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anonymous's blog

anonymous

**The Effects Of AIDS On The Fudge-Packer, & Fairy-Fondler:**

Pseudomembranous Candidiasis
Oral candidiasis is a common fungal infection in HIV disease. It may be asymptomatic or cause a bad taste in the mouth or dysphagia. The most frequent manifestation is this pseudomembranous form, also known as thrush, which is characterized by white, curd-like plaques on the tongue, buccal mucosa, palate, or posterior pharynx. Diagnosis is made by potassium hydroxide (KOH) preparation. Oral candidiasis is treated with topical agents such as nystatin swish and swallow or clotrimazole troches. Refractory cases may require systemic therapy with oral fluconazole.
 
Atrophic Candidiasis
This form of candidiasis is less common than thrush. It is manifested by an erythematous, glistening mucosal surface with a few erosions. Patients may complain of pain when eating acidic, spicy, or extremely hot or cold foods.
 
 
Hairy Leukoplakia
Hairy leukoplakia is a characteristic oral lesion associated with HIV infection. It presents as white, raised, vertical corrugations, most often on the lateral margins of the tongue. This lesion is believed to be caused by Epstein-Barr virus and often regresses in response to antiviral therapy. While hairy leukoplakia by itself is neither painful nor dangerous, it has a negative prognostic implication for HIV disease progression.
 
 
Herpes Zoster
With varicella-zoster virus reactivation, clinically known as "shingles," HIV-infected persons may experience recurrent or disseminated cutaneous disease. Rarely the infection may spread to internal organs. Diagnosis is made by the clinical appearance of skin lesions and can be confirmed by viral culture or direct fluorescent antibody (DFA) testing. Treatment consists of oral acyclovir or famciclovir.
 
 
Kaposi's Sarcoma
Kaposi's sarcoma (KS) is a characteristic manifestation of HIV infection occurring primarily in gay and bisexual men. It often presents when the CD4 count is between 500 and 200. This tumor originates in cells which normally form capillaries and lymphatic channels, and is now known to be caused by human herpesvirus, type 8. Skin lesions can be macular, nodular, or plaque-like, are usually nontender and nonpruritic, and do not blanch with pressure. KS may spread viscerally in advanced HIV disease. Management depends upon the location and extent of lesions and may include local treatment, radiation therapy, or systemic chemotherapy. Improvement has also been noted in patients receiving combination antiretroviral therapy.
 
 
Bacillary Angiomatosis
Bartonella henselae has been recognized as the causative agent of bacillary angiomatosis in HIV-infected patients. This condition is characterized by a proliferation of blood vessels in the skin and internal organs. Skin lesions are nodular and red or purplish in color, and may eventually ulcerate and drain. Diagnosis is made by biopsy, and treatment consists of a prolonged course of an oral macrolide antibiotic such as erythromycin or azithromycin.
 
 
Eosinophilic Folliculitis
Eosinophilic folliculitis is a characteristic skin condition seen in patients with advanced HIV disease. It frequently begins as a pruritic, papular eruption that evolves into a weeping, crusting ulcer with a hypertrophic margin and central healing. Its etiology is unknown. Diagnosis is made by biopsy, and management consists of ultraviolet B phototherapy.
 
 
Seborrheic Dermatitis
Seborrhea and psoriasis are more common and sometimes resistant to therapy in HIV-infected patients. Seborrheic dermatitis typically involves the scalp, forehead, retroauricular area, moustache, beard, nipples, and perianal region. Diagnosis is made by clinical appearance. Treatment with topical steroids or antifungal agents is usually effective.
 
 
 
Oral Kaposi's Sarcoma
KS lesions of the hard palate may initially manifest as subtle red or purple macular lesions, but evolve over time into nodules. Mucosal disease is often seen in the context of cutaneous involvement.
 
