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From the Governor's speech:

“I am very happy to be here
for the inauguration of Life Force, promoted by Dr Rajesh and Dr Rupal Shah. The
service that Dr Rajesh Shah has been is rendering to the patients across the
world using homeopathy is indeed valuable. The goodness of Dr Shah lies in the
fact that he is not working for his own benefit but is working for popularizing
homeopathy all over the world.”
- Address by Mr Mohammed
Fazal, Governor of the state of Maharashtra at the inauguration of Life Force
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Dr. Rajesh Shah's advice on Acromegaly
Scope of Homeopathy:
Only symptomatic relief is offered.
Limited
role. Recommended.
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Acromegaly
Introduction:
Acromegaly is a hormonal disorder, due to excess secretion of growth hormone (GH) and occurs in middle-aged adults. This hormone in normally secreted by the 'Pituitary', a gland situated deep within the brain. Whenever there is increased secretion of GH, the clinical condition is called acromegaly (meaning enlarged extremities).
A similar excess occurring if occurring in childhood causes the condition 'gigantism'.
Acromegaly is uncommon (3-4 per 100000 people). Physical changes occur so gradually that it is easy to miss the disease altogether in the initial stages.
Few initial (early) symptoms:
Enlarged hands and feet.
Shoes do not fit, rings on fingers become tight.
Changes in facial features ->
Protrusion of lower jaw
Enlarged nose
Thickened lips
Teeth show wider spacing.
Signs & symptoms seen as the disorder progresses:
Coarse, oily, thickened skin
Excessive sweating and body odor
Small outgrowths of skin tissue (skin tags)
Fatigue and muscle weakness
A deepened, husky voice due to enlarged vocal cords and sinuses
Severe snoring due to obstruction of the upper airway
Impaired vision
Headaches
Enlarged tongue
Pain and limited joint mobility
Menstrual cycle irregularities in women
Erectile dysfunction in men
Enlarged liver, heart, kidneys, spleen and other organs
Increased chest size (barrel chest)
Causes:
The most common cause of acromegaly is a tumor. These tumors can be of two types:
Pituitary tumors: These tumors are almost always non-cancerous and benign, called 'adenomas'
This tumor secrets excess amounts of growth hormone which causes most of the symptoms.
Some symptoms like impaired vision and headaches are caused due to the tumor growing in size and pressing on nearby brain tissues.
Non-Pituitary tumors: Tumors present elsewhere in the body (pancreas, lungs, and adrenal glands) begin to secrete growth hormone resulting in excess hormone circulation.
Diagnosis
The progress of the disease being very slow, it is easy to miss acromegaly. Even with friends and family members, the condition can go unnoticed as changes are very subtle.
When there is enough reason to suspect acromegaly, the laboratory investigations required are: -
1) Growth Hormone suppression test.
GH levels in the blood are measured before and after having a fixed amount of glucose orally. If the GH levels after having glucose fail to fall, the diagnosis of acromegaly is made.
2) GH & IGF-I measurements.
Elevated levels of these hormones in spite of fasting overnight, is indicative of acromegaly.
3) Imaging.
CT and MRI scans can pinpoint the locations of pituitary as well as non-pituitary tumors.
Sequelae
Acromegaly is either a cause of or associated along with the following conditions outlined below:
Diabetes
High blood pressures
Other cardio-vascular diseases (enlargement of the heart muscles ' myopathies)
Osteoarthritis
Carpal tunnel syndrome
Sleep apnea syndrome
Carpal tunnel syndrome
Reduced secretion of other pituitary hormones (panhypopituitarism)
Spinal cord compression
Loss of vision
Formation of pre-cancerous growths (polyps) within the intestine (colon).
Benign tumors (fibroids) within the uterus.
Treatment
More than one form of treatment is usually required. Both medications and surgery are usually indicated, the aim being to reduce the total amount of GH in circulation.
A. Conventional medications
The conventional medicines have three objectives:
I. Stop excessive secretion of GH (use of drugs like octreotide)
II. Decrease the size of the tumor responsible for excess GH (use of dopamine agonists like cabercoline & bromocriptine)
III. To normalize IGF-I levels when the above (GH antagonists like pegvisomant)
B. Surgical interventions
Transsphenoidal surgery to extract the pituitary tumors.
C. Radiation
Applied in cases where there are residual tumor cells even after appropriate surgical interventions.
D. Homeopathic Treatment
Homeopathy system does not have significant treatment for Acromegaly. However,
homeopathy can successfully treat some of the end results of the disease
process.
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New book by Dr Shah on
Chronic Urticaria


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