Please Scroll Down to See Forums Below
napsgear
genezapharmateuticals
domestic-supply US-PHARMACIES UGL OZ
Raptor Labs UGFREAK OxygenPharm
napsgeargenezapharmateuticals domestic-supplyUS-PHARMACIES UGL OZUGFREAKRaptor LabsOxygenPharm

Not speaking for anyone else, but!!!!!!!!!

karson

New member
I have seen better gains and much more quality off anavar than i ever have off anything else ive takin. I feel that it is so superior to test, deca, primo, winny (again in my own opinion) that i will never touch anything again. my gains have been out of this world seriously...40 mgs a day and wow i mean wow, day and night........highly recomended if you must juice......wow
 
hey

dr prescribed. its american, but the label from the pharm just says oxandrolone....ins didnt cover it, those bastards
 
Nice.
Im thinking about trying an Anavar only cycle.
For like 16 or more weeks. 40mg ED.
Gonna cost an arm and a leg though :(
 
A real blast... LOL -- I think of a waterpark as a blast... anavar is like a pina colata on a warm sandy beach... :)

C-ditty
 
yo huck

huck, did you keep your gains well? I have put about 2.5 inchs on my arms and the rest came together nice. also my body is as hard as a rock. my friends cant beleive it. i hope i dont lose much, i read i wont.......also did you have kidney pains during? i dont know if its the up in protein or what but its kinda annoying..also canuck, to let you know, this cycle of 10 wks 40 ed cost me $3000 but worth it. glad i saved my pennies, been planning this for 2 years, cut alot of financial corners and couldnt be happier i did
 
That sounds great!

Now I'm psyched! I'm getting ready to start an Anavar only cycle (my first) in a couple of weeks. 40mg ed 8 weeks. BTG!!!! Just waiting for my last refill.

Hey Huck, you seem to be the most informed, if not the biggest advocate of Ox. I had a question about possibly running Cytomel with it, maybe in the middle or towards the end of my cyle? I'm 27(almost 28) 182lbs. 14%bf(I think)

My goals are really an overall shift in body compostion. I really don't need to put on much more than 10lbs right now. Is it true that a low dose of T3 would ramp up the protein metabolism even further while aiding in the bf reduction?

All of this is assuming my diet is in order of course.

Btw, any other suggestions, ancillaries needed etc. would be greatly appreciated.
 
Re: yo huck

karson said:
huck, did you keep your gains well? I have put about 2.5 inchs on my arms and the rest came together nice. also my body is as hard as a rock. my friends cant beleive it. i hope i dont lose much, i read i wont.......also did you have kidney pains during? i dont know if its the up in protein or what but its kinda annoying..also canuck, to let you know, this cycle of 10 wks 40 ed cost me $3000 but worth it. glad i saved my pennies, been planning this for 2 years, cut alot of financial corners and couldnt be happier i did

3,000... wow.
 
yes that is definetly your own opinion of var being the best. not near the best in my book. price to gains are just unacceptable. when i can cook up a huge batch of fina for 1/10th the price i would do that anyday over var.
 
HUCKLEBERRY FINNaplex said:
Definitely agree with you on that one.Var is one of the single best compounds I have ever ran.A real blast.

Huck, don't you usually run Anavar with a baseline test?
 
dude, never taken fina but var has changed the entire way i look. i went from a smooth blot test boy to more OF a mens health and fitness look. my size has even increased, just look waay better. not sayin its for eveyone, but my contribution to the board is that ive never seen anything like it.....it does seem to effect my kidneys and liver more than injections though, the only downside
 
Karson-I kept nearly 100% of the gains I made.Lost just a tad bit of strength,but gained it back after a few weeks.

Oxman.The T-3 would work okay,but is not really necessary,oxandrolone will ramp up protein synthesis to a huge degree all on its own,and it is quite potent at helping you get leaner(if diet is in order)as well.
 
I dont get this though.

Doesn't Var shut you down?

So, when you guys speak of these great Var-only cycles, are you just sort of "dealing" with the fact that your Unit won't function for a while?

I have never understood this.
 
I am interested in hearing more about this...Does it shut you down???
 
I had no problem with libido on it Riker,but that does not mean it's not possible for anyone.I think the fact that it has a very low androgenic profile and zero conversion to E makes it a little less harsh on endocrine function.
 
Here's a study you anavar fans should like:

(3) : J Clin Endocrinol Metab 1990 Oct;71(4):846-54
Testosterone and oxandrolone, a nonaromatizable androgen, specifically amplify the mass and rate of growth hormone (GH) secreted per burst without altering GH secretory burst duration or frequency or the GH half-life.
Ulloa-Aguirre A, Blizzard RM, Garcia-Rubi E, Rogol AD, Link K, Christie CM, Johnson ML, Veldhuis JD
 
How much can one expect to gain of 12 weeks at 40mgs...If you've done a couple stronger cycles??
 
