I was taught that stuff by the late Snagency on here - a good mentor, as well as Danger Dave. Lots to be learned from those who came before!
I’m just trying to do it all the best I know how, like you lol
I can see why you would think that when you are starting to see/feel effects and sides is when you think a compound is kicking in, but I assure you all orals, even SARMs, are active right away. It’s in your blood and it’s causing physiological process changes immediately.
My suggested layout causes the slowest shutdown of natural test production as well as produces the biggest, strongest, fullest package at the finale of the cycle - the greatest peak result, with the fastest hormonal recovery time from the available scenario. With only Rad starting out, production will begin declining immediately but you will not be at 0 for some time. 1-3 weeks probably before things are totally offline. And a dry DHT like 3AD isn’t very suppressive either. But a 19-Nor like YK certainly will be, as will such a potent compound as Msten.
The liver will also only be under strain for the 4-6 weeks you run the YK (which encompasses the Msten blast), vs starting with Msten, then finishing with YK has you on 7-9 total weeks of methylated compounds. 4-6 a bit more intense vs 7-9 more continuous load.
You could run it that way if you prefer, and it will be easier on sides at the end, but realize the gains from this cycle will be a flatter curve. This may be desirable for longterm gain-retention, or for someone not interested in producing as dramatic a transition. Maybe milder is the way to go for you - it’s individual preference. The lone drawback is being totally shut off by end of week 1 vs perhaps week 3, and implications for ease of HPTA recovery afterward.
Greg “I’m NOT a doctor” Doucette, IFBB Pro