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2021-05-27

How do you decrease red blood cells?

How do you decrease red blood cells?

Treatment

  1. Exercise to improve heart and lung function.
  2. Eat less red meat and iron-rich foods.
  3. Avoid iron supplements.
  4. Keep yourself well hydrated.
  5. Avoid diuretics, including coffee and caffeinated drinks.
  6. Stop smoking, especially if you have COPD or pulmonary fibrosis.

Is bright red blood healthy?

You may see bright red blood on your heaviest days. This doesn’t mean that all changes in color are normal. If you see a shade that’s unfamiliar or gray — especially if you have other symptoms — there’s no harm in making an appointment to get checked out.

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What is the negative effects of having a high red blood cell count?

If too many RBCs are produced and released, then you can develop polycythemia. This can cause thicker blood, decreased blood flow and related problems, such as headache, dizziness, problems with vision, and even excessive clotting or heart attack.

What should I eat if I have polycythemia?

Polycythemia vera diet Eat well-balanced meals complete with fresh fruits and vegetables, whole grains, lean protein, and low-fat dairy. Ask your doctor how many calories you should consume each day to maintain a healthy weight. Also, watch how much salt you eat.

What foods to avoid if you have polycythemia?

Cut – sugar, processed “white’ flour, junk food. Add – garlic, onion, curcumim, brocolis. I try to eat whole vegies and lots of fruits.

Does polycythemia go away?

There’s no cure for polycythemia vera. Treatment focuses on reducing your risk of complications. These treatments may also ease your symptoms.

Can PV be cured?

There’s no cure for PV, but there are treatments. Most people with PV live a normal life when they get the care they need.

What are the symptoms of PV?

Some possible signs and symptoms of PV include:

  • blurred or double vision.
  • headaches.
  • congestion.
  • fatigue.
  • itching.
  • weight loss.
  • burning sensation in the skin, especially in hands and feet.
  • facial skin redness.
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What is the best treatment for PV?

The most common drug used to treat PV is hydroxyurea (Hydrea®, Droxia®). This medicine helps slow the production of red blood cells. Some people with PV take aspirin every day because it helps thin the blood.

Can you live a normal life with PV?

Polycythemia Vera: Prognosis and Life Expectancy. Polycythemia vera (PV) is a rare blood cancer. While no cure exists for PV, it can be controlled through treatment, and you can live with the disease for many years.

Does polycythemia get worse?

Polycythemia vera treatments help reduce your risk of symptoms and complications. But for some people, the disease still gets worse and turns into another blood cancer, despite treatment.

Is PV hereditary?

Most cases of polycythemia vera are not inherited. This condition is associated with genetic changes that are somatic, which means they are acquired during a person’s lifetime and are present only in certain cells. In rare instances, polycythemia vera has been found to run in families.

What is the difference between polycythemia and polycythemia vera?

Secondary polycythemia is defined as an absolute increase in red blood cell mass that is caused by enhanced stimulation of red blood cell production. In contrast, polycythemia vera is characterized by bone marrow with an inherent increased proliferative activity.

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Who is most at risk for polycythemia?

Polycythemia vera can occur at any age, but it’s more common in adults between 50 and 75. Men are more likely to get polycythemia vera, but women tend to get the disease at younger ages.

How can you conclude that the person has polycythemia?

How can we conclude that the person has polycythemia? We can conclude that the person has polycythemia because it has a high number if red blood cells than the normal one. 3. The rank of blood cell in a normal person and one with sickle cell anemia is the same.

How long can you live with polycythemia?

Median survival in patients with polycythemia vera (PV), which is 1.5-3 years in the absence of therapy, has been extended to approximately 14 years overall, and to 24 years for patients younger than 60 years of age, because of new therapeutic tools.