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Welcome to Hunter's Heart...
Discover the life of Duchenne Muscular Distrophy
What We Know~
Duchenne muscular dystrophy (DMD) is a genetic disorder characterized by progressive muscle degeneration and weakness due to the alterations of a protein called dystrophin that helps keep muscle cells intact. DMD is one of four conditions known as dystrophinopathies. The other three diseases that belong to this group are Becker Muscular dystrophy (BMD, a mild form of DMD); an intermediate clinical presentation between DMD and BMD; and DMD-associated dilated cardiomyopathy (heart-disease) with little or no clinical skeletal, or voluntary, muscle disease.
DMD symptom onset is in early childhood, usually between ages 2 and 3. The disease primarily affects boys, but in rare cases it can affect girls.
Who is Hunter?
Hunter Guillmeno is an amazingly brave and courageous young boy that was diagnosed with Duchenne Muscular Dystrophy (DMD) on 03/03/02016. Hunter lost his ability to walk during the summer of 2020 due to muscle and skeletal regression which has left him now fully dependent on his wheelchair for mobility.
In spite of the many medical appointments, medication management, hospitalization, challenges, and unexpected setbacks, Hunter continues to press on, and has a strong desire to engage in and with life as much as his body will allow him to. Hunter has the biggest heart and has always showed compassion and empathy for those he loved, cared about, the homeless, and underprivileged children, while having courage beyond measure.
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