testarea genetica in timpul sarcinii deoarece doresc sa mai aiba un copil. Cuplul are o fetita de 4 ani cu Fibroza Chistica. Cum credeti ca au ajuns sa solicite consultatia? Ce lucruri anticipati ca doresc sa discute? Cum ati incepe consultatia? Ce lucruri ati dori sa abordati? O tanara de 23 de ani, aflata la prima sarcina si insarcinata in 14 saptamani, a solicitat o consultatie pentru a discuta riscul de a avea un copil cu sindromul Down. In urma unei ecografii a fost semnalata transulcenta nucala si li s-a comunicat un risc estimat de 1 la 50. Cuplul este nehotarat in privinta testarii invazive. Cum ati incepe consultatia? Ce ati avea nevoie sa stiti pentru a intelege mai bine situatia cu care se confrunta? Cum puteti interveni pentru a le facilita decizia? Setting Getting started Programare / Trimitere Breaking the ice Small talk (ex. Finding the place, Ipod) Other people coming with the patient Greeting Names, Relationships Working environment Shared vision of what is to come Expectations / Hopes Setting realistic goals “I want to know if my baby is going to be healthy” Aggenda setting Feedback Verbal / Non verbal communication mutatie, aberatie, retard(at), handicap, autist, etc What is and is not being said! Interview Questionning (ex. Family / Children; Information given during the session) Open ended Focused Closed Rephrasing Redirecting “It is very important… but let’s go back to…” “Before moving on to…” “Let’s slow down / go back to…” Reflecting Shared language “Non working / Bad” gene Neurofibromatosis = NF Silence Key assessment points Family / Personal history Support system Understanding / Previous knowledge Attitudes Beliefs Religion Education Emotional state