I read yesterday that it against the law in Australia for siblings (or anyone) to find out if they are a carrier of CF until they are 18. This makes me angry as I have been thinking about getting J and Em tested so that they and we know. So when they are teenagers you can start talking about the implications of that. I don't understand why you can't find out. What would the harm be? I also don't know if this is actually the truth as it was just something I read online so will have to check with the clinic.
Prayers today for Rebecca who is taking her two kids for their annual cf reviews. Clinic appointments are always stressful for me and then the week after waiting for phone calls of results is like torture! (which is where we are at the moment). I thought perhaps it would get better, but I don't think the fear of the unknown will ever go away.
CF Sucks!
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