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Time
tested remedies | Most affordable prices
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Cystic Fibrosis
| Treatment No. : |
RD0167 |
| Dosage & Instructions: |
15 drops in 15 ml of plain water twice a day,
mornings and evenings.
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| Composition: |
Echinacea D1+10C
Iris vers D1+10C
Viola tri D1+10C
Donovansol D10+100C
Amalaki D1+10C |
| 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.
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| 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.
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| Storage: |
Store in a cool and dry place |
| Precautions: |
Keep away from the reach of children |
| Standard Packaging : |
30 ml Drops |
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Order Online:
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One 30 ml bottle for $79.99
Two 30 ml bottles for $129.99
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Condition Overview: Cystic fibrosis is a genetic disease that affects approximately 30,000 children and adults in the United States. Because of a defective gene, mucus-secreting glands within the lining of the lung’s airways (bronchi) produce unusually thick, sticky secretions. This clogs the air passages, promotes bacterial growth, and leads to chronic obstruction, inflammation, and infection of the airways. These thick secretions also obstruct the pancreas, keeping digestive enzymes from reaching the intestines to help break down and absorb food.
In many cases, this disorder is apparent soon after birth, but 10% of the people with cystic fibrosis do not receive a diagnosis until age 18 or older. There is variation in the severity of symptoms, which may include salty-tasting skin, cough, shortness of breath, excessive appetite but poor weight gain, and greasy, bulky stools.
According to the Cystic Fibrosis Foundation, more than 10 million Americans are symptomless carriers of the defective cystic fibrosis gene. An individual must inherit two defective genes, one from each parent, to have cystic fibrosis.
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