I am 17 weeks and am seeing my peri because I was so unhappy with my OB that delivered my DD. They missed a lot of my symptoms and were very dismisive with me. He failed to diagnose or treat my postpartum HELLP Syndrome, and it would scare me to go back there. On the one hand, I feel like I am in good hands at the perinatologist group/MFM group. They have run some extra tests and are very watchful in case I develop signs of preeclampsia again (which of course, led to HELLP Syndrome). I also had a postpartum rash called a pupps rash, I also had preterm contractions starting at 23 weeks. I have already noticed contractions in the past few weeks which are a little scary, they did check me to make sure my cervix is still long and closed, which it is. I think I might have more contractions as I progress, I am just now starting to show. I had shots of terbutaline with my last pregnancy to stop contractions, multiple multiple times, but never went into preterm labor. And I have Celiac, so i am gluten free, and I had abdominal surgery last year. So those are the reasons they have qualified me as "High Risk". other than that though, there is a chance, it could be a normal pregnancy this time, which is what I am hoping.
I am just second guessing if I should be at an OB group where I can kno very well the doctor that will eventually deliver me. I don't want to be so overly expecting a complication, if there is none and everything goes well. I have our big anatomy scan in three weeks at our 20 week appointment. Maybe I will know more then....???
Re: Does anyone see a perinatologist *only*
I didn't read your whole post - too long with no breaks, but in answer to your subject line question, yes, we only see an MFM, but not by our choice. When I was admitted to the hospital at 23w,5d for PTL, our MW and high risk OB said we should just see the MFM for now on. They don't have privileges at the hospital with the level 3 NICU, but the MFM is based here, so it made sense.
Dx: balanced translocation and LPD
TTC since Oct 2011
BPF 02/19/12, EDD 10/31/12, natural m/c 02/28/12 (4w6d)
IVF (BCPs starting 10/30/12, ER 11/18/12, 5dt of 1 beautiful, healthy embryo 11/23/12)
BFP 12/02/12, u/s @ 6w,5d showed 2 HBs! Identical twins!!
Bed rest from 21w-35w due to short cervix, hospital bed rest from 23w-32w due to PTL
Our rainbows were born 07/19/13 (36w, 5d)
BFP #2 - Sylvie V. Q. born and died on 10.28.11 at 21w.
BFP #3 - Evie V. Q. Fetal demise @ 16w. DC 7.8.12
BFP #4 - Beatrix V. Q. Born 6.2.13 at 23w6d.
My blog My chart
Anovulatory cycles, increased Synthroid Diagnosed Sep 2010
1 Clomid/Ovidrel BFN May 2011
Natural cycle Aug 2011 BFP M/C 4 Weeks
1 IUI Sept 2011 BFP M/c 7 weeks
Provera Dec 2011 BFP M/C 3 Weeks
IVF March 2012 BFP m/c 4weeks 5 days (IL, Prednisone)
IVF#2w/DS July 2012 MEGA FAILURE BFN (IL, Dexamethasone)
Diagnosed No real HLA Match, DQ Beta Triad, High TNF, Low NK Cells
Oct 2012 Natural Cycle m/c 4wks (Lovenox, Prednisone)
Went to Beer Center- high tnf, low lad, implantation failure
Jan 2013 BFP
Humira,LIT,Prednisone, Lovenox, IVIG, Baby Aspirin
Miracle Born August 2013 Premature
Yours doesn't have to be a sad story
DOR and AMA
2/12-5/12: 4 IUI cycles = all BFN;
7/12: DE IVF # 1 (with ICSI)- 20R, 16M, 14F, 5DT of 2 blasts; 6 frosties = BFN;
Lupus anticoagulant initially high, then found to be normal on hematology consult;
Follow up testing in September all clear;
Started synthroid for "high normal" TSH;
FET # 1- late October 2012- BFP on FRER; beta # 1- 21(low), beta # 2- 48 (still low), beta # 3- 132, beta # 4- 1,293; beta # 5- 5,606; last beta- over 100,000. First u/s 11/21- heard heartbeat
12/12- Officially an OB patient!
Level 2 ultrasound at 20 weeks shows vasa previa and VCI
Referral to MFM and mandatory c section for delivery
Beautiful baby girl born at 34 weeks
Finally home after 15 day NICU stay!
Trying for sibling: FET # 2- May 2014; beta 5/31, BFN
FET #3, early July 2014; beta 7/14, BFN
DE IVF # 2- August 2014; 14R, 13M, 11F, 5dt of 2 blasts (3 AA), 5 frosties = BFN
FET #4- December 2014, yet another BFN
Dr. KK work up shows borderline uterine blood flow, elevated NK cells, and MTHFR mutation (homozygous for c677t)
Added baby aspirin, prednisone, supplements, Metanx, and intralipids
Switched to large clinic for final attempt; had endometrial receptivity testing in January; FET March 2015 = yet another BFN
Likely OAD- NBC