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Phil Heath Explains Why He Can't Train Heavy Like RONNIE COLEMAN


AE AE AE

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HGH 2vials 10iu/vial free sample

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The Power of The Mind - Placebo Pills Cure Chronic Pain Patients

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September 12, 2018

Northwestern University

Someday doctors may prescribe sugar pills for certain chronic pain patients based on their brain anatomy and psychology. And the pills will reduce their pain as effectively as any powerful drug on the market, according to new research. Scientists have shown they can reliably predict which chronic pain patients will respond to a sugar placebo pill based on the patients' brain anatomy and psychological characteristics.

Someday doctors may prescribe sugar pills for certain chronic pain patients based on their brain anatomy and psychology. And the pills will reduce their pain as effectively as any powerful drug on the market, according to new research.

Northwestern Medicine scientists have shown they can reliably predict which chronic pain patients will respond to a sugar placebo pill based on the patients' brain anatomy and psychological characteristics.

"Their brain is already tuned to respond," said senior study author A. Vania Apkarian, professor of physiology at Northwestern University Feinberg School of Medicine. "They have the appropriate psychology and biology that puts them in a cognitive state that as soon as you say, 'this may make your pain better,' their pain gets better."

There's no need to fool the patient, Apkarian said.

"You can tell them, 'I'm giving you a drug that has no physiological effect but your brain will respond to it,'" he said. "You don't need to hide it. There is a biology behind the placebo response."

The study was published Sept. 12 in Nature Communications.

The findings have three potential benefits:

Prescribing non-active drugs rather than active drugs. "It's much better to give someone a non-active drug rather than an active drug and get the same result," Apkarian said. "Most pharmacological treatments have long-term adverse effects or addictive properties. Placebo becomes as good an option for treatment as any drug we have on the market."
Eliminating the placebo effect from drug trials. "Drug trials would need to recruit fewer people, and identifying the physiological effects would be much easier," Apkarian said. "You've taken away a big component of noise in the study."
Reduced health care costs. A sugar pill prescription for chronic pain patients would result in vast cost savings for patients and the health care system, Apkarian said.
How the study worked

About 60 chronic back pain patients were randomized into two arms of the study. In one arm, subjects didn't know if they got the drug or the placebo. Researchers didn't study the people who got the real drug. The other study arm included people who came to the clinic but didn't get a placebo or drug. They were the control group.

The individuals whose pain decreased as a result of the sugar pill had a similar brain anatomy and psychological traits. The right side of their emotional brain was larger than the left, and they had a larger cortical sensory area than people who were not responsive to the placebo. The chronic pain placebo responders also were emotionally self-aware, sensitive to painful situations and mindful of their environment.

"Clinicians who are treating chronic pain patients should seriously consider that some will get as good a response to a sugar pill as any other drug," Apkarian said. "They should use it and see the outcome. This opens up a whole new field."

https://www.sciencedaily.com/release...0912133542.htm

JINTROPIN.US HGH Serial Numbers Don't Match

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Hello,

I ordered hygetropin 100iu from www.jintropin.us and they refer you to the website [url=http://www.hygetropin.biz] for validation of the serial number.

The legitimate manufacturer website is wwww.hygetropin.cn and lists HYGETROPIN as a SCAM WEBSITE.

The serial number on the box is an 8 digit number and does validate on the www.jintropin.us directed scam website HYGETROPIN.

However real Hygetropin has a 16 digit serial number does not validate on the legitimate www.hygetropin.cn website.

In addition there should be threads within the holographic seal on the box in real Hygetropin and that is also proof that WWW.JINTROPIN.US IS FAKE.

Sorry guys I am out money and surprised you guys endorse this website. If you delete this post then I guess this website is part of this scam.

Mike

SSRIs and AAS

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Does anyone have any experience with combining antidepressants and anabolics?

I am prescribed zoloft and wondered if it would have any negatives or perhaps maybe even prevent some negative mental sides caused by anabolics? Ex; equipoise and anxiety, tren and depression etc

Sent from my SM-N950U1 using Tapatalk

No Representative from now on!!!

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Nevada professor shoots himself on campus to protest President Trump

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Healthy Mind here folks..

______________

LAS VEGAS —

While his reasoning wasn’t made clear, a sociology professor in Nevada shot himself in the arm while on campus to protest President Donald Trump, according to a police report.

Mark J. Bird, 69, a professor at the College of Southern Nevada since 1993, is facing felony gun charges, the Las Vegas Review-Journal reported.

