Broad support in one location.
Patient support available for you
Ultragenyx is committed to patients with rare diseases, which is why we created UltraCare Patient Services for DOJOLVI—your guide throughout your treatment journey.
Our UltraCare Guides have varied backgrounds, including social workers, healthcare professionals, and patient advocates, and are ready to help you gain and maintain access to DOJOLVI.
UltraCare Guides can help you to:
Utilize patient support program resources, including help with billing and coding
Find and navigate available financial assistance and patient assistance programs that can help to cover co-pay and other out-of-pocket expenses
Start and stay on DOJOLVI treatment through personalized counseling and education based on the recommendations, advice, and prescription of your healthcare team
Take the first step
Step 1: Ask your healthcare
provider to fax your completed*
Start Form to 1-415-723-7474.
Step 2: Sign up by visiting UltraCare Patient Services or call 1-888-756-8657 to connect with our UltraCare Guides.
*Please note that a completed form is required for patient enrollment.
Download DOJOLVI materials
Step-by-step instructions for storing, administering, and keeping track of DOJOLVI doses
A tool you can use to keep track of your DOJOLVI doses and notes for your healthcare team
An overview of the UltraCare Patient Services program and the resources available to you
Learn more and find your community
Metabolic disease information and advocacy
A scientific organization specifically dedicated to research and education about fatty acid oxidation disorders
An advocacy organization working to educate and support patients with mitochondrial disease and their families
Rare disease information and advocacy
A center within the National Institutes of Health (NIH) that maintains a list of rare diseases and related terms to help people find reliable information about their disease
An advocacy organization that provides support, education, and resources to the rare disease community
A patient advocacy organization dedicated to individuals with rare diseases and the organizations that serve them