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Jesse

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Mit navn er Patches Hester. Min søn er Jesse Caden Hester. Han blev født den 30. marts 2007. Han var en stor fyr, der vejede 12 kg, 12 oz og 21 1/2 inch lang. Ingen større problemer ved fødslen undtagen, han bestod ikke sin høretest. Vi var ikke for bekymrede i starten, og han fortsatte med at vokse som normalt. Ved hans fjerde kontrol, bemærkede vi, at han ikke mødte nogle af de typiske milepæle som at holde hovedet meget godt op og meget lidt øjenkontakt. Han havde også konsekvent undladt alle de normale høretests. Vi blev sendt til en genetiklæge, og han fik diagnosen PKS kl. 8 måneder. gammel. Ved hjælp af vores stats tidlige indgrebsprogram og rehabiliteringstjenester til børn er Jesse begyndt at få alle de ting, han har brug for. Han sidder næsten alene, han vælter så godt på hver side, han udvikler øjenkontakt bedre og med sine høreapparater kan han ordligt bestemte lyde meget godt. Ingen kan virkelig forklare, hvordan det er at få et barn med særlige behov. Som mor vil du ordne alt, sørg for at de ikke har smerter, trøst dem, men du kan ikke ordne dette. Han har imidlertid åbnet en helt ny vidunderlig verden, som jeg aldrig ville have oplevet, hvis Gud ikke har givet ham til mig og min familie. Vores tålmodighed er steget, den mindste præstation, han opnår, bringer så meget glæde, at hans smil kan lyse et rum op. Han er ikke fordømmende, han er bare simpelthen glad. Jesse har en ældre bror, Levi, og jeg kan allerede fortælle, at han er meget beskyttende og meget medfølende over for ham og andre mennesker (et smukt træk). Vores familie gør ikke, hvad fremtiden bringer, men Jesse vil være der lige med os hele vejen.

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PKS Kids giver håb og hjælp til familier. Uanset om det er at dele information og support eller give tilskudsdollar til udstyr og terapier, vil vi hjælpe.

E-mail : gretchen.peters@pkskids.net

Telefon : 269-967-7175

Skatte-ID: 20-5653-043

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