Millions of people in the United States live with a rare disease. While each individual disease may be uncommon, the people they affect often face similar challenges. Finding reliable information, getting a diagnosis, and locating resources can feel overwhelming.
That’s where NIH’s Genetic and Rare Diseases (GARD) Information Center can help.
Easy-to-understand information at your fingertips
GARD is a comprehensive resource for anyone affected by a rare disease. On their website, you’ll find current, reliable, and easy-to-understand information on thousands of rare diseases. Information is available in both English and Spanish. It is presented in a clear and actionable way, giving you the information you may need to get a diagnosis, manage your care, or find a supportive community.
Connect with a GARD Information Specialist
Getting a diagnosis for a rare disease can be challenging and, for some patients, may take months to years. GARD offers free support through its team of dedicated Information Specialists.
GARD Information Specialists can provide individualized help with:
- Finding or understanding information about a rare disease
- Navigating the process of getting a rare disease diagnosis
- Finding resources, disease experts, and clinical trials
- Connecting with patient communities
While GARD Information Specialists can’t give you medical advice or make a diagnosis, they can help you find someone to answer your questions.
Contacting GARD
GARD Information Specialists are available Monday through Friday from 12 p.m. to 6 p.m. Eastern Time (except federal holidays).
Get in touch by calling toll-free at 888-205-2311 or by filling out a contact form on their website.
Tip: Be as specific as possible when describing your information needs to a GARD Information Specialist. It’s a good idea to have some questions prepared ahead of time.
With GARD's support, you won't have to face a rare disease alone.