80 mg winstrol ga je wel voelen in je gewrichten. Had er met 40 al een beetje last van de laatste week.
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Originally posted by niet_hier View Post
Bedankt, nu voel ik me nog weer ouder met m'n 45.Originally posted by niet_hier View PostJe bent zo oud als je je zelf voelt.
Originally posted by STED View Postwtf zit er nog zoveel zout in kip?
Originally posted by bruce View Postsnuf, je bent gek. met je hoeveelheden, maar ja.
tren en deca zoveel opgeteld zit je ook op 1000mg, die hcg is dus wel op zn plek.
ben benieuwd naar je sides.
echt, de gains geloof ik wel. ik ga de sides bijhouden, als je die op wil schrijven iig.
dus:
hair loss
pimples
moisture
agression
horny (bility?)
gewrichts pijntjes
etc.
Misschien wat agressie op de sportschool, that's all.
Ben benieuwd wat de toevoeging van tren, deca en winstrol gaat bewerkstelligen.
Vergeet de proviron niet kerel, die zorgt voor een androgene toevoeging. Icm HCG zal ik als het goed is geen last ondervinden van libido-verlaging en/of deca-dick.
De reden voor de hoeveelheden heb ik al meerdere keren uitgelegt. Ten eerste wil ik gewoon ervaren wat het teweegbrengt. Ten tweede weet ik dat ik een hoge roid-tolerantie heb, dwz geen last van bijwerkingen met gemiddelde doseringen dus kan ik het stapje hoger in inname gemakkelijk maken.
Originally posted by Shredmaster View Post80 mg winstrol ga je wel voelen in je gewrichten. Had er met 40 al een beetje last van de laatste week.
Tis persoonsgebonden Timmetje.
Originally posted by bruce View Postna 6 weken winny op 40 leek ik wel een hond qua uitharen
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Originally posted by Snuff-Sann View PostVergeet de proviron niet kerel, die zorgt voor een androgene toevoeging.The Sky Ain't The Limit
"Permanence, perseverance and persistence in spite of all obstacles, discouragement, and impossibilities: It is this, that in all things distinguishes the strong soul from the weak."
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Originally posted by Snuff-Sann View Post???
Geloof dat de discussie vorige keer over het meer vrije testosteron verhaal ging.
En bij nader inzien, tevens veel meer erover gelezen te hebben, ben ik van mening dat proviron dat inderdaad bewerkstelligt.▬▬▬▬▬▬▬▬▬▬▬ஜ۩۞۩ஜ▬▬▬▬▬▬▬▬▬▬▬▬▬
We like it
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Originally posted by Snuff-Sann View PostVooral deca mist het androgene gedeelte. Daarom ook het probleem met het libido en het krijgen van een deca-dick. Proviron kan uitkomst bieden omdat het deze eigenschap wel bezit.The Sky Ain't The Limit
"Permanence, perseverance and persistence in spite of all obstacles, discouragement, and impossibilities: It is this, that in all things distinguishes the strong soul from the weak."
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Met alle respect hoor Snuff en weet dat jij echt van de weinige bent die echt veel van as af weet hier.
Maar ik vind het erg naief als je denkt dat je geen bijwerkingen hebt omdat je ze niet voelt, ik waarschuw mensen altijd erg voor as omdat de kater altijd later gaat komen en je cholesterol helemaal naar de klote gaat en dat zijn de meest gevaarlijke bijwerkingen die je helaas niet meteen voelt.Face your demons...........
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Originally posted by Kevster View PostInteresting. Heb je ergens een linkje hoe progesteron en DHTs enzo allemaal werkt op het deca-dick gebeuren? Als ik zoek krijg ik voornamelijk wanhopige pannekoeken die hun pum niet meer de lucht in krijgen.
Proviron has four distinct uses in the world of bodybuilding. The first being the result of its structure. It is 5-alpha reduced and not capable of forming estrogen, yet it nonetheless has a much higher affinity for the aromatase enzyme (which converts testosterone to estrogen) than testosterone does. That means in administering it with testosterone or another aromatizable compound, it prevents estrogen build-up because it binds to the aromatase enzyme very strongly, thereby preventing these steroids from interacting with it and forming estrogen. So Mesterolone use has the extreme benefit of reducing estrogenic side-effects and water retention noted with other steroids, and as such still help to provide mostly lean gains. Its also been suggested that it may actually downgrade the actual estrogen receptor making it doubly effective at reducing circulating estrogen levels.
