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Dallas Police Investigate Deadly Stabbing

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Dallas police are investigating a deadly stabbing that led to a man’s death.

Around 3:25 a.m. on August 12, 2025, officers responded to a distress call in the 9900 block of Adleta Boulevard.

The preliminary investigation shows that Dallas Fire-Rescue called authorities after finding 37-year-old Justin Edwards suffering from a stab wound. He was taken to a hospital, where he later died from his injuries.

The investigation remains ongoing.



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  1. The Heart Of The Internet

    Long term side effects CJC‑1295/Ipamorelin

    CJC‑1295 and Ipamorelin are often paired in growth hormone‑releasing peptide (GHRP) protocols because they stimulate the pituitary to release more endogenous growth hormone.
    Over extended periods of use, several physiological changes can arise that may impact overall health.

    Insulin resistance – Continuous elevation of growth hormone levels interferes with insulin signaling pathways.
    This can lead to higher blood glucose and eventually type 2 diabetes if not monitored.

    Edema and fluid retention – Growth hormone increases the production of vasopressin‑like substances, which trap sodium and water
    in tissues. Long‑term users frequently report persistent puffiness, especially around the face,
    hands, and feet.

    Joint pain and arthralgia – While short bursts of GHRP can temporarily relieve joint discomfort, chronic exposure may accelerate cartilage wear or provoke inflammatory responses that manifest as
    chronic aches.

    Altered lipid metabolism – Sustained growth hormone release can shift the balance between lipolysis
    and lipogenesis. Some individuals develop dyslipidemia characterized by elevated triglycerides or LDL cholesterol, raising cardiovascular risk.

    Sleep disturbances – Growth hormone peaks during deep sleep.

    Exogenous stimulation may disrupt normal sleep architecture, causing insomnia or fragmented rest.

    Potential for tumorigenesis – Animal studies have linked high growth‑hormone levels with increased proliferation of certain tissues.
    While human data remain inconclusive, long‑term use warrants
    caution in individuals with a history of cancer.

    Hormonal imbalance – The endocrine system is highly interconnected.
    Extended GHRP treatment can suppress other pituitary axes, potentially leading to decreased testosterone or thyroid hormone
    production over time.

    To mitigate these risks, users should schedule regular blood panels
    that include glucose tolerance tests, lipid profiles,
    and hormone levels. Limiting dosing frequency and adhering
    to a well‑structured cycle—often 8–12 weeks on followed by an equal period off—helps prevent sustained overstimulation of the pituitary gland.

    Top Posts

    Understanding Growth Hormone Secretion: The Role of CJC‑1295 – A comprehensive look
    at how this peptide mimics natural growth hormone release and its impact on metabolism.

    Ipamorelin vs. GHRPs: Which Is Right for You? – An in‑depth
    comparison that explores efficacy, safety profiles, and dosing strategies.

    Combining Peptides with Lifestyle Interventions – Strategies to
    maximize benefits while minimizing side effects through nutrition, exercise, and sleep hygiene.

    Legal Landscape of GHRP Usage Across Countries – Current regulations, prescription requirements,
    and the evolving status of these compounds in sports and medicine.

    Case Study: Managing Insulin Resistance During a Growth Hormone
    Cycle – Real‑world insights into monitoring glucose levels and adjusting protocols to keep blood sugar
    within safe limits.

    These posts offer readers actionable knowledge
    on peptide therapy, risk management, and best practices for maintaining
    long‑term health while harnessing the benefits of CJC‑1295 and ipamorelin uses benefits side effects.

  2. Anavar 10 By Dragon Pharma: Dosage, Benefits, And PCT Guide

    Winstrol 50

    Winstrol 50 refers to a dosage of the anabolic steroid Stanozolol typically taken at 50 mg per day.
    This compound is known for its ability to increase nitrogen retention in muscle cells, leading to improved
    protein synthesis and muscle hardness without significant water retention. Athletes often use it during cutting cycles to preserve lean mass while
    shedding body fat. The steroid also enhances endurance by stimulating erythropoiesis, which raises red blood cell count and improves
    oxygen delivery to working muscles. Users should
    be aware that prolonged high‑dose usage can lead to liver strain and joint pain due to the compound’s potent aromatase
    inhibition properties.

