I haven't been around much lately, though I used to post a lot here. I am going through a bit of a tough time at the moment with IF. Our second FET with frozen embryos just failed and I am having trouble believing that this is ever going to work.
We live abroad and laws here mandate that embryos are transfer back after 2 days, so we have no way of knowing how the embryos would develop. PGD is also forbidden here (Welcome to the Land that makes IF hell). I suspect that this is our problem. In Dec., we transferred two "perfect embryos" (both Grades 1) at Day 2 and got BFN. In March, same thing. In May, again. What is going on? There is not even remotely a sign of implantation (i.e. Beta = <5) and I am looking for advice. The RE also doesn't have an idea and is surprised that it is not working in the least bit.
A little background: DH has a microdeletion and subsequent severe Oligospermia (ca. .1 -.3 Million). We had 10 eggs out of 12 fertilise with ICSI. Everything on my end came back normal.
We are looking at going abroad for treatment now, since we are legally not able to pursue more aggressive treatment here. But before that we have two more rounds, each with two embryos.
My questions: What should I be asking my RE at this point? (We didn't even get a WTF appt. this time around, which really upset me.) Is there anything that we should look for on my side (for example, something that might be keeping the embryos from implanting or killing them off in utero)?
I am so sad and lost at the moment. I didn't expect that with IVF it would be the same story over and over again. To top it all off, my MIL informed me the other day that DH younger cousin is pregnant and that maybe I am just "not meant to have children." I am obviously not talking to her about IVF again.
You could look into immune issues to see if there is anything on your end, but honestly with your DH sperm issues I think pgd/ccs testing is your best bet.
TTC#1 since April 2011 IVF#1 July 2012 5R, 3 made it to blast, sET c/p FET#1 Aug 2012 2 blasts transferred BFN IVF#2 Oct 2012 16R/6M/6F/2-8 cell grade 1 transfer Beta 1-237.9, Beta 2-566, Beta 3-8657 US 6w3d shows one baby w/ HB 115 US 7w1d no more heartbeat/ D&C 11/30/12 normal karyotype IVF#3 Mar 2013 6R/4M/4F 1 compacting and 2-8 cell transfer ectopic pg MTX given 3 month break from TTC
IVF#4 Sept 2013--BFN IVF#5-7 Apr 2014, Jun 2014 and Aug 2014 banking embryos for CCS testing. Praying for normals!
I'm sorry you are still fighting IF.
You could look into immune issues to see if there is anything on your end, but honestly with your DH sperm issues I think pgd/ccs testing is your best bet.
I agree with all of this. Also you could look into testing your DH's sperm DNA fragmentation. Sometimes even if they pick a normal looking sperm the DNA is still messed up. There isn't much you can do for this, but sometimes lifestyle changes can help.
DH (32): SA is ok, slightly low morph, normal SCSA Me (32): Slightly low progesterone, hostile CM, carrier for CF, Moderately high NKC, High TNFa, heterozyogous mutated Factor XIII, and +APA
October 2012-May 2014: 4 failed IUIs, 3 failed IVFs, and 1 failed FETw/donor embryos
November 2014: IVF w/ICSI #4 Agonist/Antagonist with EPP and Prednisone, Baby Aspirin, Lovenox, and IVIG for immune issues. Converted to freeze all due to lining issues. 2 blasts frozen on day 6!
January 2015: FET #2 Cancelled due to lining issues
I am so sorry you are having to deal with this. And the MIL on top of it? That's completely uncalled for. I'm not sure I'm any help other than to say I'm sorry and still very hopeful for you.
*** Siggy/Ticker Warning *****
TTC June 2011 /// RE Jan 2013 /// DX: DH (30) - low morph, Me (30) - irregular ovulation
Clomid cycle March 2013 - BFN /// IUI #1 April 2013 - BFN /// IUI #2 June 2013 - BFN
IVF w/ICSI- Oct 2013 - ER Oct. 15 (10 mature, 6 fertilized)
I'm sorry you're so frustrated. I will say from experience they need to at LEAST grow to day 5 before transfer. I had a similair experience as you with my previous RE who only transferred on day 3. We always had PEREFECT embryos on day 3 but I always ended with a BFN. We switched clinics. He said that between day 2-5 a lot of embryos will not make it and you want to wait to transfer b/c the "strongest of the fittest" will make it to day 5. We also added PGD testing and that was the lucky trick for us. I think you're making a good decision to to abroad where you have more options. I went through 5 transfers before it worked! Someimtes it just takes more time to find the right embryo. GOod luck to you!