The second use is in enhancing the potency of testosterone. Testosterone in the body at normal physiological levels is mostly inactive. As much as 97 or 98 percent of testosterone in that amount is bound to sex hormone binding globulin (SHBG) and albumin, two proteins. In such a form testosterone is mostly inactive. But as with the aromatase enzyme, DHT has a higher affinity for these proteins than testosterone does, so when administered simultaneously the mesterolone will attach to the SHBG and albumin, leaving larger amounts of free testosterone to mediate anabolic activities such as protein synthesis. Another way in which it helps to increase gains. Its also another part of the equation that makes it ineffective on its own, as binding to these proteins too, would render it a non-issue at the androgen receptor.
Thirdly, mesterolone is added in pre-contest phases to increase a distinct hardness and muscle density. Probably due to its reduction in circulating estrogen, perhaps due to the downregulating of the estrogen receptor in muscle tissue, it decreases the total water build-up of the body giving its user a much leaner look, and a visual effect of possessing “harder” muscles with more cuts and striations. Proviron is often used as a last-minute secret by a lot of bodybuilders and both actors and models have used it time and again to deliver top shape day in day out, when needed. Like the other methylated DHT compound, drostanolone, mesterolone is particularly potent in achieving this feat.
Lastly Proviron is used during a cycle of certain hormones such as nandrolone, with a distinct lack of androgenic nature, or perhaps 5-alpha reduced hormones that don’t have the same affinities as DHT does. Such compounds, thinking of trenbolone, nandrolone and such in particular, have been known to decrease libido. Limiting the athlete to perform sexually being the logical result. DHT plays a key role in this process and is therefore administered in conjunction with such steroids to ease or relieve this annoying side-effect. Proviron is also commonly prescribed by doctors to people with low levels of testosterone, or patients with chronic impotence. Its not perceived as a powerful anabolic, but it gets the job done equally well if not better than other anabolic steroids making it a favorite in medical practices due to its lower chance of abuse.
Mesterolone is generally well liked nonetheless as it delivers very few side-effects in men. In high doses it can cause some virilization symptoms in women. But because of the high level of deactivation and pre-destination in the system (albumin, SHBG, 3bHSD, aromatase) quite a lot of it, if not all simply never reaches the androgen receptor where it would cause anabolic effects, but also side-effects. So its relatively safe. Doses between 25 and 250 mg per day are used with no adverse effects. 50 mg per day is usually sufficient to be effective in each of the four cases we mentioned up above, so going higher really isn’t necessary. Unlike what some suggest or believe,
I will post an abstract to refute these next statements at the bottom of the page
Its not advised that Proviron be used when not used in conjunction with another steroid, as it too is quite suppressive of natural testosterone, leading to all sorts of future complications upon discontinuation. Ranging from loss of libido or erectile dysfunction all the way up to infertility. One would not be aware of such dangers because Proviron fulfills most of the functions of normal levels of testosterone.
Stacking and Use:
Mesterolone is an oral alkylated steroid. If used primarily as an anti-aromatase drug, using it throughout a longer cycle (10-12 weeks) of injectables may elevate liver values a little bit, though much, much less than one would expect with a 17-alpha-alkylated steroid. Eventhough instead of inhibiting gains, mesterolone may actually contribute to gains. So that’s a bit of a shame. Its not quite as toxic since its not alkylated in the same fashion, but at the 1 position, which reduces hepatic breakdown, but not like 17-alpha alkylation. The reason for the change of position I assume, is because alkylating at the 17-alpha position has been shown to reduce affinity for sex hormone binding proteins. This would in turn decrease its ability to free testosterone. Nonetheless the delivery rate is quite good. Its taken daily in 50-100 mg doses.
