7 common symptoms of acid reflux in infants Acid reflux is a condition in which the acid produced by the stomach moves to the esophagus, causing a burning sensation of the stomach and discomfort in the chest that we normally refer to as heartburn. If you experience acid reflux twice a week or more, you may be suffering from a condition known as gastroesophageal reflux disease (GERD).

Acid reflux during pregnancy: Symptoms and lifestyle changes to avoid them Acid reflux is a condition wherein one experiences pain in the lower chest area, which is commonly referred to as heartburn. When the acids of the stomach travel back to the esophagus, this condition arises. During pregnancy, hormonal changes may cause the LES or lower esophageal sphincter to not function properly; this is the valve to carry food to the stomach.

Eczema is a skin condition that becomes worse due to allergies. Food is one of the factors that cause allergies. Hence, those suffering from eczema need to adhere to a diet that includes certain food items and excludes others. Eczema diet Those who have eczema are prone to allergies. Food allergies can worsen the situation.

Hemophilia is a rare genetic condition in which a person experiences a deficiency in blood clotting proteins called clotting factors. If one injures oneself, these clotting factors create a sticky paste to eventually stop the bleeding. In hemophilia, people experience excessive bleeding internally and externally, and the blood can take longer than a healthy person’s to clot.

Cystic fibrosis is an inherited disease that affects the lungs and the digestive system. This condition is associated with cells that produce mucus, sweat, and digestive juices and impels them to turn the fluid into a thick and sticky one. The fluid clogs up the lungs and possibly obstructs the pancreas, causing discomfort.

Leukemia is a type of cancer that affects the blood and bone marrow. Bone marrow is a soft, spongy tissue that produces red blood cells, white blood cells, and platelets. Typically, leukemia affects the leukocytes or white blood cells, making them function abnormally. These blood cells play a crucial role in protecting the body against external bacteria, viruses, fungi, and other foreign substances.

Kawasaki disease is also sometimes referred to as mucocutaneous lymph node syndrome. It was first detected in Japanese children in the 1960s. It is a rare disease that typically affects children under the age of five. This rare disease affects 9-20 children among 100,000, which makes it more crucial to know its causes and look for the following symptoms.

Hyperhidrosis is a condition that causes excessive sweating in one or many parts of the body. The symptoms of this condition can get severe to the point where one may need a frequent change of clothes. For some people, this condition can trigger serious psychological problems like anxiety and depression.

Leukemia is classified on the basis of two factors: the speed at which it progresses and the type of cells it affects. Acute myeloid leukemia is an aggressive form of leukemia that spreads rapidly and affects the functioning of the White Blood Cells (WBCs). The WBCs, which are disease-fighting cells of the immune system, grow abnormally under the effect of this condition, and it can turn fatal if left unchecked.

Lupus is an autoimmune condition that causes the body’s immune system to be hyperactive and attack healthy tissue. This complex condition has rightly earned the moniker “a disease with a thousand faces”. Research shows that at least 1.5 million individuals in the country suffer from lupus. Symptoms of lupus This condition can affect many organs and its symptoms differ from person to person.

Psoriasis is an unusual skin condition that influences the skin cells to multiply a lot faster than usual. It is marked by the development of red, bumpy patches covered in white scales. The condition usually occurs during early adulthood and affects either a small or large area of the body.

Spinal muscular atrophy is a neurological condition that affects an individual’s movement. The rare genetic condition causes the muscles to weaken due to improper functioning of the spinal cord and brainstem cells, and it is the leading genetic cause of infant mortality. Despite its prominence, there is a general lack of awareness about this degenerative disorder.