Heart Disease
Self Help Clearinghouse
Arrhythmia Alliance (The Heart Rhythm Charity)
International network. Founded 2004. A network of sufferers, medical professionals, various UK based charities and related industries promoting better understanding, diagnosis, treatment and quality of life for individuals with cardiac arrhythmias.
Write:
Arrhythmia Alliance
P.O. Box 3697, Stratford upon Avon
Warwickshire, UK CV37 8YL
Voice: 44-01 78904
Website: http://www.heartrhythmcharity.org
E-mail: info@heartrhythmcharity.org
Verified: 10/13/2010
Mended Hearts
National. 285 chapters. Founded 1951. Mutual support for persons who have heart disease, their families, friends and other interested persons. Quarterly magazine and chapter development kit.
Write:
Mended Hearts
8150 N. Central Expressway
M2075
Dallas, TX 75206
Voice: 1-888-432-7899 or 214-296-9252
Fax: 214-295-9552
Website: http://www.mendedhearts.org
E-mail: info@mendedhearts.org
Verified: 10/13/2010
National Society for MVP and Dysautonomia
National. 54 affiliated groups. Founded 1987. Assists individuals suffering from Mitral Valve Prolapse syndrome and dysautonomia to find support and understanding. Education on symptoms and treatment. Newsletter and literature.
Write:
National Society MVP and Dysautonomia
880 Montclair Rd., Suite 370
Birmingham, AL 35213
Voice: 205-592-5765 or 1-800-541-8602
Fax: 205-592-5707
Website: http://www.mvprolapse.com
E-mail: staff@mvprolapse.com
Verified: 12/2/2009
Society for Mitral Valve Prolapse Syndrome
International. 23 affiliated groups. Founded 1991. Provides support and education to patients, families and friends about mitral valve prolapse syndrome. Newsletter, phone support, literature, conferences and support group meetings. Publishes 'Survival Guide.' Offers guidelines to start similar groups.
Write:
Society for MVP Syndrome
P.O. Box 431
Itasca, IL 60143-0431
Voice: 630-250-9327
Fax: 630-773-0478
Website: http://www.mitralvalveprolapse.com
E-mail: bonnie0107@aol.com
Verified: 10/14/2010
Kids With Heart
National. 3 affiliated groups. Founded 1985. Mutual support for families and adults affected by congenital or acquired heart defects. Also provides bereavement services. Matches parents together for support, referrals to local support groups nationwide. Promotes public awareness of congenital heart defects. Books, awareness products, advocacy assistance and assistance in starting groups.
Write:
Kids With Heart NACHD, Inc.
1578 Careful Dr.
Green Bay, WI 54304
Voice: 1-800-538-5390 or 920-498-0058 (voice/fax) (Mon.-Fri., 8am-3pm CST)
Website: http://www.kidswithheart.org
E-mail: michelle@kidswithheart.org
Verified: 10/13/2010
Adult Congenital Heart Association
National. Founded 1998. Seeks to improve the quality of life and extend the lives of adults with congenital heart defects. Education, outreach, advocacy and promotion of research. Online support, quarterly newsletter and national conferences.
Write:
Adult Congenital Heart Association
6757 Greene St., Suite 335
Philadelphia, PA 19119
Voice: 1-888-921-2242 or 215-849-1260
Fax: 245-849-1261
Website: http://www.achaheart.org
E-mail: info@achaheart.org
Verified: 10/13/2010
Congenital Heart Anomalies-Support, Education, Resources (CHASER)
National network. Founded 1992. Opportunity for parents of children born with heart defects to network with other parents with similar needs and concerns. Education on hospitalization, surgeries, medical treatments, etc. Phone support, information and referral. Heart surgeons and facilities directory.
Write:
CHASER
2112 N. Wilkins Rd.
Swanton, OH 43558
Voice: Jim and Anita 419-825-5575 (day)
Verified: 10/14/2010
SADS Foundation
International. 5 affiliated groups. Founded 1992. Works to save the lives of young persons who are predisposed to sudden death due to cardiac arrhythmia. Offers networking, newsletter, literature, advocacy, information, phone support and referrals.
