I was wondering if anyone has experience with MCAD deficiency, and if so, has it been a big adjustment? Our newborn screening flagged for that and I am of course freaaaaaking out. It's still a preliminary positive, and I know it's not the worst that could happen by any means, but I feel so terrible for C.
We've had a really rough last two days, between terrible phone calls and horrific attempts at lab work, I am really hoping it is just a false positive and we can forget this ever happened!
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