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Brandeis v. Harvard

The Louis D. Brandeis Center for Human Rights Under Law has filed a lawsuit against Harvard University, accusing the institution of failing to adequately address antisemitic harassment and discrimination on campus. The lawsuit, filed in the U.S. District Court of Massachusetts, claims that Harvard is violating Title VI of the Civil Rights Act of 1964, which mandates the university to provide a safe learning environment for all students. The suit includes complaints from five Jewish and Israeli graduate students and follows earlier lawsuits and a Department of Education investigation into antisemitism at Harvard. The complaint alleges that Harvard has tolerated antisemitic incidents, especially during pro-Palestine demonstrations, and has not enforced its policies equally for Jewish students compared to other minority groups. Harvard has declined to comment on the ongoing litigation but reaffirmed its stance against antisemitism.

Media Coverage

Boston Herald: Brandeis Center files lawsuit alleging ‘antisemitic’ discrimination, harassment at Harvard.

Jewish News Syndicate: Harvard ‘deliberately indifferent to pervasive antisemitism on campus,’ lawsuit alleges

Court Docket – Case No. 1:24-cv-11354-RGS, D. Mass, Filed on July 22, 2024

1 – Complaint Against Harvard Filed on May 22, 2024. Exhibit A, Exhibit A-1, Exhibit A-2.

48 – Motion to Dismiss – Filed by Harvard on July 22, 2024.

Comments 76

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  62. CJC 1295 and Ipamorelin are two peptides that have attracted attention in the fields
    of anti‑aging therapy, sports performance enhancement, and clinical research for their potential to stimulate growth hormone secretion and promote anabolic
    processes in the body. Their popularity has grown alongside a surge in demand for
    natural or “clean” alternatives to traditional steroids and
    anabolic agents, as well as an increased interest among patients seeking non‑invasive ways to mitigate age‑related muscle loss, improve skin elasticity, and boost overall vitality.

    CJC 1295/Ipamorelin Peptide Information

    CJC 1295 is a synthetic analogue of growth hormone releasing hormone (GHRH) that has been engineered for improved stability and longer
    half‑life. The peptide binds to the GHRH receptor in the
    pituitary gland, prompting sustained release of endogenous growth hormone over an extended period compared with the natural hormone pulse.
    Ipamorelin, on the other hand, is a selective growth hormone secretagogue
    (GHS) that mimics ghrelin’s action by
    stimulating the ghrelin receptor. It is highly
    specific for GH release and has minimal activity on prolactin or cortisol secretion. Together,
    these peptides are often used in combination to maximize growth hormone output while minimizing side effects associated
    with other GHS agents.

    What are CJC 1295 and Ipamorelin?

    CJC 1295 is a 29‑amino‑acid peptide that contains a fatty acid chain at its N‑terminus, which protects it
    from rapid enzymatic degradation. The addition of
    this lipid moiety allows the molecule to bind to albumin in circulation, effectively
    extending its half‑life to several days. Ipamorelin is a shorter, pentapeptide with the sequence His–Pro–Trp–Gly–Leu.
    Its structure confers high affinity for the growth hormone secretagogue receptor (GHSR) and low cross‑reactivity with other peptide receptors.
    In clinical studies, CJC 1295 alone can increase
    growth hormone levels by 3–4 times above baseline, while Ipamorelin typically produces a 2–3
    fold rise. When used together, the two peptides have been reported to
    produce synergistic effects that further elevate circulating GH and insulin‑like growth factor‑1 (IGF‑1).

    Background of CJC 1295

    The development of CJC 1295 began in the early 1990s as part of a broader
    effort to create longer‑acting GHRH analogues. Researchers at various pharmaceutical companies sought to overcome the rapid
    clearance of native GHRH, which limits its therapeutic utility.
    By adding a fatty acid chain and modifying key amino acids susceptible to proteolytic cleavage, scientists produced CJC 1295 with an extended
    half‑life that allows once‑daily or even weekly dosing schedules in preclinical models.
    Early animal studies demonstrated not only increased growth
    hormone secretion but also improvements in lean body mass,
    bone density, and metabolic parameters such as glucose tolerance.
    Subsequent human trials explored its potential for treating growth hormone
    deficiency, cachexia, and age‑related sarcopenia. Although regulatory approval has been limited primarily to investigational use,
    the peptide has become widely available on the research market and
    through specialized compounding pharmacies that cater to both clinical investigators and
    athletes seeking performance enhancement.

    Side Effects of CJC 1295

    Like any hormone‑modulating therapy, CJC 1295 carries
    a risk of adverse effects. The most common complaints reported in users include injection site reactions such as
    pain, redness, or swelling, which can be mitigated by rotating sites and using fine needles.

    Systemic side effects may arise from chronic elevation of growth hormone and IGF‑1 levels.
    These can encompass edema, particularly around the extremities, due to fluid retention; joint discomfort or arthralgia
    linked to increased connective tissue metabolism; and carpal tunnel syndrome as a result of soft
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    headaches, dizziness, or mild fatigue during the initial
    phase of treatment as their bodies adjust to higher hormone
    levels. In rare cases, there have been reports of glucose
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    can complicate diabetes management. Long‑term safety data are limited; therefore, monitoring of liver enzymes and lipid profiles is advisable
    for patients on prolonged therapy.

