Today we met with Dr. S, a new-to-us RE within our current practice (our former clinics merged back in April). It was a good move on our part to get a fresh set of eyes on our case. She really seemed to take an interest, and was genuine when expressing her condolences for our recent loss.
I liked her a lot. She listened to everything we had to say, answered our questions honestly and professionally, and overall had an excellent bedside manner. She offered to reach out to the other doctors on our team, including my rheumatologist and the MFM doctor from CHOP. When I mentioned that the genetic counselor from CHOP would be willing to consult regarding our frozen embryos, she was very pleased to hear that and said absolutely they would work together. I really that she is willing to go out of her way to help us. We are a bit complicated and puzzling, so we really need doctors who are willing to work together and think outside the box.
We reviewed our history and past protocols. As I expected, she was open to all of the medications I was on with the exception of the high dose of Prednisone and the use of IVIG. All the other medications and supplements were fine by her.
She recommends a diagnostic hysteroscopy prior to a transfer and testing our embryos. The hysteroscopy is a no-brainer. Testing the embryos to me is too, but John is afraid about the risk of losing viable embryos in the thaw and refreeze... Dr. S said that the survival rate at their lab is 97% for the first thaw, and then the second thaw would go down to 95%. She said that usually the embryos that don't survive are not good quality... our embryos are of very good quality. But still, I can see John's hesitation because someone has to be the unlucky 5%. We have proven to be the unlucky percentage almost every time in the past... is it worth it to take any unnecessary risks? I don't know if I could proceed with a pregnancy knowing that the embryo had not been tested... That's something we'll have to think about before making a decision.
Dr. S recommends waiting at least six months postpartum before transferring another embryo. She said given our history, we could transfer two embryos if we wanted, however she'd feel more comfortable with a single embryo transfer. We agree... as much as I have always dreamed of being a twin mama, it is not worth the risk to our precious babies. Besides, I already am a twin mama... Rosa & Robin made it so <3
I asked if she had any recommendations for my diet & lifestyle. She referred me to the nutritionist, so we'll schedule a consultation. She said that running is not a problem for a future cycle nor a potential pregnancy. I like that very much. VERY MUCH. I can't begin to tell you how important it is to have the option to go for a run through all of this... I need to feel like myself in order to keep my head on my shoulders.
I asked her when my period should return. I'm still not sure if the bleeding I had 5 weeks postpartum was my period, and even still, it has been 32 days since that bleeding. She said that right about now is when I should be getting my period again, and then said she'd do an ultrasound and blood work to see where I'm at in my cycle right now.
The physical exam showed that I have high blood pressure (what the what?! 138/82... so out of the norm for me). I gave blood and urine samples for testing. My weight has gone up 5 lbs (which to this marathon runner is a win! I know it's the muscle mass that I've gained over the past several weeks of training). The ultrasound showed possible calcification in my uterine lining. And, get this, my lining measured 9.8mm and was Type III. NEVER in all of my documented cycles has my lining been that thick. I know it doesn't bear any significance, but I am kinda proud of that. My ovaries are doing their typical thing. Righty had 6-8 follicles measuring under 10mm and a 22mm cyst, Lefty had 4 follicles measuring under 10mm. The cyst might mean that I ovulated. We're waiting for blood results to see what's what. Depending on my blood work, I will probably be prescribed Provera to induce a period. Then I'll go in for another baseline on CD3 to see what's going on with my uterus.
The final question we asked was to look up the sex of Frostie Ninja. We had him/her CCS tested after IVF #3. S/he was normal, but we didn't want to know the sex at that time. Now, I think we're ready to find out. Though, I have to say, I am a little nervous to know. I have a gut feeling, but what if I'm wrong? I have been operating under the assumption that Robin was a boy. We won't know until we get to heaven... if I was wrong about Frostie, then it'll make me wonder if I am wrong about Robin too. I hope I am right!!