Weight goes up, strength goes up, I'd say on par with dbol. It's good in low dose range 5-10 mg, I don't see a need to go above this ( I did, and didn't notice anything other then increase sides; cramps, puffines, heart burn). The heart burn from it is atrocious.
Wow you got some great advice!!M1T was my first and favorite oral compound. i ran M1T 30mg's a day wek 1-3 week 4-10 40 mg's M1T AND 50 mg's winny. didn't use any test cause i was told test made your balls small. loved M1T. put on 18lbs first4weeks. now thanks to deca, M1T and D-BOL both give me puffy big nips.
not advice, just my experience!!!Wow you got some great advice!!
isnt m1t like dbol and only supposed to be ran for like 3-4 weeks? lol 10 weeks seems excessive
Lol I meant about not using test because it will shrink your balls. I remember the pre Internet days when the biggest dude at the gym "obviously knew everything about gear. No disrespect bro.not advice, just my experience!!!
my advice, don't fuck with it!! take some creatine and drink lots of water, eat a bunch of mcdonalds! cuase thats the after affects of M1T. but if you can handle it and deal with the headaches. M1T is some great shit.
20x if you dissolve it in your rectum
How is that possible? The 17-a methylation makes it up to 98% bio-available orally, not to mention increases the molecular weight which would make absorption into the buccal membranes under the tongue more difficult.Short half life, and did you guys know M-1-T is absorbed in far greater quantities if you dissolve it under your tongue?
http://toxnet.nlm.nih.gov/cgi-bin/sis/search/r?dbs+hsdb:@term+@rn+58-18-4
I thought that went without sayingYeah, but with that route absorption only occurs if application is done via penis
How is that possible? The 17-a methylation makes it up to 98% bio-available orally, not to mention increases the molecular weight which would make absorption into the buccal membranes under the tongue more difficult.
I agree with your thinking, but...
Sublingual methyltestosterone is absorbed faster and its bioavailability is
double that from orally admin drug in humans...[The Chemical Society.
Foreign Compound Metabolism in Mammals Volume 3. London: The
Chemical Society, 1975., p. 166]