 
 
Gingivitis
Acute necrotizing ulcerative gingivitis (ANUG) presents as painful, swollen gums associated with an erythematous line at the gingivodental border. ANUG can lead to rapidly progressive periodontal disease and tooth loss. HIV-infected patients with gingival disease should be empirically started on oral antibiotic therapy and promptly referred for dental evaluation.
 
 
 
Aphthous Ulceration
Aphthous ulcerations or "canker sores" are recurrent, painful, clean-based oral lesions of unknown etiology. This condition is generally self-limited but may persist in HIV-infected patients. It generally responds to topical steroid therapy, but some refractory cases have required thalidomide. Mouth ulcers in HIV disease have a broad differential diagnosis, including herpes simplex infection, syphilis, neoplasia, and drug toxicity.
 
 
 
Atrophy on CT Scan
Neural destruction in the brain associated with HIV infection may lead to global cortical dysfunction known as HIV encephalopathy. This syndrome is characterized by a general decline in cognitive skills, behavioral capacity, and muscular coordination. Early manifestations include difficulties with short-term memory and concentration. Combination antiretroviral therapy may result in symptomatic improvement.
 
 
 
Cryptococcus on India Ink
Cryptococcus neoformans meningitis in HIV-infected patients presents subacutely over several weeks. Symptoms may include fever, headache, malaise, photophobia, meningismus, nausea, vomiting, altered mental status, and/or seizures. This India ink preparation under high power shows a thick polysaccharide capsule surrounding the yeast, the organelles of which can be identified. Diagnosis is made by lumbar puncture, and management consists of systemic antifungal therapy, generally intravenous amphotericin B followed by maintenance oral fluconazole.
 
 
 
Toxoplasmosis on CT Scan
Toxoplasma gondii, a protozoan associated with asymptomatic infection in many normal adults, can reactivate in patients with advanced HIV disease to produce central nervous system mass lesions. Symptomatology ranges from subtle personality changes to major motor and sensory deficits, seizures, and coma. Diagnosis is made by CT scan with contrast or by MRI scan, which typically shows multiple enhancing brainstem lesions. Treatment consists of sulfadiazine and pyrimethamine.
 
 
 
PML on MRI Scan
JC virus causes progressive multifocal leukoencephalopathy (PML), an infrequent progressive demyelinating central nervous system disease in patients with advanced HIV disease. Symptoms include dementia and a wide variety of focal neurologic abnormalities. MRI scan shows nonenhancing white matter lesions. No treatment has been demonstrated to be effective for this condition, but combination antiretroviral therapy may be beneficial.
 
 
 
CNS Lymphoma on CT Scan
Central nervous system lymphoma, which occurs in advanced HIV disease, presents with rapidly evolving neurologic symptoms. Ring enhancement and surrounding edema can be seen on this CT scan with contrast, making the lesion difficult to distinguish from toxoplasmosis. Management consists of radiation therapy.
 
 

AIDS-Related Lymphoma Treatment (PDQ®) - Stages of AIDS-Related Lymphoma

After AIDS-related lymphoma has been diagnosed, tests are done to find out if cancer cells have spread within the lymph system or to other parts of the body.

 

The process used to find out if cancer cells have spread within the lymph system or to other parts of the body is called staging. The information gathered from the staging process determines the stage of the disease. It is important to know the stage in order to plan treatment, but AIDS-related lymphoma is usually advanced when it is diagnosed. The following tests and procedures may be used in the staging process:

