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Did elijah get a free trip to hell

question4u
Posts: 492
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6/3/2013 9:41:27 AM
Posted: 3 years ago
Did elijah the prophet get a free ride on a fire chariot straight to hell? He did not believe in coming messiah or godman or even believe jesus.. So where did he go, also david as well. According to my old faith anyone that is anyone who die without christ will go to hell...what do you think
Sower4GS
Posts: 1,718
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6/3/2013 9:52:06 AM
Posted: 3 years ago
cid...
Lysergic acid diethylamide
From Wikipedia, the free encyclopedia
"LSD" redirects here. For other uses, see LSD (disambiguation).

Lysergic acid diethylamide

Systematic (IUPAC) name
(6aR,9R)- N,N- diethyl- 7-methyl- 4,6,6a,7,8,9- hexahydroindolo- [4,3-fg] quinoline- 9-carboxamide
Clinical data
Pregnancy cat.C (US)
Legal statusProhibited (S9) (AU) Schedule III (CA) CD (UK) Schedule I (US)
Dependence liabilityVery low
RoutesOral, Intravenous, Ocular, Intramuscular
Pharmacokinetic data
MetabolismHepatic
Half-life3"5 hours[1][2]
ExcretionRenal
Identifiers
CAS number50-37-3
ATC code ?
PubChemCID 5761
IUPHAR ligand17
DrugBankDB04829
ChemSpider5558
UNII8NA5SWF92O
ChEBICHEBI:6605
ChEMBLCHEMBL263881
SynonymsLSD, LSD-25,
lysergide,
D-lysergic acid diethyl amide,
N,N- diethyl- D- lysergamide
Chemical data
FormulaC20H25N3O
Mol. mass323.43 g/mol
SMILES[show]
InChI[show]
Physical data
Melt. point80"85 "C (176"185 "F)
(what is this?) (verify)
Lysergic acid diethylamide, abbreviated LSD or LSD-25, also known as lysergide (INN) and colloquially as acid, is a semisynthetic psychedelic drug of the ergoline family, well known for its psychological effects which can include altered thinking processes, closed and open eye visuals, synesthesia, an altered sense of time and spiritual experiences, as well as for its key role in 1960s counterculture. It is used mainly as an entheogen, recreational drug, and as an agent in psychedelic therapy. LSD is non-addictive, is not known to cause brain damage, and has extremely low toxicity relative to dose. However, adverse psychiatric reactions such as anxiety, paranoia, and delusions are possible.[3]
LSD was first synthesized by Albert Hofmann in 1938 from ergotamine, a chemical derived by Arthur Stoll from ergot, a grain fungus that typically grows on rye. The short form "LSD" comes from its early code name LSD-25, which is an abbreviation for the German "Lysergs"ure-diethylamid" followed by a sequential number.[4][5] LSD is sensitive to oxygen, ultraviolet light, and chlorine, especially in solution, though its potency may last for years if it is stored away from light and moisture at low temperature. In pure form it is a colorless, odorless, tasteless solid.[6] LSD is typically delivered orally, usually on a substrate such as absorbent blotter paper, a sugar cube, or gelatin. In its liquid form, it can also be administered by intramuscular or intravenous injection. LSD is very potent, with 20"30 "g (micrograms) being the threshold dose. New clinical LSD experiments in humans started in 2009 for the first time in 40 years.[7]
Introduced by Sandoz Laboratories, with trade-name Delysid, as a drug with various psychiatric uses in 1947, LSD quickly became a therapeutic agent that appeared to show great promise.[8] In the 1950s, officials at the U.S. Central Intelligence Agency (CIA) thought the drug might be applicable to mind control and chemical warfare; the agency's MKULTRA research program propagated the drug among young servicemen and students. The subsequent recreational use of the drug by youth culture in the Western world during the 1960s led to a political firestorm that resulted in its prohibition.[9] Currently, a number of organizations"including the Beckley Foundation, MAPS, Heffter Research Institute and the Albert Hofmann Foundation"exist to fund, encourage and coordinate research into the medicinal and spiritual uses of LSD and related psychedelics.[10]
question4u
Posts: 492
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6/3/2013 10:15:29 AM
Posted: 3 years ago
L: At 6/3/2013 9:52:06 AM, Sower4GS wrote:
cid...
Lysergic acid diethylamide
From Wikipedia, the free encyclopedia
"LSD" redirects here. For other uses, see LSD (disambiguation).