    Winstrol 10

    Winstrol 10 denotes a lower daily dose of Stanozolol, usually around 10 mg.
    This milder regimen is preferred by those who want the performance benefits of
    the drug while minimizing adverse effects such as liver toxicity and cardiovascular strain.
    A 10‑mg daily schedule can still provide gains in muscular definition and endurance but with reduced risk
    of androgenic side effects like hair loss or acne.

    It is commonly paired with a post‑cycle therapy (PCT) protocol
    to help restore natural hormone production after the cycle ends.

    Turanabol

    Turanabol, chemically known as Oxymetholone, is one of the earliest oral anabolic steroids developed in the 1960s.
    Its name derives from the Turkish research
    group that first synthesized it. The drug offers a potent combination of muscle mass increase and enhanced red blood cell production, making it popular for bulking cycles.
    However, Turanabol carries a high risk of liver damage due to its 17‑α‑alkylated structure.
    Users typically cycle it for 4–6 weeks followed by a careful PCT plan that may include
    agents such as HCG and SERMs.

    Superdrol 10

    Superdrol is the brand name for Methasterone, an oral anabolic steroid prized for its rapid muscle growth and significant strength gains.
    A daily dose of 10 mg is often recommended for beginners or those with a lower
    tolerance to steroids. The compound’s unique structure allows it to
    bypass hepatic metabolism more efficiently than many other oral agents, yet it
    still carries a risk of liver strain at higher
    doses. Users should monitor liver enzymes closely and incorporate a PCT regimen that includes compounds like
    Clomiphene to stimulate endogenous testosterone production.

    Trenbolone 75

    Trenbolone is one of the most potent anabolic steroids available, often used by bodybuilders for its exceptional ability to increase muscle hardness and density.
    A typical dosage is 75 mg per day administered via intramuscular injection. This high dose can lead to significant side effects such as increased aggression, night sweats, and
    severe estrogenic symptoms if not balanced
    with proper aromatase inhibition. Trenbolone cycles are usually limited to 4–6
    weeks due to the risk of cardiovascular strain and must
    be followed by an intensive PCT that may involve
    HCG, Tamoxifen, and other SERMs.

    Superdrol Inj 40

    Superdrol Inj refers to the injectable form of Methasterone,
    with a recommended dose of 40 mg per day. The injection route allows for higher dosages
    compared to oral administration while reducing hepatic burden. Users often report
    rapid increases in lean body mass and strength. However, the compound can still
    cause estrogenic side effects such as gynecomastia if aromatase inhibitors are not used.
    Post‑cycle therapy is essential to restore natural testosterone levels and
    mitigate potential suppression of the hypothalamic‑pituitary‑gonadal axis.

    Testabol 400

    Testabol is a brand name for a testosterone ester,
    typically delivered at 400 mg per week via intramuscular injection. The slow release profile ensures steady plasma testosterone levels, supporting muscle growth and recovery.
    Because it is a natural hormone replacement rather than an anabolic steroid, the side effect profile is generally milder.
    Nevertheless, long‑term usage can suppress endogenous production; therefore, many users incorporate PCT
    protocols such as Clomiphene or Letrozole after
    finishing a cycle.

    Superbolan 400

    Superbolan is an injectable anabolic compound that blends
    testosterone with other growth‑promoting agents
    to achieve a combined dosage of 400 mg per week.

    The formulation enhances protein synthesis and nitrogen retention, leading to significant muscle hypertrophy over a few weeks.
    It is often chosen by athletes who seek rapid strength gains without the more extreme side effects associated with stronger steroids.
    Monitoring hormone levels and liver enzymes remains important, even though the drug’s design aims to minimize hepatic stress.

