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Brayden

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Brayden blev diagnosticeret med PKS 3 dage gammel. Han blev født efter 35 uger og placeret i NICU i 34 dage. Heldigvis så lægerne noget andet ved den måde, Brayden holdt på hans hænder, så de kontrollerede hans DNA. Sikker på, at vi var velsignede, at der var et svar, og at svaret var PKS. Brayden viste ikke meget af symptomerne på PKS dengang, og det gør han heller ikke nu. Brayden tager skridt hver dag. Han kan sidde, tage skridt med hjælp, spise alt, trække sig op i sin vugge og til vores bord og elsker at gribe ting og smide dem. Han har lav muskeltonus, men ikke sammenlignet med hvad andre børn har, han er meget stærk i underlivet.
Brayden er forsinket udviklingsmæssigt. Vi ville placere ham omkring et år bag andre børn i hans alder. Han kravler og ruller, som vi lige startede et par uger før hans 2-års fødselsdag. Hans foretrukne ting at gøre er enten at spise eller være sammen med bedsteforældre.
Som en ung familie er vi velsignet med, at der var et svar på, hvad der gjorde Brayden så speciel. Vi lever vores liv fuldt ud og lader ikke noget holde vores familie tilbage. Gud velsignede os med dette specielle barn, og nogle dage har vi måske lyst til at give op, men til sidst fik vi dette barn af en grund, og vi ved måske ikke årsagen nu, men i sidste ende vil vi. Jeg føler, at Gud kun vælger specielle mennesker til at give specielle børn også.

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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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