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158 Pleasant Street
N. Andover, MA 01845-2797
Phone: (978) 685-4477 or
1-800- 394-2747
Fax: (508) 685-4488
ABOUT KIDS is the pediatric branch of the International Foundation for Functional Gastrointestinal Disorders. ABOUT KIDS was formed to answer the needs of families, patients and health care professionals facing the many challenges posed by gastrointestinal motility disorders in infants and children. Since 1988, APHS, has been developing various programs to address its organizational objectives of research, education and family support. As a national and international not for profit charitable organization, APHS promotes public awareness of gastrointestinal motility disorders; these include, but are not limited to chronic intestinal pseudo-obstruction (CIP), Hirschsprung's disease (HD) and gastroesophageal reflux (GER).
American Heart Association
7272 Greenville Avenue
Dallas, TX 75231
Phone: (800) AHA-USA-1 or
The American Heart Association is a national voluntary health agency whose mission is to reduce disability and death from cardiovascular diseases and stroke.
Air Charity Network
Air Charity Network is a national network of charitable medical air transportation resources. The organization uses FAA-certified volunteer pilots who fly their own private aircraft. Also available are donated or deep discount airline tickets from airline partners through the National Patient Travel Center ( Eligibility for Air Charity Network assistance includes a verifiable medical travel need and patient situation where resources for commercial transportation are perhaps non-existant or very limited, at best. The Air Charity Network will likely administer 80% of all charitable medical travel trips in the United States this year. Actual transportation costs are donated by the volunteer pilots or special airline ticket funds. Donations to administer the program come from individuals, service clubs, foundations and corporations.
Birth Defect Research for Children Inc.
930 Woodcock Road, Suite 225
Orlando, FL 32803
(407) 895-0802
BDRC serves as a national clearinghouse to provide parents and professionals with information about birth defects and services for children with disabilities. BDRC sponsors the National Birth Defect Registry and parent matching service. They offer newsletters, Birth Defect Fact Sheets, and treatment and support group information. They also provide a Birth Defect Registry.
Children's Hospital Boston, Esophageal and Airway Treatment Center
Founded by Russell Jennings, MD, the Esophageal and Airway Treatment Center at Boston Children's Hospital is dedicated to the care of infants, children and young adults with complex esophageal and airway problems. For our team, these very rare esophageal conditions are not rare at all. Since 2010, our clinicians have cared for more than 600 patients, making us the most experienced institution in the world when it comes to treating these complex conditions.
March of Dimes Birth Defect Foundation
1275 Mamaroneck Ave.
White Plains, NY 10605
(888) 663-4637
March of Dimes offers a Catalog of Public Health Education Materials (booklets, information sheets and videos) available for purchase.
MARCI Kids (Midwest Acid Reflux Children's Institute)
MARCI-Kids is comprised of a team of experts with extensive experience treating children with Gastro Esophageal Reflux Disease (GERD). Pediatricians, pharmacology experts, and researchers from the University of Missouri-Columbia have come together to share the latest information available for treating this disease. The MARCI-Kids team includes health care providers who want to help children and families affected by this treatable disease.

Medicaid provides health coverage to millions of Americans, including eligible low-income adults, children, pregnant women, elderly adults and people with disabilities. Medicaid is administered by states, according to federal requirements. The program is funded jointly by states and the federal government.

National Fathers Network
16120 NE 8th St.
Bellevue, WA 98008-3937
(425) 747-4004 ext.218
The National Fathers Network (NFN) provides support and resources to fathers of children with developmental disabilities and chronic illness and the professionals who serve them. NFN develops materials in both English and Spanish.
NORD Inc. - National Organization for Rare Disorders
P.O. Box 1968
Danbury, CT 06813-1968
(800) 999-6673 (voicemail only)
Fax: 203.798.2291
One of NORD's main objectives is to encourage, promote and fund scientific research on the cause, control and ultimate cure of rare disorders (any disorder affecting fewer than 200,000 people). They act as a clearinghouse for information about rare disorders and facilitate networking of families with similar disorders for mutual support.
The Oley Foundation
214 Hun Memorial, A-28
Albany Medical Center
Albany, NY 12208-3478
(518) 262-5079 or (800) 776-OLEY
The Oley Foundation provides free information and emotional support to patients (consumers) requiring home nutrition support and their families. This includes enternal (tube) nutrition, for those who cannot eat but have at least a partially functioning intestinal tract; and parenteral (intravenous) nutrition for those who cannot absorb nutrients into their systems because of a damaged or removed intestinal tract. Support services include an information clearinghouse, bimonthly newsletter, local grassroots support networks, conferences and research on health outcomes.
Pediatric/Adolescent Gastroesophageal Reflux Association (PAGER)
Main Office
P.O. Box 1153
Germantown, MD 20875-1153
(301) 601-9541

West Coast Office
2329 Fallbrook Place
Escondido, CA 92027
(760) 747-5001

PAGER is a parent-led, nonprofit organization providing information and support to parents of children with GE Reflux. PAGER offers telephone support, literature on GER, a monthly newsletter, a library of technical information, lecture series (video tape), list of parent-tested, practical care techniques, and monthly meetings for local families.
The Pull-Thru Network
2312 Savoy St.
Hoover, AL 35226
(205) 978-2930
The Pull-Thru Network is a nonprofit national support and information network for families of children born with anorectic malformations and their associated defects, or who have had a pull-thru surgery for any reason. They publish a quarterly newsletter with medical information, new research, bowel management issues, helpful tips and personal stories.
Ronald McDonald Houses
The idea behind Ronald McDonald House is simple: provide a “home-away-from-home” for families of seriously ill children who are receiving treatment at nearby hospitals. Some children have to travel great distances to get the medical attention they need. In-hospital treatment may last one day, one year, or even longer. For the families of these children, accommodations can be hard to come by; options are often limited to costly hotels or unforgiving hospital chairs and benches. The Ronald McDonald House provides a comfortable, supportive alternative for these families. It serves as a temporary residence near the medical facility where family members can sleep, eat, relax and find support from other families in similar situations. In return, families are asked to make a donation ranging from $5 to $20 per day; if that isn’t possible, their stay is free.

The Sibling Support Project
A Kindering Center program
Don Meyer, Director
6512 23rd Ave NW, #213
Seattle, WA 98117
phone (206) 297-6368
fax (509) 752-6789

The Sibling Support Project is a national program dedicated to the interest's of brothers and sisters of people with special health and development needs. It includes newsletters, workshops and lots of resources for and about brothers and sisters.

St. George's Center
91 Victoria Road
Nottingham, NG4 2NN
TOFS is a support group based in England for families who have children with Esophageal Atresia, TEF and VATER. They publish a newsletter every two months and a magazine, CHEW, once a year.
United Ostomy Association, Inc. (UOA) - Parents of Ostomy Children (POC)
19772 MacArthur Blvd., suite 200
Irvine, CA 92612-2405
(800) 826-0826
The primary purpose of Parents of Ostomy Children is to support parents whose child has had or may have ostomy related bowel/bladder surgery. POC provides parent-to-parent support in person or by telephone from "parents who have been there." POC also coordinates educational sessions and social events at the national United Ostomy Association Conference. UOA publishes a quarterly magazine and POC publishes a national newsletter for parents.
Working With Kids
WorkingWithKids was formed to offer a unique reference point on working with children as a career or in voluntary work. Working with children is both demanding and rewarding. We examine potential child-focused roles, the legal requirements and the qualifications you need to work with children. Our concern was that there was no single UK resource for interesting features and practical advice on this subject. Our features and articles are written by professional journalists and experts - who have a particular interest, or a background in this area.