Active campaign · Playa del Carmen
Pato Manzi

STAY STRONG

Pato deserves the chance to grow up.

Every donation, every share, and every act of kindness brings Pato one step closer to the treatment he needs

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His story
8
Years old
HIGM
Diagnosis
1 in 500k
Affected worldwide
BMT
Only known cure

About Pato

Meet Pato

Patrizio — everyone calls him Pato — is one of those children who makes a room brighter just by being in it. At 8 years old, he is kind, happy, and somehow still finds reasons to laugh every single day. He has a beautiful smile and an amazing heart.

Pato was diagnosed with Hyper IgM Syndrome, a rare and life-threatening immune deficiency that leaves his body unable to fight infections on its own. He depends on regular immunoglobulin treatments to stay healthy — without them, even a common infection can become dangerous.

Pato also carries his big brother Massimo with him. In his own quiet way, he keeps Massimo's memory alive every day.

His father

Jonathan's story

My name is Jonathan, and I am the proud father of two incredible boys.

Several years ago, both of my sons were diagnosed with Hyper IgM Syndrome. Four years ago, we lost my oldest son, Massimo. He was only 11. That loss changed everything — and it made me more determined than ever to give Pato every chance possible.

Caring for Pato is my priority above everything else. Over the past few years, that has meant reducing my ability to work, navigating a system that doesn't always have the medication Pato needs, and covering the gaps myself — travel to specialists, medications, and all the unexpected costs that come with raising a child with a rare condition.

I am not asking for sympathy. I am asking for help so that Pato can have the stable, healthy childhood every child deserves.

Pato's older brother Massimo also lived with Hyper IgM Syndrome. He passed away four years ago at age 11. Pato talks to him still. Jonathan carries them both.

The diagnosis

What is Hyper IgM Syndrome?

Hyper IgM Syndrome (HIGM) is a rare primary immunodeficiency disorder. The immune system cannot produce the antibodies needed to fight common infections, leaving patients entirely dependent on external treatment to survive.

What it is

A rare genetic disorder affecting the immune system's ability to produce immunoglobulins (antibodies). Patients have elevated IgM but little or no IgG, IgA, or IgE.

What it means

Without proper antibodies, ordinary infections — pneumonia, gut infections, fungal disease — can become life-threatening. Constant medical supervision is required.

The treatment

Regular immunoglobulin infusions help replace the antibodies Pato's body cannot produce. These treatments must happen every month without interruption.

How rare

HIGM affects approximately 1 in 500,000 people. Government programs help when available — but gaps in supply force families to cover the cost privately.

ℹ️

While a bone marrow transplant is the only known cure for Hyper IgM Syndrome, Pato's immediate need is ensuring his monthly immunoglobulin treatments are never interrupted. That is what this campaign is focused on.

On-chain transparency

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23aoTXta6FtoPPPV3EV7AaXGBUDTK6p84WjkZboUCM8Z
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Updates

Campaign timeline

The family posts updates here as the campaign progresses. Every entry is dated and transparent.

Full updates on GoFundMe ↗
August 5, 2026Announcement

Campaign launched

The official campaign to support Pato's monthly treatments is now live. Thank you to everyone who has already shared and donated. Every bit of support reaches Jonathan and Pato directly.

Future updates will appear here

FAQ

Common questions

We want this campaign to be as transparent as possible. If you have a question that isn't answered here, the full story is on GoFundMe.

Yes. The GoFundMe campaign is the official fundraising platform, managed directly by Jonathan, Pato's father. The Solana wallet is Jonathan's own wallet — every transaction is publicly verifiable on-chain.

What happens next

Roadmap

NOW
1

Awareness

Reach as many people as possible with Pato's story through social media, press, and community.

Campaign launch
Social media outreach
Press contacts
First fundraising milestone
2

Community

Build a sustained support network around the family and keep donors informed with regular updates.

Telegram support group
Weekly updates from Jonathan
Community ambassadors
Token launch
3

Stability

Reach the funding goal and ensure Pato's treatments are covered without interruption for 6 months.

6 months of treatments secured
Reduced financial pressure on Jonathan
Pato living a normal childhood
Regular medical updates
4

Future

With stability achieved, explore long-term options including the bone marrow transplant that could cure Pato.

Sustained treatment plan
Transplant evaluation
Long-term donor community
Pato thriving

Community initiative

$Stay Strong Token

Stay Strong is a community initiative created to support Pato's fight against Hyper IgM Syndrome, raise awareness, and bring more people to the official donation campaign.

Important notice

Stay Strong ($PATO) is a community initiative created to raise awareness of Pato's campaign. It is not an investment, does not represent ownership or equity, and does not promise financial returns. To support Pato directly, please donate through the official GoFundMe campaign or the verified Solana wallet shown on this website.

Not an investment of any kind
No financial returns promised or implied
Does not represent equity in anything
No guarantees of any economic benefit

Want to actually help Pato? Donate directly through GoFundMe or send SOL to the official wallet above. That is the only way your support reaches the family.

Contract: Ghp8smazq181JaKp15TSwBUu6vBLYFJvrkP9GhwJpump

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You don't need money to help Pato. Sharing his story with your network could reach the person who does. Every share matters.

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