Hi everyone, I am feeling a bit lost & confused and wondered if anyone may be able to offer some advice.
I’m currently going through a chemical pregnancy which is my 5th loss in 1.5 years and first loss on Dr Shehata’s complex plan for high NK cells. My other losses have been at 8.5 weeks and then 4 between 4-6 weeks. Being on prednisolone this time, I thought things would be different but this pregnancy lasted no longer than the others.
I wondered if others have had losses on Dr Shehata’s plan or similar and might have advice? I’m currently thinking about 3 potential options:
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Try again (naturally) on an amended treatment plan with Dr S. I’ve read he prescribes hydroxy to people who miscarry on pred so maybe this will help? Also i was only taking 15mg of pred which they said was suitable as I’m quite small but maybe they’ll increase as the standard dose is 25mg? This would be the cheapest/easiest plan but worried something else is going on and it will happen again.
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Do more extensive tests with Dr Gorgy (eg uterine NK cells, LADs, uterine infections, EMMA/ALICE etc). This would be expensive and delay TTC again (as I believe uterine NK cells must be tested at least 6 weeks after the last miscarriage) but it may give a more complete picture and avoid future losses. Partner not keen on this option though due to costs.
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Try IVF with genetic testing. We usually conceive quite easily so have been told IVF is a waste of money and time, but I’m wondering if having more control over the process (hormones etc) and only putting in genetically normal embryos will reduce the risk of miscarriage. We may be able to get one round free through my partner’s health insurance.
I’ve had the NHS RM tests and all were clear except PCOS which I’m taking metformin for. I’m 32 and been taking coq-10 for a year so wouldn’t necessarily expect egg quality to be poor unless it’s badly affected by my PCOS. My partner’s sperm and dna frag is all fine.
If anyone can offer any advice or insights I’d be super grateful. I’ve also posted this question on the NK cells thread but thought starting a thread would be useful to reach people who aren’t on that thread.
Lily xx