Supporting people affected by Systemic Mastocytosis

Learn more about Systemic Mastocytosis

Supporting people affected by Systemic Mastocytosis

Systemic Mastocytosis (SM) is a very rare disease, but Novartis believes that No Disease is Too Small to receive support and guidance.

Systemic Mastocytosis (SM)

SM is a rare blood disease that is often underdiagnosed or misdiagnosed for years. Finding support and information can be difficult for patients and their loved ones. These resources are specifically created to empower patients and educate about the complexities of SM.
 

  • Get the facts about Systemic Mastocytosis

    Get the Facts

    Early identification of SM by a health care provider can be critical. Learn more about SM symptoms, diagnosis and treatment options.

  • Learn more about Systemic Mastocytosis, Symptoms and Diagnosis

    A Patient Guide

    SM is difficult to diagnose and treat. An educated SM patient and physician can work together to develop a treatment plan.

  • Having an informed conversation with your doctor about Systemic Mastocytosis

    Talking to Your Doctor

    Making the most of your doctor’s appointment can be a challenge. Use these questions to start a conversation with your doctor about SM and its impact on your life.