Features

Surgery with general anesthesia has an increased risk of anaphylaxis for people living with SM. But there are alternatives.

Learning to manage stress levels with SM is key to avoiding symptom episodes and enjoying a better quality of life.

Have a carefully prepared SM medical kit to use in unexpected situations, such as the unexpected rapid onset of symptoms.

Clonal and nonclonal mast cell diseases have a different disease course and entail different therapeutic strategies.

People living with SM may benefit from having access to clinical trials that test innovative therapies still under research.

Closely monitor triggers and use antihistamines and topical skin treatments to help manage SM’s itchy rashes and flushing.

The loss of smell is less common in SM, but when it occurs, it can have implications for personal safety as well as one’s sense of taste.

Systemic mastocytosis (SM) rarely affects the eyes, but if it does, it can lead to loss of vision.

It’s an important part of disease management to monitor disease progression and the effectiveness of SM treatment.

SM-related anaphylaxis can happen suddenly and be life-threatening if not treated immediately. Have a plan to ensure a positive outcome.