What best describes your hereditary ATTR (hATTR) amyloidosis experience?

hATTR amyloidosis is a rare, hereditary condition that can progress rapidly

Quote About Hope for the hATTR Amyloidosis Community
Quote About Hope for the hATTR Amyloidosis Community

Get to know the symptoms and the effects they can have on you and your family

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Your health and hereditary ATTR amyloidosis

A brochure to learn more about hATTR amyloidosis

Hear about David’s journey to diagnosis

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Watch David's Story
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Start creating your support system

Quote About Acceptance After an hATTR Amyloidosis Diagnosis
Quote About Acceptance After an hATTR Amyloidosis Diagnosis
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Find tips on talking with your family about your diagnosis and helping them understand the condition

Your Family Brochure

Your family and hereditary ATTR amyloidosis

A brochure to help guide important discussions with family and loved ones

Q&A Booklet

Our hATTR amyloidosis journey

A collection of personal experiences from people living with hATTR amyloidosis

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Learn how you can best support your loved one

Quotes About Mentally Coping with hATTR Amyloidosis
Quotes About Mentally Coping with hATTR Amyloidosis
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Get to know the symptoms and the effects they can have on you and your family

Your Family Brochure

Your family and hereditary ATTR amyloidosis

A helpful guide for both those with hATTR amyloidosis and their caregivers

Roland and his wife Nicky share their experience of living with hATTR amyloidosis

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Watch Roland's Story
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Learn how the condition occurs, what the symptoms are, and how it may affect your family

Read about the next steps after diagnosis and tips on how to talk to your family

Hear from people about their experiences living with hATTR amyloidosis

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Information and Support Groups

Amyloidosis Alliance logo

Amyloidosis Alliance is an international umbrella patient advocacy organisation, aiming to raise awareness and improve the quality of care of amyloidosis patients.

Click here to visit their website to find out more about the work they are doing to help patients across Europe and beyond.

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