Archive for August, 2010

Alternative Diabetic Medicine Neuropathy

August 31st, 2010
Conny Hanson asked:




With the right alternative diabetic medicine neuropathy effects can be reduced. Peripheral diabetic neuropathy is one of the four categories that can develop after the onset of diabetes. It is a result of poor blood circulation and damage to nerve endings caused by high blood sugar levels and affects the hands, legs, feet, fingers and toes of patients. It can also cause pain in these areas but with the right alternative diabetic medicine neuropathy effects can be reduced.

This type of diabetic neuropathy can result in cutting, tingling or burning pain in each leg, foot, hand or toe of the patient. This could surprisingly also be accompanied by numbness. Patients should therefore take adequate care to inspect the soles of their feet at regular intervals for any cuts, bruises or punctures that they might not have felt. The tingling pain can cause severe physical and mental discomfort to diabetics and while analgesics could be taken, they could lead to drowsiness while narcotics usually have a nasty habit of becoming addictive over a longer period of time. On the other hand medicines derived from natural ingredients can provide an improved alternative to alleviating muscle pain and even regulating blood glucose levels to a certain extent.

An antioxidant by the name of alpha lipoic acid has shown great promise in reducing the painful effects of diabetic neuropathy. Alpha lipoic acid is found naturally in food sources such as potatoes, spinach, broccoli, liver, kidneys and beef. Its effects have been studied in detail in Europe including Germany. It is available in tablet and capsule form and a dosage of up to 50mg on a daily basis could be a safe way to start the treatment. Diabetic patients should however, ask their doctor before embarking on any supplemental course since any medicine that they consume should not interfere with their present medication. Alpha lipoic acid is found to act quickly on elderly patients although it is beneficial for younger ones too. Diabetic pets such as dogs, hamsters and horses can also benefit from this wonder antioxidant although cats cannot be given these supplements due to the negative effects that it has on the cat’s liver.

Alpha lipoic acid can also enhance the effectiveness of other important vitamins required by the body such as vitamin C and E. A healthy diet along with these natural supplements should help patients stay within the prescribed blood sugar range. Diabetics should specifically take extra care in monitoring blood sugar levels when they start any alternative diabetic medicine program since some components can raise or lower blood sugar levels upon entering the body. Dosages too should be adjusted to achieve the perfect balance between reducing pain along with maintaining ideal blood sugar levels. Antioxidants such as alpha lipoic acids are much more effective if diabetic neuropathy has not progressed to a very late stage.

Hence, although alternative diabetic medicines might be taboo in the eyes of certain doctors and hospitals, some medications derived from natural sources can truly help the patient by reducing muscle pain and numbness. Hence, with the right alternative diabetic medicine neuropathy effects can certainly be reduced to a great extent.

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Prostate Pain

August 31st, 2010
Marcus Peterson asked:




Prostate pain is caused by the inflammation of the prostate gland, which is an exocrine gland of the male reproductive system. Its main function is to secrete and store a fluid that constitutes up to one-third of the volume of semen. This inflammation of the prostate is also known as prostatitis. If the prostate grows too large, it may constrict the urethra and impede the flow of urine, making urination extremely difficult and painful and in extreme cases, completely impossible. Prostatitis is usually treated with antibiotics, prostate massage or in extreme cases, surgery.

In older men, the prostate gland often enlarges to the point where urination becomes very difficult. This is known as benign prostatic hyperplasia and can be treated with medication or with surgery that removes a part of the prostate gland. The surgery technique most often used in such cases is called transurethral resection of the prostate. In this case, an instrument is inserted through the urethra to remove excess prostate tissue that is pressing against the upper part of the urethra and restricting the flow of urine.

Prostate cancer is one of the most common cancers affecting elderly men in developed countries and a major cause of death among them. Regular rectal exams are recommended for elderly men to detect prostate cancer in its early stages. There is also a blood test that measures the concentration of a protein, Prostate Specific Antigen (PSA), which is normally very low.

Elevated and more sophisticated test results may be an indicator of disorder within the prostate either prostatitis or benign hyperplasia or prostate cancer. The PSA test cannot distinguish between them, but can certainly lead a doctor to investigate further. Prostate cancer is treated with hormone manipulation, which is the prevention of production of testosterone, with radiation and surgery. It has recently been found that a drug known as Docetaxel can be effective in the treatment of prostate cancer.

Pain Medications

Pain medications generally deal with painkillers, medically known as analgesics. They are a member of the diverse group of drugs used to relieve pain. The word analgesic is derived from the Greek word ‘an’ which means ‘without’, and ‘algia’ which means ‘pain.’

Analgesic drugs act in different ways on the peripheral and central nervous system of the body. They include paracetamol (acetaminophen), nonsteroidal anti-inflammatory drugs (NSAIDs) such as the salicylates, narcotic drugs such as morphine, synthetic drugs with narcotic properties such as tramadol, and various others. Some other classes of drugs, not otherwise considered analgesics, are also used to treat neuropathic pain syndromes, which include tricyclic antidepressants and anticonvulsants.

