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Real members of MyAmyloidosisTeam have posted questions and answers that support our community guidelines, and should not be taken as medical advice. Looking for the latest medically reviewed content by doctors and experts? Visit our resource section.
August 9
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That's a really important question to raise, and it's worth understanding why early genetic testing can matter — even before heart symptoms appear.

With wild-type ATTR, genetic testing isn't typically needed since it's not inherited. However, if your hATTR typing was ambiguous, that changes things a bit. Here's why earlier Show Full Answer

That's a really important question to raise, and it's worth understanding why early genetic testing can matter — even before heart symptoms appear.

With wild-type ATTR, genetic testing isn't typically needed since it's not inherited. However, if your hATTR typing was ambiguous, that changes things a bit. Here's why earlier genetic clarity can be valuable:

- Treatment options differ between wild-type and hATTR — some medications are only approved for one type
- Early treatment works best before organ damage occurs, as most therapies can slow progression but can't reverse existing damage
- A confirmed hATTR mutation could also have implications for blood relatives who may want to be tested Waiting until the heart is affected could mean missing a window for more effective treatment. It may be worth getting a second opinion from an amyloidosis specialist, as they see this condition more regularly than general cardiologists and may have a different perspective on the timing of genetic testing.

A MyAmyloidosisTeam member in a similar situation found that seeking care at a dedicated amyloidosis center helped them get clearer answers much sooner.

August 9

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