Me (28) DH (32) Endometriosis IVF #1 (1/2013) - 17 Retrieved, 16 Mature, 14 Fertilized- 2 transferred- BFN FET #1 (7/2013) - 2 embryos - BFN FET #2 (9/2013) - 2 emrbyos - BFN New RE. Fresh Start IVF #2 (2/2014) - 25 Retrieved, 19 Mature, 16 Fertilized, 9 blasts. CGH Testing: 6 Normal FET #3 (4/2014) -1 embryo - BFP! Beta#1: 35 Beta #2: 16 FET #4 (5/2014) -1 embryo - BFP! Beta#1: 321!!! Beta #2: 727.9!6/5/2014 Heartbeat! 144bpm It's a girl! Due January!
I'm so sorry you are dealing with this and a tough MIL too. Our clinic has some research that has led them to move towards the 5 day transfer more and more because of they are stronger, similar to what another poster said earlier too. Good luck with your next steps and I'm sorry it's been so tough!
TTC since March 2010, BFP #1 11.09.10, ectopic, m/c 12.14.10 (10w) Clomid + TI=BFN, IUIs 1-6= BFN Application for domestic adoption submitted 4/18/12, matched 8/12/12, DD born 10/31/12
I'm so sorry you're going through this. If financially possible I would really seek treatment abroad where you can let the embryos grow to day 5. It's so important to see which ones can make it to blast and still look good. ((( big hugs))) good luck!
Me: 30 DH: 30 ~ TTC #1 Since August 2011
BFP #1 2/28/13, Ectopic, Tubal surgery 3/25
Began RE testing 8/8, Dx Unexplained,
IUI #1 11/1=BFN
Moving on to IVF
IVF #1 12/2 ER 8R 7M 4 fertilized
12/7 Transferred 2 "perfect" little blasts 12/17 BFN
New DX= DOR, I fu*kng hate IF
1/14 Hysteroscopy, new clean uterus!
IVF #2: bcp, Lupron, follistim 300, menopur 225. 2/21 8R 4M 3F. 3dt of 2 perfect embryos. 1 little penguin
3/10 BFFN
Regrouping. Seeing reproductive immunologist Dr. Kwak Kim 6/10
Kwak Kim protocol: Metformin 1000mg, vitamin D 4000iu, vitamin E 400iu, baby aspirin, Metanx, levothyroxine 75mcgs
Absolutely ditto all the previous posters. "Perfect" at Day-2 tells you nothing; find a place that will allow you to transfer at Day 5.
You might consider doing an endometrial biopsy, just to make sure you don't have implantation issues. But honestly, I don't know that I would do it until I'd had a chance to see what Day-5 embryos look like.
Finally, I'm so sorry about what your MIL said to you. That was so completely out of line.
Me: 34 / DH: 33
19-year history of endometriosis. Multiple surgeries and cyst removals. Forced directly into IVF due to blocked tubes and severe adhesions.
IVF w/ICSI and CCS #1 - Dec 2013 - Only 1 normal. Ended in CP
Since most pre-implantation pregnancy loss is immunological,
treatment by appropriate immunotherapies are applied and have been quite
successful.
· Intravenous Immunoglobulin (IVIg) treatments have
been shown to be quite effective in the treatment of implantation
failure. It has been most beneficial to women who have been good embryo
producers. Good producers are those who fertilized at least 50% of eggs
retrieved and generated at least three embryos for transfer. It is
usually administered six to seven days before embryo transfer, and again
after a positive pregnancy test. Sometimes it is necessary to
administer IVIg every three weeks until the end of the first trimester.
The problems with IVIg are that it is a blood product that is obtained
from pooled donor blood and each infusion costs between $2,000 and
$3,000.
