Ds 2 (6) and ds 3 (23 months) both have sn and dyspraxia. Went to see the neuro disability pead today who gave us paperwork for the bloods and genetics.
When I handed it to the nurse it only asked for fragile x. I told the nurse as baby is not yet two couldn't he have a more comprehensive genetics screen as I know dyspraxic kids who have rare deletions. I don't want to have bloods drawn twice for fragile x then a full screen at a later date.
The nurse said she will ask the pead for me. So has anyone had a full genetics screen on nhs or am I asking for to much? I didn't ask for the screen it was offered to us but I don't see the point in only looking for fragile x?
I asked if they could draw a vial and I pay for private screening but my hospital won't draw bloods for private tests.
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Genetics testing - any experiences on the nhs?
48 replies
2boysnamedR · 24/02/2014 13:28
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