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Isabella

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Isabella blev født 23. oktober 2010. Jeg havde en perfekt graviditet og fødsel. Vi var i fuldstændig chok, da hun blev født for at finde ud af, at hun havde en duplikatå på højre fod og andre ulige egenskaber. Det er meget ødelæggende at pludselig blive ramt af den virkelighed, at din dyrebare nye baby pige måske har noget galt med hende. Jeg undtagen det faktum, at hun havde en ekstra tå, der kunne ordnes, men hendes genetik kunne ikke. Hun blev diagnosticeret med PKS en uge gammel. Den dag ændrede vores liv for evigt. Isabella er 15 måneder nu og vores livs stolthed. Vi elsker hende så meget! .Hun er fysisk og mentalt forsinket. Hun kan ikke sidde alene, kravle eller gå endnu. Men vi tror snart, det vil hun. Hun ser ud til at høre godt, men vi er usikre på hendes vision. Hun ser ikke direkte på os, bare rundt omkring. Hun ELSKER lys !. Hun blev ammet i 14 måneder og klarede sig godt !. Hun kan ikke lide at spise en ske, men hun gør en indsats. Hun elsker badetid !. Nu og da får vi et fnise ud af hende, og vi værner om det !. Hun er netop for nylig blevet brugt på anfaldsmedicin for det, jeg ser som svage, men MR siger, at de er anfald. Forhåbentlig hjælper medserne. Hvis du nogensinde har spørgsmål om PKS, eller hvis du bare har brug for en samtale med en PKS-mor, så send mig en e-mail på brooketurner08@yahoo.com

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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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