College employees found Bird collapsed and bleeding from a self-inflicted gunshot wound outside a bathroom on campus around 8:15 a.m. Aug. 28.

Campus police discovered a $100 bill taped to a mirror inside the bathroom with a note that said, “For the janitor,” police said. The pistol Bird reportedly used was found on the bathroom floor.

He's been charged with discharging a gun in a structure within a prohibited area, among other charges, according to online court records.

Bird was still employed with the college as of Tuesday, college spokesman Richard Lake told the Review-Journal, although he wasn’t scheduled to teach any classes during the current semester.

https://www.wcvb.com/article/nevada-...e-say/23119734

Tren out of the question.!? NPP could be what you need.

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Tren out of the question.!? NPP could be what you need.

Nandrolone Phenylpropionate (NPP) - 100mg/ml 10ml/vial EP

Condition: New product

Supplier:Euro-Pharmacies
Chesh Dragmical Name:Nandrolone PhenylPropionate
Presentation:10ml vial, 100 mg/ml
Active Life:5 days
Drug Class:Anabolic/Androgenic Steroid
Average Dose:100-400mg/EOD

Nandrolone Phenylpropionate (NPP) - 100mg/ml 10ml/vial EP - Puritysourcelabs

(NPP)Nandrolone Phenylpropionate was the first Nandrolone compound ever sold commercially. NPP emerged in the1950’s by Organon under the name Durabolin. Not long after Organon released its long estered cousin Deca Durabolin.
Nandrolone Phenylpropionate has many therapeutic and performance benefits. The Nandrolone hormone is the most commonly prescribed anabolic steroid other than testosterone, but the long estered Decanoate version is the most commonly prescribed Nandrolone form. It is one of the most well tolerated steroids.

Nandrolone Phenylpropionate is identical to Nandrolone Decanoate. Both npp and deca are comprised of the same active hormone. With NPP we have a shorter ester that kicks ins faster after injection, but also carries a shorter half-life. This means Nandrolone Phenylpropionate has to be injected more frequently for blood levels to remain stable vs deca.

Nandrolone Phenylpropionate is slightly more anabolic than testosterone with a rating of about 125 compared to testosterone’100. It is also significantly less androgenic with a rating of 37 compared to test with 100. The reduced androgenicity is due to the Nandrolone hormone reducing to dihydronandrolone (DHN) instead of dihydrotestosterone (DHT). This is one of the reasons Nandrolone Phenylpropionate can be tolerated so well at higher doses in comparison to higher doses of testosterone in some men.

Nandrolone Phenylpropionate is also significantly less estrogenic than testosterone. Both Nandrolone and testosterone aromatize, but Nandrolone does so at about 20% the rate of testosterone.
Nandrolone Phenylpropionate carries a progestin nature, and this will play into the side effects.
Some positive effects of nandrolone are:
Increased IGF-1 production
Increased nitrogen retention
Inhibition of glucocorticoids(cortisol)
Increased rbc
Increased protein synthesis
Increased collagen synthesis
Increased bone mineral density

This is one of the best mass builders available and for many bodybuilders is used in every bulking plan. Despite being a faster acting Nandrolone growth will not only occur rapidly, but it will be steady, even and significant.
You should also notice you stay leaner during your off season due to the metabolic effects of the hormone. And when it comes to recovery from strenuous training very few things will beat Nandrolone Phenylpropionate.

Nandrolone Phenylpropionate can also be used for cutting cycles.
Npp will protect lean muscle mass better than many steroids. When we diet/cut we burn more calories than we consume. Unfortunately, this puts lean muscle tissue at risk, and NPP can provide the protection We need and minimize muscle loss. And again the recovery benefits will be tremendous, even when in a caloric deficit.
Again Many athletes will use low doses of Nandrolone Phenylpropionate for the recovery and joint relief benefits alone.

For the athlete or bodybuilder doses can vary greatly. 200mg per week is commonly seen for therapeutic relief.
cycle doses will range from 200-800mg a week. Usually for 12weeks.
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ARIMIDEX - 1mg/tab EP



Condition: New product

Supplier:Euro-Pharmacies

Chemical Name:Anastrozole

Comes In: 1mg tab

Dosage: 0.25-0.5mg/eod

Active time: 48 hours

Class:Type-II Aromatase Inhibitor



Anastrozole (A-dex)





History: Considered revolutionary at the time of its introduction, Anastrozole was brought to the market by Astra Zeneca for the treatment of breast cancer. It was the 1st next-generation A.I. and since its release, multiple similar AI’s have been produced, but Arimidex continues to remain one of the most effective.