· Intralipid is now being used to help circumvent
immunological pre-implantation pregnancy loss in women who have had
abnormal natural killer (NK) cell levels or functions. Intralipid has
the ability to suppress the NK cytotoxicity and stimulate the immune
system to remove faulty signals from cytokines that can lead to
pregnancy loss. It is also effective in enhancing live birth rates in
women with elevated NK cells and a history of pre-implantation pregnancy
loss. The advantages to Intralipid are its track record of being used
for decades without side effects, the fact that it is not a blood
product and it is relatively inexpensive - costing $450 to $700 per
infusion.
Many fertility specialists are now recommending Intralipid infusions
for their patients who are plagued with pre-implantation pregnancy loss
due to immunological factors.
It stinks that you can't do PGD. It could be a problem with the eggs, which would only be proven with PGD. I had 3 perfectly rated embryos during my first round of IVF and after PGD we found out that all 3 were unhealthy.
Hi ladies, thank you so much for all the support, insight and advice. Many of you confirmed what I already suspected, which is that we are probably going to have to go abroad for treatment, adding another complicating dimension to this whole IVF thing.
@jbasore1123, thanks for the information about pre-implantation pregnancy loss - do you happen to know how they would test for immunological issues? Is it something long and invasive or a quick blood test?
I am worried about going abroad for treatment, spending the time and resources (both financial and emotional) and then finding out that the problem is something altogether different and being bumped back to square one.
Thanks, again, for all the help and advice. You are amazing.
@Twinkie0612, do you have any information/websites you could recommend about DNA fragmentation and lifestyle changes?
DH was on FHS injections for three months prior to our Dec. IVF cycle with the idea that this should improve his sperm quality (no idea what the scientific basis is for this, but medicine in Europe is a bit different - feels like voodoo magic sometimes...in a bad way). This did nothing for his numbers but he had a fertilisation rate that was way higher than expected (10 out of 12).
So I guess my question is would the DNA fragmentation show up with a low fertilisation rate or later in the development process of the embryos? With DH's DX, I think that there is a high chance of fragmentation being a problem, but I am just not sure what can be done about that. It seems unlikely that I will truly be able to convince DH to make lifestyle changes without evidence to back it up.
@Twinkie0612, do you have any information/websites you could recommend about DNA fragmentation and lifestyle changes?
DH was on FHS injections for three months prior to our Dec. IVF cycle with the idea that this should improve his sperm quality (no idea what the scientific basis is for this, but medicine in Europe is a bit different - feels like voodoo magic sometimes...in a bad way). This did nothing for his numbers but he had a fertilisation rate that was way higher than expected (10 out of 12).
So I guess my question is would the DNA fragmentation show up with a low fertilisation rate or later in the development process of the embryos? With DH's DX, I think that there is a high chance of fragmentation being a problem, but I am just not sure what can be done about that. It seems unlikely that I will truly be able to convince DH to make lifestyle changes without evidence to back it up.
@Margritli From what I understand the first few days of an embryos development is dependent on the egg, this is why we suspect an egg quality issue for us, our embryos are always very poor quality by day 3. After day 3 the sperm takes over. I have read that embryos that look good on day 3, but arrest between day 3 and 5 can be a sign of a sperm issue. Honestly I haven't done much research into sperm DNA fragmentation or the treatment, but I think most recommended antioxidants, which may or may not have an impact. Sperm DNA fragmentation assay is on our list of tests if DH decides that he wants to try using his sperm if we move on to donor eggs. Here is a study that I found that looked into treating high DNA fragmentation: https://www.ncbi.nlm.nih.gov/pubmed/15867002.
DH (32): SA is ok, slightly low morph, normal SCSA Me (32): Slightly low progesterone, hostile CM, carrier for CF, Moderately high NKC, High TNFa, heterozyogous mutated Factor XIII, and +APA
October 2012-May 2014: 4 failed IUIs, 3 failed IVFs, and 1 failed FETw/donor embryos
November 2014: IVF w/ICSI #4 Agonist/Antagonist with EPP and Prednisone, Baby Aspirin, Lovenox, and IVIG for immune issues. Converted to freeze all due to lining issues. 2 blasts frozen on day 6!
January 2015: FET #2 Cancelled due to lining issues
IVF prep September 2013 cancelled due to Ovarian Cyst IVF #1 October 2013 Antagonistic Protocol with ICSI ER 10/31/13 (18R 16M 11F- 6 blasts to freeze) ET delayed due to OHSS FET scheduled for July 8. Delayed due to a crazy high TSH (it had been under control for YEARS!) FET #1 8/5/14 sET BFN
Re: "Perfect Embryos" (x 2) = BFN? Any Advice?
