@GingerRCD I had a AMH of around 4 pmol when starting with Create and got advised natural modified would be beneficial, especially as my failed NHS cycle at another clinic led to only 2 mature eggs of which neither fertilised (high dose stims). Create asked if I agreed, which after my disaster NHS round I completely did. I did the following with Create:
Cycle 1: natural modified, 5 eggs collected, 4 mature, 3 fertilised successfully:
1 x day 3 (as yet to culture once thawed to see if it gets to blastocyst or not) and 1 x blastocyst frozen
Cycle 2; natural modified, 2 eggs collected, both mature, both fertilised, both reach blastocyst:
1 x frozen, the other discarded on day 6 as poor.
Notes from this cycle were that I had a number of follicles that could have possibly caught up; so more eggs (possibly 4 in total could have been collected but the follicles were not big enough and eggs would have been immature, so mild advised for next time to see if it was possible)
Cycle 3 1st attempt: false start, cycle cancelled. I did back to cycles and in hindsight shouldn't have done (I pushed for it). I developed a polyp later which needed a Hysteroscopy, and in all hoensty I'm glad I had the Hysteroscopy as my periods have improved since as adhesions were removed too (better flow, no period pain), seen it as a prep for FET. But I do believe the polyp arose because of the stims and back to back cycles...hence now doing natural FETs to avoid meds where possible. So if you get a good response with natural modified, you may want to consider a one month break between cycles as natural is only meant to collect 1 or 2 eggs.
Cycle 3: mild, 7 eggs collected, all mature and fertilsed, 5 reached blastocyst:
4 x day 5 and 1 x day 6 blastocyst frozen
So overall, I got 8 embryos frozen - we were prognosed to only get 2-3, so whatever happens, it was more than we could have hoped or expected at this stage.
I just completed my FET of the best grade from cycle 3 but unfortunately that was a BFN so I'm now going straight into my next natural FET with an embryo that is the same quality from cycle 1. I did not do PGTA.
Overall, I have found the clinical care with Create good, I have done my own research along the way too and am making my own decisions on how to approach which they are in support of.
How have you found it?