Analgesics can be broadly categorised into three groups. The first one comprises of Paracetamol and NSAIDs. The exact mechanism for action of paracetamol is uncertain, but it apparently acts centrally. Aspirin and the NSAIDs inhibit cyclo-oxygenase, leading to a decrease in prostaglandin production. This improves pain and also inflammation, in contrast to paracetamol and the opioids. Paracetamol has few side effects, but dosing is limited by possible hepatotoxicity (potential for liver damage). NSAIDs may predispose to peptic ulcers, renal failure, allergic reactions, and hearing loss, and may also increase the risk of hemorrhage.

The second group is of Opiates and morphinomimetics. Tramadol and buprenorphine are considered to be partial agonists of the opioid receptors. Morphine, the common opioid, and various other substances like pethidine, oxycodone, hydrocodone and diamorphine, all exert a similar influence on the cerebral opioid system. Dosing may be limited by toxicity caused by opoids leading to confusion, myoclonic jerks and pinpoint pupils, but there is no dose ceiling in patients who can tolerate this. Opioids, though very effective analgesics, may have some unpleasant side-effects. Up to 1 in 3 patients starting morphine, may experience nausea and vomiting, which is generally relieved by a short course of antiemetics. Pruritus or itching may require switching to a different opioid. Constipation occurs in almost all patients on opioids, and laxatives such as lactulose, macrogol-containing or co-danthramer are typically co-prescribed. When used appropriately, opioids and other similar narcotic analgesics are safe and effective, carrying relatively little risk of addiction. Occasionally, gradual reduction of the dose is required to avoid withdrawal symptoms.

The third category is of the specific agents consumed by patients suffering from chronic or neuropathic pain. Tricyclic antidepressants, especially amitriptyline, have been shown to improve pain in apparently a central manner. The exact mechanism of carbamazepine, gabapentin and pregabalin is unclear as well, but these anticonvulsants are used to treat neuropathic pain with modest success.

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Pain Relief Machines – How They Work

August 31st, 2010
Bob G Johnson asked:




The term “pain relief machine” is a very confusing phrase and it’s understandable how people can not differentiate a “muscle stimulator” from a “tens unit” to an “interferential unit” or “pulsed galvanic stimulator” or a “micro amperage stimulator”.

Four of the 5 listed units are actually intended to be used for the treatment of chronic and acute pain.

On the internet the following terms are searched on and the patient often gets some reference to a “pain machine” as a solution and then the confusion really begins.

* neck traction
* sciatic nerve pain
* sciatic nerve pain relief
* back pain relief machine
* pain relief machine
* sciatic nerve treatment
* painreliefmachine.com
* sore neck stretches
* stretches for sore neck

Of the 5 machines listed the only one that is not intended for pain relief is a “muscle stimulator” which should be correctly called a “functional electrical stimulator” – FES. The purpose of a muscle stimulator is to help a patient restore function or prevent atrophy to muscles. All of the listed “pain machines” can literally be adjusted to the point that a muscle contraction can be elicited but that is not the purpose of a “pain machine”.

There are basically three methods of controlling pain that each of the pain machines relies upon.

1. Melzack/Wall Gate Control Theory:

This is simply the process of stopping the transmission of the pain impulse to the spinal cord for transmission to the brain where the pain is perceived. The method of operation is to stimulate non-pain fibers so the actual pain message is not transmitted and the pain impulse is not transmitted. When that happens the brain does not receive the message therefore there is no pain. In reality though for the chronic pain patient the actual results are less transmissions rather than 100% total cessation meaning pain reduction, not total pain elimination.

2. Sjolund Opioid Peptide Production ( Pain Killers)

In this application, which rarely ever works, the actual pain fibers, c fibers, are stimulated for 20 – 30 minutes and that stimulation by the pain machine results in the brain increasing the production of pain killers, aka endorphins and enkaphlins are the general terms used. As long as there is an increased amount of the peptides in the blood stream then the pain is not felt. As the peptides wear off and decrease in total volume then the pain reappears. This is not theory but has been proved however as stated earlier this application rarely is effective for the vast preponderance of chronic pain patients.

3. Glial Dysregulation of Pain and Opioid Actions

This is very recent, appearing in research being done by Linda Watkins, PhD. – Univ. of Colorado – Boulder. Her work involves the blocking of pathological pain by inhibiting glial activation in the spinal column where the glial cells exist. The glial cells actually release many neuroexcitatory substances which can lead to pain amplification.

The latter explanation helps to clarify what is now occurring with the use of interferential pain machines, unlike the other tens, micro, PGS machines where there is no carryover or residual pain relief once the pain machine is turned off. With interferential therapy there is residual or carryover pain relief during and following the treatment for hours or in some situations days/weeks. Glial cell inhibition may explain the effects of portable interferential units as well as replicate the clinical interferential treatments.

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