  • CT scan (CAT scan): A procedure that makes a series of detailed pictures of areas inside the body, taken from different angles. The pictures are made by a computer linked to an x-ray machine. A dye may be injected into a vein or swallowed to help the organs or tissues show up more clearly. This procedure is also called computed tomography, computerized tomography, or computerized axial tomography.
  • PET scan (positron emission tomography scan): A procedure to find malignant tumor cells in the body. A small amount of radioactive glucose (sugar) is injected into a vein. The PET scanner rotates around the body and makes a picture of where glucose is being used in the body. Malignant tumor cells show up brighter in the picture because they are more active and take up more glucose than normal cells do.
  • MRI (magnetic resonance imaging): A procedure that uses a magnet, radio waves, and a computer to make a series of detailed pictures of areas inside the body. A substance called gadolinium is injected into the patient through a vein. The gadolinium collects around the cancer cells so they show up brighter in the picture. This procedure is also called nuclear magnetic resonance imaging (NMRI).
  • Bone marrow aspiration and biopsy: The removal of bone marrow, blood, and a small piece of bone by inserting a hollow needle into the hipbone or breastbone. A pathologist views the bone marrow, blood, and bone under a microscope to look for abnormal cells.
  • Lumbar puncture: A procedure used to collect cerebrospinal fluid from the spinal column. This is done by placing a needle into the spinal column. This procedure is also called an LP or spinal tap.

    Lumbar puncture. A patient lies in a curled position on a table. After a small area on the lower back is numbed, a spinal needle (a long, thin needle) is inserted into the lower part of the spinal column to remove cerebrospinal fluid (CSF, shown in blue). The fluid may be sent to a laboratory for testing.
  • Blood chemistry studies: A procedure in which a blood sample is checked to measure the amounts of certain substances released into the blood by organs and tissues in the body. An unusual (higher or lower than normal) amount of a substance can be a sign of disease in the organ or tissue that makes it. The blood sample will be checked for the level of LDH (lactate dehydrogenase).
 
Drug Resistant AIDS Strain
Radio-Canada
1-25-2000
 
 
 
 
MONTREAL - Researchers in Montreal say drug-resistant strains of the AIDS virus are being transmitted to new patients through unsafe sex or misuse of needles.
 
In a recently published study, researchers found that nearly 17 per cent of newly infected AIDS patients were immune to most common AIDS drugs such as AZT and 3TC.
 
They want Health Canada to approve an experimental test that would allow doctors to detect resistance to drugs.
 
Dr. Mark Wainberg is the director of the McGill University AIDS centre in Montreal. He says patients who have had the virus for a long time are passing their resistance on to people who have never even taken medication.
 
Wainberg says that resistance is being transmitted through sexual intercourse or contaminated needles. Researches say drug-resistance tests are needed to prevent doctors from prescribing medication that won't be effective.
 
Wainberg wants those tests to be approved by Health Canada.
 
"Now that we have the results we're hopeful that the governments at the various levels will want to approve this because as we've all agreed today, it makes good sense."
 
Wainberg says there are enough treatments on the market to offer alternatives to patients that have the drug-resistant strain of HIV. But he can't guarantee how well those drugs will work in the future.
 
"We simply have no way of knowing how long our drugs will remain efficient over long periods of time. But one thing is for sure: the development of this technology is something that will enable us to potentially identify resistance before it becomes a clinical problem."
 
Wainberg says developing countries will suffer most as the number of drug-resistant AIDS viruses increase. He says these nations may not have the money to pay for the $500 drug-resistance test.
 
Researchers say the problem isn't acute at the moment but they say it may proliferate if nothing is done to detect mutant strains of HIV in newly infected patients.
 
 
 
 
 
 

FIRST PART SUMMARY OF 5 CASE HISTORIES OF

LAST STAGE AIDS PATIENTS
TREATED by
Nick Tsilimigakis, MD

1. S.T. Female 30 years of age.

 

A. Therapy Method:

a. Use of Device for determining patients Bioenergy Condition;

b. Use of Micro-currents Device;

c. Use of PAP IMI Device since August 1994. At the beginning of treatment (November 1992) the patient was additionally receiving AZT.

 

B. Clinical picture before therapy beginning: Significant loss of energy, Lymphadenitis, Hodgkin, Emaciation, Weight down to 46 Kgr.

