According to research, if there was a way to effectively increase nitric oxide production in the body, people suffering from sickle cell anemia would finally be able to do something to relieve and eliminate their painful symptoms. There are speculations that sometime in the future there will be a way to produce adequate amounts of nitric oxide.
Nitric oxide in gaseous form can be delivered through breathing it in through the lungs. The effects are limited because nitric oxide is highly reactive so concentrations must be kept low or it would cause damage.
There is a safe and natural product that has been developed a decade ago that effectively produces nitric oxide in your body. It is called Hemoxide.
Hemoxide contains two important types of nutrients. One supplies the molecular building blocks needed to produce nitric oxide in the body. The other stimulates nitric oxide production. Hemoxide works to produce nitric oxide in your body, which in turn improves the circulation and helps to relieve the symptoms caused by having sickle cell anemia.
In addition to Hemoxide, another recommended product is Rejuvin, The water of Life.
Rejuvin can rejuvenate and refresh your blood cells so the sickle cells work more efficiently.
It is a top product for every autoimmune disease, Alzheimer's, arthritis, diabetes, osteoporosis, cancer and more.
Hemoxide Is Unique and Rejuvin Heals And Prevents Disease.
Get Clear Skin
Tuesday, December 1, 2009
Tuesday, November 17, 2009
Sickle Cell Crisis Precautions For Children And Adults
General Precautions
Have regular physical examinations every three to six months.
Have periodic and careful eye examinations.
Have sufficient rest, warmth, and increased fluid intake.
Avoid conditions, such as crowds, that increase risk for infections.
Avoid excessive demands on the body that would increase oxygen needs. Low impact exercise may be useful and safe for maintaining strength, particularly in the legs and hips, but patients should consult their physician about any exercise program.
Avoid high altitudes if possible. If flying is necessary, be sure that the airline can provide oxygen.
Do not smoke, and avoid exposure to second-hand smoke.
Dietary Factors and Supplements
You should drink as much water as possible each day to prevent dehydration. Females should include cranberry juice to help prevent urinary tract infections.
It is important to have 5 to 9 daily servings of green, red, and yellow vegetables, fruits, or juices that are rich in antioxidants and other important nutrients.
Protein is important for people living with sickle-cell.
Have regular physical examinations every three to six months.
Have periodic and careful eye examinations.
Have sufficient rest, warmth, and increased fluid intake.
Avoid conditions, such as crowds, that increase risk for infections.
Avoid excessive demands on the body that would increase oxygen needs. Low impact exercise may be useful and safe for maintaining strength, particularly in the legs and hips, but patients should consult their physician about any exercise program.
Avoid high altitudes if possible. If flying is necessary, be sure that the airline can provide oxygen.
Do not smoke, and avoid exposure to second-hand smoke.
Dietary Factors and Supplements
You should drink as much water as possible each day to prevent dehydration. Females should include cranberry juice to help prevent urinary tract infections.
It is important to have 5 to 9 daily servings of green, red, and yellow vegetables, fruits, or juices that are rich in antioxidants and other important nutrients.
Protein is important for people living with sickle-cell.
Sunday, November 15, 2009
Different Types Of Sickle Cell
Sickle Cell Anemia
Sickle cell anemia is a serious disease in which the body makes sickle-shaped red blood cells.
Normal red blood cells are disc-shaped and look like doughnuts without holes in the center. They move easily through your blood vessels. Red blood cells contain the protein hemoglobin. This iron-rich protein gives blood its red color and carries oxygen from the lungs to the rest of the body.
Sickle cells contain abnormal hemoglobin that causes the cells to have a sickle shape. Sickle-shaped cells don’t move easily through your blood vessels. They’re stiff and sticky and tend to form clumps and get stuck in the blood vessels.
The masses of sickle cells block blood flow in the blood vessels that lead to the limbs and organs. Blocked blood vessels can cause pain, serious infections, and organ damage.
People who have this form of sickle cell disease inherit two sickle cell genes, one from each parent.
Sickle-Hemoglobin C Disease
People who have this form of sickle cell disease inherit one sickle cell gene and one gene from an abnormal type of hemoglobin called ?C.? Hemoglobin is a protein that allows red blood cells to carry oxygen to all parts of the body. This is usually a milder form of the disease.
Sickle Beta-Plus Thalassemia and Sickle Beta-Zero Thalassemia.
Sickle Beta-Plus Thalassemia - People who have this form of sickle cell disease inherit one sickle cell gene and one gene for beta thalassemia, another type of anemia. There are two types of beta thalassemia. Those with Sickle Beta Zero Thalassemia usually have a severe form of the disease. People with Sickle Beta Plus Thalassemia tend to have a milder form of the disease.
