Months ago doctor from department of child development recommended us to bring janelle for a genetics test. Didn't think too much and followed the flow..
J and hus asked why would I want to go for genetics test?? what can I do after knowing if it is a genes problem?? will there be an solution of its a genes issue?? All the why came out from them..
After more than 3 months of wait.. spending nearly a thousand of dollar.. The result is finally out. Hus was not avaliable so i went alone. Early morning before i left house, hus told me the result doesnt mean anything. Whether is it normal or not.. its no longer mean anything to him cos he know it very well that there wouldnt have any change to janelle life anymore. He asked me not to worry too much and don't take the result too hard.
With a heavy heart and in a messy mind, I went in to hear the result. Everything is normal.. High level and commonly dna that causes seizures was tested and everything is normal. Of cos there are more detailed test that can ve taken and deep dive into each cells but decided not to further presume for gens test, like hus shared.. what can u do if it is gens problem? Bascially is Nothing.. is FYI kind of test, so save the money and janelle blood. Doctor also shared that I would have a 25% as compared to average of 1% chamce to have other children having the same condition as janelle. That's the take away from these test.
I shared with my mom, she says the chances not high can try. I shared with my mil, she says if you scare then don't. And I agreed with my mil, both hus and myself heart are too fragile now to have another janelle.