Yes, and I discovered that I had very low AMH for my age, went on to appointments at fertility clinic and had several Antral Follicle Count ultrasounds which confirmed Diminished Ovarian Reserve.
I will say, please have a good idea in your head about how you might proceed with the information provided. How old are you? What are your plans regarding children? Do you have a partner? Are you in a position to start TTC asap if you get low results?
Of course, the vast majority of people who do these tests for “reassurance” will get those reassuring results, but you need an idea of what your plan would be if you get bad results.
I got my Superdrug AMH results January last year, and I’m not kidding when I say it absolutely consumed the last year of my life with appointments, scans, decisions, etc.
Do you have the money to proceed with private fertility investigations/treatment if you get bad results? Because the NHS/your GP wont suddenly jump in to investigate or act on a low AMH result sought privately. The NHS don’t really even recognise it as a valid test, not because it isn’t, but because it isn’t relevant to any of the NHS infertility pathways. You’ll find that they’ll still only investigate further if you’ve met the standard criteria of TTC with your partner for 6 or 12 months depending on age.
If you don’t have a partner and aren’t TTC, there is no NHS provision for egg freezing/embryo freezing as a solo person (unless in certain types of cancer treatment that run the risk of infertility).
AMH alone doesn’t tell the full story either, it’s simply a measure of potential reproductive lifespan, it doesn’t tell you about egg quality, etc. Even with very low AMH you can still fall pregnant naturally, it only takes one egg. Or you could have a good AMH but poor quality eggs that don’t fertilise or create viable embryos.
Given the last year of my life, and the investigations and money I’ve spent, the cost to my emotional wellbeing and stress levels, I think if I’d had no money to investigate further or pursue treatment privately myself, I’d prefer not to have known about my AMH. Knowing that something is so time critical, but without the practical means to act on it, would be hellish.