Lysergic acid diethylamide

Systematic (IUPAC) name
(6aR,9R)- N,N- diethyl- 7-methyl- 4,6,6a,7,8,9- hexahydroindolo- [4,3-fg] quinoline- 9-carboxamide
Clinical data
Pregnancy cat.C (US)
Legal statusProhibited (S9) (AU) Schedule III (CA) CD (UK) Schedule I (US)
Dependence liabilityVery low
RoutesOral, Intravenous, Ocular, Intramuscular
Pharmacokinetic data
MetabolismHepatic
Half-life3"5 hours[1][2]
ExcretionRenal
Identifiers
CAS number50-37-3
ATC code ?
PubChemCID 5761
IUPHAR ligand17
DrugBankDB04829
ChemSpider5558
UNII8NA5SWF92O
ChEBICHEBI:6605
ChEMBLCHEMBL263881
SynonymsLSD, LSD-25,
lysergide,
D-lysergic acid diethyl amide,
N,N- diethyl- D- lysergamide
Chemical data
FormulaC20H25N3O
Mol. mass323.43 g/mol
SMILES[show]
InChI[show]
Physical data
Melt. point80"85 "C (176"185 "F)
(what is this?) (verify)
Lysergic acid diethylamide, abbreviated LSD or LSD-25, also known as lysergide (INN) and colloquially as acid, is a semisynthetic psychedelic drug of the ergoline family, well known for its psychological effects which can include altered thinking processes, closed and open eye visuals, synesthesia, an altered sense of time and spiritual experiences, as well as for its key role in 1960s counterculture. It is used mainly as an entheogen, recreational drug, and as an agent in psychedelic therapy. LSD is non-addictive, is not known to cause brain damage, and has extremely low toxicity relative to dose. However, adverse psychiatric reactions such as anxiety, paranoia, and delusions are possible.[3]
LSD was first synthesized by Albert Hofmann in 1938 from ergotamine, a chemical derived by Arthur Stoll from ergot, a grain fungus that typically grows on rye. The short form "LSD" comes from its early code name LSD-25, which is an abbreviation for the German "Lysergs"ure-diethylamid" followed by a sequential number.[4][5] LSD is sensitive to oxygen, ultraviolet light, and chlorine, especially in solution, though its potency may last for years if it is stored away from light and moisture at low temperature. In pure form it is a colorless, odorless, tasteless solid.[6] LSD is typically delivered orally, usually on a substrate such as absorbent blotter paper, a sugar cube, or gelatin. In its liquid form, it can also be administered by intramuscular or intravenous injection. LSD is very potent, with 20"30 "g (micrograms) being the threshold dose. New clinical LSD experiments in humans started in 2009 for the first time in 40 years.[7]
Introduced by Sandoz Laboratories, with trade-name Delysid, as a drug with various psychiatric uses in 1947, LSD quickly became a therapeutic agent that appeared to show great promise.[8] In the 1950s, officials at the U.S. Central Intelligence Agency (CIA) thought :-) the drug might be applicable to mind control and chemical :-) :-) :-) warfare; the agency's MKULTRA research program propagated the drug among young servicemen and students. The subsequent recreational use of the drug by youth culture in the Western world during the 1960s led to a political firestorm that resulted in its prohibition.[9] Currently, a number of organizations"including the Beckley Foundation, MAPS, Heffter Research Institute and the Albert Hofmann Foundation"exist to fund, encourage and coordinate research into the medicinal and spiritual uses of LSD and related psychedelics.[10]

Maybe I can go with the method you gave me since it is coming from the sower of yhshua godman but I will rather go with a more holistic method YAHWEH Only
AlbinoBunny
Posts: 3,781
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6/3/2013 10:16:02 AM
Posted: 3 years ago
At 6/3/2013 9:56:06 AM, Sower4GS wrote:

Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall.
bladerunner060 | bsh1 , 2014! Presidency campaign!

http://www.debate.org...
http://www.debate.org... - Running for president.
http://www.debate.org... - Running as his vice president.