Method of Administration: Anastrozole is administered in oral form.

Drug Class: Aromatase Inhibitor.





Primary Use: Anastrozole, like all anti-estrogens, is used to help normalize/maintain estrogen levels within the body. Aside from the prevention of estrogenic side effects, estrogen management can assist users in maintaining a hard & dry appearance when using aromatizable drugs. This is especially useful prior to a contest, when displaying this looks is essential to success. Anastrozole accomplishes this function by binding with the aromatase enzyme, which is responsible for converting testosterone (and other aromatizable drugs) into estrogens. Unlike a suicide aromatase inhibitor, Anastrozole does not permanently bind with the aromatase enzyme, but will detach after a certain period of time. This opens up the individual to the possibility of estrogen rebound, which is when the user experiences a brief period of elevated estrogen levels after cessation of the drug. In most cases, this rebound is not significant enough to cause any issues, but for those who do find this to be problematic, it is easily dealt with by gradually reducing the dosage of Anastrozole over a couple of weeks before finally discontinuing the drug. One advantage of Anastrozole is its relatively infrequent dosing schedule.





Anabolic-Androgenic Ratio: N/A.

Aromatizable: No. Exhibits anti-estrogenic activity.

Progestagenic Activity: No.

Methylated: No.






Standard Dosing Range and Cycle Length: Anastrozole is commonly administered at a dosage of .5 mg every other day to 1 mg per day. Dosing requirements will be determined by the number, type, and amount of aromatizable drugs being used.





Frequency of Administration: Due to Anastrozole’s long active life, it can be dosed as infrequently as every other day, although more even blood concentrations are achieved with daily dosing. The drug is typically administered as long as aromatizable drugs are present







AROMASIN - 20mg/tab EP



Condition: New product

Supplier:Euro-Pharmacies

Chemical Name:Exemestane

Comes In: 20mg tab

Dosage: 20mg/day

Active time: 14-17 hours

Class:Type-I Aromatase Inhibitor



Exemestane (Aromasin)





History: Initially researched as a treatment option for breast cancer in the late 90’s, Aromasin was demonstrated to be superior to Tamoxifen and was subsequently released by Pfizer. A fairly recent addition to the anti-estrogen marketplace, Aromasin’s clinical success transferred over into the BB’ing community, where it is now considered standard fare on UGL products lists the world over.





Method of Administration: Aromasin is administered in oral form.





Drug Class: Suicidal Aromatase Inhibitor.





Primary Use: Aromasin, like all anti-estrogens, is used to help normalize/maintain estrogen levels within the body. Aside from the prevention of estrogenic side effects, estrogen management can assist users in maintaining a hard & dry appearance when using aromatizable drugs. This is especially useful prior to a contest, when displaying this looks is essential to success. Aromasin accomplishes this function by binding with the aromatase enzyme, which is responsible for converting testosterone (and other aromatizable drugs) into estrogens. Once bound, Aromasin will permanently deactivate the aromatase enzyme, preventing any further interaction and eliminating the possibility of experiencing estrogen rebound. This ability to permanently deactivate the aromatase enzyme is what classifies Aromasin as a suicide inhibitor, as not all anti-estrogens have this effect. This advantage is one of the key differences between Aromasin and several other anti-estrogens. However, Aromasin needs to be dosed frequently in order to maintain adequate blood levels of the drug; preferably twice per day, or every 12 hours. This is in significant contrast to several other AI’s, which only need to be dosed every few days. Additionally, unlike all other AI’s, which have been shown to potentially have a negative impact on cholesterol levels, Aromasin is neutral in this regard, making it the more heart health alternative.





Anabolic-Androgenic Ratio: N/A.

Aromatizable: No. Exhibits anti-estrogenic activity.

Progestagenic Activity: No.

Methylated: No.





Standard Dosing Range and Cycle Length: Aromasin is commonly administered at a dosage of 12.5-50 mg per day. Dosing requirements will be determined by the number, type, and amount of aromatizable drugs being used. The drug is typically administered as long as aromatizable drugs are present.





Frequency of Administration: Daily usage; split into 2 equally divided doses.







LETROZOLE (Femara) - 2.5 mg/tab EP



Condition: New product

Supplier: Euro-Pharmacies

Chemical Name: Letrozole

Comes In: 2.5mg tab

Dosage: 2.5-5 mg every day

LETROZOLE (Femara) is a powerful aromatase inhibitor.





