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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.
A MyAmyloidosisTeam Member asked a question 💭
Great BRITAIN
December 8, 2025
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A MyAmyloidosisTeam Member

Well Jim7 I think you are doing great as I can only walk about 25 ft with a walker. All exertion causes rapid fatigue followed by bp drop. I have wild type.

December 9, 2025
A MyAmyloidosisTeam Member

I asked my heart specialist when I was diagnosed. He said “5-7 years, but I am not very good at this guessing thing”. I’m 2.5 years on now and I have always taken Vyndamax 61 mg. As far as I can tell, I was diagnosed early, which helps. I feel very much like I did 2.5 years ago. I have also read in this site about a guy from England who is doing well 10 years after diagnosis and he was also on Vyndamax 61. I’m 83 years old, so how long might I live, with or without Amyloidosis? Good question. At present, I’m in good shape and workout every day by walking a mile on a treadmill and go to a workout class once a week. I’ve been happily married for 56 years, I think, happy wife, happy life…….and maybe a tad longer…….lol!
Jim7 😎🇨🇦

December 9, 2025
A MyAmyloidosisTeam Member

There is no real answer, there are to many factors. You can't go with answers from the internet, just to many personal factors involved.

December 9, 2025
A MyAmyloidosisTeam Member

Yes it is very complicated. I’ve read that there are three blood tests that contribute to making an informed guess for people diagnosed. It gives a median number of years for the three stages. Which means half are above and half are below. So the numbers are a guess.

December 8, 2025
MyAmyloidosisTeam

What is the life expectancy with wild-type ATTR amyloidosis?

Wild-type ATTR amyloidosis (ATTRwt) generally has a more favorable prognosis compared to hereditary forms of the condition. Since it develops slowly over time, people with ATTRwt often have a better outlook.

ATTRwt is typically diagnosed in men who are 60 or Show Full Answer

What is the life expectancy with wild-type ATTR amyloidosis?

Wild-type ATTR amyloidosis (ATTRwt) generally has a more favorable prognosis compared to hereditary forms of the condition. Since it develops slowly over time, people with ATTRwt often have a better outlook.

ATTRwt is typically diagnosed in men who are 60 or older. The condition affects the same protein as hereditary ATTR amyloidosis but is not inherited. Instead, the normal protein becomes unstable and misfolds on its own.

The amyloid deposits in ATTRwt most often affect the heart, though they can also impact nerves and soft tissues. This can sometimes cause carpal tunnel syndrome or peripheral neuropathy.

Many of the same medications used to treat hereditary ATTR amyloidosis can also be used for wild-type ATTR amyloidosis, which helps manage symptoms and slow disease progression.

While specific survival numbers weren't provided for ATTRwt alone, the more favorable prognosis and slower progression suggest better outcomes than some other forms of amyloidosis, especially when diagnosed and treated early.

December 8, 2025

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A MyAmyloidosisTeam Member asked a question 💭
Paris, AR