Most Frequently Asked Questions about T-BOL

  • What is T-BOL?

    T-BOL is the strongest natural testosterone boosting formula on the market today. Working WITH your body, rather than against it, T-BOL was designed to massively increase BOTH total testosterone and free testosterone for unsurpassed advancements in lean mass acquisition and strength enhancement. T-BOL is not a pro-hormone and does not require a post cycle therapy.

  • How do I use T-BOL?

    Using T-BOL is easy. Preferably on an empty stomach, take 2 capsules in the morning, another 2 capsules mid-day, and 2 capsule in the evening. Why should you take 2 capsules in the morning? That's a great question. Many supplements offer stronger benefits when strategically taken at key points throughout the day. When you are sleeping, your body naturally produces testosterone. When you wake up, testosterone production is at its peak. By taking 2 capsules of T-BOL immediately upon waking, you will be able to create a lot more FREE testosterone in your body for maximum muscle growth throughout the day.

    One strategy that many T-BOL users have reported to be extremely effective is to consume 2 capsules of T-BOL pre-workout. Doing so will help increase your training intensity levels as more free testosterone is created, in addition to NOS (nitric oxide synthase). NOS is the enzyme responsible for producing nitric oxide, a potent vasodilator that can massively increase muscular pumps and endurance.

    After using T-BOL for 50 days (2 bottles), we recommend that you discontinue using T-BOL for 3-4 weeks prior to using T-BOL again.

  • What is "free" testosterone and how is it different from "testosterone?"

    Testosterone can exist in two states; bound and unbound (free). The unbound, or "free" form of testosterone is what builds muscle mass. The more you have, the greater your anabolic potential.

    Testosterone becomes bound when a globular protein called sex hormone binding globulin (SHBG) binds to testosterone. It's like gum getting stuck to a key. When gum is stuck to the teeth on a key, that key cannot properly fit into the lock and unlock the door. The same principle applies to unlocking muscle growth. When SHBG (gum) binds to testosterone (key), testosterone cannot bind to your androgen receptors (key hole) and open the door to muscle growth.

    However, while free testosterone builds muscle, focusing only on boosting free testosterone values is not the answer. In fact, if you only increase free testosterone, it is not uncommon to experience a decrease in total testosterone production. This occurs because your body senses an imbalance in your testosterone to free testosterone ratio. In response, your body will lower its testosterone output in an attempt to re-establish a normal ratio. This is a major downfall of many testosterone boosters on the market, as they focus only on increasing free testosterone. So the key is to use a formula, like T-BOL, that increases BOTH total testosterone production and free testosterone for a true testosterone boosting experience.

  • Will I keep all of my gains when I am done using T-BOL?

    That depends on you! After you are finished using T-BOL your natural testosterone levels will gradually return to baseline over the course of 2-3 weeks. This slow transition back down to baseline values makes coming off T-BOL incredibly easy. To keep all of your hard earned gains, here is what we recommend you do. Make sure that you are consuming enough calories to support the new mass, strength, and performance you have achieved. Incorporating ThermoLife's Vasodianabolic protein matrix, Vasolate, makes this goal easy to achieve. If however you fail to provide your body with the necessary calories needed to sustain your new muscle, you may notice a decrease in your muscularity, strength, and performance as you are not giving your body the protein and calories it needs to sustain your new growth.

    Also, it is exceedingly important to continue training hard and heavy. Your body will only hold onto your new muscle mass and strength IF it has a need to, and that requires continually progressive effort in the gym.

  • Is T-BOL safe to use?

    Yes, absolutely. Formulating T-BOL to be rich with healthy benefits was our number one priority. After all, if you don't have your health, you don't have anything. Just how healthy you ask? Unlike pro-hormones, powerful ingredients inside T-BOL are scientifically verified to possess strong anti-oxidant properties. They offer liver protective and cardiovascular benefits in addition to being anti-hypertensive. One key ingredient displays incredibly healthy benefits to the prostate, while others have even been shown to possess antimalarian, antiviral, and anti-anxiety benefits. Hands down T-BOL is not only the most complete natural testosterone booster on the market, but it is also the smartest choice on the market too.

  • What does T-BOL stack best with?

    For athletes who are looking to pack on lean mass and gain strength as fast as possible, there is no better compliment to T-BOL than ThermoLife's Non-Hormonal, Super Anabolic matrix, E-BOL!

