Il est fort probable que les contribuables de l’ONA perdent toutes les cotisations qu’ils ont en caisse ou les cotisations mensuelles de 12% des employés (6% de l’employeur plus les 6% de l’employé).
2 min read
Il est fort probable que les contribuables de l’ONA perdent toutes les cotisations qu’ils ont en caisse ou les cotisations mensuelles de 12% des employés (6% de l’employeur plus les 6% de l’employé).
L’ONA est de plus en plus très mal vu par les contribuables et aussi par la population qui, depuis quelque temps, ont de la répugnance à l’égard de cette vache à lait institutionnelle, espace des hommes corrompus, notamment le personnage à la tête, Chesnel Pierre.
Il arrive que le directeur général de l’ONA, Chesnel Pierre, est entre le marteau et l’enclume pourvu qu’il ne sait quoi faire pour ne pas franchir la route du pénitencier national après l’éclatement des informations de l’ONA.
Depuis la nomination de Chesnel pierre à la tête de la direction de l’ONA, cette noble institution dans le temps est devenue de nos jours un bordel et ne cesse de faire faillite.
Prenons en exemples les trois dernières années :
en 2014, l’ONA a fait des dépenses en terme de subventions (donation), 23,429.45 gourdes
En 2017—> 108, 210.49 gourdes
En 2018—> 177,960.62 gourdes
En 2019-> 208,873.54 gourdes
À vous de faire la somme.
Seulement pour subvention, sans parler des autres dépenses .
Des subventions approuvées par le directeur général de l’ONA Chesnel Pierre qui ne respecte aucun règlement interne de l’institution, Ni les lois de la république, Ni les lois morales, Ni les lois naturelles.
Il faut noter que ses dépenses ne proviennent pas des fonds publics , ce sont les cotisations des entreprises pour leurs employés déjà mal payés et qui travaillent parfois dans des conditions critiques.
Alors que les cotisants n’ont pas accès à des prêts minimals à l’ONA! On se demande maintenant pourquoi cotiser le mois prochain ?
puisque cette cotisation sera distribuée à des Gangs armés pour faire répression contre mes concitoyens (ennes) qui exigent de meilleures conditions de vie et que leur cotisation puisse demeurer disponible en cas de besoin pour propulser les petites et moyennes entreprises.
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bodybuilders, and fitness enthusiasts looking to enhance muscle definition and strength
while minimizing fat gain. Its reputation for being relatively mild compared to other steroids makes it
especially attractive for those who want noticeable improvements without severe side effects.
Below is an in‑depth look at what users can expect from Anavar, focusing on results after two weeks
of use for both women and men, reasons why people choose this compound,
and some related posts that might interest you.
—
Anavar Results After 2 Weeks On Woman & Man (Before/After)
Women
Muscle Definition: Within the first fortnight, many female users
notice a subtle increase in muscle firmness. The lean muscle mass grows slightly, giving the appearance of tighter hips and thighs.
Fat Loss: Women often report a modest reduction in body fat, particularly around the abdomen. This
occurs because Anavar can elevate metabolic rate without drastically altering hormone levels that affect estrogen.
Strength Gains: Though the increase is not dramatic, women may experience an uptick in power during resistance
training—especially for exercises like squats and deadlifts—helping them lift slightly heavier weights than before starting.
Side Effects: Mild acne or mild headaches are possible but typically less severe than with stronger steroids.
Some users might notice a slight change in libido, though this is usually minimal.
Men
Muscle Hypertrophy: Two weeks into an Anavar cycle can bring noticeable gains in muscle
size, especially in the upper body—arms, chest,
and shoulders. The compound promotes protein synthesis, which contributes to muscle
growth.
Strength Boost: Many men experience a significant increase in lifting capacity.
Bench presses, rows, and overhead presses often feel
easier, allowing for higher volume training sessions.
Fat Loss: Men typically observe more pronounced fat loss compared to women. Anavar’s
effect on metabolism can help burn calories stored as body fat, resulting in a leaner appearance.
Recovery Speed: Users report quicker recovery between workouts.
The steroid reduces muscle damage and inflammation, so soreness is less
intense after sessions.
Before/After Comparison
Weight Gain: Men may gain 2–3 pounds of lean mass, while women might see a
gain of 1–2 pounds.
Body Fat Reduction: Both genders often experience a drop in body fat percentage ranging from 0.5%
to 1.5%, depending on diet and training intensity.
Strength Increase: Men can lift roughly 10–15% more
than before, whereas women may see a similar percentage increase, though absolute numbers are lower.
Why Use Anavar?
1. Mild Side‑Effect Profile
Anavar is known for being one of the gentlest anabolic steroids.
Unlike stronger compounds that often cause significant liver stress or drastic hormonal imbalances, Anavar
typically offers fewer side effects, making it a popular choice for beginners and
experienced users alike.