You could look into immune issues to see if there is anything on your end, but honestly with your DH sperm issues I think pgd/ccs testing is your best bet.
TTC#1 since April 2011
IVF#1 July 2012 5R, 3 made it to blast, sET c/p
FET#1 Aug 2012 2 blasts transferred BFN
IVF#2 Oct 2012
16R/6M/6F/2-8 cell grade 1 transfer
Beta 1-237.9, Beta 2-566, Beta 3-8657
US 6w3d shows one baby w/ HB 115
US 7w1d no more heartbeat/ D&C 11/30/12 normal karyotype
IVF#3 Mar 2013
6R/4M/4F 1 compacting and 2-8 cell transfer
ectopic pg MTX given 3 month break from TTC
IVF#4 Sept 2013--BFN
http://i61.tinypic.com/34zll06IVF#5-7 Apr 2014, Jun 2014 and Aug 2014 banking embryos for CCS testing. Praying for normals!
TTC #1 since August 2011
My Blog
September 2012: Start IF testing
DH (32): SA is ok, slightly low morph, normal SCSA Me (32): Slightly low progesterone, hostile CM, carrier for CF, Moderately high NKC, High TNFa, heterozyogous mutated Factor XIII, and +APA
October 2012-May 2014: 4 failed IUIs, 3 failed IVFs, and 1 failed FETw/donor embryos
November 2014: IVF w/ICSI #4 Agonist/Antagonist with EPP and Prednisone, Baby Aspirin, Lovenox, and IVIG for immune issues. Converted to freeze all due to lining issues. 2 blasts frozen on day 6!
January 2015: FET #2 Cancelled due to lining issues
April 2015: FET #2.1
PAIF/SAIF Welcome!
FET #1 (7/2013) - 2 embryos - BFN
FET #2 (9/2013) - 2 emrbyos - BFN
New RE. Fresh Start
IVF #2 (2/2014) - 25 Retrieved, 19 Mature, 16 Fertilized, 9 blasts.
CGH Testing: 6 Normal
FET #3 (4/2014) -1 embryo - BFP! Beta#1: 35 Beta #2: 16
FET #4 (5/2014) -1 embryo - BFP! Beta#1: 321!!! Beta #2: 727.9! 6/5/2014 Heartbeat! 144bpm It's a girl! Due January!
TTC since March 2010, BFP #1 11.09.10, ectopic, m/c 12.14.10 (10w)
Clomid + TI=BFN, IUIs 1-6= BFN
Application for domestic adoption submitted 4/18/12, matched 8/12/12, DD born 10/31/12
Since most pre-implantation pregnancy loss is immunological, treatment by appropriate immunotherapies are applied and have been quite successful.
· Intravenous Immunoglobulin (IVIg) treatments have been shown to be quite effective in the treatment of implantation failure. It has been most beneficial to women who have been good embryo producers. Good producers are those who fertilized at least 50% of eggs retrieved and generated at least three embryos for transfer. It is usually administered six to seven days before embryo transfer, and again after a positive pregnancy test. Sometimes it is necessary to administer IVIg every three weeks until the end of the first trimester. The problems with IVIg are that it is a blood product that is obtained from pooled donor blood and each infusion costs between $2,000 and $3,000.
· Intralipid is now being used to help circumvent immunological pre-implantation pregnancy loss in women who have had abnormal natural killer (NK) cell levels or functions. Intralipid has the ability to suppress the NK cytotoxicity and stimulate the immune system to remove faulty signals from cytokines that can lead to pregnancy loss. It is also effective in enhancing live birth rates in women with elevated NK cells and a history of pre-implantation pregnancy loss. The advantages to Intralipid are its track record of being used for decades without side effects, the fact that it is not a blood product and it is relatively inexpensive - costing $450 to $700 per infusion.
Many fertility specialists are now recommending Intralipid infusions for their patients who are plagued with pre-implantation pregnancy loss due to immunological factors.
It stinks that you can't do PGD. It could be a problem with the eggs, which would only be proven with PGD. I had 3 perfectly rated embryos during my first round of IVF and after PGD we found out that all 3 were unhealthy.
