Hi all,
On 4/1, I found out at my 7w sonogram there was no heartbeat. Opted for a D&C, which I had on 4/4. Healing well, spotting as normal, very limited pain/cramping. Because partner and I are both data-driven, we opted to get carrier screening done at that appointment and to have the tissue from the D&C genetically tested.
Husband and I are not carriers for the same thing (we're each carriers for one thing, but since there's no overlap I was told the chances of our passing anything on are very slim). So that's good. Genetics from the tissue collected came back, and were all normal. Some kind of minor irregularity on chromosome 9 which is apparently not a cause of demise and not clinically significant.
I'm feeling frustrated that there's no answer. Since the MMC I decided to get my husband on a multivitamin, focus on losing a couple pounds, and bought some Brazil nuts, plus scheduled a GP appt since it's been a couple years since I've had regular bloodwork done. I know it's insane to rush to a specialist at this point, but part of me wants to because of the lack of a genetic explanation. This makes me feel like there must be something wrong with me, and that I just don't know what it is.
So, mixed emotions: happy about the fact that the carrier testing came back clear, but frustrated we've got no answers at this point. Interested in advice, similar stories, or anything really. Having to restart this whole process combined with the frustration and anxiety that this will happen again is really...a lot.
On 4/1, I found out at my 7w sonogram there was no heartbeat. Opted for a D&C, which I had on 4/4. Healing well, spotting as normal, very limited pain/cramping. Because partner and I are both data-driven, we opted to get carrier screening done at that appointment and to have the tissue from the D&C genetically tested.
Husband and I are not carriers for the same thing (we're each carriers for one thing, but since there's no overlap I was told the chances of our passing anything on are very slim). So that's good. Genetics from the tissue collected came back, and were all normal. Some kind of minor irregularity on chromosome 9 which is apparently not a cause of demise and not clinically significant.
I'm feeling frustrated that there's no answer. Since the MMC I decided to get my husband on a multivitamin, focus on losing a couple pounds, and bought some Brazil nuts, plus scheduled a GP appt since it's been a couple years since I've had regular bloodwork done. I know it's insane to rush to a specialist at this point, but part of me wants to because of the lack of a genetic explanation. This makes me feel like there must be something wrong with me, and that I just don't know what it is.
So, mixed emotions: happy about the fact that the carrier testing came back clear, but frustrated we've got no answers at this point. Interested in advice, similar stories, or anything really. Having to restart this whole process combined with the frustration and anxiety that this will happen again is really...a lot.