Snake River Hemophilia & Bleeding Disorders Association Inc.

The Snake River Hemophilia and Bleeding Disorders Association’s mission statement is, “Improve the quality of care and life for persons with inherited bleeding disorders, including Hemophilia and Von Willebrand Disease, through education, peer support, resources, and referrals.” 

We meet every other month and have annual events for women, men, family, and the holidays!

Our Goals

EDUCATING FAMILIES

The main goals of the Association will be educating families about bleeding disorders and their treatment options, advocacy for patient’s best care, and peer support for both individuals and families.

Insurance concerns, parental and school support for children with bleeding disorders, sibling issues, treatment options (both concerning medicine and treatment facilities) and extended health care needs are some of the issues that affect the bleeding disorder community.

Current Board Members

Angie Boling

President

Curtis Jaussi

Vice President

Chad Stevens

Treasurer

Kymm Shaw

Executive Director

Upcoming Events

Next Meeting: Wednesday, April 26th
Bees Knees Restaurant at 6:00PM

Snake River Hemophilia Meetings

How Often? Every Other Month

Camp Sunrise Family Camp
Where: Sawtooth United Methodist Campground
Fairfield, Idaho
When: June 22nd – 24th

Parnering with Idaho Chapter National Hemophilia Foundation