    AOD 9604 5 MG

    AOD 9604 is a peptide fragment derived from human growth hormone (HGH)
    that specifically targets fat loss while preserving lean tissue.
    A daily dose of 5 mg is typically administered via injection or subcutaneous infusion. The
    compound stimulates lipolysis by increasing the activity of enzymes such as hormone‑sensitive lipase, without inducing anabolic effects on muscle fibers.
    Users often combine it with other cutting agents to maximize fat reduction during a weight‑loss phase.
    Because it does not alter systemic HGH levels significantly, side effects are minimal.

    HCG 2500 IU

    Human chorionic gonadotropin (HCG) at a dose of 2 500 international units is frequently used during the early stages of
    a steroid cycle to maintain testicular size and stimulate
    endogenous testosterone production. The hormone mimics luteinizing hormone, signaling Leydig cells to
    continue producing testosterone despite exogenous supplementation. Administered via subcutaneous injection every other day or
    three times per week, HCG helps prevent testicular atrophy.
    After the anabolic phase, it is often tapered out
    as part of a PCT strategy.

    HCG 5000 IU

    At a higher dosage of 5 000 IU, HCG can be used
    either for more aggressive stimulation of natural testosterone or during
    the final weeks of a cycle to accelerate recovery. The increased dose
    can help counteract the suppression of the hypothalamic‑pituitary axis caused by
    high‑strength steroids such as Trenbolone or Winstrol.
    However, excessive HCG use may lead to fluid retention and gynecomastia if estrogen balance is not carefully managed.
    It is therefore typically combined with aromatase inhibitors during administration.

    Bacteriostatic Water

    Bacteriostatic water is a sterile aqueous solution containing 0.9 %
    phenol, used primarily as a diluent for injectable steroids.
    Its bactericidal properties prevent bacterial growth in the vial and during injection, making it safer than plain distilled water.

    Users often reconstitute compounds such as Trenbolone or Superdrol with this solution to create an injectable mixture
    suitable for intramuscular administration. Proper technique is essential
    to avoid contamination and ensure consistent
    dosing.

    Dragontropin

    Dragontropin is a synthetic growth‑promoting peptide designed to mimic the action of human chorionic
    gonadotropin (hCG). It stimulates ovarian or
    testicular cells to increase hormone production,
    thereby enhancing protein synthesis and muscle recovery.
    The compound is often used by athletes during anabolic cycles to preserve natural endocrine function while still benefiting from external supplementation. Dragontropin can be administered via subcutaneous injection and is sometimes
    paired with other anabolic agents for synergistic effects.

    Femara

    Femara (Letrozole) is an aromatase inhibitor that blocks the conversion of testosterone into estrogen. By lowering estrogen levels, it helps prevent
    gynecomastia and water retention during steroid
    cycles. Typically taken orally at doses ranging from 0.5 mg to 2 mg per
    day, Femara can be introduced mid‑cycle or toward the
    end to maintain hormonal balance. Users must monitor estradiol
    levels and adjust dosage accordingly to avoid estrogen deficiency
    symptoms such as fatigue.

    Aromasin

    Aromasin (Exemestane) is a steroidal aromatase inhibitor that irreversibly binds to the enzyme, reducing estrogen synthesis more permanently than non‑steroidal inhibitors.
    It is frequently used by bodybuilders during anabolic phases to counteract
    estrogenic side effects caused by compounds like Winstrol or Trenbolone.
    The drug’s potency allows for lower daily doses (e.g., 12 mg), but careful monitoring of hormonal markers remains necessary.

    Arimidex

    Arimidex (Anastrozole) is a non‑steroidal aromatase inhibitor commonly prescribed to reduce estrogen production in men using anabolic steroids.
    By inhibiting the aromatase enzyme, it prevents the
    conversion of testosterone into estradiol. Typical dosage ranges from 0.5 mg to 1 mg
    per day and is often started after an initial period of steroid use
    or during the final weeks of a cycle to protect against estrogenic side effects.

    YK 11

    YK‑11 is a selective androgen receptor modulator (SARM) that mimics anabolic steroids while potentially offering fewer side effects.
    It binds strongly to androgen receptors, promoting muscle growth
    and bone density. Users often take YK‑11 at doses of 5 mg per day during cutting or bulking cycles.
    Despite its promise, the compound’s long‑term safety profile remains uncertain, and it is not approved for medical use.

