ACHA logo

The Adult Congenital Heart Association (ACHA) is a nonprofit organization that seeks to improve the quality of life and extend the lives of adults with congenital heart defects. Through education, outreach, advocacy, and promotion of research, ACHA serves and supports the more than one million adults with congenital heart defects, their families and the medical community.

6757 Greene Street, Suite 335
Philadelphia, PA 19119-3508

(888) 921-2242


ACS logo

The American Cancer Society is a nationwide, community-based voluntary health organization dedicated to eliminating cancer as a major health problem. Headquartered in Atlanta, Georgia, the ACS has 12 chartered Divisions, more than 900 local offices nationwide, and a presence in more than 5,100 communities. Saving lives by helping people stay well, get well, find cures, & fight back.

250 Williams Street NW
Atlanta, Georgia, 30303



AHA logo

Our mission is to build healthier lives, free of cardiovascular diseases and stroke. That single purpose drives all we do. The need for our work is beyond question.

7272 Greenville Ave.
Dallas, TX 75231



ALS logo

Established in 1985, The ALS Association is the only national non-profit organization fighting Lou Gehrig's Disease on every front. By leading the way in global research, providing assistance for people with ALS through a nationwide network of chapters, coordinating multidisciplinary care through certified clinical care centers, and fostering government partnerships, The Association builds hope and enhances quality of life while aggressively searching for new treatments and a cure.

1275 K Street NW, Suite 1050
Washington, DC 20005

(800) 782-4747


ALZ logo

The Alzheimer's Association is the leading, global voluntary health organization in Alzheimer's care and support, and the largest private, nonprofit funder of Alzheimer's research.

225 N. Michigan Ave., Fl. 17
Chicago, IL 60601-7633

(800) 272-3900


PSP logo

Increase awareness of progressive supranuclear palsy, corticobasal degeneration, and other atypical Parkinsonian disorders; fund research toward treatment, cure and prevention; educate healthcare professionals; and provide support, information, and hope for affected persons and their families.

30 E. Padonia Road, Suite 201
Timonium, MD 21093



HDSA logo

The Huntington's Disease Society of America is the largest 501(c)(3) non-profit volunteer organization dedicated to improving the lives of everyone affected by Huntington's Disease. Founded in 1968 by Marjorie Guthrie, wife of folk legend Woody Guthrie who lost his battle with HD, the Society works tirelessly to provide the family services, education, advocacy and research to provide help for today, hope for tomorrow to the more than 30,000 people diagnosed with HD and the 200,000 at-risk in the United States.

505 Eighth Avenue, Suite 902
New York, NY 10018



IBC logo

"The Inflammatory Breast Cancer Foundation is a group of concerned citizens who came together with the hope of making a difference in the way Inflammatory Breast Cancer ( IBC ) is perceived by both the general public and the medical community.

Our mission is to change the perceived notion that all breast cancers have a lump. The medical community has not been educated to a degree where they can catch this deadly form of breast cancer earlier than stage IIIB. This is not acceptable"

P.O. Box 16
Milford, Michigan 48381

(866) 944-4223


NMSS logo

The National MS Society is a collective of passionate individuals who want to do something about MS now—to move together toward a world free of multiple sclerosis. MS stops people from moving. We exist to make sure it doesn't. We help each person address the challenges of living with MS through our 50-state network of chapters. The Society helps people affected by MS by funding cutting-edge research, driving change through advocacy, facilitating professional education, and providing programs and services that help people with MS and their families move their lives forward.

1100 New York Ave.,N.W.
Suite 660
Washington, DC 20005



NORD logo

The National Organization for Rare Disorders (NORD), a 501(c)(3) organization, is a unique federation of voluntary health organizations dedicated to helping people with rare "orphan" diseases and assisting the organizations that serve them. NORD is committed to the identification, treatment, and cure of rare disorders through programs of education, advocacy, research, and service.

55 Kenosia Avenue
Danbury, CT 06810

(800) 999-6673

Contact the Compassionate Allowances Team