With more than

7,000 rare diseases rare
diseases

in the world1

including Fabry and Gaucher disease, many may not know the symptoms and are undiagnosed. When left untreated, complications can be life-threatening.2,3

A diagnosis is your first step to better care

What is Fabry and Gaucher disease?

They are both rare diseases belonging to a group of Lysosomal Storage Disorders (LSD).

LSDs are often characterized by enzyme deficiencies that cause a build-up of toxic substances in the body.4,5

Why is early diagnosis important?

Misdiagnosis for rare diseases is common, and you could take an average of 7 – 20 years to receive an accurate diagnosis.6,7

This means that appropriate treatment may be delayed which can lead to complications.3

How can I get help?

Evaluating your risk of Fabry and Gaucher diseases through the Symptom Matcher questionnaire can get you one step closer to the answers you need.

Find out your risk of
having Fabry or Gaucher disease

Find out your risk of having Fabry or Gaucher disease

  • Do you feel pain or numbness in your hands and feet?
  • Do you have frequent diarrhoea or abdominal pain?
  • Do you have hearing impairment or hear ringing in your ears?
  • Do you have heart and/or kidney problems?

You could be
at risk of Fabry Disease.

Find out at isitfabry.sg
  • Do you bleed or bruise easily?
  • Do you suffer from bone pain or fractures?
  • Do you experience chronic fatigue and often find yourself short of breath?
  • Do you have enlargement of the spleen and liver?

You could be
at risk of Gaucher Disease.

Find out at isitgaucher.sg

You could be at risk of
Fabry Disease.

Find out at isitfabry.sg

You could be at risk of
Gaucher Disease.

Find out at isitgaucher.sg

Approximately 1 in 20 people will be affected by a rare disease at some point in their life.8

You probably know at least
one person with a rare disease.

You probably know at least one person with a rare disease.

Help reach them by sharing this campaign:
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