Hi ladies. I know its been a while since i've posted. Long story short IVF#2 also ended in m/c. This time everything was right on track which makes this harder to accept.
I was wondering if anyone else had a similar experience or could guide me in a direction. I am seeing the RE in two weeks for a post op appointment where im sure we will discuss next steps. I have a list of a few things I should ask to be tested for but would like to hear anything else that I should research or ask about. I feel so clueless about this and just want answers. Also, if you did testing and found another issue, what was the treatment for it in order for you to move forward? TIA ladies!
Re: RPL Testing ? (m/c mentioned)
I would definitely request an RPL panel if your doc doesn't bring it up- IVF is simply too expensive to wait for three losses. Every doc has a different cocktail of tests they prefer but most will have the big stuff: Clotting, MTHFR, Factor V. I would request immunology and karyotyping as well if they're not offered- but a lot of places put those on the list standard.
They pulled 19 vials of blood and it took about 2 weeks to get the full panel of results (karyotyping took the longest- some stuff was back in a day or three)- my panel was very big though- number of vials/time varies widely based on the tests ordered.
My testing uncovered only 2 minor issues, neither of which my doc was prepared to say had certainly caused my miscarriage. That's something to be prepared for as well- sometimes there aren't going to be any definitive answers.
MTHFR: I have one C mutation. This is not a yes/no test- 30-40% of the population has 1 or 2 of the A or C mutation. So XXXX is normal, AXXX, XCXX, ACXX, AXAX, XCXC, ACAX, XCAC, ACAC are all possibilities. You get one set of AC from each parent. 2 copies of the C mutation is linked to recurrent miscarriage via clotting issues. Anything other than 2 copies of C can be (but is not always) linked to clotting issues. Anyone with a mutation absorbs folic acid a little less effectively than someone without a mutation- but that's not linked to miscarriage- it's linked to an increase in neural tube defects. My treatment: Take two prescription folic acid. Combined with the second issue- I also take a baby aspirin.
ACLA IgM: I have very slightly elevated anticardiolipin antibodies. If normal is 10 and aggressive treatment with blood thinners is required at 20- I have a 12. Which most docs wouldn't recommend any treatment for. My doc took a look at that combined with the single MTHFR and decided that an over the counter baby aspirin therapy would be acceptably cautious.
I'm so sorry for you loss- it's a special kind of hell to make it through IF only to have a loss. I hope they find something that can be easily treated.
Friends for 15 years. Married 8. TTC since January 2009
2010 Diagnosis: Anovulation and Severe MFI
2011 Treatment:
IVF w/ICSI #1 Antagonist: 2 blasts - c/p - BFN 04.22
FET #1: 1 blast/1 early blast - BFP 06.22 - m/c 06.30 @6w0d
07-11 RPL: MTHFR C677T Heterozygous & Slightly elevated ACLA IgM
FET #2: 1 morula - BFN: 9.02
January '12: IVF #2
Started BCP and Metformin (New!) 12-14 for stimming in January
Dum spiro, spero.
?SAIF/PAIF/PgAL/PAL always welcome?
Married 1/2/99.
TTC since 4/09.
Diagnosed PCOS. Diagnosed Hypothryoid 11/09.
SHG & SA normal. PCOS Research study started 5/10.
Clomid/Femara cycle #1 - 6/10 = BFN
Clomid/Femara cycle #2 - 7/10 = BFP #1 - Missed miscarriage 9/2/10
11/12 - BFP #2 - 11/22 - m/c
5/1/11 - BFP #3 - Pre-eclampsia, IUGR & bed rest from 32w. DD born via induction 1/4/12.
DX: 6/9/2011: Azoo ICSI/IVF only option for biological child
IVF #1: ER - 9/26 * ET - 10/1 * beta#1 10/13 - 140 * beta#2 10/17 - 477 * beta#3 10/20 - 1101
1st u/s at 6w6d - one hb * 2nd u/s at 8w3d - no hb detected 11/10/11 * natural m/c 11/13/11
FET #1 Jan/Feb 2012 - 3 delays - cancelled 2/13
FET #1.2 - May/June 2012 - ET 6/6/* beta#1 6/15 - 95 * beta #2 6/19 - 322 * beta #3 6/22 - 940
7/6 1st u/s @ 7 weeks - one beautiful hb - released from RE
EDD 2/22/2013
PAIF/SAIF/PGAL welcome
So sorry for your loss. I would definitely ask for a RPL panel before moving forward. I only had one loss, but it was in the 2nd trimester, so my RE was more concerned and ordered a RPL. She also ordered a diagnostic hysteroscopy to determine if there is a physical reason for the loss.
For the RPL, I think they took about 14 vials of blood, testing for celiac disease, anticardiolipins, and various clotting factors. I was positive for 2 copies of MTHFR, but she was not too concerned because I had normal homocysteine levels. I was also positive for the Lupus Anticoagulant, which she was concerned with. I have to get test for it again to confirm (it can be transient, and you need to test 12 weeks later) If the 2nd test is positive, she said I will need lovenox (blood thinner) injections if I get pregnant again.
The hysterocopy revealed some small polyps, which she did not think was the cause of the loss, but could make it difficult to get pregnant in the future, so I had them removed. She said if there are large polyps or fibroids, that can cause m/c.
I hope you find some answers and I wish you the best of luck!
11/2010 - Surprise BFP - m/c @ 16 weeks - dx Lupus Anticoagulant
1/2012 - Clomid & IUI #4= BFP twins! On Lovenox - m/c @ 16 weeks
9/2012 - Clomid & IUI #5= BFP! EDD 6/6/13
I may have to wait....I'll never give up.
I guess it's half timing and the other half's luck. - Buble
Thank you all for your replies. We had extensive testing before starting treatment. Before IVF we had the HIV panel run on both of us. I have family with Factor V Leiden so i was tested for that already in the beginning, and even so, he had me on a baby aspirin during treatment. I was also taking enough folic acid since that had come back low before. He does an HSG before each cycle to look for polyps. I had a lap done in Dec that removed endo and polyps and havent had any more since.
He definitely wants to run the RPL panel and ive done some reasearch and hope we can find an answer because i can not go through number 3 without some sort of answers. I guess based on my research i feel like certain things have already been eliminated because of prior testing or that we were already doing something to prevent it (like baby aspirin and folic acid). I am willing to hear him out but am also researching genetic counselors as well to see where we are with that. Thanks for all of your help. I am prepared for no answers as well, but pray that wont be the case. Thanks for all of your help!
1) Thrombophilia panel
2) Karyotyping
3) Immunological panel
I've had 1&2 & nothing was found. I don't think this cycle's going to work, and I'll push for #3.
Check this out. And this.
TTC since 6/02 (age 22) K/U instantly despite no AF for 5 months--preemie baby boy 1/03
M/C 11/04 - M/C 05 - M/C 06 - BFP 2/08--fullterm baby girl 10/08 - M/C 4/11 - went to RE at age 31
DX: crappy quality & infrequent ovulation, mild MFI
Stimmed cycle #1 C/P 7/11 - Stimmed cycle #2 C/P 8/11 - Stimmed cycle #4 C/P 10/11
On Stimmed Cycle #5
Always thought I'd be a "mom of many"--now just hoping to be a "mom of one or two more!"