For families
Explore Treatments
Find the Duchenne treatments that fit your child — matched to their stage, mutation, and where you receive care.
What treatment matching means
You shouldn't have to become a researcher to care for your child.
When a child is diagnosed with Duchenne, families are handed a wall of options overnight — corticosteroids, exon‑skipping drugs, gene therapy, cardiac and pulmonary care, physical therapy, nutrition, and a growing list of newly approved medicines. Each one comes with its own eligibility rules, side effects, schedules, and acronyms. It is overwhelming. It is supposed to feel overwhelming — and it isn't your fault.
Treatment matching is our way of cutting through that noise. Tell us about your child once, and we'll show you which approved and standard‑of‑care treatments fit their mutation, their stage, and the care available to your family — in plain language, without judgment, and without anyone trying to sell you something.
You make the decisions. We make sure you have every option in front of you.
Matched to your child
Filtered by mutation, age, ambulatory status, and the care team you already see.
Plain‑language explanations
What each treatment does, who it's for, and what to ask your neurologist.
Built for the long haul
Updated as new therapies are approved, so you're never working from old information.
Family Intake
Tell us about your child.
Share your child's situation and we'll match against approved and standard‑of‑care Duchenne treatments.
Build Your Treatment Guide
Answer a few questions so DMD Pathways can organize treatment information by country, treatment type, and what may be relevant to your family. Your answers are used only for this session and are not saved.