 

C. Laboratory findings before therapy beginning: Anemia, Leukopenia, CD4 29.

 

D. Patient Development during therapy:

a. During the first month of therapy significant improvement of physical condition, Anemia improvement, Restitution of the white cell count to normal level, weight increase by 3 Kgr, improvement of Bioenergy indexes.

b. During the end of the second month: Excellent physical condition, Normal counts for red and white blood cells, weight increase by 4Kgr, Indexes of Bioenergy Condition to normal.

c. At the end of six month therapy: Excellent physical condition, full vocational activities, complete reduction of lymph nodes swelling, weight recovery to level before illness: 56 Kgr, CD4 90

d. End of the first year Treatment: Clinical picture to excellent picture, CD4 count 120.

e. End of the second year Treatment: as above, CD4 count 165.

f. During the third year: The PAP IMI is applied around thymus. At the end of the third year CD4 clime to 350 count. During this year, no other medication was taken against HIV. Physical condition top excellent.

 

 

2. K.H. Male 60 years of age.

 

A. Method of treatment:

a. Use of Diagnostic Device for Bioenergy Condition of Body;

b. Use of Microcurrent Device,

c. Use of PAP IMI Device, d. Intaking of big doses of Vitamin C;

d. Intake of mineral traces.

 

B. Clinical picture before treatment: Significant loss of Energy, Emaciation continuous fervescence 40-42 for two months with no response to continuous antibiotic Intaking, pneumonia carini, diarrheal syndrome.

 

C. Laboratory findings before treatment: Anemia, Leukopenia, CD4 count 10.

 

D. Patient Development during the treatment application:

a. With the application of Tsilimigakis therapy and with the antibiotics being all discontinuous, during the first 10 days temperature dropped to 37-37.5 degrees C.

b. During the end of the second month of treatment patient shows complete restitution to his Bioenergy body condition. Patients physical condition becomes excellent, significant improvement to the laboratory indices. Patient returns to work. CD4 24. Complete cure from pneumonia. Weight increase by 4 Kgr.

c. During the end of the first semester: Excellent physical condition. Lung X ray examination normal, weight recovery to normal from 60 Kgr (before), to 76 Kgr (after). During all the time of the therapy no known medication against HIV was taken by the patient.

 

 

3. B.D. Male 47 years of age.

 

A. Method of treatment:

a. Use of Diagnostic Devices for the Bioenergy Condition of the Body.

b. Use of Microcurrent Device,

c. Use of PAP IMI

d. Intake of Vitamin C, Mineral Traces, multivitamins, iron.

 

B. Clinical Picture before the treatment: Significant loss of Energy, significant Emaciation, continuous diarrheal syndrome, excessive anemia.

 

C. Laboratory findings before treatment: Anemia, Ht 22, Leukopenia, CD4 count 30.

 

D. Patient development during the application of treatment:

The application of Dr Tsilimigakis treatment had resulted the significant improvement of patients physical condition during the fist month. weight increased by 4 Kgr. There was significant improvement of the laboratory findings. The Bioenergy body condition got to normal level for healthy persons. Diarrhea was discontinuous. patient returned to his work. By the end of the first semester patient had excellent physical condition, got normal body weight, CD4 count to 80. Patient was not taking any medication against HIV.

 

 

4. B.A. Male 30 years of age.

 

A. Method of treatment:

a. Use of Diagnostic Devices for Bioenergy Condition of Body;

b. Use of Microcurrent Device,

c. Use of PAP IMI Device, d. Intaking of big doses of Vitamin C;

e. Intake of vitamins and mineral traces.

 

B. Clinical picture before treatment: Significant loss of Energy, Emaciation continuous fervescence 38-39 C, diarrheal syndrome, weight 56 Kgr.

 

C. Laboratory findings before treatment: Anemia, significant reduction of plateless (28,000), Cd4 count to 70, significant loss of white cells.

