Please note that the amount listed above ($27,500) is an accumulated total since January 2024! You guys have been a huge blessing and those funds have already been used during 2024/2025!!

Dear friends and compassionate hearts,

We come to you with a plea for help and hope for 2 year old Maximo Sagrero, as a 5-month-old, this warrior was diagnosed with Menkes Disease, an extremely rare and life threatening condition.

As parents, the weight of this news was immeasurable, but despite this hardship, Juan and Katy’s spirits remain steadfast as they seek a lifeline for their precious son.

This lifeline comes in the form of a clinical trial in Columbus, Ohio. Treatment was critically urgent. Katy and Maximo traveled from their home in Merida, Mexico to DFW Texas, where he can be seen at Children’s FtWorth to continue on his trial treatment plan that is currently the only trial available for Menke’s Disease.

However, the path to this beacon of hope is fraught with financial challenges. The family is in urgent need of support as the clinical trial takes place over the course of 3 years, and will require Maximo to remain in the United States during such time. Your financial support would help with the mounting costs of travel, lodging, doctor’s visits, medication, and general living expenses during Maximo's ongoing treatment.

By contributing to this GoFundMe, you become a vital part of “Team Momo”, a community rallying behind a family in their quest for healing. Every donation, no matter the size, is a step closer to providing Maximo with the care he needs and deserves.

Thank you for opening your hearts to Maximo's story. Your love, prayers and support light the way for this brave little warrior.