Afghanistan: Don't recognise Taliban regime, resistance urges
8-09-2021, 15:19

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Anti-Taliban forces in Afghanistan have asked the international community not to recognise the new government announced by the Islamists on Tuesday.

The all-male cabinet consisting entirely of Taliban leaders or their associates is "illegal", they said.

The US has expressed concern that the interim government includes figures linked to attacks on US forces.

And the EU said the Islamist group had reneged on promises to make it "inclusive and representative".

The interim cabinet is led by Mullah Mohammad Hassan Akhund, who is on a UN blacklist. Another figure, Sirajuddin Haqqani, is wanted by the American FBI.

The National Resistance Front (NRF) said it considered the announcement of the Taliban's caretaker cabinet "a clear sign of the group's enmity with the Afghan people".

The Taliban insist they have now defeated the NRF in the Panjshir Valley north of Kabul, but NRF leaders say they are still fighting.

In a statement, the US state department said it was concerned by the "affiliations and track records of some of the individuals".

The statement said Washington would "continue to hold the Taliban to their commitments" to allow safe passage for foreign nationals and Afghans with travel documents, "including permitting flights currently ready to fly out of Afghanistan".

US Secretary of State Antony Blinken is to hold a virtual meeting of 20 Western nations to co-ordinate a set of conditions for engagement with the Taliban government.

The Taliban seized control of Afghanistan in a sweeping offensive more than three weeks ago. It now faces many tough challenges in the conflict-torn country, including stabilising the economy and gaining international recognition.

On Wednesday dozens of women marched in Kabul and in the province of Badakhshan, saying they would not accept a government without women.

The Taliban deny using violence against the demonstrations. They say protesters need permission to march and should not use abusive language.

Pakistan also denies any role in Afghanistan.

 

Ministers told to implement 'Islamic law'

 

Earlier on Tuesday, a statement attributed to Taliban Supreme Leader Mawlawi Hibatullah Akhundzada told the government to uphold Sharia law - Islam's legal system. The Taliban have been known for their extremely hardline interpretation of Sharia.

The Taliban want "strong and healthy" relations with other countries and would respect international laws and treaties as long as they did not conflict with "Islamic law and the country's national values", the group's statement said.

Hassan Akhund, the new interim prime minister, served as deputy foreign minister from 1996 to 2001, when the militants were last in power. He is influential on the religious side of the movement, rather than the military side.

His appointment is seen as a compromise, after recent reports of in-fighting between some relatively moderate Taliban figures and their hardline colleagues.

The group had previously said it wanted to form an inclusive government.

 

Interior minister on US terrorism list

 

Sirajuddin Haqqani, the acting interior minister, is head of the militant group known as the Haqqani network, who are affiliated with the Taliban and have been behind some of the deadliest attacks in the country's two-decade-long war - including a truck bomb explosion in Kabul in 2017 that killed more than 150 people.

Unlike the wider Taliban, the Haqqani network has been designated a foreign terrorist organisation by the US. It also maintains close ties to al-Qaeda.

The FBI says he is wanted for questioning over a 2008 attack on a hotel that killed an American and was behind attacks on US forces in Afghanistan.

 

BBC

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BPC‑157, short for Body Protective Compound 157, is a synthetic peptide
that mimics a naturally occurring protein fragment found in the stomach.

The full protein is involved in protecting the gastric lining from acid damage, but researchers discovered that a specific segment of 15 amino acids—hence the "157"
designation—has remarkable regenerative properties.
In laboratory settings, BPC‑157 has been administered orally or via injection to animals with promising results.




Because it is derived from a naturally occurring sequence, bpc 157 tb 500‑157 can be produced under Good Manufacturing Practice conditions
and is available in various formulations, such as
subcutaneous injections, oral capsules, and topical gels.
Its stability at room temperature and ease of dosing have contributed
to its popularity among athletes who prefer a straightforward recovery protocol.




How does BPC‑157 work?

The exact mechanisms by which BPC‑157 promotes healing are still
being elucidated, but several key pathways appear to be involved:






Angiogenesis – The peptide stimulates the growth of new blood vessels in damaged tissues.
Increased vascularization delivers more oxygen and nutrients, speeding up the repair process.





Collagen Production – BPC‑157 promotes fibroblast activity, which leads to higher collagen synthesis.
Collagen is essential for rebuilding tendons, ligaments, and other connective
tissues.



Anti‑Inflammatory Effects – By modulating inflammatory cytokines,
the peptide reduces swelling and pain at the injury site,
creating a more conducive environment for healing.




Neuroprotection – In studies involving nerve damage, BPC‑157 has been shown to protect neural tissue from degeneration and support regeneration of damaged
axons.



Stem Cell Mobilization – Some research suggests that BPC‑157 can recruit stem cells to the injury site, providing
a source of new, healthy cells for repair.



The synergy of these actions explains why many users report rapid improvements across multiple tissues—tendon, muscle, cartilage, and even nerve function. Although most evidence comes from animal models, human case reports and anecdotal reviews consistently point to similar benefits, making BPC‑157 a compelling
option for athletes seeking an edge in recovery.


