Everything you and your family need, in one place.
Whether you’re beginning treatment or looking for additional information along the way, this resource center brings together everything you need in one convenient location.
Explore the Eton Cares patient support program, ordering & pharmacy information, educational materials, downloadable guides, information about accessing HEMANGEOL, financial assistance resources, and additional tools designed to support families and caregivers throughout treatment.
We’re committed to helping make the treatment journey as straightforward and manageable as possible.
Your rare disease journey is personal. So is our support.
When your doctor prescribes HEMANGEOL, you’re automatically enrolled in the Eton Cares Patient Support—designed to support you and your family every step of the way with welcome calls, insurance verification, financial assistance, and ongoing pharmacy support.
*Restrictions, limitations, and/or eligibility requirements may apply.
When your doctor sends your prescription to our specialty pharmacy Anovo, this is what you can expect:
Welcome Call from your Care Coordinator to verify prescription, offer support, and answer questions
Medication Delivery with instructions and product-specific information
Insurance Verification to review coverage and benefits
Ongoing Pharmacy Support, including refill coordination, reminders, and 24/7 access to a pharmacist
Financial Assistance Review to explore copay programs and other support options
Nurse Ambassador Support to help you and your child stay on track with treatment, answer health or medication questions, and provide regular check-ins by phone
For questions or support, please contact us at our specialty pharmacy Anovo®:
The Pharmacy Team is always available by phone 24 hours a day, 365 days a year.
A helpful tip: We recommend saving Anovo’s phone number in your contacts so you can easily recognize important calls about your prescription, refills, or insurance updates.
Patient Education Materials
Patient Brochure
A caregiver brochure with information about HEMANGEOL and infantile hemangioma to share with families.
Instructions for Use
Parents and caregivers can follow these simple instructions to learn how to properly administer HEMANGEOL.
Getting Started Guide
Learn what to expect with your child’s HEMANGEOL prescription, including delivery, financial assistance, and ongoing support.
Medication Guide
Important safety information and usage guidance for parents and caregivers.
Physician Discussion Guide
A printable guide with key questions and talking points to help you have a productive conversation with your baby's physician.
Hemangioma FAQ (VBF)
Frequently asked questions about infantile hemangioma from the Vascular Birthmarks Foundation.
Talk to Your Baby's Physician
It is normal to feel scared or stressed about your baby's condition, but you're not alone. Your baby's doctor can answer any questions or concerns you may have and help get your baby the treatment he or she needs.
Talking to your baby's doctor is very important. It can help you develop a better understanding of infantile hemangioma, its potential impact on your baby, and the available treatment options. Bringing a list of questions to ask can help you make sure all your concerns are addressed.
Questions about Infantile Hemangioma
- What examinations and tests will my baby need?
- What should I watch out for with my baby's infantile hemangioma?
- What happens to the hemangioma over time if left untreated?
- What are the possible complications?
Questions about the Medication
- How does the medication work?
- Is this medication right for my baby?
- How quickly can I expect treatment with the medication to work?
- What are the side effects associated with this medication?
- How long will my baby need to take the medication?
- How do I get my baby started on the medication?
Caregiver Support and Patient Advocacy
When a baby first develops an infantile hemangioma, parents and caregivers may experience feelings of confusion, anxiousness, and guilt.
Below are organizations dedicated to providing education and support to all those affected by infantile hemangiomas.
The Vascular Birthmarks Foundation (VBF)
The Vascular Birthmarks Foundation is an international charitable organization that connects families affected by vascular birthmarks, tumors, or syndromes to the appropriate medical professionals. The foundation also provides informational resources, sponsors physician education, facilitates medical mission trips, and supports research and programs that promote acceptance for individuals with birthmarks.
The PHACE Syndrome Community (PSC)
PO Box 300
Willow Grove, PA 19090 USA
Phone: 1 (678) 744-3971
Email: info@phacesyndromecommunity.org
Website: phacesyndromecommunity.org
The PHACE Syndrome Community is a United States 501(c)(3) non-profit dedicated to serving those affected by PHACE syndrome along with their families, friends, and surrounding community. Its mission is to raise awareness of PHACE syndrome, build community for all affected, support research, and serve as a key source of medical information and the latest advancements.