Questions for anyone going through it. Has anyone gone through an IVF cycle, had PGS done, transferred blasts with no abnormalities and still had a failed cycle? We are just starting bcp this month with ER scheduled for any time between 3/30 and 4/3. Just wondering how much having PCS testing helps?!
Re: PGS and failed cycle?
TTC - since 2014
7 rounds of Clomid - BFN
IUI #1 - October 2015 - BFN
IUI #2 - November 2015 - BFN
IUI #3 - December 2015 - BFN
IVF #1 - March 2016
Retrieval #1 - April 2016
FET #1 - May 2016 - BFP!!! DS - Born January 2017
Trying for baby #2...
FET #2 - January 2018 - BFN
No more embryos left; switched to a new RE
IVF/Retrieval #2 - January 2019
IVF/Retrieval #3 - March 2019
FET #3 - April 2019 - BFP!!! - DD: Born December 2019
Trying for baby #3...
FET #4 - October 2021 - BFP!!! - Due June 2022
@ktrabing all the best for your journey and that it’s successful.
I know the difference a little bit, but not really sure I understand. Is PGD testing more conclusive than PGS?
Dx: low morph (1%), ANA positive, low decidualization score, high TSH and testosterone, histone antibodies
IUI #1-3 | all BFN
IVF #1 | 6.11.19 | 24R, 17M, 15F, 6B, PGT-A tested - 5 normal, 3 girls & 2 boys
FET #1 | 9.10.19 | BFN "I know you, but we've never met. I'm with you, but I don't know your name"
RPL, Receptiva, & ERA testing | all normal/negative, recommended going on gluten and dairy free diet for next FET
FET #2 | 3.31.20 | Opted to cancelled due to pandemic, continued diet and tried naturally over the summer
2nd Opinion with another RE | 8.20.20 | Not immune to measles (received 1 dose); SA results similar to 2 years ago; decided to move forward with FET #2 redo at start of next cycle
Surprise natural BFP! | 9.22.20 | MC 10.23.20 at 8 weeks
TTCAL naturally | starting 11.22.20
Initial consultation with Reproductive Immunologist | 9.14.21
Decidualization score biopsy | 10.1.21 | abnormal - low score of 1; endometrial scratch recommended and progesterone supplementation
Saline sono | 10.15.21 | normal
Bloodwork | 10.21.21 | high TSH, high testosterone, positive for anti-nuclear antibodies and histone antibodies, high protein S, multiple genetic mutations
BFP! | 11.3.21 | EDD 7.14.22
DS born 7.19.22 after induction
TTC #2 begins 6.2023
Consultation with RI | 6.6.23
Saline sono, endometritis biopsy, skin & eye check | all normal
Labs | high TSH, Factor XIII mutation, high %CD56
Follow up | 8.8.23 | prescribed metformin, prednisone, plaquenil, and levothyroxine
Repeat labs after 3 weeks on meds
Follow up | 11.9.23 | Green light!, increase in prednisone, added lovenox
Repeat labs in 8 weeks
Follow up | 1.16.24 | Green light continues
TTC ended due to filing divorce
**New relationship starting May 2024**
Surprise BFP!! | 9.7.25 | EDD 5.11.26
PGD testing generally looks for specific genetic issues and is used commonly by people who are known carriers for specific defects. We have at least one lady on the forums here who is specifically using PGD to find embryos that do not carry a certain defect so she might be able to provide more insight -- I just don't remember her name :-(
Summer 2015 - no BFP yet, labs normal, referred to RE
Fall 2015 - Summer 2016 - Further testing all normal. 3 IUI's -- BFN. Recommended move to IVF. Planned cycle for fall 2016.
September 2016 - Surprise natural BFP. MMC @ 8 weeks. RE expressed confidence that we just needed the 'right' embryo.
Fall 2016 - Spring 2017 -- Break from TTC
June 2017 - Started IVF; egg retrieval for freeze all cycle. 9 mature eggs retrieved, 5 fertilized. 2 4BB embies on ice.
August 2017 - FET transfer both embies. BFP. Twin pregnancy confirmed by ultrasound. EDD 4/28/18
September 2017 - Twin B stopped developing; Twin A doing perfectly! Graduated from RE @ 10 weeks
March 2018 - Baby Girl born via C/S due to pre-eclampsia -- strong and healthy!
TTC #2
January/Feb 2021 - Freeze-all IVF cycle
March 2021 - FET of 1 PGS normal female embryo. BFP! Beta #1 156, #2 472, #3 1241, #4 5268 EDD 12/5/21 - Christmas baby!
"When all is lost then all is found."
Currently I am awaiting FET. I had a fibroid show up in my pre FET hysteroscopy so I will undergo surgery to remove it early April.
We do have one "unaffected" which was PGD/PGS tested. Hoping to transfer in May. We also have one "no result" meaning it will need to be re-tested. One female carrier (like me) which does not have Hemophilia but carries the gene. Three PGS abnormals one of which was PGD affected,
Any other questions, Feel free to ask away! Prayers and positive thoughts to All of you on this journey.
I am a genetic carrier using PGD testing
Dec 2018 ER = 0 PGS normal embryos
Jan 2019 ER = 1 PGD/ PGS normal embryo, 1 carrier embryo, 1 no result
April 2019 Hysteroscopy to remove polyp and Fibroid
May 2019 FET = BFN
September 2019 FET = BFN
Dec 2019 ER = 1 carrier embryo
Mar ER = 0 PGS normal embryos
July 2020 ER = 0 PGS normal embryos
October 2020 Hysteroscopy to remove polyps
Nov 2020 FET = positive (little one due July 2021)