Malak said:
I am interested in hearing more about this...Does it shut you down???
"shutdown" is almost never 100%; maybe with 1g+ of test per week LH secretion will go down to nondetectable levels, but with the average cycle your testes will produce some testosterone throughout.
Only nandrolone is particularly harsh because it not only suppresses LH but also desensitizes the testes to LH.

i could not find a single study on ox's effects on adults but only on boys with growth deficiency. Ox did suppress LH at minuscule doses (as low as 2.5mg ed) but the suppression did not last the whole course; after a couple of months it rebounded even while still taking Ox. But keep in mind these boys already had a malfunctioning endocrine system.

But even with all the hoopla about Ox don't forget that is as liver toxic as any other 17aa roid. AIDS patients got problems with 20mg ed (they are running it for life without a break though)


Clin Endocrinol (Oxf) 1997 Feb;46(2):209-16

Effect of low dose oxandrolone and testosterone treatment on the pituitary-testicular and GH axes in boys with constitutional delay of growth and puberty.
Crowne EC, Wallace WH, Moore C, Mitchell R, Robertson WH, Holly JM, Shalet SM.
Department of Endocrinology, Christie Hospital Trust, Manchester, UK.
OBJECTIVE: To investigate the effect of low dose oxandrolone and testosterone on the pituitary-testicular and GH-IGF-I axes. DESIGN: Prospective double-blind placebo-controlled trial. PATIENTS: Sixteen boys with constitutional delay of growth and puberty (CDGP) with testicular volumes 4-6 ml were randomized to 3 months treatment: Group 1 (n = 5), daily placebo: Group 2 (n = 5), 2.5 mg oxandrolone daily or Group 3 (n = 6), 50 mg testosterone monthly intramuscular injections with assessment (growth, pubertal development and overnight hormone profiles) at 0, 3, 6 and 12 months. MAIN OUTCOME MEASURES: LH and GH profiles (15-minute samples) were analysed by peak detection (Pulsar), Fourier transformation and autocorrelation. Testosterone levels were measured hourly and insulin, SHBG, IGF-I, and IGFBP-3 levels at 0800 h. Statistical analysis was by multivariate analysis of variance for repeated measures. RESULTS: LH and testosterone parameters increased significantly with time in all 16 (LH AUC, P < 0.001; peak amplitude, P = 0.02; number of peaks, P = 0.02; testosterone AUC, P = 0.02; morning testosterone, P = 0.002). In Group 2, however, LH and testosterone parameters decreased at 3 months followed by a rebound increase at 6 and 12 months. SHBG levels were markedly reduced at 3 months (P = 0.006) and a wider range of dominant GH frequencies was present although GH AUC was not increased until 6 months, with an increase in GH pulse frequency but not amplitude. IGF-I levels were increased at both 3 and 12 months. In Group 3, pituitary-testicular suppression was not apparent, but GH levels increased with an increase in GH amplitude at 3 and 12 months. CONCLUSION: Oxandrolone transiently suppressed the pituitary-testicular axis and altered GH pulsatility. Testosterone increased GH via amplitude modulation.
 
Wow! Great post bro...Karma
 
Malak said:
Wow! Great post bro...Karma
thank you.
here is a link to the medibolics article about the experiences with Ox, Winny and abombs from AIDS patients:
http://www.medibolics.com/oxandrin2.htm

there is talk about ox, winny and anadrol in there. interestingly, abombs @ 150mg ed did not produce more liver problems than ox @ 40mg ed. Ox got the (false) reputation of being safe because sci. studies alway use it in ultra low doses like 2.5mg while anadrol is taken at 100mg upwards ed. on a mg-to-mg comparison the orals all seem to have the same toxicity.

one must also take notice about unfavorable blood lipid value changes from oxandrolone. in the following study, they even switched one group from ox to deca because blood lipids got so bad; ox demonstrated superior fat-loss qualitites though (my guess: the fat-loss advantage over test and deca is estrogen related since ox does not aromatize at all):