In summary, BPC‑157 is a promising regenerative peptide that
offers tendon repair, joint protection, and broad tissue healing.
Its mechanism involves stimulating blood vessel growth, enhancing collagen production, dampening inflammation, protecting nerves, and mobilizing
stem cells—all of which contribute to faster, more complete recovery for
athletes and active individuals.
6 October 2025 23:56
#1   Stormy
      
CJC‑1295 and Ipamorelin are two peptides that have attracted attention in the fields of anti‑aging research, muscle
growth, and metabolic health. They are often combined because each peptide stimulates the release of growth
hormone (GH) while having complementary safety profiles.
Understanding their side effects is essential for anyone considering these compounds as part of a therapeutic or performance regimen.



CJC 1295 Ipamorelin:
The Ultimate Guide to Peptide Research

The combination of CJC‑1295 and Ipamorelin offers a potent stimulus
for growth hormone secretion while minimizing the risk of excessive prolactin release.
CJC‑1295 is a long‑acting analog that binds to somatostatin receptors, thereby prolonging GH release over several hours.

Ipamorelin, on the other hand, mimics ghrelin but with high specificity for the ghrelin receptor,
producing a rapid surge in GH without significant appetite stimulation. Together, they create a sustained yet balanced
hormonal environment that can aid tissue repair, fat loss, and overall vitality.




Key Takeaways: Research Insights on CJC‑1295 & Ipamorelin

Clinical studies have shown that when administered subcutaneously at doses ranging from 100 to 250 micrograms per injection, the
pair elevates serum GH levels by up to five times baseline.
The rise in insulin-like growth factor 1 (IGF‑1) follows suit, contributing to anabolic effects on muscle and bone.

Importantly, side effect profiles differ from older analogs like GHRP‑6 or
Sermorelin: nausea, headache, transient dizziness,
and mild injection site reactions are the most frequently reported adverse events.
The combination does not typically raise
prolactin levels, which reduces risks such as gynecomastia or sexual
dysfunction that have been documented with other GH secretagogues.




What is CJC‑1295?

CJC‑1295 is a synthetic peptide comprising 29 amino acids engineered to resist degradation by the enzyme dipeptidyl peptidase
IV. Its design includes a fatty acid tail that binds to albumin, extending its half‑life from
minutes to days. This prolonged circulation allows for less frequent dosing
(often twice weekly) compared to other GH secretagogues. The peptide specifically targets somatostatin receptor
subtypes 2 and 5, thereby modulating the inhibitory signals that normally curb GH release.

By suppressing this inhibition, CJC‑1295 facilitates a more robust
and sustained secretion of growth hormone.



Side Effect Landscape





Injection Site Reactions: Swelling, redness, or mild pain at the needle entry point is
common, especially with higher volumes. Proper injection technique and rotating sites can mitigate these effects.



Fluid Retention: Some users report puffiness in the extremities or face due to vasodilatory actions of GH.

This usually resolves within a few days after
stopping treatment.


Hyperglycemia: Growth hormone has counter‑insulin properties, so elevated blood glucose may occur.
Monitoring fasting glucose is advised for diabetic patients.



Headache and Dizziness: A transient rise in intracranial pressure or changes in cerebral blood flow can cause mild headaches; these
are generally dose‑dependent.


Nausea and Gastrointestinal Upset: The peptides can stimulate ghrelin receptors,
leading to an increased sense of fullness or discomfort in the stomach.




Long‑Term Considerations

While short‑term studies have not identified severe
toxicities, long‑term safety data remain limited.
Potential concerns include alterations in lipid metabolism,
changes in body composition, and rare reports of tumor promotion due to IGF‑1 stimulation. Regular health check‑ups, including blood panels for liver enzymes,
lipid profiles, and hormone levels, are recommended for
prolonged use.



Comparisons with Other Peptides

Unlike GHRP‑2 or GHRP‑6, which can significantly raise prolactin and cause sexual side
effects, CJC‑1295 paired with Ipamorelin maintains a lower prolactin profile.
Compared to Sermorelin, the combination offers extended duration of action without the need for daily
dosing. However, users should weigh the higher cost and potential for increased fluid retention when choosing between these agents.




Practical Guidance for Safe Use





Start at low doses (e.g., 100 micrograms) and gradually increase as tolerated to identify personal sensitivity.




Administer injections in a clean environment; use sterile needles and alcohol prep to reduce infection risk.



Monitor body weight, blood pressure, and glucose levels before
and during treatment to catch any metabolic shifts early.




Allow adequate recovery time between cycles (typically
4–6 weeks) to prevent receptor desensitization.



In summary, CJC‑1295 and Ipamorelin provide a scientifically grounded method for
enhancing growth hormone secretion with a favorable side
effect profile compared to older analogs. Nonetheless, careful dosing, vigilant monitoring, and an understanding of potential long‑term implications are essential components of responsible peptide therapy.
6 October 2025 01:45
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