Giannina
OnePath Patient
Support Manager
Tools & Support
Find resources to help you make the most of OnePath support for your prescribed Takeda treatment.
Giannina
OnePath Patient
Support Manager
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Find enrollment forms for Takeda treatments here.
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Find the OnePath brochure
that’s right for you
If you’re prescribed a Takeda treatment for primary immunodeficiency (PI) or multifocal motor neuropathy (MMN), you can now find information and resources at Takeda Patient Support.
Alpha-1 antitrypsin deficiency (Alpha-1)
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Hereditary angioedema (HAE)
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Hunter syndrome (MPS II)
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Short bowel syndrome (SBS)
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Type 1 Gaucher disease
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Stay connected with OnePath
Use the OnePath App and Portal to update insurance information, log how you or your loved one is feeling with our convenient Health Events Log, and much more.
Discover inspiring real-life stories
Hear from people living with or caring for someone with Gaucher disease or Hunter syndrome. Their journeys of self-discovery, full of purpose and grit, are sure to move you.
Community resources*
If you’re prescribed a Takeda treatment for primary immunodeficiency (PI) or multifocal motor neuropathy (MMN), you can now find information and resources at Takeda Patient Support.
Uncover Alpha-1 is an online resource for navigating life with Alpha-1, full of information on genetic testing, diagnosis, lifestyle changes, management, and more—designed for both those living with the condition and their loved ones. Uncover Alpha-1 also offers a closer look at the alpha-1 antitrypsin protein with a video about the role it plays in the body.
The Alpha-1 Foundation is a not-for-profit Florida corporation created to promote research and the development of new therapies for improving the quality of life for those diagnosed with Alpha-1. The website contains patient support resources, healthcare provider (HCP) locator tools, ongoing grants offered, and links to events.
NORD (National Organization for Rare Disorders) is a rare disease umbrella organization that provides advocacy, research, education, and patient services in the US. See how they help and find out how you can get involved.
DiscoverHAE.com from Takeda offers information for people living with HAE. Topics include HAE symptoms, triggers, diagnosis, management, and more. You’ll also find downloadable tools and guides, patient videos, and links to support resources.
American Academy of Allergy, Asthma & Immunology (AAAAI)
Check out current research and connect with experts. See what today’s allergists, immunologists, and other healthcare professionals are talking about.
Hereditary Angioedema Association (HAEA) is a non-profit patient advocacy organization founded and staffed by HAE patients and caregivers. HAEA provides a wide range of HAE resources and personalized patient support.
NORD (National Organization for Rare Disorders) is a rare disease umbrella organization that provides advocacy, research, education, and patient services in the US. See how they help and find out how you can get involved.
American College of Allergy, Asthma & Immunology (ACAAI)
Explore the resources available through this wide network of healthcare professionals dedicated to improving the quality of patient care.
HunterPatients.com from Takeda offers information for people living with Hunter syndrome and those who care for them. There are links to websites and informative videos, and downloadable tools. You’ll also find inspiring family stories and much more.
The National MPS Society provides hope and support for individuals and families affected by MPS through research, advocacy, and awareness. Browse MPS resources, apply for family support programs, or get involved in fundraising.
NORD (National Organization for Rare Disorders) is a rare disease umbrella organization that provides advocacy, research, education, and patient services in the US. See how they help and find out how you can get involved.
ShortBowelSyndrome.com from Takeda provides education and tips for people living with SBS. It also offers a healthcare provider discussion guide, information about advocacy groups, insightful videos from patients, and much more.
Crohn’s & Colitis Foundation of America (CCFA) is a non-profit, volunteer-fueled organization dedicated to finding cures for Crohn’s disease and ulcerative colitis and improving the quality of life of patients and caregivers.
The Oley Foundation serves patients on home parenteral (IV) and enteral (tube-fed) nutrition. Their website contains a variety of medical and practical information such as troubleshooting guides, travel tips, networking and educational opportunities, as well as printable tools.
NORD (National Organization for Rare Disorders) is a rare disease umbrella organization that provides advocacy, research, education, and patient services in the US. See how they help and find out how you can get involved.
International Foundation for Functional Gastrointestinal Disorders (IFFGD) informs, assists, and supports people affected by gastrointestinal (GI) disorders.
United Ostomy Associations of America (UOAA) promotes quality of life for people with ostomies and continent diversions through information, support, advocacy, and collaboration.
KnowGaucherDisease.com from Takeda offers information about Gaucher disease, such as symptoms, testing methods, treatment options, and more. You’ll also find downloadable guides, links to advocacy organizations, and patient testimonials.
Gaucher Community Alliance (GCA) is a non-profit organization for the patient community by the patient community. GCA’s mission is to support patients with Gaucher disease and their families through peer-to-peer support and education, advocacy, patient and family resources, and networking.
National Gaucher Foundation (NGF) helps support the Gaucher community through financial, educational, and research programs. Follow them for the latest information and explore the resources on their website.
NORD (National Organization for Rare Disorders) is a rare disease umbrella organization that provides advocacy, research, education, and patient services in the US. See how they help and find out how you can get involved.
*The above links are provided as a resource. This is not an endorsement, and Takeda has no control over the content found on any website not owned by Takeda.