This compound is appropriately required when running substantial amounts of aromatizing steroids , also when one is prone to gynecomastia and using moderate amounts of steroids.

Don`t buy from selectHGH.com

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Gut bacteria's shocking secret: They produce electricity

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September 12, 2018

University of California - Berkeley

To date, most electricity-generating bacteria have come from weird environments, but researchers have found more than 100 in the human microbiome, both pathogenic and probiotic. They were unsuspected because they employ a different and simpler extracellular electron transfer system, which may prove useful in creating bacterial batteries. Their electrogenic ability may be important in infectivity, or in how they ferment cheese and yogurt.

While bacteria that produce electricity have been found in exotic environments like mines and the bottoms of lakes, scientists have missed a source closer to home: the human gut.

University of California, Berkeley, scientists discovered that a common diarrhea-causing bacterium, Listeria monocytogenes, produces electricity using an entirely different technique from known electrogenic bacteria, and that hundreds of other bacterial species use this same process.

Many of these sparking bacteria are part of the human gut microbiome, and many, like the bug that causes the food-borne illness listeriosis, which can also cause miscarriages, are pathogenic. The bacteria that cause gangrene (Clostridium perfringens) and hospital-acquired infections (Enterococcus faecalis) and some disease-causing streptococcus bacteria also produce electricity. Other electrogenic bacteria, like Lactobacilli, are important in fermenting yogurt, and many are probiotics.

"The fact that so many bugs that interact with humans, either as pathogens or in probiotics or in our microbiota or involved in fermentation of human products, are electrogenic -- that had been missed before," said Dan Portnoy, a UC Berkeley professor of molecular and cell biology and of plant and microbial biology. "It could tell us a lot about how these bacteria infect us or help us have a healthy gut."

The discovery will be good news for those currently trying to create living batteries from microbes. Such "green" bioenergetic technologies could, for example, generate electricity from bacteria in waste treatment plants.

The research will be posted online Sept. 12 in advance of Oct. 4 print publication in the journal Nature.

Breathing metal

Bacteria generate electricity for the same reason we breathe oxygen: to remove electrons produced during metabolism and support energy production. Whereas animals and plants transfer their electrons to oxygen inside the mitochondria of every cell, bacteria in environments with no oxygen -- including our gut, but also alcohol and cheese fermentation vats and acidic mines -- have to find another electron acceptor. In geologic environments, that has often been a mineral -- iron or manganese, for example -- outside the cell. In some sense, these bacteria "breathe" iron or manganese.

Transferring electrons out of the cell to a mineral requires a cascade of special chemical reactions, the so-called extracellular electron transfer chain, which carries the electrons as a tiny electrical current. Some scientists have tapped that chain to make a battery: stick an electrode in a flask of these bacteria and you can generate electricity.

The newly discovered extracellular electron transfer system is actually simpler than the already known transfer chain, and seems to be used by bacteria only when necessary, perhaps when oxygen levels are low. So far, this simpler electron transfer chain has been found in bacteria with a single cell wall -- microbes classified as gram-positive bacteria -- that live in an environment with lots of flavin, which are derivatives of vitamin B2.

"It seems that the cell structure of these bacteria and the vitamin-rich ecological niche that they occupy makes it significantly easier and more cost effective to transfer electrons out of the cell," said first author Sam Light, a postdoctoral fellow. "Thus, we think that the conventionally studied mineral-respiring bacteria are using extracellular electron transfer because it is crucial for survival, whereas these newly identified bacteria are using it because it is 'easy.'"

To see how robust this system is, Light teamed up with Caroline Ajo-Franklin from Lawrence Berkeley National Laboratory, who explores the interactions between living microbes and inorganic materials for possible applications in carbon capture and sequestration and bio-solar energy generation.

She used an electrode to measure the electric current that streams from the bacteria -- up to 500 microamps -- confirming that it is indeed electrogenic. In fact, they make about as much electricity -- some 100,000 electrons per second per cell -- as known electrogenic bacteria.

Light is particularly intrigued by the presence of this system in Lactobacillus, bacteria crucial to the production of cheese, yogurt and sauerkraut. Perhaps, he suggests, electron transport plays a role in the taste of cheese and sauerkraut.

"This is a whole big part of the physiology of bacteria that people didn't realize existed, and that could be potentially manipulated," he said.

