OPERATION HUNTER

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Help fund the search for a cure.

Hunter syndrome (MPS II) is a rare, progressive disease, and there is no cure today. Operation Hunter backs every credible scientific path toward one — funding research coordination, recruiting investigators, and winning grants — and prioritizes approaches that can reach the brain, where this disease does its cruelest work.

We are the catalyst, not the clinic. Your gift funds the grunt work that helps qualified teams get to a trial faster. Donations are processed by a secure third-party platform — Operation Hunter never sees or stores your card or bank details.

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Donations will be handled by a vetted third-party platform so that Operation Hunter never touches your payment details. Check back shortly, or reach the team through the mission console.

Where your gift goes

Coordination, not treatment

Donations fund the catalyst work: screening and applying for research grants, scouting publicly-published MPS II investigators, synthesizing the scientific literature, and drafting the legal and tax structure (for a licensed attorney and CPA to sign off). Any science happens only inside qualified institutions under FDA and IRB oversight — Operation Hunter does not perform medicine.

Want the detail? See the campaign plan and our cited grant radar and financial strategy.

How your donation is handled

We never see your card

Payments are processed entirely by a hosted third-party donation platform. Card and bank details go directly to that platform's secure systems; they never pass through, and are never stored on, this website. We receive only the funds and the platform's standard reporting.

Tax status

Not yet tax-deductible

Operation Hunter is not yet a registered 501(c)(3) tax-exempt organization. Unless and until contributions are processed through a fiscal sponsor or a recognized tax-exempt entity, gifts are generally not tax-deductible. We are exploring fiscal sponsorship to enable deductible giving. Please consult your own tax advisor about your situation.

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A personal share from someone people trust reaches further than any ad. Pass this campaign to one person who cares about rare disease, research, or kids. Nothing posts automatically — each button just opens the app with a ready-to-edit message.

You can also read the plan, explore the treatment landscape, or dig into the cited research library.

About the science we want to fund

Operation Hunter supports multiple credible scientific routes toward a cure, with a priority on therapies that can cross the blood–brain barrier. One direction we find promising — an encapsulated-cell / iPSC-gene-corrected approach to delivering the IDS enzyme — is a proposed research direction only. It is not approved, not human-tested, and not proven, and it is not available as a treatment. Nothing on this page is a medical claim, a promise of any outcome, or an offer of therapy.

Background, attributed to primary sources: Hunter syndrome (mucopolysaccharidosis type II) is a rare, X-linked condition caused by a shortage of the enzyme iduronate-2-sulfatase, leading to a progressive buildup of complex sugars in the body's cells — per MedlinePlus Genetics (U.S. National Library of Medicine). There is no cure, and current care focuses on managing the disease — see the National MPS Society and our cited research library.