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Support for Jill LoMonaco & Family

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Since fall of 2022, Jill has been hoping for a diagnosis to explain fainting spells and other neurological problems. In March 2024, at the Mayo Clinic Hospital in Phoenix, she finally got some answers. Jill has been diagnosed with POEMS. POEMS syndrome (Polyneuropathy, Organomegaly, Endocrinopathy, Monoclonal plasma cell disorder, Skin changes) is a paraneoplastic process characterized by the presence of a monoclonal plasma cell disorder, peripheral neuropathy, and other features. It is incredibly rare.

While insurance covers some of Jill's medical bills, it does not cover everything, and the Mayo Clinic is NOT cheap (but was the only place that FINALLY gave Jill some answers!). She is looking at treatments for the next six months, and is unsure when she will be able to go back to work. Jill has lost complete functional use of her hands and the ability to walk independently. (She cannot claim disability until she's been unable to work for a year.)

On top of that, Ryan had a recent career change, and their income for the household has decreased.

If you feel led to give, every little bit will help the LoMonaco family through this tough time and the medical bills ahead. Thanks in advance!
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Donations 

  • Amy Skaalen
    • $25
    • 6 mos
  • Christina Garnier
    • $100
    • 7 mos
  • Christine Denardo
    • $50
    • 8 mos
  • Raquel Bradley
    • $25
    • 8 mos
  • Katrina Kaeser
    • $100
    • 8 mos
Donate

Organizer and beneficiary

Natalie Trout
Organizer
Litchfield Park, AZ
Jill LoMonaco
Beneficiary

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