2. Lean Muscle Gain Without Bulk
The steroid is ideal for those who want to add muscle definition without adding excessive
bulk. Athletes in sports like gymnastics, wrestling, or bodybuilding
competitions that emphasize aesthetics often rely on Anavar to achieve a shredded look while maintaining agility.
3. Fat Loss and Metabolic Boost
Anavar increases metabolic rate, helping the body burn calories more efficiently.
When paired with a calorie‑controlled diet,
users can lose fat quickly while preserving muscle mass—a desirable combination for many fitness enthusiasts.
4. Strength Enhancement
The compound provides significant strength improvements without the
heavy water retention seen in some other steroids. This means athletes can push harder during
training sessions and potentially reach new personal bests.
5. Shorter Cycle Length
Because of its mild nature, Anavar cycles are often shorter—typically two
to four weeks for women and up to eight weeks for men. Shorter cycles reduce the risk of long‑term side effects and
make it easier to incorporate into a broader
training plan.
6. Compatibility with Other Stacks
Anavar is commonly used in combination with other steroids or performance
enhancers. Its mildness allows it to act as a « maintenance » drug,
helping users maintain gains while using more potent compounds for muscle growth.
—
Related Posts
« Understanding the Difference Between Anavar and Winstrol: Which Is Better for Cutting? » – A comparative analysis of two popular cutting
steroids, focusing on side‑effect profiles and effectiveness.
« The Ultimate Guide to Post‑Cycle Therapy (PCT) After Using Anavar »
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« Dietary Strategies to Maximize Fat Loss While Taking Anavar » – Meal
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have gained popularity among athletes, bodybuilders, and researchers looking for ways to enhance muscle growth, fat loss, and overall recovery.
These peptides act on the growth hormone axis by stimulating the
release of growth hormone from the pituitary gland.
They are often used together because their combined effect can lead to a more robust increase in circulating growth hormone levels while minimizing potential side effects that can occur when each is used alone.
CJC 1295 and Ipamorelin dosage: benefits, mechanisms,
and research applications
The most common dosage regimen for CJC 1295 involves a
subcutaneous injection of 2 to 3 micrograms per kilogram of
body weight. For an average adult weighing around 70 kilograms this translates to roughly 140 to
210 micrograms daily. Ipamorelin is typically administered at a dose of 100 to 200
micrograms per kilogram, which would be about 7 to 14 milligrams for the
same individual. In many protocols participants receive both peptides simultaneously, with injections spaced
either once or twice per day depending on their goals and tolerance.
The benefits reported in studies and anecdotal evidence include significant
increases in lean body mass, improvements in muscle strength, enhanced fat loss, better sleep quality, faster recovery from injury, and a general boost in energy levels.
CJC 1295 works by binding to growth hormone‑releasing hormone
receptors, thereby increasing the release of endogenous growth
hormone. Ipamorelin is a selective ghrelin receptor agonist that also
stimulates growth hormone secretion but does so with less impact on cortisol
or prolactin levels. When combined, they provide a synergistic
effect: CJC 1295 supplies a sustained stimulus while Ipamorelin offers rapid spikes
of growth hormone release, leading to a more consistent overall elevation.
In research settings, these peptides have been used to study the physiology
of aging, muscle wasting diseases such as sarcopenia, and metabolic disorders.
Preclinical trials in rodents have shown that chronic administration can improve insulin sensitivity,
reduce inflammatory markers, and promote cardiovascular health.
Human clinical trials are still limited but have demonstrated safety when used
at recommended dosages for short periods.
Long‑term data remain sparse, so most practitioners advise cycling these peptides to avoid potential
receptor desensitization.
What is CJC 1295 Ipamorelin?
CJC 1295 is a synthetic analogue of growth hormone‑releasing hormone (GHRH) that has been modified to increase its half‑life
in the bloodstream. The original GHRH peptide is rapidly
degraded, but CJC 1295 contains a stabilizing sequence that allows it to remain active for up to 48
hours after injection. This extended duration means patients can receive fewer injections while still maintaining high
levels of growth hormone.
Ipamorelin, on the other hand, is a pentapeptide that mimics ghrelin, the « hunger hormone. » It selectively activates the growth hormone secretagogue receptor (GHS‑R1a) without significantly affecting appetite or cortisol secretion. Because it is highly specific, Ipamorelin tends to produce
fewer side effects such as water retention, increased
blood pressure, or changes in glucose metabolism that are sometimes
seen with other ghrelin mimetics.
When combined, CJC 1295 and Ipamorelin provide a balanced approach:
CJC 1295 offers a sustained, low‑level growth hormone stimulus while Ipamorelin delivers short
bursts of hormone release. This dual mechanism is believed to maximize the anabolic benefits while minimizing
peaks that could lead to undesirable side effects.
