Fight Cystic Fibrosis With Vitamins And Over The Counter Products

Cystic fibrosis is a hereditary disease that affects thereason is unknown.
entire body, causing progressive disability and earlyUse a mask nebulizer and other inhalations treatments
death. Cystic fibrosis affects the entire body andare the most common forms of treatments for cystic
impacts growth, breathing, digestion, and reproduction.fibrosis. The goal is the treating and limiting the amount
Difficulty breathing and insufficient enzyme productionof lung damage caused by thick mucus and infection.
in the pancreas are the most common symptoms.Albuterol and ipratropium bromide are inhaled to
The Pancreas of patients with Cystic Fibrosis fails toincrease the size of the small airways by relaxing the
produce enough enzymes that are necessary tosurrounding muscles. As lung disease worsens,
break down food. As a result the food eaten retainsbreathing support from machines may become
its fats and most of its nutrients as it passes throughnecessary.
the body.Most individuals with cystic fibrosis take additional
The bronchial tubes in the lungs also malfunction andamounts of vitamins A, D, E, and K and eat high calorie
produce a thick, sticky mucus. Germs multiply in thismeals.
mucus and cause respiratory infection such asCommon Vitamins and over the counter products can
pneumonia, accompanied by a cough and high feverhelp with treating Cystic Fibrosis such as Vitamin E,
that is more severe than normal.Vitamin K, Vitamin A, Lactase Enzyme, Papaya,
A multitude of other symptoms, including sinusProtein Tablets, Vitamin B, Amino Acid and L-Carnitine.
infections, poor growth, diarrhea, and potential infertilityDr. Harry Schwachman reported "most patients with
(mostly in males) result from the effects of cysticcystic fibrosis have low levels of vitamin E". Vitamin E
fibrosis on other parts of the body. Patients with Cysticprotects lung tissue form inhaled pollutants and aids the
Fibrosis also sweat profusely and their perspirationsfunctioning of the immune system.
also contains an unusually high percentage of salt.Vitamin K helps the blood to clot after and injury.
Cystic fibrosis is the most common life-limitingA number of studies have suggested that taking
recessive disease among people of Europeanantioxidants such a Vitamin A reduces the risk of
heritage. Two copies of the recessive mutated gene,bronchoconstriction. Vitamin A is stored in the liver and
one from each parent is needed by the human bodyfat cells of the human body and can reach toxic levels.
to develop Cystic Fibrosis.DO NOT take more than the recommended dosage
Because cystic fibrosis testing is expensive, testing isof Vitamin A.
often performed on just one parent initially. If thatLactase Enzyme makes milk products more readily
parent is found to be a carrier of a CFTR genedigestible.
mutation, the other parent is then tested to calculatePapaya contains lipase, which assists in Fat and
the risk that their children will have cystic fibrosis.Cellulose digestion.
Cystic fibrosis can result from more than a thousandProtein tablets increase protein intake.
different mutations and, as of 2006, it is not possible toAll of the different Vitamin Bs taken together as
test for each one. Most commercially available testsB-Complex work together as a team to perform vital
look for 32 or fewer different mutations.biological processes, such as energy production and
Couples who are at high risk for having a child withefficient metabolic function. Vitamin B boost energy
cystic fibrosis; i.e. cystic fibrosis has developed in familylevels and help fight fatigue.
members, will often opt to perform further testingAmino Acid help regulate growth, digestion and
before or during pregnancy. After birth cystic fibrosismaintaining the body's immune system.
may be diagnosed in newborn with sweat testing, orL-Carnitine is essential for the body's ability to turn food
genetic testing.into energy. L-Carnation increases energy at the cell
Most states and countries do not screen for cysticlevel by increased fat burning, increases the body's
fibrosis routinely at birth. Children with cystic fibrosisability to remove toxic disease-causing compounds
typically do not gain weight or height at the same rateand helps cells live longer.
as their peers and occasionally are not diagnosed untilAlways consult your doctor before using this
investigation is initiated for poor growth. Males tend toinformation.
have a longer life expectancy than females but the