कांग्रेसले ८४ को निर्वाचको लागि संवेदनशील र सक्रिय भएन:एनपी साउद

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नेपाली कांग्रेसका नेता एनपी साउदले आइतबार ललितपुरको सानेपामा जारी केन्द्रीय कार्यसमिति बैठकमा बोल्दै वर्तमान राजनीतिक परिदृश्यमा कांग्रेसले संवेदनशील र सक्रिय भूमिका निर्वाह गर्न नसकेका कारण पार्टी कम्जोर भएको आरोप लगाएका छन्। 

यति मात्र होइन उनले भने, ०८४ सालमा हुने भनिएको आम निर्वाचनका लागि पार्टी तयारनभएको छैन। राजनीतिक दलहरूमा आक्रमण बढ्दै गएको छ।अरुलाई आक्रमण गरेर आफ्नो दल माथि पुग्दैन। यो केवल दलहरूमा होइन, संविधानमाथि नै आक्रमण गर्ने प्रयास भइरहेको छ। यस्तो अवस्थामा नेपाली कांग्रेसले स्पष्ट आवाज उठाउनुपर्थ्यो। तर कांग्रेस त्यसका लागि तयारी अवस्थामा छैन। गैरकांग्रेस मतहरूसँगको दूरी पनि बढिरहेको छ, जुन हाम्रो मत घट्ने संकेत हो।

काँग्रेस पार्टी भित्रको अनुशासन, गुटबन्दी र असमान व्यवहारप्रति उनको असन्तुष्टि जनाउँदै साउदले अनुशासनका नाममा एक पक्षीय कारबाही भएको, पार्टीका शीर्ष नेताहरू देशभर घुमिरहे पनि सङ्गठन बलियो नबनेको, पार्टीलाई समय अनुकूल अपडेट गर्दै गुटबन्दी अन्त्य गर्न र सङ्गठन मजबुत बनाउनेतर्फ तुरुन्त ध्यान दिन नेतृत्वलाई आग्रह गरे।

6 thoughts on “कांग्रेसले ८४ को निर्वाचको लागि संवेदनशील र सक्रिय भएन:एनपी साउद

  1. The out there scientific literature describes that short-term administration of those drugs by athletes can increase strength and body weight.

    Energy gains of about 5–20% of the preliminary power and increments of 2–5kg body weight, that could be attributed to a rise of the
    lean physique mass, have been observed. Although AAS administration may have an result on erythropoiesis and blood haemoglobin concentrations, no effect on endurance efficiency was observed.
    Little data concerning the results of AAS on metabolic responses during
    train training and restoration are available and, therefore, do
    not allow firm conclusions. Antiandrogens comprise a comparatively massive group of compounds that intrude with the traditional organic exercise of T and varied mechanisms have been proposed for their perform.
    Some antiandrogens compete with androgens similar to
    T for binding to androgen receptors, preventing receptor activation and the consequent organic results.

    You might have them to treat conditions such as bronchial asthma, eczema, muscle and joint situations, lupus, or a number of sclerosis.
    AAS are most commonly administered by intramuscular (i.m.) injection or
    by oral ingestion. Injection are primarily based on vegetable oils, such as arachis oil,
    by which AAS are dissolved. Aromatic compounds similar to benzoyl benzoate (BB) or benzyl alcohol (BA) are sometimes added as excipients for their bacteriostatic properties and to
    extend the oil solubility of AAS.
    Examine along with your physician or pharmacist to ensure these medicine don’t cause any harm if you take them together with different medicines.
    Never cease taking your treatment and never change
    your dose or frequency with out consulting your doctor.
    In youthful adolescents, steroids can interfere with the development of arm and leg bones.
    Men over forty years of age with baseline prostate-specific antigen (PSA) of greater than zero.6
    ng/mL should have their PSA levels measured and a prostate
    examination at 3 to six months. Treatment must be withheld in men with a palpable prostate nodule or prostate-specific antigen of more than four ng/mL
    and in sufferers at excessive danger of prostate malignancy with prostate-specific antigen of more than three
    ng/mL.
    Substitution of the 17α-H with an ethynyl group on nandrolone,
    a 19-nor anabolic steroid with some progestational exercise, will lead to a potent orally lively progestogen, this being
    referred to as norethisterone (norethindrone), a steroid that’s still used in some contraceptives today.
    Nevertheless, substitution with an ethyl group on nandrolone quite than ethynyl group results in one other anabolic steroid known as norethandrolone, which also has oral exercise.
    Gestrinone, is a pharmaceutically out there progestogen that lacks the C-19 angular methyl
    group but has a 17α-ethynyl group, and it follows
    that discount of this ethynyl group to the tetrahydro product ought
    to make THG a ‘potent’ androgen. This is certainly the case, as subsequently THG was found to be
    a extremely potent androgen (and progestogen) in an in vitro bioassay system expressing human steroid receptors (Death
    et al., 2004), and it promotes muscle accretion in orchidectomized male rats (Jasuja et al.,
    2005). With structural modifications to testosterone,
    the anabolic results of androgens may be enhanced but, even so, these can’t be divorced totally from their androgenic effects.

