Resources
ARC provides patients and healthcare professionals with the latest, up-to-date resources to
help improve treatment and care of patients with amyloidosis.
Webinars
ARC Talks
Patients
ARC Talks
Patients
GI Disturbances and Symptom Relief for Amyloidosis
Dr. John Clarke, a gastroenterologist and motility specialist with Stanford Medicine, covers everything that patients need to know about GI involvement and symptom management in amyloidosis, followed by a Q&A session.
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Webinars
ARC Talks
Physicians
Physicians
ARC Talks: Managing Amyloidosis during COVID-19 for Physicians
This physician webinar covers the treatment of amyloidosis patients during the COVID-19 pandemic. With guidelines from the International Society of Amyloidosis, high-risk patient considerations, an update on clinical trials, and policy changes, we cover everything HCPs need to know.
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ARC Talks
AL Amyloidosis
Webinars
Hereditary ATTR Amyloidosis
Wild-Type Amyloidosis
ARC Talks
Other Types of Amyloidosis
Patients
Webinars
Hereditary ATTR Amyloidosis
Wild-Type Amyloidosis
ARC Talks
Other Types of Amyloidosis
Patients
Caregivers: A Guide to Self-Care
Nancy Verel, a nurse at the Cleveland Clinic, shares her story about her family's journey through her husband's AL amyloidosis diagnosis and treatment. Robert David from BMC Cancer Support Programs provides coping and support strategies for caregivers.
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AL Amyloidosis
AL Amyloidosis
Patient Stories
Patient Stories
AL Amyloidosis: Dan’s story
Dan, a patient with AL amyloidosis, describes his journey to diagnosis. A once very active athlete, Dan found himself not able to do his favorite activities anymore. After 10-15 doctors misdiagnosed Dan with GERD, emphysema, and athlete's heart, he finally received the correct diagnosis of AL amyloidosis and started on the road to recovery.
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AL Amyloidosis
Patient Stories
Wild-Type Amyloidosis
Wild-Type Amyloidosis
Wild-type ATTR: James’ story
James' only concerning symptom leading up to his diagnosis was bilateral edema. But, after a stroke, James spent a month in the hospital and received a surprising diagnosis of Wild-Type Transthyretin Amyloidosis. James shares his story and optimism just months after his diagnosis.
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Patient Stories
Hereditary ATTR Amyloidosis
Patient Stories
Patient Stories
Hereditary ATTR: Cece’s story
Despite having many of the "red flag" symptoms of amyloidosis, Cece still experienced a delay in diagnosis. Cece shares her story, how a genetic condition has impacted her family, and how a heart transplant changed her life.
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Hereditary ATTR Amyloidosis
AL Amyloidosis
Patient Stories
Patient Stories
AL Amyloidosis: Greg’s story
Greg Foster, 4-time world champion and Olympic Silver medalist, discusses his journey to diagnosis. Learn more about his initial symptoms, multiple doctors visits, and what drove him to continue pursuing an accurate diagnosis of AL Amyloidosis, despite being told he had Athlete's Heart.
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AL Amyloidosis
Publications
[Poster] The Amyloidosis Forum: A Public-Private Partnership to Advance Drug Development in AL Amyloidosis
Isabelle Lousada, Vaishali Sanchorawala, Angela Dispenzieri, Kristen Hsu, Robyn Himick, Preston Dunnmon, Mathew Maurer. International Society of Amyloidosis, Annual Meeting 2020
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Publications