    E-BOL is considered the "holy grail" in muscle building sports supplementation, mimicking the potent anabolic properties of hormones and pro-hormones without any of the unwanted androgenic side effects. The revolutionary E-BOL matrix signals muscle cells into an anabolic (growth) state, increasing nitrogen retention and converting more of your dietary protein intake into lean muscle mass. E-BOL also possesses dual adaptogenic effects that effectively "auto adjust" your physiological systems according to your own individual needs. In turn, this permits anabolism to excel and your physique and performance to break through previous "sticking points". This adaptogenic-anabolic effect is uniquely elicited by E-BOL, defining it as a breakthrough category in bodybuilding supplements.

  • When I come off my T-BOL cycle, what can I use to ensure that I am making continually progressive gains?

    Excellent question. In designing the entire ThermoLife product lineup, ThermoLife scientists have developed products that not only stack perfectly together, but also function as supercharged follow-ups to any cycle you create. If you chose not to stack E-BOL with T-BOL, using E-BOL following your cycle of T-BOL will be your absolute BEST choice to ensure continued gains in muscle growth, strength enhancement, and athletic performance.

  • Is T-BOL a pro-hormone

    No, it is not. T-BOL is 100% natural and does not contain any steroidal ingredients.

  • How old must I be to use T-BOL?

    We are glad you asked. T-BOL is recommended for those who are 18 years of age and older.

  • I am subject to drug testing. Should I use T-BOL?

    That is always a great question to ask. While T-BOL is 100% natural, it is always best to check FIRST with your testing organization and obtain approval and permission before using T-BOL.

  • Do you offer a 100% Money Back Guarantee?

    Yes, we do.

    As the president of ThermoLife International I have made sure that every one of our products meets label claims and does exactly what it is intended to do. I am so sure of this that we offer a 100% money back guarantee on every product that we sell. If for any reason you are not satisfied with a product purchased from this web site, just send it back with a copy of your receipt and you will receive a full refund.

    Ron Kramer
    President
    ThermoLife International

    Send returns to:
    Product Returns
    c/o ThermoLife International LLC
    3941 E. Chandler Blvd. #106-212
    Phoenix, AZ 85048

    Please include a copy of your receipt from this website, along with any unused portion of the product.

  • Got a question about one of our Products or What to know more?

    You can email your question to contact@thermolife.com and our resident experts will get an answer for you asap! And if we think that your question can help others, we will post it right here!

