Filotimo Foundation Mati
Adults with cystic fibrosis

Seen & Supported

The mati, or evil eye, is a form of protection. It offers peace and a sense of security.

So do we.

Medications covered. IVF cycles funded. Bills that were crushing you, paid.

A RIPPLE of relief.

The Filotimo Family

We’ve never met a stranger. Adults with CF, social workers, doctors, fertility clinics, friends. They’re all part of the Filotimo Family, where every connection creates a ripple that reaches far beyond one person.

  • Grace Jenkins

    “I’ve been a CF mom to my son Elliot since 2022.”

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    Grace Jenkins
    CF Ally
    Parent of a person with CF

    Glenside,

    Pennsylvania

    “I’ve been a CF mom to my son Elliot since 2022.”

    Grace Jenkins
    CF Ally
    Parent of a person with CF

    Glenside,

    Pennsylvania

    “I’ve been a CF mom to my son Elliot since 2022.”

  • Lauren Shallah

    “My husband has nonclassic CF & we are expecting our first child through IVF in January!”

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    Lauren Shallah
    CF Ally
    Spouse of a person with CF

    Blue Mound,

    Kansas

    “My husband has nonclassic CF & we are expecting our first child through IVF in January!”

    Lauren Shallah
    CF Ally
    Spouse of a person with CF

    Blue Mound,

    Kansas

    “My husband has nonclassic CF & we are expecting our first child through IVF in January!”

  • Brian Donahoe

    “Proud Filotimo Family member with a beautiful family thanks to the support of the foundation. Adult living and advocating for CF!”

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    Brian Donahoe
    Adult with CF
    Person with CF

    Pittsburgh,

    Pennsylvania

    “Proud Filotimo Family member with a beautiful family thanks to the support of the foundation. Adult living and advocating for CF!”

    Brian Donahoe
    Adult with CF
    Person with CF

    Pittsburgh,

    Pennsylvania

    “Proud Filotimo Family member with a beautiful family thanks to the support of the foundation. Adult living and advocating for CF!”

  • Pierce Chaseley

    “I have a cousin in his 30s with CF who I don't get to see very often, so I have been running for Filotimo as a way of connecting and supporting him.”

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    Pierce Chaseley
    CF Ally
    Friend of a person with CF

    Highland Park,

    Illinois

    “I have a cousin in his 30s with CF who I don't get to see very often, so I have been running for Filotimo as a way of connecting and supporting him.”

    Pierce Chaseley
    CF Ally
    Friend of a person with CF

    Highland Park,

    Illinois

    “I have a cousin in his 30s with CF who I don't get to see very often, so I have been running for Filotimo as a way of connecting and supporting him.”

  • Lanazha Hammond

    “I navigate life with a chronic illness ( CF) that affects my health and requires ongoing care. I continue to do my best to keep moving forward.”

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    Lanazha Hammond
    Adult with CF
    Person with CF

    Denver,

    North Carolina

    “I navigate life with a chronic illness ( CF) that affects my health and requires ongoing care. I continue to do my best to keep moving forward.”

    Lanazha Hammond
    Adult with CF
    Person with CF

    Denver,

    North Carolina

    “I navigate life with a chronic illness ( CF) that affects my health and requires ongoing care. I continue to do my best to keep moving forward.”

Pete and his wife dancing at their wedding

Our Story

Filotimo was founded by Pete Proimos, who has CF himself.

Everything we build comes from lived experience and from seeing how broken the system is for adults with CF. The system is built around survival, not possibility.

We exist to close that gap.

Our Impact

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hospital partners
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families supported

Need support?

Hardship Support

If you are struggling, we’re here.

Family Building

If you’re ready to build your family, we’re ready to help.