Larsons' Homeo - Prader Willi Syndrome


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Prader Willi Syndrome

Treatment No. :	RD0697
Dosage & Instructions:	One tea spoon twice a day, mornings and evenings.
Composition:	Natr sulfuricum D3 Silicea D3 Calcarea carb D2 Calcarea iodata D4 Natrum phos D2 Magnesia phos D2 Ferrum phos D2 Rubia D2 Juglans regia pulv D2
Treatment Type:	This remedy is a symptomatic treatment. A symptomatic treatment cannot eliminate the disease from its root but is able to considerably improve the patient's condition by easing his or her symptoms.
Contra-indications:	None established
Special Instructions:	Whereas this remedy can be safely used by teenagers, its use has not been evaluated in children under 12 years of age. Please do not administer to children under this age.
Storage:	Store in a cool and dry place
Precautions:	Keep away from the reach of children
Standard Packaging :	350 gm Granule
Order Online:	One 350 gm bottle for $79.99 Two 350 gm bottles for $129.99

Condition Overview:

Prader-Willi syndrome is a genetic disorder characterized in infancy by diminished muscle tone (hypotonia), feeding difficulties, and failure to grow and gain weight (failure to thrive). In childhood, features of the disorder include short stature, genital abnormalities and an excessive appetite. Progressive obesity results because of a lack of feeling satisfied after completing a meal (satiety) that leads to overeating. Without appropriate treatment, individuals with severe progressive obesity may have an increased risk of cardiac insufficiency, diabetes or other serious conditions that may lead to potentially life-threatening complications. All individuals with Prader-Willi syndrome have some cognitive impairment that ranges from borderline normal with learning disabilities to mild mental retardation. Behavior problems are common and can include temper tantrums, obsessive/compulsive behavior, and skin picking.

Prader-Willi syndrome occurs when the genes in a specific region of chromosome 15 do not function. The abnormal genes usually result from random errors in development, but are sometimes inherited.

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Larsons Homeo
Suite 3587
SE-111 74 Stockholm
Sweden