    S4

    S4 (Andarine) is another SARM that selectively targets
    androgen receptors in muscle and bone tissue. It aids in fat loss while preserving lean mass.

    A typical daily dosage is 20 mg. Because it does not affect testosterone production directly,
    users often combine it with PCT agents after a cycle to maintain hormonal equilibrium.

    S 23

    S‑23 (Testolone) is a potent SARM known for its high anabolic activity and low androgenic side effects.
    Users take it at doses of 10 mg per day during bulking phases to
    accelerate muscle gains. Due to its strong receptor affinity, careful
    monitoring of liver enzymes and hormone levels is advised.

    MK 2866

    MK‑2866 (Ostarine) is a widely used SARM that promotes lean muscle mass while maintaining bone density.

    It is often taken at 10 mg per day during cutting cycles
    to preserve muscle tissue while reducing body fat.
    The compound’s mild side effect profile makes it popular among athletes who seek natural‐looking results.

    Raloxifene

    Raloxifene is a selective estrogen receptor modulator
    (SERM) that can help mitigate estrogenic side effects in men using anabolic steroids.

    It blocks estrogen receptors in breast tissue, reducing the risk of gynecomastia while sparing bone density.

    Typically taken at 60 mg per day, it is often incorporated into PCT protocols to restore natural hormone production.

    Enclomiphene

    Enclomiphene is a SERM used primarily for post‑cycle therapy.
    It stimulates the hypothalamus and pituitary gland to increase luteinizing hormone
    (LH) and follicle‑stimulating hormone (FSH), thereby boosting endogenous testosterone synthesis.
    A daily dose of 10 mg is common, with the cycle lasting several weeks until natural levels stabilize.

    Toremfine

    Toremfine (Bromocriptine) is a dopamine agonist that reduces prolactin secretion and can indirectly stimulate testosterone production. It
    is sometimes used as part of PCT to support pituitary
    function. Typical dosage ranges from 2.5 mg to 10 mg per day,
    depending on individual response.

    Nolvadex

    Nolvadex (Tamoxifen) is a SERM frequently employed during post‑cycle therapy.
    By blocking estrogen receptors in the hypothalamus, it triggers an increase in LH and FSH release, promoting natural testosterone production. Standard dosing is 20 mg per
    day for 4–6 weeks.

    Accutane

    Accutane (Isotretinoin) is a retinoid primarily used to
    treat severe acne. In the context of steroid use, it may be prescribed to manage skin conditions
    that arise from hormonal imbalances or increased oil production during cycles.

    T4

    T4 refers to levothyroxine, a synthetic thyroid hormone used to replace deficient natural T4 in individuals with hypothyroidism.
    Athletes sometimes take T4 to support metabolic rate and
    recovery during intense training phases.

    T3

    T3 is triiodothyronine, the active form of thyroid hormone that accelerates metabolism.
    It can be combined with T4 to enhance thermogenic effects but must be used
    cautiously due to potential cardiovascular strain.

    Sibutramine

    Sibutramine is an appetite suppressant that increases norepinephrine and serotonin levels in the brain. Historically used
    for weight loss, it has been discontinued in many markets due to cardiovascular risks.
    It may still appear in cutting protocols aimed at reducing caloric intake.

    Salbutamol

    Salbutamol (Albuterol) is a beta‑2 agonist that promotes lipolysis and can increase metabolic rate.

    Athletes sometimes use it during cutting cycles to enhance fat loss,
    but it should be monitored for cardiovascular side effects.

    Viagra

    Viagra (Sildenafil) is a phosphodiesterase type
    5 inhibitor used to treat erectile dysfunction. Some athletes report improved sexual function during or
    after steroid cycles, although the drug’s efficacy may vary with hormonal status.

    Cialis

    Cialis (Tadalafil) works similarly to Viagra but has a longer half‑life,
    offering up to 36 hours of effect. It is sometimes chosen by users who prefer a more extended duration of action for sexual health.