 

D. Patient development during the application of treatment:

a. During the first two weeks, the patient shows improvement of his physical condition, weight increased by 2 Kgr, reduction to the frequency of diarrhea.

b. By the end of the first month of therapy patient shows sufficient good physical condition, weight increased by 3 Kgr (total increase in the fist month 5 Kgr). Diarrhea stopped completely. laboratory verified improvement of anemia, Ht 31, restitution of white cells to normal healthy level. Plateless increase to 48,000. Patient got out of Hospital to receive the Tsilimigakis treatment and was receiving combinations of AZT, DDI, 3TC.

 

 

5. M.K male. 30 years of age.

 

A. Method of treatment:

a. Use of Diagnostic Devices for Bioenergy Condition of Body;

b. Use of Microcurrent Device,

c. Use of PAP IMI Device,

d. Intaking of big doses of Vitamin C;

e. Intake of mineral traces.

 

B. Clinical picture before treatment: Significant loss of Energy, Excessive lymphadenitis of cervical lymph nodes due to non Hodgkin lymphoma.

 

C. Laboratory findings before treatment: Anemia, Reduction of White cells, CD4 count 300.

 

D. Patient Development during the treatment application:

 

a. By the end of two weeks, the patient shows improvement of his physical condition, reduction of the swelling of cervical lymph nodes.

 

b By the end of the first month: Excellent physical condition, farther reduction of swollen cervical lymph nodes. Laboratory examinations for red and white cells normal. The patient was taking AZT, DDI and had been through chemotherapy process without patient's organism positive response.

 

Notice for optimizing the method

 

A. Patients usually after a two month treatment, because:

1. they are encouraged by the significant improvement of their physical condition; and

2. because of financial difficulty to self cover the treatments (not yet covered by health insurance policies), do not follow recommendation and drop the number of treatments they receive.

 

B. Similarly, there is a problem of follow up and retrieving laboratory examinations taken in major hospitals the AIDS patients initial report and receive treatments. Major Hospitals are unwilling to corporate in carrying recommended by us examinations, as well as in providing existing results.

I suggest two solutions to this problem.

 

The first is a short time solution by supplementing patients expenses, for their therapy and required examinations.

The second solution is the set up of a specialized center in the form of a clinic or Hospital for the correct self application of the method.

 

Presently, the application of the method incurs a lot of problems and difficulties, and results in abstaining from optimum efficacy, which otherwise could have been achieved.

 

B. For patient follow up treated for AIDS and other major diseases, the patients body Bioenergy condition is very significant. During, many years of experience and research stages, it has been understood what daily is realized in curative medicine, i.e., many times patients with more serious adverse prognosis carry a more successful follow up with respect to others with less serious adverse prognosis. A decisive factor is the patients General Bioenergy

 

Body condition, which does not show in the partial laboratory findings and prognosis.

If we call with A the patient state defined by all the laboratory and clinical findings; and B the state of Bioenergy condition of the patient, not included in the previous laboratory and clinical description of the patient, then patient's true Condition is the resultant of both states A and B, given by their product AxB.

 

This is confirmed in the above cases which show that the patient's General Condition right after Bioenergy treatments is much higher and too optimistic than the condition expected by the laboratory findings alone.

In the present situation, it is considered very important the diagnosis of Patients Bioenergy Condition for setting the plan for his therapy.

 

C. Applications of the present therapeutic method, other than the applications to various types of cancer and AIDS with impressive and increasing number of successes, appear to give similar results and achievements in:

Rheumatoid Diseases,

Asthma,

Intestinal and Stomach Ulcers,

Burning and various Edemas,

Fractures with impressive healing speed,

Eye problems and conditions,

Brain Damages,

Dermatopathy and Skin Diseases,

Various Inflammatory Diseases,

Cosmetology,

 

The method may provide also significant results in prognosis and preventing decreases as well as in retarding the process of aging of body cells.

Nick Tsilimigakis, MD, December 12, 1995.

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anonymous 1133 days agocomment permalink
 
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Sincerely,

Andrew Friedman

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