Write:
SADS Foundation
508 E. South Temple, Suite 202
Salt Lake City, UT 84102
Voice: 1-800-786-7723 or 801-531-0937
Fax: 801-531-0945
Website: http://www.stopsads.org
E-mail: sads@sads.org
Verified: 10/13/2010
SVT (Supra Ventricular Tachycardia) Support
Online. Founded 2002. E-mail list support. Mutual aid support from and for persons with supra ventricular tachycardia or any type arrhythmia. Newsletter.
Website: http://groups.yahoo.com/groups/svtsupport
Verified: 10/13/2010
Pacemaker Club
Online. Founded 2000. Regular exchange of messages, listserv and newsgroup. Chat meetings. E-mail pen pal program to support new members. Offers support, information and encouragement in a fun and interactive environment. Also provides information on local groups.
Website: http://www.pacemakerclub.com
Verified: 10/13/2010
Children's Cardiomyopathy Foundation
Online. Provides support and information on pediatric cardiomyopathy. Offers website discussion forum and biannual newsletter. Working on plans to start community support groups.
Website: http://www.childrenscardiomyopathy.org
Verified: 10/13/2010
Congenital Heart Information Network
Online. Offers support, information and resources to families of children with congenital heart defects, acquired heart disease and adults with congenital heart defects. Also open to interested professionals.
Website: http://www.tchin.org
Verified: 10/13/2010
Little Hearts, Inc.
National. Provides support, resources, networking and hope to families affected by congenital heart defects. Provides newsletter, literature, phone support, annual picnic and advocacy.
Write:
Little Hearts, Inc.
P.O. Box 171
110 Court St., Suite 3A
Cromwell, CT 06416
Voice: 1-866-435-4673
Fax: 860-635-0006
Website: http://www.littlehearts.org
E-mail: info@littlehearts.org
Verified: 10/13/2010
It's My Heart
National. 15 groups. Founded 2005. Mutual-aid support provided via family matching program (matches families with others that have a similar congenital heart defect diagnosis or by proximity), moderated online message board and listserv. Provides support, education and advocacy for those affected by congenital heart defects by creating alliances with fellow families, hospitals, support groups and the community. Newsletter, online support group and assistance in starting local support groups available.
Write:
It's My Heart
1775 St. James Pl., Suite 130
Houston, TX 77056
Voice: 1-888-432-7807
Fax: 866-222-0334
Website: http://www.itsmyheart.org
E-mail: info@itsmyheart.org
Verified: 10/14/2010
Sudden Cardiac Arrest Association Online Community
Online. Support community connecting those who have suffered sudden cardiac arrest, have an implantable defibrillator, are family or caregivers of someone who suffered a cardiac arrest and all who want to interact with others interested in reducing sudden cardiac arrest.
Website: http://www.suddencardiacarrest.org
Verified: 5/3/2010
HAMA (Hypertrophic Cardiomyopathy Association)
Online. 225+ active members. Message board that offers mutual support and exchange of information for persons with hypertrophic cardiomyopathy and their families and friends. Website has resource information.
Website: http://www.4hcm.org
Verified: 10/11/2010
This information does not replace the advice of a doctor. Healthwise disclaims any warranty or liability for your use of this information. Your use of this information means that you agree to the Terms of Use. How this information was developed to help you make better health decisions. |
Topic Contents
- Arrhythmia Alliance (The Heart Rhythm Charity)
- Mended Hearts
- National Society for MVP and Dysautonomia
- Society for Mitral Valve Prolapse Syndrome
- Kids With Heart
- Adult Congenital Heart Association
- Congenital Heart Anomalies-Support, Education, Resources (CHASER)
- SADS Foundation
- SVT (Supra Ventricular Tachycardia) Support
- Pacemaker Club
- Children's Cardiomyopathy Foundation
- Congenital Heart Information Network
- Little Hearts, Inc.
- It's My Heart
- Sudden Cardiac Arrest Association Online Community
- HAMA (Hypertrophic Cardiomyopathy Association)

Feedback