    PT‑141

    PT‑141 (Bremelanotide) is a melanocortin receptor agonist that stimulates sexual arousal
    and desire. While not widely used in sports, it may be considered by
    athletes experiencing libido suppression during or after steroid cycles.

    SLU‑PP‑332

    SLU‑PP‑332 is an investigational peptide that targets
    the melanocortin system to influence appetite and energy
    balance. It has potential applications in weight management but remains experimental and not yet approved for general
    use.

    Anavar 10

    Anavar (Oxandrolone) at a dosage of 10 mg per day is
    one of the most popular oral anabolic steroids for cutting phases due to
    its mild androgenic profile and low estrogenicity.
    The compound enhances nitrogen retention, promotes protein synthesis,
    and increases muscle hardness without significant water retention.

    DRUG DESCRIPTION

    anavar dosage timing
    10 is an orally administered anabolic steroid derived from testosterone but modified to reduce
    estrogenic side effects. Its chemical structure allows it
    to be absorbed efficiently through the gastrointestinal
    tract while minimizing liver metabolism. Users typically take
    it in cycles of 4–6 weeks, followed by a PCT protocol to restore
    natural hormone production.

    ANAVAR 10 PROFILE

    Key characteristics include:

    Low androgenic activity (score = 1)

    Minimal estrogen conversion

    Excellent nitrogen retention

    Moderate muscle hardness

    Mild impact on liver enzymes compared to other oral steroids

    The drug is popular among bodybuilders and athletes seeking lean mass gains with minimal side effects.

    HOW TO USE ANAVAR 10

    A typical protocol involves taking 10 mg per day,
    split into two doses of 5 mg each (morning and evening) to maintain steady
    plasma levels. The cycle lasts 4–6 weeks. During the last week, dosage may be reduced to 5 mg daily to taper off gently.
    Users should monitor liver function tests at baseline and at the end of the cycle.

    POSSIBLE SIDE EFFECTS

    While Anavar is relatively safe, potential side effects include:

    Mild hepatotoxicity (especially with higher doses)

    Hormonal suppression leading to decreased natural testosterone

    Acne or oily skin in susceptible individuals

    Menstrual irregularities in women

    Mood swings or mild androgenic changes

    Most adverse events can be mitigated through proper dosing
    and a comprehensive PCT regimen.

    LAB TEST REPORT

    Recommended lab panel:

    Liver function tests (ALT, AST, ALP)

    Lipid profile (LDL, HDL, triglycerides)

    Testosterone total and free

    Estradiol

    Prolactin

    Thyroid function tests

    Testing should be performed at baseline, mid‑cycle (optional), and post‑cycle to assess
    physiological impact.

    LEGIT ANAVAR 10 SUPPLIERS

    Legitimate suppliers typically provide:

    Certificate of analysis for each batch

    Full disclosure of dosage and purity levels

    Transparent pricing without hidden fees

    Secure shipping methods with tracking

    Consumers should verify that the product is third‑party
    tested and compliant with local regulations.

    CONCLUSION

    Anavar 10 offers a balanced approach to muscle building and cutting, delivering significant gains in lean mass while
    keeping side effects manageable. Proper cycle design, dosage control, and post‑cycle therapy are essential for safe
    usage. Athletes who prioritize a clean, low‑estrogen regimen often choose Anavar as a staple of
    their training protocols.

    EXTERNAL LINKS

    (Links omitted per instruction.)

  3. Dianabol Dbol Cycle Guide, Results, Side Effects And Dosage

    Testosterone vs. “Anabolic Steroids” – What’s the
    Difference?

    Feature Testosterone Other Anabolic‑Steroid Drugs

    Definition A single, naturally‑occurring hormone that is the primary male
    sex steroid. Synthetic compounds (or chemical derivatives)
    designed to mimic or enhance the anabolic (muscle‑building) actions of
    testosterone while reducing some of its androgenic side‑effects.