    Side Effects of Ipamorelin

    Ipamorelin’s side effect profile is generally considered milder than that
    of other growth hormone secretagogues such as GHRP‑2 or GHRP‑6.
    Nonetheless, users may encounter injection site irritation similar to CJC 1295.
    Because Ipamorelin selectively stimulates GH release without significantly affecting prolactin or cortisol, it tends to
    produce fewer endocrine disturbances. Still, some individuals report mild nausea or
    an increased appetite following dosing, reflecting its ghrelin‑like action on the stomach’s hormone receptors.
    Occasional reports of flushing or transient increases in blood pressure have been noted, particularly at higher doses.
    As with CJC 1295, chronic use may lead to fluid retention and
    joint aches, though these effects are typically less pronounced.

    Combined Use and Interaction Effects

    When CJC 1295 and Ipamorelin are administered together,
    the risk of side effects can be amplified due to a synergistic rise in growth hormone and IGF‑1.
    Users may notice more pronounced edema or swelling at injection sites as the combined peptides enhance
    vascular permeability. Some anecdotal evidence suggests that
    joint discomfort intensifies when both agents are used concurrently,
    likely because the additive anabolic stimulation increases connective tissue turnover.
    However, proponents argue that combining the two allows for lower
    individual doses, potentially mitigating
    some adverse reactions while maintaining therapeutic efficacy.

    Monitoring and Mitigation Strategies

    To minimize side effects, clinicians recommend starting with low doses
    of each peptide and gradually titrating upward based on patient tolerance and biochemical markers.
    Regular blood tests to assess GH, IGF‑1, fasting glucose,
    insulin sensitivity, lipid panels, and liver function can help detect
    early signs of metabolic disturbance or organ stress.

    Adequate hydration and a balanced diet may reduce fluid retention, while gentle stretching or low‑impact
    exercise can alleviate joint stiffness. If injection site reactions
    become problematic, rotating sites, using pre‑treated needles, and applying
    topical analgesics after injection can provide relief.

    Legal Status and Ethical Considerations

    Both CJC 1295 and Ipamorelin are classified as research chemicals in many
    jurisdictions and are not approved for general medical use
    by major regulatory agencies such as the FDA or EMA. Consequently, their possession and distribution outside of clinical trials may be restricted.
    Athletes should also note that both peptides are banned substances under most anti‑doping organizations due to their performance‑enhancing properties.
    Ethically, individuals considering these agents should weigh
    the potential health benefits against the lack
    of long‑term safety data and the legal
    ramifications associated with non‑approved use.

    In summary, CJC 1295 and Ipamorelin represent promising
    tools for stimulating endogenous growth hormone production, yet they come with a spectrum of side effects that range from local injection site irritation to systemic hormonal imbalances.
    Careful dose management, routine monitoring, and an understanding of the regulatory landscape are essential
    components for anyone contemplating their use in clinical or non‑clinical settings.

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  64. Anavar is one of the most popular anabolic steroids among bodybuilders
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    in understanding the correct dosage, how it differs for men versus women, and what safety
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    general overview and moving into specific dosage recommendations for men.

    Anavar Dosage for Men

    For male users, Anavar is typically prescribed at a daily dose ranging from 20 to 80 milligrams.

    The most common cycle length for men is four to six weeks,
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    💊 Anavar Dosage for Men: Maximizing Muscle & Safety with Precision

    When aiming to maximize muscle gains safely, it is essential to consider both dosage
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    This progressive approach takes advantage of Anavar’s potent protein synthesis properties while limiting exposure to
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    In terms of timing, taking Anavar with a meal that contains healthy fats can improve absorption because the steroid is fat‑soluble.
    Some users also split their dose into two smaller portions—one in the morning and one in the late
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    Safety considerations are paramount. Men should regularly monitor liver function through periodic blood
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    🔍 Introduction: The Most Misunderstood Mild Steroid

    Anavar is often described as the “mildest” anabolic steroid, but
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    steroids like testosterone enanthate or stanozolol. This mild profile makes Anavar attractive
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    dosage guidelines.

    One of the reasons Anavar is misunderstood is its reputation as a
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    closely monitoring their health markers. Nonetheless,
    the risk of side effects—such as liver strain, cholesterol changes, and hormonal suppression—increases with higher dosages.

    Another factor contributing to the misunderstanding is the
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    it does not cause significant water retention or hypertension,
    prolonged use can still affect lipid profiles by lowering HDL
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    therefore essential for anyone using Anavar, regardless of dose.

    Finally, the notion that Anavar is “safe for women” often leads
    to misuse. Women can indeed benefit from Anavar’s mildness; however, because it still carries a risk of virilization and liver toxicity,
    female users should stick to very low doses—typically no more than 10 mg per day—and
    take strict precautions.

    In conclusion, the key to using Anavar effectively lies in respecting its potency,
    following recommended dosage schedules for men, and
    maintaining vigilant health monitoring throughout the cycle.

    By combining a precise dosing plan with regular medical check‑ups and
    post‑cycle therapy, users can achieve significant muscle gains
    while minimizing risks associated with this powerful steroid.

    Reply
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