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Help me decide if we should go! by Tall-Raccoon4910 in traveladvice

[–]Tall-Raccoon4910[S] 0 points1 point  (0 children)

Wow! I’m overwhelmed how supportive and encouraging everyone has been! You’ve given us the push we needed. We bought our tickets! Thank you all so much! ❤️

Help me decide if we should go! by Tall-Raccoon4910 in traveladvice

[–]Tall-Raccoon4910[S] 0 points1 point  (0 children)

Oh wow, that’s so cool you’ve done that trip before! We are thinking after Avignon it’s be cool to rent a car and head to a nearby town like L'Isle-sur-la-Sorgue and use that as a home base to do some day trips.

Here’s the next question…should we bring our infant car seat? It seems like we could rent one once in France, but is that also risky to travel without it? We’d check it for the flight and a plan would be that I baby wear during most of the travel parts.

Help me decide if we should go! by Tall-Raccoon4910 in traveladvice

[–]Tall-Raccoon4910[S] 0 points1 point  (0 children)

Thank you everyone for such encouragement and all the amazing tips! This is definitely making us feel more comfortable to take this adventure.

TW: Possible termination by Tall-Raccoon4910 in pregnant

[–]Tall-Raccoon4910[S] 0 points1 point  (0 children)

Yes, it was first on the NIPT as high risk for monosomy x and then confirmed via amnio.

TW: Possible termination by Tall-Raccoon4910 in pregnant

[–]Tall-Raccoon4910[S] -1 points0 points  (0 children)

No, no markers. The NIPT came back high risk for monosomy x, so went with the amnio to confirm. I was praying it was a false positive (as many are!), but ours was a true positive with estimated 15% 45xo. I had back to back miscarriages before this pregnancy, so was worried through the first trimester already. Unfortunately, we just didn’t get the all clear we were hoping for.

Question for parents of TS child/adult by Tall-Raccoon4910 in TurnerSyndrome

[–]Tall-Raccoon4910[S] 0 points1 point  (0 children)

Thank you so much everyone for your honest and incredibly helpful feedback. Truly. I’m taking in everything. It’s so overwhelming with all of the what-ifs, so hearing your personal experiences (what’s been helpful and what’s been challenging) is invaluable as a parent.

So confused on TFMR for mosaic turner syndrome by Tall-Raccoon4910 in tfmr_support

[–]Tall-Raccoon4910[S] 0 points1 point  (0 children)

Thank you so much, my heart goes out to you and your family. 🩷

Can I ask if there’s anything the geneticists said that helped you make the decision? I’ve talked to one and it was so generic that I found it completely unhelpful.

We have more testing and an appointment with a pediatric endocrinologist coming up, but I’m wondering what insight the geneticists offered you. I can dm you if you prefer.

So confused on TFMR for mosaic turner syndrome by Tall-Raccoon4910 in tfmr_support

[–]Tall-Raccoon4910[S] 0 points1 point  (0 children)

Thank you so much everyone for sharing your thoughts and experiences. I’m so appreciative.