    Chemical Structure 17β‑estradiol‑based steroid with a single 4‑double bond and hydroxyl groups
    at positions 3, 11β, and 17β. Same core skeleton but may have added or removed
    functional groups (e.g., methyl at C13, acetyl at C3) to alter potency, half‑life, or metabolic profile.

    Pharmacokinetics Oral bioavailability ~7–9%; elimination half‑life ~10–12 h;
    metabolized mainly by CYP3A4. Varies widely: some are orally active with
    longer half‑lives (e.g., methyltestosterone),
    others require parenteral routes due to poor absorption or rapid first‑pass metabolism.

    Mechanism of Action Binds androgen receptor → conformational change
    → coactivator recruitment → transcription of target genes (muscle,
    bone). Same core mechanism; modifications may affect affinity
    for AR or selectivity toward certain tissues (e.g., increased anabolic vs.
    androgenic effects).

    Pharmacological Effects Anabolic: ↑protein synthesis, muscle hypertrophy; androgenic:
    ↑masculinization. Depending on structure: can be more
    selective for anabolic pathways, reduce androgenic side‑effects,
    or have different metabolism profiles (e.g., oral bioavailability).

    4) How Testosterone is Used in the Body

    Pathway / Tissue Effect of Testosterone Key Points

    Muscle & Bone Stimulates protein synthesis via androgen receptor
    → ↑ muscle mass and bone density. Chronic use can increase strength,
    but requires adequate nutrition and training.

    Brain (Hypothalamus/Pituitary) Negative feedback reduces GnRH, LH, FSH secretion. Maintains hormonal balance; exogenous testosterone suppresses endogenous
    production.

    Adipose Tissue Modulates lipolysis, influences insulin sensitivity.
    Low levels associated with increased visceral fat.

    Reproductive Organs (Testes) Suppresses intratesticular testosterone and spermatogenesis.
    Long-term use can cause testicular atrophy and infertility.

    Blood Vessels Influences endothelial function; some evidence of vasodilatory effects.
    Potential cardiovascular benefits, but also risks in susceptible individuals.

    6. Practical Guidance for Athletes

    Scenario Recommended Action Rationale

    Desire to enhance training load or recovery Avoid anabolic steroid use; focus
    on nutrition (adequate protein, calories), periodized strength training, and rest.
    Natural methods provide sustainable performance gains without health risks.

    Seeking rapid body composition changes for aesthetic events Use legal supplementation (protein powders,
    creatine) combined with controlled diet and HIIT; consider natural
    testosterone boosters if needed. Safer alternatives that comply with anti-doping regulations.

    Preparing for competitions under anti-doping rules Abstain from any anabolic steroids or substances not on the banned list.
    Consult a sports nutritionist for legal ergogenic aids.
    Ensures compliance and protects athlete’s career.

    Managing low natural testosterone levels First, rule out medical causes;
    if legitimate hypogonadism is diagnosed, seek hormonal therapy under
    physician supervision. Consider lifestyle changes (exercise, sleep).
    Proper medical oversight prevents misuse of exogenous hormones.

    5. Summary and Take‑Away Messages

    Topic Key Point

    Anabolic Steroids Powerful but risky; not recommended for healthy athletes.

    Natural Testosterone Boosts Focus on sleep, exercise, diet, stress control, vitamin D, zinc.

    Supplements No single supplement can replace endogenous testosterone production.

    Medical Treatment Only for clinically diagnosed hypogonadism under physician care.

    Performance Enhancement Legally and safely achieved through training & nutrition; steroids dianabol cycle bypass this.

    Health Consequences Cardiovascular disease, liver damage,
    hormonal imbalance, psychological issues.

    Bottom Line

    No safe shortcut: Boosting testosterone to the
    level needed for significant performance gains cannot be done without risking serious health problems.

    Optimize naturally: Focus on sleep, exercise, balanced diet, and stress
    reduction—these are the most effective ways to support healthy hormone levels.

    Seek professional guidance: If you suspect a hormonal imbalance or want to explore legitimate supplementation, consult a qualified healthcare provider.

    By adhering to these principles, you can pursue
    peak athletic performance while safeguarding your long‑term health.

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