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Maya's Hope: Sponsor a Child - Gordiy with 3-Methylglutaconic Aciduria & Klinefelter's Syndrome (UA)
Maya's Hope: Sponsor a Child - Gordiy with 3-Methylglutaconic Aciduria & Klinefelter's Syndrome (UA)

Gordiy's medical profile is quite complex: 

- Atypical form of 3-methylglutaconic aciduria: A metabolic disorder characterized by difficulties in breaking down certain amino acids, resulting in the accumulation of 3-methylglutaconic acid in the blood and urine.

- Klinefelter's syndrome: A genetic condition affecting physical and developmental characteristics due to an extra X chromosome (XXY).

- Mitochondrial dysfunction: Impairment in cellular energy production and bodily functions, often leading to various health challenges.



Considering the intricacies of his diagnosis, Gordiy's medical needs remain our top priority. To manage his health effectively, Gordiy heavily relies on a regimen of daily vitamins and mineral supplements, including vitamin D3, coenzyme Q10, calcium, trimethylglycine (TMG), etc.



His mom's raising him solo, and you can imagine the financial strain that comes with covering all the necessary medical expenses. You can help with these needs and ensure he receives the necessary support by covering essential medication, lab work, and medical tests to monitor his well-being closely.

Will you be Gordiy's superhero?