numbness and paralysis from the waist down, and pins and needles numbness in the right shoulder, making it almost impossible to get up at times.


Normally the Specialists do not treat the problems and leave it up to the primary care Doctor, or they want to give me Medications that have Beta-glucan or Cornstarch Inert Ingredients that will raise my ANA Level and make it worse, like they have repeatable done in the Past. I can take Penicillin and Bicillin by shot forms or IV, they have no inert ingredients that cause me harm, Erythromycin by shot or IV may be ok, (I had adverse reactions when they gave it to me, but that most likely was from the TAB medications that they gave me at the same time,) but I have adverse reactions to the same Antibiotics and Antiseizure Drugs that people with Porphyria do. That should be and is not noted in my Medical Records to cause me more Medical Harm.



In service of Yahweh and Country

Lord Joseph
Heir by birthright of the house of Israel.

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