The best thing to stack it with is testosterone of course. Its most easily bound to SHBG and albumin, and deactivated for up to 98%. Since the DHT can compete for these structures with higher affinity it would naturally lead to a higher yield of whatever testosterone product you stacked it with. Since DHT levels are notably higher now there is also more stimulation of the androgen receptor causing more strength gains, and because of its affinity for aromatase the overall estrogen level decreases as well. This has as a result that gains are leaner, and once again the overall testosterone yield is increased as less I converted at the aromatase enzyme.
It’s of course used in other stacks with products such as methandrostenolone, boldenone and nandrolone to reduce estrogenic activity and increase muscle hardness. The addition of proviron makes boldenone a dead lock for a cutting stack and for some may even make it possible to use nandrolone while cutting, although the use of Winstrol or a receptor antagonist in conjunction is wishful as well. The benefit of adding it to a nandrolone stack is that it may also help you reduce the decrease in libido suffered from nandrolone, since the latter is mostly deactivated by 5-alpha reductase, an enzyme that makes other hormones more androgenic.
Proviron is an anti-aromatase, so obviously anti-estrogens would be futile and redundant. Blood pressure medication for those prone to hypertension may be wise, as this DHT can increase the blood pressure.
Abstract refuting that Proviron is not highly suppressive
Here is the study I was referring to. Only 85 men out of 250 showed any suppression. Proviron did not shut down the HPTA in any of the subjects and that was at 150mg for 1 year. I would say its pretty safe and has very little effect on one’s HPTA
This study shows no effect on normal LH and FSH with 100-150mg/ d mesterolone, and decrease of FSH/LH that were elevated.
Proviron doesn’t substitute Clomid as hpta therapy, but doesn’t get in the way, either.
The effect of mesterolone on sperm count, on serum follicle stimulating hormone, luteinizing hormone, plasma testosterone and outcome in idiopathic oligospermic men.
Varma TR, Patel RH.
Department of Obstetrics & Gynaecology, St. George’s Hospital Medical School London, U.K.
Two hundred fifty subfertile men with idiopathic oligospermia (count less than 20 million/ml) were treated with mesterolone (100-150 mg/day) for 12 months. Seminal analysis were assayed 3 times and serum follicle stimulating hormone (FSH) luteinizing hormone (LH) and plasma testosterone were assayed once before treatment and repeated at 3, 6, 9 and 12 months after the initiation of treatment. One hundred ten patients (44%) had normal serum FSH, LH and plasma testosterone, 85 patients (34%) had low serum FSH, LH and low plasma testosterone. One hundred seventy-five patients (70%) had moderate oligospermia (count 5 to less than 20 million/ml) and 75 patients (30%) had severe oligospermia (count less than 5 million/ml). Seventy-five moderately oligospermic patients showed significant improvement in the sperm density, total sperm count and motility following mesterolone therapy whereas only 12% showed improvement in the severe oligospermic group. Mesterolone had no depressing effect on low or normal serum FSH and LH levels but had depressing effect on 25% if the levels were elevated. There was no significant adverse effect on testosterone levels or on liver function. One hundred fifteen (46%) pregnancies resulted following the treatment, 9 of 115 (7.8%) aborted and 2 (1.7%) had ectopic pregnancy. Mesterolone was found to be more useful in patients with a sperm count ranging between 5 and 20 million/ml. Those with severe oligospermia (count less than 5 million) do not seem to benefit from this therapy.
PMID: 2892728 [PubMed - indexed for MEDLINE]One more…
Effect of non aromatizable androgens on LHRH and TRH responses in primary testicular failure.
Spitz IM, Margalioth EJ, Yeger Y, Livshin Y, Zylber-Haran E, Shilo S.
We have assessed the gonadotropin, TSH and PRL responses to the non aromatizable androgens, mesterolone and fluoxymestrone, in 27 patients with primary testicular failure. All patients were given a bolus of LHRH (100 micrograms) and TRH (200 micrograms) at zero time. Nine subjects received a further bolus of TRH at 30 mins. The latter were then given mesterolone 150 mg daily for 6 weeks. The remaining subjects received fluoxymesterone 5 mg daily for 4 weeks and 10 mg daily for 2 weeks. On the last day of the androgen administration, the subjects were re-challenged with LHRH and TRH according to the identical protocol. When compared to controls, the patients had normal circulating levels of testosterone, estradiol, PRL and thyroid hormones. However, basal LH, FSH and TSH levels, as well as gonadotropin responses to LHRH and TSH and PRL responses to TRH, were increased.
