LE GROUPE DES QUATRE (4) A RAISON: Tous les ministres et secrétaires d’ETAT qui faisaient partie du Gouvernement de Jean Henry CÉANT ont besoin de décharge pour intégrer un nouveau Cabinet ministériel.
2 min readLE GROUPE DES QUATRE (4) A RAISON: Tous les ministres et secrétaires d’ETAT qui faisaient partie du Gouvernement de Jean Henry CÉANT ont besoin de décharge pour intégrer un nouveau Cabinet ministériel.
C’est tout à fait inacceptable de reconduire des ministres qui faisaient partie d’un gouvernement censuré. Si cela était juridiquement possible, on pourrait , sans décharge, revenir avec Jean Henry Céant dans un nouveau Gouvernement.
La constitution est claire : le vote de censure met fin à la fonction de tous les membres du Gouvernement, premier ministre, ministres et secrétaires d’Etat. La constitution est formelle : Après un vote de censure, le premier Ministre remet sa démission et celle de son Gouvernement au Président de la République. Reconduire des ministres qui faisaient partie d’un Gouvernement censuré par le Parlement , c’est vassaliser le parlement; c’est attaquer son autorité.
Les gens qui disent qu’il y a des précédents dans la mesure où cela a été le cas avec Jean Max Bellerive qui faisait du Gouvernement de Michèle D Pierre Louis, font fausse route. Et je leur réponds ceci : la violation de la loi ne peut pas servir de précédent. Une décision de justice qui viole la loi ne doit pas servir de Jurisprudence.
La violation de la loi, c’est la violation de la loi.
La nomination de Jean Max Bellerive comme premier ministre alors qu’il faisait partie du Gouvernement censuré de Michèle D Pierre Louis était tout simplement une violation de la constitution.
La défaite du Droit est provisoire.
Pour toutes ces raisons, je supporte la position et le Combat du Groupe des 4 sénateurs de l’Opposition tout en rappelant que la solution à la crise Politique actuelle passe d’abord et avant tout par la démission du président Jovenel Moïse, la réalisation du PROCÈS PETROCARIBE et l’organisation de la Conférence Nationale Haïtienne Souveraine .
André Michel, Av, porte parole du Secteur Démocratique et Populaire
LAKAYINFO
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While they can provide significant increases in circulating growth hormone
levels, their use is not without risks. Understanding
the potential side effects, especially from a medical perspective, helps users make informed decisions about whether to incorporate these peptides into their regimen.
—
Understanding Ipamorelin Side Effects: A Comprehensive
Review
Hormonal Imbalance and Endocrine Disruption
Ipamorelin stimulates the pituitary gland to release growth hormone (GH) and insulin‑like growth factor 1 (IGF‑1).
Prolonged or high‑dose exposure can upset the delicate balance of other hormones.
Users may experience:
Elevated prolactin levels, which can lead to lactation in women, decreased
libido, and sexual dysfunction.
Alterations in thyroid hormone production; some individuals report mild hypothyroidism symptoms such as fatigue, weight gain, or cold intolerance.
Changes in cortisol rhythm, potentially contributing to mood swings or sleep disturbances.
Metabolic Effects
Because growth hormone has lipolytic properties, it can influence glucose metabolism.
The main metabolic concerns include:
Insulin resistance: Some users develop higher fasting insulin levels and decreased
glucose tolerance over time, which may predispose
them to type‑2 diabetes.
Increased triglycerides: Elevated fat breakdown can sometimes raise
circulating lipid intermediates, potentially impacting cardiovascular risk.
Local Injection Site Reactions
Ipamorelin is typically administered subcutaneously. Common local reactions involve:
Redness and swelling at the injection site that generally resolves within 24 to 48 hours.
Pain or tenderness during needle insertion or withdrawal.
Rarely, users develop a mild inflammatory reaction that may require topical steroids
or antihistamines.
Cardiovascular Concerns
Growth hormone exerts effects on blood vessels. In susceptible individuals, ipamorelin can cause:
Peripheral edema: Fluid retention in extremities, especially when combined
with high GH levels.
Hypertension: Elevated blood pressure readings may appear after prolonged use, necessitating regular monitoring.
Neurological and Psychological Effects
Some users report changes in mood or cognition, which may include:
Anxiety or irritability during the first weeks of therapy as the body adapts to increased GH.
Sleep disturbances such as insomnia or vivid dreams due to hormonal
fluctuations.
Headaches, particularly if water retention leads to increased intracranial pressure.
Rare but Serious Complications
Although uncommon, there are serious adverse events that can arise:
Acromegalic changes: Long‑term overstimulation of GH can lead
to soft tissue swelling and bone overgrowth in the hands,
feet, or face.
Tumor growth stimulation: Certain tumors may respond to higher IGF‑1 levels by accelerating proliferation.
Key Takeaways
Dose Matters – The likelihood and severity of side effects increase with higher dosages or extended
treatment periods. Adhering to recommended protocols (e.g., 100–200 µg daily) reduces risk.
Monitoring is Crucial – Regular blood work for
GH, IGF‑1, insulin, thyroid hormones, and lipid panels helps catch imbalances
early.
Injection Technique Affects Comfort – Using a new sterile needle each time and rotating injection sites
can minimize local reactions.
Lifestyle Factors Influence Outcomes – Adequate sleep, balanced nutrition, and avoiding excessive alcohol or caffeine help mitigate many
side effects.
Consult Healthcare Professionals – Prior to starting ipamorelin,
especially if you have pre‑existing medical conditions, a thorough evaluation by an endocrinologist is advisable.
Ipamorelin Cancer Risk Assessment
The relationship between growth hormone secretagogues and cancer risk remains
under investigation. Several points are important:
Biological Rationale
Growth hormone drives the production of IGF‑1,
a mitogenic factor that can promote cell proliferation. Elevated IGF‑1 levels have been linked in epidemiological studies to increased risks
for certain cancers such as breast, prostate, and colorectal.
Evidence from Animal Studies
Rodent models treated with GH secretagogues occasionally show accelerated tumor growth in pre‑existing tumors or enhanced development
of benign nodules. However, translating these findings to humans is not straightforward due to species differences.
Human Data
Clinical trials involving ipamorelin are limited and typically short‑term (a
few weeks). No large‑scale randomized controlled studies have definitively
shown an increase in cancer incidence among users. Long‑term observational data
are sparse.
Current Consensus
Low to Moderate Risk: For healthy individuals using standard therapeutic doses, the risk appears low but cannot be dismissed entirely.
Higher Risk with Pre‑Existing Conditions: People who already have hormone‑responsive cancers or a strong
family history may face an elevated risk if GH/IGF‑1 levels rise.
Practical Recommendations
Screening Before Use – A baseline evaluation of tumor markers and imaging
for those with personal or familial cancer histories
can identify hidden lesions.
Periodic Surveillance – Annual check‑ups, including PSA testing in men over 50, mammography
in women, and colonoscopy as indicated, are
prudent while on therapy.
Limit Duration – Shorter courses (no more than three to six
months) reduce cumulative exposure to elevated IGF‑1.
In summary, while ipamorelin offers tangible benefits for growth hormone deficiency or anti‑aging protocols, it carries a spectrum of side effects ranging
from mild injection site reactions to serious endocrine and cardiovascular disturbances.
Its potential link to cancer remains an area of active
research; thus, users should proceed with caution, maintain rigorous monitoring, and consult
healthcare providers before initiating therapy.
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