Amyloidosis Support Group

For Patients, Families, & Friends

JOIN US FOR

Q & A sessions with Amyloidosis experts.
Tips to maintain quality of life with amyloidosis Information about clinical trials & therapies, and
Group discussions

Saturday, Oct 19, 2024

7:30–3:30 pm | 1st Floor Auditorium
The Primary Children’s and Families’ Cancer Research Center at Huntsman Cancer Institute

Keynote Speaker

About

The annual Utah Amyloidosis Support Group in Salt Lake City is provided by Amyloidosis Support Groups, Inc. in conjunction with the Utah Amyloidosis Program. We welcome patients, family members, friends, and anyone else effected by amyloidosis to join us. Group discussions, presentations and Q & A will focus on topics related to amyloidosis as well as caregiver concerns. The majority of topics will focus on AL Amyloidosis and TTR Amyloidosis (hereditary and age-related) but topics surrounding other diagnoses of amyloidosis will be discussed as well. Complementary breakfast and lunch will be provided courtesy of the Utah Amyloidosis Program.

Location

Map shows Huntsman Cancer Center buildings in a row starting with cancer hospitals left and research buildings right.

New location at Primary Children’s and Families’ Cancer Research Center (also called the Cancer Research South building)

Parking

Parking is available directly in front of the Primary Children’s and Families’ Cancer Research Center in the outdoor strip parking. Do not park in stalls marked as 24-hour reserved.

This parking lot can be accessed by driving up North Medical Drive past University Hospital and taking the next right in front of the parking terrace. Go straight past the Clinical Neurosciences Center and stay left where the road will curve back into a parking lot directly in front of the Primary Children’s and Families’ Cancer Research Center.

Otherwise, visitors are welcome to park in the patient parking terrace however be aware that the walk will take approximately 5–10 minutes from this location.

Contact Us

RSVP, questions, comments, and concerns can be directed to Muriel Finkel, President of Amyloidosis Support Groups.

E-mail: Muriel@AmyloidosisSupport.org

Thank you to Muriel Finkel from Amyloidosis Support Groups Inc. for helping us put on this successful event for patients and others affected by amyloidosis on an annual basis.

Patient Resources