Mesterolone administration produced no changes in steroids, thyroid hormones, gonadotropins nor PRL.
There was, however, a reduction in the integrated and incremental TSH secretion after TRH.
Fluoxymesterone administration was accompanied by a reduction in thyroid binding globulin (with associated decreases in t3 and increases in t3 resin uptake). The free T4 index was unaltered, which implies that thyroid function was unchanged.
In addition, during fluoxymesterone administration, there was a reduction in testosterone, gonadotropins and LH response to LHRH.
Basal TSH did not vary, but there was a reduction in the peak and integrated TSH response to TRH. PRL levels were unaltered during fluoxymesterone treatment.
Originally posted by bruce View PostDus proviron zorgt voor een proviron Dick. Tevens een Dick head. Vol pukkels gege
Originally posted by Kevin72 View PostMet alle respect hoor Snuff en weet dat jij echt van de weinige bent die echt veel van as af weet hier.
Maar ik vind het erg naief als je denkt dat je geen bijwerkingen hebt omdat je ze niet voelt, ik waarschuw mensen altijd erg voor as omdat de kater altijd later gaat komen en je cholesterol helemaal naar de klote gaat en dat zijn de meest gevaarlijke bijwerkingen die je helaas niet meteen voelt.
Je doet net alsof ik niet goed weet waar ik mee bezig ben.
Dacht je nu werkelijk dat ik alleen naar de buitenkant van mijn lichaam kijk om te zien of alles goed gaat?
Sorry maar daar neem ik geen genoegen mee. Ik en mijn dokter begrijpen elkaar en zij is er wel niet zo blij mee dat ik steroiden gebruikt maar ze staat me wel bij en ik kan 4x per jaar een bloedtest laten uitvoeren waarin alle belangrijke punten worden onderzocht.
Zal je even wat info verschaffen.
Heb nog geen twee weken geleden een bloedonderzoek gehad.
Zal ff vertellen wat er loos is.
Ze heeft ook m'n bloeddruk nog ff opgemeten en die was toppie, geen last van de verhoging van rode bloedcellen, want dat is het eerste wat met een standaard test verschilt, slechts een kleine verhoging, 5,75. Mag normaal gesproken niet boven de 5,70.
Witte bloedcellen zijn lager dan standaard, 1,10. Mag niet lager dan 1,50.
Oestrogeen ligt te hoog, 305, mad niet hoger dan 206, maarja dat is ook niet zo vreemd als je 5x meer test in je lichaam hebt rondcirculeren, bridgte op dat moment met 250mg test-e. Zat op dat moment op 25mg provi, dit is nu verhoogd naar 50mg, maw zal dit de oestrogeen nog wat meer drukken. Tevens dien je altijd oestrogeen te bezitten.
Urea level te hoog, hebben alle krachtsporters die veel proteinen innamen.
BMI lift te hoog, jah gek he!
Plasma glucose level ligt net iets te laag, 3,4. Mag niet lager dan 3,5.
Heeft te maken met een enorm tekort aan suiker in mijn strak dieet.
Dan is er een leverwaarde-verhoging echter zeer laag en duid dit enkel maar op gewichtstraining en niet op ernstige leverschade.
En als laatste liggen het LH en FSH hormoon plat op hun gat. Tsja, daar ontkom je niet aan als je teveel test in je lichaam pompt.
Is helemaal niet erg. Ik heb het LH hormoon vervangen voor HCG en het FSH hormoon zorgt enkel voor je 'spermcount' met de sertoli-cellen.
Echter heb ik een betrouwbaar en tevens zeer goedkoop adres weten te vinden en zal ik spoedig met HMG, imitaat voor FSH, gaan starten.
Hierdoor zal ik beide hormonen vervangen hebben.
Kort samengevat weet ik heel erg goed waar ik mee bezig en ook van binnen.
Maak je niet druk bro, ik heb allang voorgenomen dat mocht er serieus iets ernstig mis zijn zal ik onherroepelijk ophouden met kuren.
Kijk ik ben wel goed maar niet gek.
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