About Company
The peptides are produced by several biotechnology firms specializing in peptide synthesis and
research chemicals. One of the leading manufacturers is a company based in Europe that has
received regulatory approval for producing high‑purity, GMP‑grade peptides.
Their production process involves solid‑phase
peptide synthesis followed by rigorous purification steps such as
reverse‑phase HPLC and mass spectrometry verification. The company’s product line includes both CJC 1295
and Ipamorelin as separate items, as well as pre‑mixed formulations that
allow users to combine the two in a single vial for convenience.
The firm offers detailed dosage guidelines on its website and provides safety data sheets outlining potential risks.
They also maintain an online forum where researchers share protocols, dosing schedules,
and personal experiences with side effects. The company’s commitment to transparency
has helped build trust among clinicians and athletes who
rely on precise peptide therapy for performance enhancement or medical research.
Side Effects of CJC 1295 Ipamorelin
Although both peptides are generally well tolerated at recommended doses, users can experience a range of side effects that vary in severity.
Commonly reported adverse reactions include:
Local injection site reactions – redness, swelling, or mild pain where the
peptide is injected. These symptoms usually resolve within a
few hours and do not require medical intervention.
Water retention and bloating – particularly with higher doses
of CJC 1295. The sustained release of growth hormone can lead to an increase in extracellular fluid
volume, resulting in a puffy appearance or mild edema around the ankles
and face.
Headaches – some users report tension headaches after the first few
injections. This is thought to be related to rapid changes
in blood flow and hormonal fluctuations.
Increased appetite – while Ipamorelin does not strongly stimulate hunger,
the overall rise in growth hormone can sometimes trigger a mild increase in caloric
intake. Users who are trying to lose weight should monitor their diet closely.
Joint pain or stiffness – higher levels of growth hormone
may lead to increased collagen turnover, which can cause temporary discomfort
in joints and tendons.
Fatigue or lethargy – paradoxically, some people feel more tired after starting peptide
therapy. This could be due to altered sleep architecture; many users report deeper but longer periods of rest.
Hormonal imbalances – rare cases of elevated prolactin levels have been observed when CJC 1295 is
used at very high doses for extended periods.
Monitoring hormone panels can help detect this early.
Rare allergic reactions – in a small number of individuals, hypersensitivity
to the peptide or its excipients has led to itching, rash, or anaphylaxis.
Immediate medical attention is required if such symptoms occur.
Potential impact on insulin sensitivity – growth hormone antagonizes insulin action, so users with diabetes or pre‑diabetes may
see worsening glycemic control. Regular blood glucose checks are recommended for this population.
Long‑term safety data are limited; chronic use could
theoretically influence cancer risk because growth hormone
promotes cell proliferation. Most studies focus on short‑term cycles (4–12 weeks), and long‑lasting effects remain under investigation.
Mitigating Side Effects
To reduce the likelihood of adverse reactions, many users adopt a cycling strategy:
8 to 10 weeks of therapy followed by a break of 2 to 4
weeks. This approach allows the body’s receptors to reset and
reduces the risk of desensitization. Hydration is
also crucial; drinking ample water can counteract fluid
retention and help flush out metabolic waste. Pairing peptide therapy
with a balanced diet low in processed sugars and high in protein helps maintain muscle gains while preventing
unwanted fat storage.
Monitoring
Regular blood work, including growth hormone levels, IGF‑1 (insulin‑like growth factor 1),
prolactin, cortisol, thyroid function, and lipid panels, provides insight into how the body is responding.
If any of these markers deviate significantly from baseline, dose adjustments or discontinuation may be necessary.
In summary, CJC 1295 and Ipamorelin can offer powerful benefits for muscle growth, fat loss, and recovery when used responsibly.
However, users must remain vigilant about potential side
effects ranging from mild injection site reactions
to more serious hormonal changes. Careful dosing, proper monitoring, and adherence to recommended cycling protocols are essential for achieving the desired outcomes while minimizing risks.
and nerve injuries, as well as gastrointestinal healing.
While anecdotal reports suggest remarkable benefits,
it is essential to understand that the use of BPC 157 may carry various side effects and
risks. These adverse reactions can range from mild local symptoms at the injection site
to more systemic complications depending on dosage, frequency, and individual sensitivity.
Side Effects of BPC 157
Local Injection Site Reactions
The most common complaints involve discomfort or pain at the area
where the peptide is administered. Some users
experience redness, swelling, or a mild inflammatory response that typically resolves within a few hours to days.
In rare cases, more pronounced inflammation or even infection can occur if aseptic technique is not strictly followed.
Hormonal and Metabolic Impact
BPC 157 may influence several hormonal pathways.
Elevated levels of growth hormone, insulin-like growth
factor‑1, and changes in cortisol have been reported in animal studies.
