Feronia
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Im nervous about ultrasounds and really want to limit my exposure (Im 13 weeks). However, Ive already had 3 scans due to a subchorionic hematoma and bleeding. Each time I thought I had miscarried, and it was a relief to see the baby doing well each time, but I feel a bit guilty about them nonetheless. Now I havent had any bleeding, spotting, or cramping for 5 weeks, so I really think the SCH has absorbed and my midwife agrees. However, now Im thinking about the 20-week anomaly scan. My midwife gave me plenty of alternatives (like only checking the placenta and the SCH, or avoiding measuring the head, or avoiding all measurements, or not doing the scan at all). With my daughter, they belittled my request to keep the scan short, but my midwife said that if they put my requests on the report they will honour them.
(Note: I am planning my second home water birth.)
So my questions are:
-How important is it to check the SCH to see whether it has absorbed, and the placenta location? I know 98% of low-lying placentas diagnosed in the second trimester move up, so would this information be important?
-I am doing both quad screening tests (10 weeks and 16ish weeks), so how likely is it that an ultrasound would diagnose downs syndrome, trisomy 18, or neural tube defects when the quad screen would miss it? I would really like to know about these things ahead of time to consider my option.
-Are there any other common (or fairly common) anomalies found on scans? I dont care about minor defects, but Id want to know about severe defects or conditions incompatible with life ahead of time though I am a very healthy, 27-year old who doesnt smoke or drink so I think my risks are low.
-How important is it to diagnose growth, or growth-related conditions like IUGR?
-What about checking the baby's heart if I have no family history of heart problems?
So conflicted! Thanks so much!
(Note: I am planning my second home water birth.)
So my questions are:
-How important is it to check the SCH to see whether it has absorbed, and the placenta location? I know 98% of low-lying placentas diagnosed in the second trimester move up, so would this information be important?
-I am doing both quad screening tests (10 weeks and 16ish weeks), so how likely is it that an ultrasound would diagnose downs syndrome, trisomy 18, or neural tube defects when the quad screen would miss it? I would really like to know about these things ahead of time to consider my option.
-Are there any other common (or fairly common) anomalies found on scans? I dont care about minor defects, but Id want to know about severe defects or conditions incompatible with life ahead of time though I am a very healthy, 27-year old who doesnt smoke or drink so I think my risks are low.
-How important is it to diagnose growth, or growth-related conditions like IUGR?
-What about checking the baby's heart if I have no family history of heart problems?
So conflicted! Thanks so much!