Where can I find out more about how to cope with an undiagnosed condition?
Where can I find out how to cope with an undiagnosed condition? Back to Top
GARD Information Specialists developed the following video tutorial to provide tips and resources to help you with the process of getting a diagnosis.
Tips for the Undiagnosed
To learn more about how to deal with genetic or rare conditions that have no definitive diagnosis, see:
- Learning about an Undiagnosed Condition in a Child
- Learning about an Undiagnosed Condition in an Adult
The Global Genes Project has developed a resource for people with undiagnosed conditions called "Becoming An Empowered Patient: A Toolkit For The Undiagnosed."
Are there research programs available for people without a diagnosis? Back to Top
Yes. If an individual’s health care providers and specialists have not been able to make a definite diagnosis so far, participating in a research study or clinical trial may be another option. See below for a description of some of the National Institutes of Health (NIH) research programs that are going on now:
The Undiagnosed Diseases Network (UDN) is a research study funded by the National Institutes of Health Common Fund. The UDN is made up of clinical and research centers across the United States working to improve diagnosis and care of patients with undiagnosed diseases. Physicians and patients with additional questions may call 1-844-746-4836 (1-844-Ring-UDN).
ClinicalTrials.gov is database that provides current information on clinical research studies. You can search ClinicalTrials.gov for research studies looking at general categories of diseases (e.g. neurological disease or eye disease) or specific symptoms. Some studies accept individuals without a diagnosis with the research goal of making a diagnosis.
One study that is enrolling individuals who do not have a diagnosis is entitled "Studies of Children with Metabolic and Other Genetic Diseases". This study is evaluating individuals with known or suspected genetic diseases, including metabolic diseases. Despite the name, people of all ages may be eligible for this study.
To find out more about clinical trials that take place at the NIH, you can call the NIH Clinical Center to talk to a specialist.
Patient Recruitment and Public Liaison Office
NIH Clinical Center
National Institutes of Health
Bethesda, Maryland 20892-2655
Toll-free: (800) 411-1222
Fax: (301) 480-9793
How can I learn more about clinical trials? Back to Top
If you or someone you know is interested in enrolling in a clinical trial, you can find helpful general information on clinical trials at ClinicalTrials.gov.
Resources on many charitable or special-fare flights to research and treatment sites and low-cost hospitality accommodations for outpatients and family members, as well as ambulance services, are listed in the Travel and Lodging Assistance section of this Web site.
Are there any advocacy groups for people with an undiagnosed condition? Back to Top
Yes. See below for additional information and supportive resources for individuals with an undiagnosed condition and their families.
In Need of Diagnosis (INOD) provides help and support to individuals with undiagnosed conditions.
Syndromes Without A Name (SWAN) is a supportive organization for families of children who have undiagnosed, unnamed conditions, or who are still looking for a diagnosis.
The National Organization for Rare Disorders (NORD) is a federation of more than 130 nonprofit voluntary health organizations serving people with rare disorders. The NORD Web site includes information on medication assistance programs and networking programs, a resource guide, and links to other online resources. You can get this information through NORD's Web site or by calling or writing the NORD offices.
National Organization for Rare Disorders
55 Kenosia Avenue
PO Box 1968
Danbury, CT 06813-1968
Toll free: 800-999-6673 (voicemail only)
Web site: http://www.rarediseases.org/
Who should I talk to if I have financial concerns? Back to Top
It can sometimes take many years of specialized appointments and testing for a condition to be diagnosed, and this affects many individuals and families financially.
The Patient Advocate Foundation is a non-profit organization that serves as a liaison between families and their insurer, employer or creditors to resolve insurance, job retention and/or debt crisis matters related to their medical conditions. You can contact the Patient Advocate Foundation for further information.
Patient Advocate Foundation
700 Thimble Shoals Boulevard
Newport News, VA 23606
Web site: http://www.patientadvocate.org
Are there organizations that can help with the cost of travel? Back to Top
Yes. Traveling to specialized centers for testing and diagnosis can be costly; the following organizations help organize free travel for patients within the US.
National Patient Travel Center
4620 Haygood Rd, Ste. 1
Virginia Beach, VA 23455
Web site: http://www.patienttravel.org
Where can I find out more about financial assistance? Back to Top
The National Organization for Rare Disorders (NORD) provides information on financial and medication assistance programs, health insurance, medicare/medicaid programs, and links to additional online resources. Most of these resources are available only to individuals in the United States.
The National Human Genome Research Institute (NHGRI) at the National Institutes of Health (NIH) has information about financial assistance resources for people who need help paying for medical care.