References

  • Hypoglycemic and hypolipidemic effects of alcoholic extract of Tribulus alatus in streptozotocin-induced diabetic rats: a comparative study with T. terrestris (Caltrop).
  • Free serum testosterone level in male rats treated with Tribulus alatus extracts. El-Tantawy WH, Temraz A, El-Gindi OD.Drug Bioavailability Center, National Organization For Drug Control and Research, Cairo, Egypt. wldhmdy@yahoo.com
  • Phytochemistry. 2006 May;67(10):1011-8. Epub 2006 May 2 Steroidal saponins from the aerial parts of Tribulus alatus Del. Temraz A, El Gindi OD, Kadry HA, De Tommasi N, Braca A. Dipartimento di Chimica Bioorganica e Biofarmacia, Università di Pisa, Via Bonanno 33, 56126 Pisa, Italy.
  • Gimlette, J.D. and Thomson, J.W. (eds). “A dictionary of Malaysian medicine.” (1977).
  • Ang HH, et al. “Effects of Eurycoma longifolia jack on laevator ani muscle in both uncastrated and testosterone-stimulated castrated intact male rats.” Arch Pharm Res. 24(5), (2001): Pages 437-40.
  • Ang, H.H. Chan, K.L. and Mak, J.W. J.Ethnopharmacol. 49 (1995): Pages 171-175
  • Bansiddhi J. and Pecharaply D. Botanical Report of Some Thai Medicinal Plants, Department of Medical Sciences, Bangkok, Thailand. (1988): Pages 21-23
  • Chan, K.L. Lee, S.P and Yuen, K.H. “Antipyretic Activity of Quassinoids from Eurycoma Longifolia Jack”. (1995).
  • Morita, H. Kishi, E., Takeya, K. Itokawa, H., and Iitaka, Y. 1993. Chem. Lett. 5:749-752
  • Morita, H. Kishi, E., Takeya, K. Itokawa, H., and Iitaka, Y. 1993 Phytochem 34:765-771
  • Ang HH, et al. “Aphrodisiac evaluation in non-copulator male rats after chronic administration of Eurycoma longifolia Jack.” Fundam Clin Pharmacol. 15(4), (2001): Pages 265-8.
  • Ang HH, et al. “Evaluation of the potency activity of aphrodisiac in Eurycoma longifolia Jack.” Phytother Res. 15(5), (2001): Pages 435-6.
  • Ang HH, et al. “Effects of Eurycoma longifolia Jack (Tongkat Ali) on the initiation of sexual performance of inexperienced castrated male rats.” Exp Anim. 49(1), (2000): Pages 35-8.
  • Ang HH, et al. “Studies on the anxiolytic activity of Eurycoma longifolia Jack roots in mice.” Jpn J Pharmacol. 79(4), (Apr 1999): Pages 497-500.
  • Ang HH, et al. “Eurycoma longifolia Jack enhances libido in sexually experienced male rats.” Exp Anim. 46(4) (Oct 1997): Pages 287-90.
  • Ang HH, et al. “Sexual arousal in sexually sluggish old male rats after oral administration of Eurycoma longifolia Jack.” J Basic Clin Physiol Pharmacol. 15(3-4), (2004): Pages 303-9.
  • Ang HH, et al. “Eurycoma longifolia Jack enhances sexual motivation in middle-aged male mice.” J Basic Clin Physiol Pharmacol. 14(3), (2003): Pages 301-8.
  • Ang HH, “Effects of Eurycoma longifolia Jack on sexual qualities in middle aged male rats.” Phytomedicine. 10(6-7), (2003): Pages 590-3.
  • Ang HH, “Effect of Eurycoma longifolia Jack on orientation activities in middle-aged male rats.” Fundam Clin Pharmacol. 16(6), (Dec 2002): Pages 479-83.
  • Ang HH, et al. “Effect of Eurycoma longifolia Jack on libido in middle-aged male rats.” J Basic Clin Physiol Pharmacol. 13(3), (2002): Pages 249-54.
  • Low BS, “Bioavailability and pharmacokinetic studies of eurycomanone from Eurycoma ongifolia.” Planta Med. 71(9), (Sep 2005): Pages 803-7.
  • Chan KL, et al. “Semisynthetic 15-O-acyl- and 1,15-di-O-acyleurycomanones from Eurycoma longifolia as potential antimalarials.” Planta Med. 71(10), (Oct 2005): Pages 967-9.
  • Belguendouz L., et al. “Resveratrol inhibits metal ion-dependent and independent peroxidation of orcine low-density lipoproteins.” Biochem.Pharmacol., 53(9) (May 1997): Pages 1347-1355.
  • Bertelli A.A, et al. “Resveratrol, a natural stilbene in grapes and wine, enhances intraphagocytosis in human promonocytes: a cofactor in anti-inflammatory and anti-cancer chemopreventive activity.” Int. J. Tissue React., 21, (1999): Pages 93-104.
  • Ewa Ignatowicz, Wanda Baer-Dubowska. “RESVERATROL, A NATURAL CHEMOPREVENTIVE AGENT AGAINST DEGENERATIVE DISEASES”. Polish journal of pharmacology, 53(6), (2001): Pages 557- 569.
  • Juan ME, et al. “Trans-Resveratrol, a Natural Antioxidant from Grapes, Increases Sperm Output in Healthy Rats” J. Nutr. 135(4), (Apr 2005): Pages 757-760.
  • Piver B, et al. “Differential inhibition of human cytochrome P450 enzymes by epsilon-viniferin, the dimer of resveratrol: comparison with resveratrol and polyphenols from alcoholized beverages.” Life Sci. 73(9), (Jul 2003): Pages 1199-213.