These shifts could potentially lead to increased appetite, fluid retention, or
altered blood glucose control, particularly in individuals with underlying endocrine disorders.
Cardiovascular Effects
While the data are limited, there is evidence that BPC 157
can affect vascular tone and blood pressure regulation. Users
may experience transient fluctuations in systolic or
diastolic readings, especially when taken in higher doses or combined with other vasoactive substances.
Gastrointestinal Symptoms
Some users report mild nausea, bloating, or abdominal discomfort
after oral ingestion of the peptide. These symptoms are generally short‑lived but can be bothersome for people
who already have digestive sensitivities.
Allergic Reactions
Though rare, hypersensitivity to BPC 157 has been documented.
Signs include itching, rash, hives, and in severe cases anaphylaxis.
Immediate medical attention is required if any allergic response occurs.
Immune System Modulation
By interacting with inflammatory cytokines, BPC 157 may alter immune function. This modulation could theoretically reduce the
body’s ability to fight infections or, conversely, provoke an overactive immune response in susceptible individuals.
Potential for Interaction with Medications
The peptide can interact with various drugs such as NSAIDs, anticoagulants, and hormonal therapies.
These interactions might either diminish therapeutic effects or increase side‑effect
risk, underscoring the importance of consulting
a healthcare professional before combining BPC 157 with other medications.
Unknown Long‑Term Effects
Because clinical trials are scarce, long‑term safety data are incomplete.
Prolonged use could conceivably lead to unforeseen complications such as organ toxicity
or endocrine disruption that have not yet been identified in the
limited available studies.
Best Form of BPC 157 Revealed: Injectable, Capsule, or Oral?
Choosing the optimal form of BPC 157 depends on several factors
including the desired therapeutic outcome, convenience, and risk
tolerance. Each delivery method has its own profile:
Injectable BPC 157
The injectable formulation is considered the most potent because it bypasses the digestive tract and achieves higher bioavailability.
It is commonly used for acute injuries or when rapid
tissue repair is required. However, self‑injection carries
a risk of infection if proper sterility is not maintained, and users may experience local pain or swelling at the injection site.
Capsule (Oral) BPC 157
Oral capsules offer greater convenience and lower risk of needle‑related complications.
Nonetheless, gastrointestinal degradation reduces the amount of
peptide that reaches systemic circulation,
potentially diminishing efficacy for conditions requiring high concentrations.
Some users still report benefits, especially for mild to moderate GI issues or general healing support.
Sublingual or Buccal Forms
While not as widely available, sublingual tablets or solutions allow absorption through the oral mucosa, providing a middle ground between injection and capsule routes.
Bioavailability is higher than capsules but lower than injections.
Users may experience rapid onset of action with fewer local side effects.
What to Consider When Choosing a BPC 157 Form
Medical Condition and Desired Outcome
If you are treating a serious tendon or nerve injury, an injectable form might offer the most direct and robust effect.
For general gut health or mild musculoskeletal pain, oral capsules may suffice.
Skill Level and Comfort with Self‑Administration
Those comfortable with injections can benefit
from the potency of the injectable route. Individuals who
prefer minimal handling or have needle phobia should consider oral or
sublingual forms.
Safety Profile and Risk Tolerance
Injectables carry a higher risk of infection or local tissue damage if not handled properly.
Oral or buccal formulations reduce this risk but also come with
lower systemic potency, which may be acceptable for some users.
Cost and Availability
Injectable BPC 157 often costs more due to
the need for sterile packaging and higher purity. Capsules are
generally cheaper and easier to obtain, though quality
control can vary between manufacturers.
Regulatory Status and Legal Considerations
In many jurisdictions, peptides like BPC
157 are not approved by major regulatory bodies such
as the FDA or EMA for therapeutic use. Users
should verify legal restrictions in their region before purchasing or
using any form of the peptide.
Monitoring and Medical Guidance
Regardless of the chosen route, regular monitoring
of blood pressure, glucose levels, and liver function may be prudent if
you are taking BPC 157 over an extended period.
Consulting with a healthcare professional can help identify potential drug interactions and manage side effects effectively.
Quick Takeaways
BPC 157 is linked to several possible side effects including injection site
reactions, hormonal changes, cardiovascular fluctuations, mild GI discomfort, allergic responses, immune modulation, drug
interactions, and unknown long‑term risks.
Injectable forms provide the highest potency but come with infection risk and require sterile technique.
Oral capsules are more convenient but less bioavailable;
sublingual options offer intermediate benefits.
The choice of form should be guided by the specific
medical need, personal comfort with self‑administration, safety considerations, cost, legal status, and ongoing medical supervision.
Monitoring for side effects and consulting a qualified professional
can mitigate risks and help maximize potential therapeutic benefits.
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