Behcet’s Disease

Explore the complexity of Behçet’s Disease in this concise presentation by Prof. Dr. Mike Chan, designed for rheumatologists and immunology specialists. Behçet’s is a chronic, multisystem vasculitis marked by recurrent oral and genital ulcers, uveitis, and skin or joint inflammation. Diagnosis is clinical, based on recurrent mucocutaneous and systemic features. Beyond immunosuppressive therapy, a holistic approach integrates Autologous Active Specific Immunotherapy (AASI), PSC (Precursor Stem Cells), GcMAF Forte, Thymus Therapy, and systemic modulators like MO/NOP Thymus and MO/NOP STF to regulate immunity, reduce flares, and preserve long-term vascular and organ health.