  • Piver B, et al. “Inhibition of CYP3A, CYP1A and CYP2E1 activities by resveratrol and other non volatile red wine components.” Toxicol Lett. 125(1-3), (Dec 2001): Pages 83-91.
  • Wang Y, et al. “The red wine polyphenol resveratrol displays bilevel inhibition on aromatase in breast cancer cells.” Toxicol Sci. 92(1), (Jul 2006): Pages 71-7.
  • Randall C, et al. “Randomized controlled trial of nettle sting for treatment of base-of-thumb pain.” J R Soc Med. 93(6), (Jun 2000): Pages 305-9.
  • Bnouham M, et al. “Antihyperglycemic activity of the aqueous extract of Urtica dioica.” Fitoterapia. 74(7-8), (Dec 2003): Pages 677-81.
  • Cetinus E, et al. “The role of urtica dioica (urticaceae) in the prevention of oxidative stress caused by tourniquet application in rats.” Tohoku J Exp Med. 205(3), (Mar 2005): Pages 215-21.
  • Uncini Manganelli RE, et al. “Antiviral activity in vitro of Urtica dioica L., Parietaria diffusa M. et K. and Sambucus nigra L.” J Ethnopharmacol. 98(3), (Apr 2005): Pages 323-7.
  • Kanter M, et al. “Hepatoprotective effects of Nigella sativa L and Urtica dioica L on lipid peroxidation, antioxidant enzyme systems and liver enzymes in carbon tetrachloride-treated rats.” World J Gastroenterol. 11(42), (Nov 2005): Pages 6684-8.
  • Daher CF, et al. “Effect of Urtica dioica extract intake upon blood lipid profile in the rats.” Fitoterapia. 77(3), (Apr 2006): Pages 183-8.
  • El Haouari M, et al. “Inhibition of rat platelet aggregation by Urtica dioica leaves extracts.” Phytother Res. 20(7), (Jul 2006): Pages 568-72.
  • Gansser D, et al. “Plant constituents interfering with human sex hormone-binding globulin. Evaluation of a test method and its application to Urtica dioica root extracts.” Z Naturforsch [C]. 50(1-2), (Jan-Feb 1995): Pages 98-104.
  • Schottner M, et al. “Lignans from the roots of Urtica dioica and their metabolites bind to human sex hormone binding globulin (SHBG).” Planta Med. 63(6), (Dec 1997): Pages 529-32.
  • Hryb DJ, “The effect of extracts of the roots of the stinging nettle (Urtica dioica) on the interaction of SHBG with its receptor on human prostatic membranes.” Planta Med. 61(1), (Feb 1995): Pages 31-2.
  • Chris Kilham. “Ali is the Greatest.” Physical Magazine, (Mar 2004).
  • Chris Kilham. “Tongkat Ali: Sexual Treasure of Southeast Asia.” Let's Live, (Feb 2004).
  • “Jungle Herbs: Rev Up Romance.” Prevention Magazine, (Nov 2003).
  • Valenti, S, Guido, R, Giusti, M, Giordano, G. (1995) In vitro acute and prolonged effects of melatonin on purified rat Leydig cell steroidogenesis and adenosine 3',5'-monophosphate production Endocrinology 136,5357-5362 [Abstract]
  • Valenti, S, Fazzuoli, L, Giordano, G, Giusti, M. (2001) Changes in binding of iodomelatonin to membranes of Leydig cells and steroidogenesis after prolonged in vitro exposure to melatonin Int J Androl. 24,80-86 [Medline]
  • Serotonin secretion from rat Leydig cells.Tinajero JC, Fabbri A, Ciocca DR, Dufau ML.Section on Molecular Endocrinology, National Institute of Child Health and Human Development, National Institute of Health, Bethesda, MD 20892.
  • Expression of testicular 3 beta-hydroxysteroid dehydrogenase/delta 5----4-isomerase: regulation by luteinizing hormone and forskolin in Leydig cells of adult rats. Keeney DS, Mason JI. Cecil H. and Ida Green Center for Reproductive Biology Sciences, Department of Biochemistry, University of Texas Southwestern Medical Center, Dallas 75235-9051.
  • Dissolution of steroids in bile salt solutions is modified by the presence of lecithinAuteur(s) / Author(s) NAYLOR L. J. (1) ; BAKATSELOU V. ; RODRIGUEZ-HORNEDO N. ; WEINER N. D. ; DRESSMAN J. B. ; Affiliation(s) du ou des auteurs / Author(s) Affiliation(s) Abbott Laboratories, North Chicago IL, ETATS-UNIS
  • J Pharmacol Exp Ther. 1986 Feb;236(2):488-93. Piperine-mediated inhibition of glucuronidation activity in isolated epithelial cells of the guinea-pig small intestine: evidence that piperine lowers the endogeneous UDP-glucuronic acid content.
  • Body Composition and Hormonal Adaptations Associated with Forskolin Consumption in Overweight and Obese Men. Michael P. Godard, Brad A. Johnson and Scott R. Richmond. Obesity Research (2005) 13, 1335-1343; doi: 10.1038/oby.2005.162

Only Loyal T "trustees" will be entitled to:
* Exclusive Deals & Discounts
* Free Training & Nutrition Tips
* Pre-release Supplement Offers
* Scientific Bulletins
* Plus Much Much Much MORE!