ASG booth at ASH (American Society of Hematology) in Atlanta GA December 2012. Courtesy of Paula Schmitt and Carole Harber.


Website www.amyloidosissupport.com

Toll Free Hot/Help Line 866-404-7539


ON LINE AMYLOIDOSIS SUPPORT www.amyloidosisonline.com
OVER 1370 HAVE JOINED OUR "FAMILY" IN 6 YEARS. This group is for patients, caregivers, friends, family and those who have lost someone to this rare disease amyloidosis.

We hope you can also attend our meetings. Details are on our website.
We have a lot to give each other as well as receive and our expert doctor
guests are so educational, supportive and helpful.

If you have the familial form of the disease we have another on line group
www.familialonline.com. We have on this group, AL, familial, localized, Wild Type TTR (Senile), CAA, ILE 122, African American Variant, AA, and
others. All are welcome.

We have on our home page www.amyloidosisonline.com
Archives of previous posts;

Click on messages and type in key words (i.e. edema, velcade, tongue)
and find all posts referring to these items of interest

Links:
Items of common interest

Polls:
Take part in these anonymous polls and be counted

Files:
Articles of interest to all

Photos:
See who you are talking to

This is your group and if you can not find what you are looking for on the website www.amyloidosissupport.com someone on this list or one of our medical advisors will be able to help. Come to a support meeting near you soon.

Our website also features the most common symptoms of
Systemic amyloidosis.

LLS and Entitlements
Contact Paula pschmitt_98@yahoo.com

Survivor Stories
See link on website www.amyloidosissupport.com