TTC since April 2012
BFP #1, 10/03/2012 - EDD 6/15/2013 - MMC 11/15/2012 - D&C 01/04/2013
BFP #2, 04/06/2013 - EDD 12/17/2013 - MC 04/19/2013
6/12/2013 Diagnosed with Balanced Translocation (12 & 16)
IVF #1 with PGS: 10/2013: Canceled 9/27/2013 for issues with genetic lab
IVF #1.5 with PGS: 11/16/2013: Canceled. 11 eggs retrieved, 9 mature & 9 fertilized, all unhealthy embryos
IVF #2: 1/22/14: Canceled. 16 eggs retrieved, 14 mature, 7 fertilized, all unhealthy embryos
IVF #3 with PGS: 5/10/2014: Switched to FET in July. 10 eggs retrieved, 9 mature, 8 fertilized, 2 healthy embryos!
FET #1: 7/31/2014: Transferred 2 nearly perfect (6AA, 6BA) healthy embryos- BFFN
Laproscopy: 10/2014: Healthy uterus
IVF #4: 12/8/2014: Canceled. 17 eggs retrieved, 15 mature, 10 fertilized, all unhealthy embryos
Everyone welcome on my posts
@Margritli From what I understand the first few days of an embryos development is dependent on the egg, this is why we suspect an egg quality issue for us, our embryos are always very poor quality by day 3. After day 3 the sperm takes over. I have read that embryos that look good on day 3, but arrest between day 3 and 5 can be a sign of a sperm issue. Honestly I haven't done much research into sperm DNA fragmentation or the treatment, but I think most recommended antioxidants, which may or may not have an impact. Sperm DNA fragmentation assay is on our list of tests if DH decides that he wants to try using his sperm if we move on to donor eggs. Here is a study that I found that looked into treating high DNA fragmentation: https://www.ncbi.nlm.nih.gov/pubmed/15867002.
TTC #1 since August 2011
My Blog
September 2012: Start IF testing
DH (32): SA is ok, slightly low morph, normal SCSA Me (32): Slightly low progesterone, hostile CM, carrier for CF, Moderately high NKC, High TNFa, heterozyogous mutated Factor XIII, and +APA
October 2012-May 2014: 4 failed IUIs, 3 failed IVFs, and 1 failed FETw/donor embryos
November 2014: IVF w/ICSI #4 Agonist/Antagonist with EPP and Prednisone, Baby Aspirin, Lovenox, and IVIG for immune issues. Converted to freeze all due to lining issues. 2 blasts frozen on day 6!
January 2015: FET #2 Cancelled due to lining issues
April 2015: FET #2.1
PAIF/SAIF Welcome!
TTC since April 2012
BFP #1, 10/03/2012 - EDD 6/15/2013 - MMC 11/15/2012 - D&C 01/04/2013
BFP #2, 04/06/2013 - EDD 12/17/2013 - MC 04/19/2013
6/12/2013 Diagnosed with Balanced Translocation (12 & 16)
IVF #1 with PGS: 10/2013: Canceled 9/27/2013 for issues with genetic lab
IVF #1.5 with PGS: 11/16/2013: Canceled. 11 eggs retrieved, 9 mature & 9 fertilized, all unhealthy embryos
IVF #2: 1/22/14: Canceled. 16 eggs retrieved, 14 mature, 7 fertilized, all unhealthy embryos
IVF #3 with PGS: 5/10/2014: Switched to FET in July. 10 eggs retrieved, 9 mature, 8 fertilized, 2 healthy embryos!
FET #1: 7/31/2014: Transferred 2 nearly perfect (6AA, 6BA) healthy embryos- BFFN
Laproscopy: 10/2014: Healthy uterus
IVF #4: 12/8/2014: Canceled. 17 eggs retrieved, 15 mature, 10 fertilized, all unhealthy embryos
Everyone welcome on my posts
Me: 32 H: 31
IVF #1 October 2013 Antagonistic Protocol with ICSI ER 10/31/13 (18R 16M 11F- 6 blasts to freeze)
ET delayed due to OHSS
FET scheduled for July 8. Delayed due to a crazy high TSH (it had been under control for YEARS!)
FET #1 8/5/14 sET BFN