Autoimmune & Inflammation

Autoimmune diseases are not just physical conditions—they reflect an imbalance in the body's systems.

Holistic medicine seeks to restore harmony by addressing the root causes, not just managing symptoms, and recognizing the interconnectedness of mind, body, and environment in the healing process."

Autoimmune & Inflammation conditions we treat

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Henoch-Schönlein purpura (HSP) is a form of vasculitis, which is the inflammation of blood vessels. It primarily affects small blood vessels and is most commonly seen in children, though it can occur in adults as well. HSP is characterized by a group of symptoms that include a purplish rash, joint pain, abdominal pain, and kidney problems.

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Herpes Gestationis (Pemphigoid Gestationis)Herpes gestationis, also known as pemphigoid gestationis (PG), is a rare, autoimmune blistering skin disorder that occurs during pregnancy. Despite its name, it is not related to the herpes virus, but rather to an autoimmune reaction in which the body’s immune system attacks the skin, leading to the formation of blisters.

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IgA NephropathyIgA nephropathy, also known as Berger's disease, is a kidney disorder that occurs when immunoglobulin A (IgA), a type of antibody, builds up in the kidneys, leading to inflammation and potential damage to kidney tissues. This condition is one of the most common causes of glomerulonephritis (inflammation of the glomeruli, the filtering units of the kidneys).

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Hidradenitis Suppurativa (HS), also known as Acne Inversa, is a chronic skin condition characterized by the formation of painful bumps, abscesses, and fistulas (tunnel-like structures) under the skin, usually in areas where skin rubs together. These areas include the armpits, groin, buttocks, and under the breasts. HS is a long-term (chronic) condition that can significantly impact a person’s quality of life, causing physical discomfort and emotional distress.

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IgG4-related sclerosing disease is a rare, systemic autoimmune condition characterized by the inflammation and hardening (sclerosis) of various organs in the body, which is driven by elevated levels of a specific subclass of antibodies called IgG4. The condition is part of a broader spectrum known as IgG4-related disease (IgG4-RD), which involves multiple organs and often presents with a combination of inflammation, fibrosis, and tumor-like masses that can mimic cancers.

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Immune Thrombocytopenic Purpura (ITP) is a rare autoimmune disorder characterized by a low platelet count (thrombocytopenia), which can lead to easy bruising, bleeding, and the appearance of purple spots (purpura) on the skin. In ITP, the body's immune system mistakenly attacks and destroys its own platelets, which are essential for blood clotting.

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Immune Thrombocytopenic Purpura (ITP) is a rare autoimmune disorder characterized by a low platelet count (thrombocytopenia), which can lead to easy bruising, bleeding, and the appearance of purple spots (purpura) on the skin. In ITP, the body's immune system mistakenly attacks and destroys its own platelets, which are essential for blood clotting.

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Juvenile Arthritis (JA)Juvenile arthritis refers to a group of autoimmune and inflammatory conditions that affect children under the age of 16. It involves chronic inflammation of the joints, leading to pain, swelling, and stiffness. Unlike arthritis in adults, juvenile arthritis may also cause growth problems, joint damage, and other systemic issues.

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Juvenile Diabetes, also known as Type 1 Diabetes (T1D), is a chronic autoimmune condition where the body's immune system mistakenly attacks and destroys the insulin-producing cells in the pancreas, called beta cells. This leads to a lack of insulin, a hormone essential for regulating blood sugar (glucose) levels.

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Inclusion Body Myositis (IBM)Inclusion Body Myositis (IBM) is a rare, progressive muscle disorder that primarily affects the muscles in the arms and legs. It is one of the inflammatory myopathies, which are conditions where the immune system mistakenly attacks muscle tissue. IBM is characterized by muscle weakness, muscle wasting, and inflammation that slowly worsen over time. Unlike other forms of muscular dystrophy or autoimmune diseases, IBM typically affects people over the age of 50 and progresses gradually.

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