Sickle Cell Trait
People who have this form of sickle cell disease inherit one sickle cell gene and one normal gene. This is called sickle cell trait. People with sickle cell trait usually do not have any of the symptoms of the disease and live a normal life, but they can pass the disease on to their children.
Sickle cell anemia is a serious disease in which the body makes sickle-shaped red blood cells.
Normal red blood cells are disc-shaped and look like doughnuts without holes in the center. They move easily through your blood vessels. Red blood cells contain the protein hemoglobin. This iron-rich protein gives blood its red color and carries oxygen from the lungs to the rest of the body.
Sickle cells contain abnormal hemoglobin that causes the cells to have a sickle shape. Sickle-shaped cells don’t move easily through your blood vessels. They’re stiff and sticky and tend to form clumps and get stuck in the blood vessels.
The masses of sickle cells block blood flow in the blood vessels that lead to the limbs and organs. Blocked blood vessels can cause pain, serious infections, and organ damage.
People who have this form of sickle cell disease inherit two sickle cell genes, one from each parent.
Sickle-Hemoglobin C Disease
People who have this form of sickle cell disease inherit one sickle cell gene and one gene from an abnormal type of hemoglobin called ?C.? Hemoglobin is a protein that allows red blood cells to carry oxygen to all parts of the body. This is usually a milder form of the disease.
Sickle Beta-Plus Thalassemia and Sickle Beta-Zero Thalassemia.
Sickle Beta-Plus Thalassemia - People who have this form of sickle cell disease inherit one sickle cell gene and one gene for beta thalassemia, another type of anemia. There are two types of beta thalassemia. Those with Sickle Beta Zero Thalassemia usually have a severe form of the disease. People with Sickle Beta Plus Thalassemia tend to have a milder form of the disease.
Sickle Cell Trait
People who have this form of sickle cell disease inherit one sickle cell gene and one normal gene. This is called sickle cell trait. People with sickle cell trait usually do not have any of the symptoms of the disease and live a normal life, but they can pass the disease on to their children.
Friday, November 13, 2009
Treatment
Treatment
Health maintenance for patients with sickle cell disease starts with early diagnosis, preferably in the newborn period and includes penicillin prophylaxis, vaccination against pneumococcus bacteria and folic acid supplementation.
Treatment of complications often includes antibiotics, pain management, intravenous fluids, blood transfusion and surgery all backed by psychosocial support.
Blood transfusions help benefit sickle cell disease patients by reducing recurrent pain crises, risk of stroke and other complications.
Bone marrow transplantation can cure the disease.
Health maintenance for patients with sickle cell disease starts with early diagnosis, preferably in the newborn period and includes penicillin prophylaxis, vaccination against pneumococcus bacteria and folic acid supplementation.
Treatment of complications often includes antibiotics, pain management, intravenous fluids, blood transfusion and surgery all backed by psychosocial support.
Blood transfusions help benefit sickle cell disease patients by reducing recurrent pain crises, risk of stroke and other complications.
Bone marrow transplantation can cure the disease.
What Is Sickle Cell?
Sickle cell disease is an inherited blood disorder that affects red blood cells. Sometimes these red blood cells become sickle-shaped (crescent shaped) and have difficulty passing through small blood vessels.
Types of Sickle Cell Disease
There are several types of sickle cell disease. The most common are: Sickle Cell Anemia (SS), Sickle-Hemoglobin C Disease (SC)
Sickle Beta-Plus Thalassemia and Sickle Beta-Zero Thalassemia.
What is Sickle Cell Trait?
Sickle Cell trait (AS) is an inherited condition in which both hemoglobin A and S are produced in the red blood cells, always more A than S. Sickle cell trait is not a type of sickle cell disease. People with sickle cell trait are generally healthy.
Inheritance
Sickle cell conditions are inherited from parents just like blood type, hair color and texture, eye color and other physical traits. Hemoglobin genes are inherited in two sets;one from each parent.
Types of Sickle Cell Disease
There are several types of sickle cell disease. The most common are: Sickle Cell Anemia (SS), Sickle-Hemoglobin C Disease (SC)
Sickle Beta-Plus Thalassemia and Sickle Beta-Zero Thalassemia.
What is Sickle Cell Trait?
Sickle Cell trait (AS) is an inherited condition in which both hemoglobin A and S are produced in the red blood cells, always more A than S. Sickle cell trait is not a type of sickle cell disease. People with sickle cell trait are generally healthy.
Inheritance
Sickle cell conditions are inherited from parents just like blood type, hair color and texture, eye color and other physical traits. Hemoglobin genes are inherited in two sets;one from each parent.
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