Hereditary Hemorrhagic Telangiectasia (HHT) is a rare genetic disorder causing abnormal blood vessels, leading to frequent nosebleeds and internal bleeding.
Ehlers-Danlos Syndrome (EDS)
Ehlers-Danlos Syndrome (EDS) is a genetic disorder characterized by joint hypermobility, skin elasticity, and often fragile tissues. It can cause pain, fatigue, and other complications.
Embolus & Embolism
An embolus is a traveling blood clot that can block blood flow, causing serious complications like pulmonary embolism or stroke. Early detection and treatment are crucial to prevent these life-threatening risks.

Pulmonary Embolism (PE)
A pulmonary embolism (PE) is a life-threatening blockage in lung arteries, often from a leg clot. Urgent diagnosis and treatment are vital.

Peripheral Artery Disease (PAD)
PAD: Narrowed leg arteries causing pain, slow healing. Risk factors include smoking & diabetes. Early detection is key to prevent complications.

HELLP Syndrome
HELLP syndrome: A serious pregnancy issue with hemolysis, elevated liver enzymes, and low platelets. Requires urgent care.
Activated Partial Thromboplastin Time (aPTT) Blood Test
The APTT assay measures how long it takes for a blood clot to form by measuring the amount of time it takes for fibrinogen to be converted to fibrin.
Prothrombin Time (PT) & INR
The PT assay is used to diagnose and monitor a variety of bleeding and clotting disorders by measuring how long it takes a blood clot to form.
Immune Thrombocytopenia (ITP)
Immune thrombocytopenia (ITP) is a rare autoimmune disorder in which the body’s immune system destroys its own platelets.
Disseminated Intravascular Coagulation (DIC)
Disseminated intravascular coagulation (DIC) occurs when the blood coagulation system is overwhelmed causing widespread blood clots and bleeding throughout the body.
Hemophilia
Hemophilia is a rare inherited blood disorder that affects the ability of blood to clot. People with hemophilia often bleed for longer than usual after an injury or surgery.
Hemorrhagic Disease of the Newborn
Hemorrhagic disease of the newborn is a bleeding disorder that occurs in newborns due to a deficiency of vitamin K.