The variety of signs and symptoms associated with Fabry disease means that both its diagnosis and treatment require input from a number of different healthcare specialists.
In the first instance, you may be referred to a specialist centre or genetic laboratory for confirmation of the diagnosis. This may be because another member of the family has been diagnosed, or because a certain combination of symptoms may lead your doctor to suspect Fabry disease.
Once a diagnosis of Fabry disease has been made, you may be referred to a specialist centre for co-ordinated consultations and ongoing treatment. In Australia, patients need to be referred to one of the specialist centres for confirmation of the diagnosis and appropriate treatment and monitoring. All centres have been designated by the Department of Health to provide treatment and monitoring for patients with Fabry disease or other lysosomal storage disorders. The Fabry Treatment Centre in your State is experienced in the care of people with genetic disorders such as Fabry disease and will be able to help with coordinating your care across specialists.
A number of doctors, nurses, therapists and counsellors may be involved in the management of Fabry disease:
Your local GP may have been the person with whom you first discussed your symptoms and who made the initial referral to see a specialist. He or she will also be responsible for your day-to-day health and should be kept informed about the treatments you are receiving at the specialist centre.
These are hospital doctors who specialise in diseases that affect how the body makes and breaks down substances. They will also have experience in the genetic side of such diseases. These specialists will often be the doctors who confirm a diagnosis of Fabry disease and co-ordinate a patient's management and treatment.
A geneticist specializes in inherited and genetic diseases. They will often be involved in confirming the initial diagnosis of Fabry disease and may be consulted during the ongoing management programme.
As part of your initial check-up at the specialist centre, as well as at various times during your care, you may be advised to visit physicians who focus on certain areas. These include (and there may be others):
Also, it is possible that it was a physician who specialises in one of these areas who first identified that you may have Fabry disease.
You may be assigned a specialist nurse who has expertise in Fabry disease and other lysosomal storage disorders (LSDs). The nurse will potentially be the person with whom patients and their family have the most contact. They may also be responsible for organizing and monitoring treatments such as enzyme replacement therapy (ERT).
Genetic counselling may be offered, particularly if a person who has been diagnosed with Fabry disease has concerns regarding other family members that may also be affected, or if they are considering starting a family.
It is also important to develop your own support network, which you can rely on for information and help when you need it. Fabry Australia runs 4 meetings a year in Australia in different states where people with Fabry disease attend and have opportunity to meet and discuss their symptoms and concerns relating to Fabry disease. Fabry Australia also has BLOGS.
19-Jul-2010
A Dear Fabry Community Letter giving an update on the supply of Fabrazyme
06-Jun-2010
FSGA is very fortunate to have international speaker Dr Stephen Waldek present to Australian Fabry patients in 5 states.