Int J Obes Relat Metab Disord 1995 Sep;19(9):614-24

Oral anabolic steroid treatment, but not parenteral androgen treatment, decreases abdominal fat in obese, older men.
Lovejoy JC, Bray GA, Greeson CS, Klemperer M, Morris J, Partington C, Tulley R.
Pennington Biomedical Research Center, Baton Rouge, Louisiana 70808-4124, USA.
OBJECTIVE: To compare the effects of testosterone enanthate (TE), anabolic steroid (AS) or placebo (PL) on regional fat distribution and health risk factors in obese middle-aged men undergoing weight loss by dietary means. DESIGN: Randomized, double-blind, placebo-controlled clinical trial, carried out for 9 months with primary assessments at 3 month intervals. Due to adverse blood lipid changes, the AS group was switched from oral oxandrolone (ASOX) to parenteral nandrolone decaoate (ASND) after the 3 month assessment point. SUBJECTS: Thirty healthy, obese men, aged 40-60 years, with serum testosterone (T) levels in the low-normal range (2-5 ng/mL). MAIN OUTCOME MEASURES: Abdominal fat distribution and thigh muscle volume by CT scan, body composition by dual energy X-ray absorptiometry (DEXA), insulin sensitivity by the Minimal Model method, blood lipids, blood chemistry, blood pressure, thyroid hormones and urological parameters. RESULTS: After 3 months, there was a significantly greater decrease in subcutaneous (SQ) abdominal fat in the ASOX group compared to the TE and PL groups although body weight changes did not differ by treatment group. There was also a tendency for the ASOX group to exhibit greater losses in visceral fat, and the absolute level of visceral fat in this group was significantly lower at 3 months than in the TE and PL groups. There were significant main effects of treatment at 3 months on serum T and free T (increased in the TE group and decreased in the ASOX group) and on thyroid hormone parameters (T4 and T3 resin uptake significantly decreased in the ASOX group compared with the other two groups). There was a significant decrease in HDL-C, and increase in LDL-C in the ASOX group, which led to their being switched to the parenteral nandrolone decanoate (ASND) after 3 months. ASND had opposite effects on visceral fat from ASOX, producing a significant increase from 3 to 9 months while continuing to decrease SQ abdominal fat. ASND treatment also decreased thigh muscle area, while ASOX treatment increased high muscle. ASND reversed the effects of ASOX on lipoproteins and thyroid hormones. The previously reported effect of T to decrease visceral fat was not observed, in fact, visceral fat in the TE group increased slightly from 3 to 9 months, although SQ fat continued to decrease. Neither TE nor AS treatment resulted in any change in urologic parameters. CONCLUSIONS: Oral oxandrolone decreased SQ abdominal fat more than TE or weight loss alone and also tended to produce favorable changes in visceral fat. TE and ASND injections given every 2 weeks had similar effects to weight loss alone on regional body fat. Most of the beneficial effects observed on metabolic and cardiovascular risk factors were due to weight loss per se. These results suggest that SQ and visceral abdominal fat can be independently modulated by androgens and that at least some anabolic steroids are capable of influencing abdominal fat.
 
I'm also one big anavar fan, I believe that var will favorably change the physique like no other anabolic. I perfer to run var with low to moderate doses of test cyp and eq. You may not gain a lot of weight from anavar, but the weight that you do gain is quality, I also love the increases in power that you get from anavar. I used loefflar oxafort my last cycle with great results.:)
 
drveejay11 said:
Huck: which do you prefer: var +test, var+ NO test?

It's a tough call for me...Var/Test is definitely one hell of a synergistic duo,but I have to contend with the sides from test.If I'm running less than 40mgs/week of var,then I'd probably drop some test in there,but 40mgs or over,I would likely just run the var,as it givesa me outstanding results,particularly when protein intake is 2 Grams per lb of bodyweight daily.Next on tap this summer will be var/eq just to see what these 2 combined can do.
 
HUCKLEBERRY FINNaplex said:


It's a tough call for me...Var/Test is definitely one hell of a synergistic duo,but I have to contend with the sides from test.If I'm running less than 40mgs/week of var,then I'd probably drop some test in there,but 40mgs or over,I would likely just run the var,as it givesa me outstanding results,particularly when protein intake is 2 Grams per lb of bodyweight daily.Next on tap this summer will be var/eq just to see what these 2 combined can do.

What am I chopped liver? I asked you the same question and I get ignored then my good buddy drveejay11 asks you and he gets your attention...:bawling:
 
It's a tough call for me...Var/Test is definitely one hell of a synergistic duo,but I have to contend with the sides from test.If I'm running less than 40mgs/week of var,then I'd probably drop some test in there,but 40mgs or over,I would likely just run the var,as it givesa me outstanding results,particularly when protein intake is 2 Grams per lb of bodyweight daily.Next on tap this summer will be var/eq just to see what these 2 combined can do.



Anavar and eq are the dynamic duo, you get some size, you get as strong as hell, lean with veins everywhere. Its not hard to diet because the var curbs the eq hunger. I eat very high protein and pop aminos and BCAA's every couple of hours between meals.:)
 
Re: hey

karson said:
dr prescribed. its american, but the label from the pharm just says oxandrolone....ins didnt cover it, those bastards

How does one go about getting this prescribed.
 
Re: Re: hey

easy said:


How does one go about getting this prescribed.

They contract the AIDS virus or find a "juice" friendly doctor.
 
dude

to answer your question........have a friend with aids who gets them and so on and so forth......
 
Riker29 said:
I dont get this though.

Doesn't Var shut you down?

So, when you guys speak of these great Var-only cycles, are you just sort of "dealing" with the fact that your Unit won't function for a while?

I have never understood this.

I wake up every morning with wood on anavar. I don't care how it works, I'm just glad it does!
 
Dnkypnch said:
Anyone use powder var? I have some on the way and plan on runnig it at 40-50mgs for 10-12 weeks

Yep, I ran 50mg of powder a day for 10 weeks with 500mg of EQ a week. It was my first cycle, a cutting cycle, and I gained 13lbs by the end of the cycle, even while dieting. I was up over 16lbs during the cycle, but during those last few weeks I lost a good deal of fat.


liftsiron said:

Anavar and eq are the dynamic duo, you get some size, you get as strong as hell, lean with veins everywhere. Its not hard to diet because the var curbs the eq hunger. I eat very high protein and pop aminos and BCAA's every couple of hours between meals.:)

I agree, this cycle was great. Dieting is a lot more fun when you're still increasing the weights every week.
 
Top Bottom