    As suggested by Baxmann et al. (166), measuring serum cystatin C may be extra reliable to estimate GFR in healthy individuals with
    larger muscle mass and potential delicate kidney impairment.

    Cystatin C is a protein that is produced by all nucleated cells and is freely filtered on the glomerulus.
    In Contrast with serum creatinine, serum cystatin C concentrations
    are less affected by age, sex, race, and, most significantly, muscle mass (167).

    One study thus far has investigated the effect of excessive dosages of AAS on serum cystatin C concentrations
    (168). Serum creatinine and cystatin C concentrations were measured in fifty seven current AAS users, 28 past customers, and 52 non-AAS-using weightlifters.
    Unfortunately, due to its cross-sectional setup, this research does not
    allow to deduce causality.
    Lastly, we ask the patient if they’ve ever reflected on the attainable
    health consequences of their abuse, now and in the future.
    The typical person of AAS is male, aged between 20 and 40 and
    engaged in weight lifting, bodybuilding, strongman competitions or martial arts, primarily kickboxing and mixed martial arts.
    Though most physique constructing organizations have
    a drug free coverage, drug tests are mostly not
    executed. As a result, using anabolic steroids amongst opponents
    is widespread and is a necessity to be aggressive,
    particularly on the elite levels. Tensions between some AAS users and the medical community are
    nicely documented [26, sixty seven,sixty eight,69] and long established [70],
    predating anti-doping or legislative management in most nations.

    Although psychological hurt and the potential demand for interventions to handle dependence are also properly recognised
    [71,seventy two,73,seventy four,75] and diagnostic
    tools obtainable [52, 76], out there providers are few and much between. Hurt discount programmes, within the type of needle and syringe
    programmes (NSP), have clearly been profitable in participating AAS customers in Australia [42, forty three, 77, 78] and,
    in particular, the Uk [5, 30, seventy nine, 80].
    However, AAS use is still very fashionable and 1–3% of US inhabitants have
    been estimated to be AAS users [6]. Nonetheless, AASs have unwanted effects involving all organs,
    tissues and physique functions, especially long-term toxicity involving the cardiovascular system and the
    reproductive system, due to this fact, their abuse is taken into account a public
    well being problem [9,10]. In this regard, an increased consciousness
    is needed among the many population and healthcare staff, each for diagnostic, therapeutic and prevention functions.
    The purpose of the proposed review is to focus on the
    state of the art relating to the mechanisms of action of AASs
    and the opposed effects associated to AAS use/abuse.

    Nevertheless, some findings in the literature point to a potential detrimental effect.
    In the HAARLEM research, a transient small increase in serum
    creatinine concentrations of unknown clinical relevance was noticed during AAS use (from ninety three.1 μmol/L (1.05
    mg/dL) to ninety seven.8 μmol/L (1.eleven mg/dL)). Albuminuria, as measured by
    dipstick evaluation, emerged or elevated in 16% of the themes (155).
    A larger enhance in serum creatinine ranges was noticed
    in a small 4-week placebo-controlled trial with resistance-trained
    males randomized to 330 mg every day of the oral prohormone 3β-hydroxy-5α-androst-1-en-17-one (1-androsterone) or placebo (38).
    Bioactivation of the prohormone into the potent anabolic steroid 17β-hydroxy-5α-androst-1-en-3-one (1-testosterone) results from oxidation at carbon 3 of the A-ring
    and reduction at carbon 17 of the D-ring of the steroid nucleus (156).

    This estimate doesn’t accurately reflect the precise androgen exposure,
    as a result of the reality that it’s primarily based on the declared and never the actual focus
    of the abused products. Moreover, it combines oral and injectable merchandise and various varieties of androgens.
    However, it provides a sign that the weekly dose varies enormously between users and that the imply dose is very supraphysiologic.

    References:

    PedsElite

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