Light and Portnoy have many more questions about how and why these bacteria developed such a unique system. Simplicity -- it's easier to transfer electrons through one cell wall rather than through two -- and opportunity -- taking advantage of ubiquitous flavin molecules to get rid of electrons -- appear to have enabled these bacteria to find a way to survive in both oxygen-rich and oxygen-poor environments.

https://www.sciencedaily.com/release...0912133442.htm

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The Threat To Democracy From The Far Left

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This was written by Fareed Zakaria from CNN's GPS show. He's the best mind on CNN IMO. Always comes from a perspective of facts without bias or at least he tries not to have a bias. He got his BA at Yale and his PhD at Harvard. When he has something to say I usually listen..

_______________________________

By Fareed Zakaria

For several years now, scholars have argued that the world is experiencing a “democratic recession.” They have noted that the movement of countries toward democracy has slowed or stopped and even, in some places, reversed. They also note a general hollowing out of democracy in the advanced, industrial world. When we think about this problem, inevitably and rightly we worry about President Trump, his attacks on judges, the free press and his own Justice Department. But there is also a worrying erosion of a core democratic norm taking place on the left.

It has become commonplace to hear cries on the left to deny controversial figures on the right a platform to express their views. Colleges have disinvited speakers such as Condoleezza Rice and Charles Murray. Other campuses were unwilling or unable to allow conservative guests to actually speak, with protests overwhelming the events.

A similar controversy now involves Stephen K. Bannon, who, in recent months, has been making the rounds on the airwaves and in print — including an interview I did with him on CNN. Some have claimed that Bannon, since leaving the administration, is simply unimportant and irrelevant and thus shouldn’t be given a microphone. But if that were the case, surely the media, which after all is a for-profit industry, would notice the lack of public interest and stop inviting him.

The reality is that the people running the Economist, the Financial Times, “60 Minutes,” the New Yorker and many other organizations that have recently sought to feature Bannon know he is an intelligent and influential ideologist, a man who built the largest media platform for the new right, ran Trump’s successful campaign before serving in the White House, and continues to articulate and energize the populism that’s been on the rise throughout the Western world. He might be getting his 15 minutes of fame that will peter out, but, for now, he remains a compelling figure.

The real fear that many on the left have is not that Bannon is dull and uninteresting, but the opposite — that his ideas, some of which can reasonably be described as evoking white nationalism, will prove seductive and persuasive to too many people. Hence his detractors’ solution: Don’t give him a platform, and hope that this will make his ideas go away. But they won’t. In fact, by trying to suppress Bannon and others on the right, liberals are likely making their ideas seem more potent. Did the efforts of communist countries to muzzle capitalist ideas work?

Liberals need to be reminded of the origins of their ideology. In 1859, when governments around the world were still deeply repressive — banning books, censoring commentary and throwing people in jail for their beliefs — John Stuart Mill explained in his seminal work, “On Liberty,” that protection against governments was not enough: “There needs protection also against the tyranny of the prevailing opinion and feeling; against the tendency of society to impose . .  its own ideas and practices . .  on those who differ from them." This classic defense of free speech, which Supreme Court Justice Oliver Wendell Holmes later called the “freedom for the thought that we hate,” is under pressure in the United States — and from the left.

We’ve been here before. Half a century ago, students were also shutting down speakers whose views they found deeply offensive. In 1974, William Shockley, the Nobel Prize-winning scientist who in many ways was the father of the computer revolution, was invited by Yale University students to defend his abhorrent view that blacks were a genetically inferior race who should be voluntarily sterilized. He was to debate Roy Innis, the African American leader of the Congress of Racial Equality. (The debate was Innis’s idea.) A campus uproar ensued, and the event was canceled. A later, rescheduled debate with another opponent was disrupted.

The difference from today is that Yale recognized that it had failed in not ensuring that Shockley could speak. It commissioned a report on free speech that remains a landmark declaration of the duty of universities to encourage debate and dissent. The report flatly states that a college “cannot make its primary and dominant value the fostering of friendship, solidarity, harmony, civility or mutual respect. . . . it will never let these values . . . override its central purpose. We value freedom of expression precisely because it provides a forum for the new, the provocative, the disturbing, and the unorthodox.”

The report added: “We take a chance, as the First Amendment takes a chance, when we commit ourselves to the idea that the results of free expression are to the general benefit in the long run, however unpleasant they may appear at the time.” It is on this bet for the long run, a bet on freedom — of thought, belief, expression and action — that liberal democracy rests.

https://www.washingtonpost.com/opini...=.bc06541bcf9a

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Attached Images
File Type: jpg 9862DDBB-9729-4688-8107-BE4421BEA1DB.jpg (238.4 KB)

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