taysachs.net An initiative of Genetic Health Service Victoria, Murdoch Childrens Research Institute and the Jewish community
what is TSD | who it affects | carriers | Annette & Tom | Toni & Stuart | what to do | what testing involves | community screening day | student testing program |

Testing

For more than 95% of babies born with these conditions there is no family history of the condition.

What to do

Consider getting tested. Regardless of your own health, or that of your parents and even your children, you owe it to the health of your baby to be tested. Encourage your partner to get tested with you. Find out. Be sure, and remember although there is no cure, TSD and the other common genetic conditions can be avoided IF you’ve been tested.

Where do we go to have testing?

How does one determine their carrier status if they are not of Ashkenazi Jewish ancestry?

If you are not of Ashkenazi ancestry or you have mixed ancestry, a blood test is more appropriate to determine Tay Sachs disease carrier status. The type of testing required in this situation is a blood HexA level and this can be arranged by your general practitioner. If you have any questions, please call us to discuss this further.

   
Supported by The Pratt Foundation, The Besen Family foundation, The Bachrach Charitable Trust and anonymous donors
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