Welche Ratschläge sollte man einer Person geben, bei der gerade eine Chiari-Malformation diagnostiziert wurde?

Ratschläge von Fachleuten für einer Chiari-Malformation für Personen, die kürzlich mit Chiari-Malformation diagnostiziert wurden

Original


I know how awful it feels at first. As if you've been handed a death sentence. You think of all the things you wanted to be and become and do and be here for. You need to grieve for that and for what you've lost. But don't forget to be grateful for now only what you still have but what you've gained. You will look at the world differently now. Each day will be so much more important. You will see the big picture. You are not alone. By far. They say 1 in 1000 but more current estimates believe 1 in 100. Not everyone with Chiari is symptomatic. Don't compare symptoms to other people or pain. I am working on my bucket list. I don't know how much time I have and most days I don't feel up to working on my list. I start to feel bad but then remember that won't help anything. You take one hour at a time because so much changes within a day. You find out who your true friends are. You become an ambassador of knowledge yourself. You have to in order to survive. You have been fighting before you knew you were. You are strong. You are a Chiari warrior and we stand by you.

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