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I am 32yo, nl fsh, good response to stims (15-23 eggs each time), healthy, non-smoker etc. We originally went into IVF for mf (low counts, motility and morph but okay SCSA test) but it is pretty clear now that I have a true egg quality prob that cannnot be explained as with all my cycles my eggs themselves look dark, have grainy cytoplasm, thick shells and on one cycle (#3) they even had things like fragmented polar bodies, inclusion bodies, vacuoles etc. I have been on different stim protocols. Here are my IVF results. IVF w/ ICSI and AH #2-#4 have been with Dr. Schoolcraft at CCRM.
#1 at local clinic (29 years old at the time): 15eggs retrieved, 12 mature, 9 fert put back 4 poor quality (not sure of the cell #s), highly fragmented embies on day 4. BFN
Switched to CCRM #2: 16 eggs retrieved, 12 mature, 11 fert put back 1 8 cell and 2 6 cells on day 3 all of good quality (no/minimal fragmentation, even cell sizes). BFP and now have 20mo dd.
#3 (32yo): 22 eggs retrieved, 18 mature, 14 fertilized only had 1 6 cell, 1 5 cell and 1 4 cell to transfer, all good quality. BFN. This is the cycle (the only one) that the additional dysmorphic egg findings were noted and I can assume the reason for the even worse embie quality. This is the only cycle that all fsh was done.
#4: 23 eggs retrieved (mild OHSS), 16 eggs mature, 9 fertilized, put back 1 8 cell (had been 6 cells but divided prior to transfer), 1 6 cell, 2 5 cell all of good quality. BFN.
Does it sound like it is time for me to throw in the towel or move on to DE or adoption or do you think that with my young age, good response to stims, and the fact I was successful once despite poor appearing eggs that I might still have a decent shot but it may just take a few more tries? I have always heard you should switch clinics after 2 failed cycles but do you think that is true when you are already at what is considered by many a good clinic? Does your clinic offer a different type of culture medium that might help? I am thinking that is really the only thing that can be different somewhere else. Also, I have only ever tried long lupron protocols, have you ever seen any benefit in a situation like mine with an antagon protocol or mdl in terms of improving embie quality? Thanks for your time.
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