May the best man win!
Sower4GS
Posts: 1,718
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6/3/2013 10:34:29 AM
Posted: 3 years ago
At 6/3/2013 10:15:29 AM, question4u wrote:
L: At 6/3/2013 9:52:06 AM, Sower4GS wrote:
cid...
Lysergic acid diethylamide
From Wikipedia, the free encyclopedia
"LSD" redirects here. For other uses, see LSD (disambiguation).

Lysergic acid diethylamide

Systematic (IUPAC) name
(6aR,9R)- N,N- diethyl- 7-methyl- 4,6,6a,7,8,9- hexahydroindolo- [4,3-fg] quinoline- 9-carboxamide
Clinical data
Pregnancy cat.C (US)
Legal statusProhibited (S9) (AU) Schedule III (CA) CD (UK) Schedule I (US)
Dependence liabilityVery low
RoutesOral, Intravenous, Ocular, Intramuscular
Pharmacokinetic data
MetabolismHepatic
Half-life3"5 hours[1][2]
ExcretionRenal
Identifiers
CAS number50-37-3
ATC code ?
PubChemCID 5761
IUPHAR ligand17
DrugBankDB04829
ChemSpider5558
UNII8NA5SWF92O
ChEBICHEBI:6605
ChEMBLCHEMBL263881
SynonymsLSD, LSD-25,
lysergide,
D-lysergic acid diethyl amide,
N,N- diethyl- D- lysergamide
Chemical data
FormulaC20H25N3O
Mol. mass323.43 g/mol
SMILES[show]
InChI[show]
Physical data
Melt. point80"85 "C (176"185 "F)
(what is this?) (verify)
Lysergic acid diethylamide, abbreviated LSD or LSD-25, also known as lysergide (INN) and colloquially as acid, is a semisynthetic psychedelic drug of the ergoline family, well known for its psychological effects which can include altered thinking processes, closed and open eye visuals, synesthesia, an altered sense of time and spiritual experiences, as well as for its key role in 1960s counterculture. It is used mainly as an entheogen, recreational drug, and as an agent in psychedelic therapy. LSD is non-addictive, is not known to cause brain damage, and has extremely low toxicity relative to dose. However, adverse psychiatric reactions such as anxiety, paranoia, and delusions are possible.[3]
LSD was first synthesized by Albert Hofmann in 1938 from ergotamine, a chemical derived by Arthur Stoll from ergot, a grain fungus that typically grows on rye. The short form "LSD" comes from its early code name LSD-25, which is an abbreviation for the German "Lysergs"ure-diethylamid" followed by a sequential number.[4][5] LSD is sensitive to oxygen, ultraviolet light, and chlorine, especially in solution, though its potency may last for years if it is stored away from light and moisture at low temperature. In pure form it is a colorless, odorless, tasteless solid.[6] LSD is typically delivered orally, usually on a substrate such as absorbent blotter paper, a sugar cube, or gelatin. In its liquid form, it can also be administered by intramuscular or intravenous injection. LSD is very potent, with 20"30 "g (micrograms) being the threshold dose. New clinical LSD experiments in humans started in 2009 for the first time in 40 years.[7]
Introduced by Sandoz Laboratories, with trade-name Delysid, as a drug with various psychiatric uses in 1947, LSD quickly became a therapeutic agent that appeared to show great promise.[8] In the 1950s, officials at the U.S. Central Intelligence Agency (CIA) thought :-) the drug might be applicable to mind control and chemical :-) :-) :-) warfare; the agency's MKULTRA research program propagated the drug among young servicemen and students. The subsequent recreational use of the drug by youth culture in the Western world during the 1960s led to a political firestorm that resulted in its prohibition.[9] Currently, a number of organizations"including the Beckley Foundation, MAPS, Heffter Research Institute and the Albert Hofmann Foundation"exist to fund, encourage and coordinate research into the medicinal and spiritual uses of LSD and related psychedelics.[10]

Maybe I can go with the method you gave me since it is coming from the sower of yhshua godman but I will rather go with a more holistic method YAHWEH Only
YHWH and the Son are Echad (One)
Sower4GS
Posts: 1,718
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6/3/2013 10:35:25 AM
Posted: 3 years ago
At 6/3/2013 10:16:02 AM, AlbinoBunny wrote:
At 6/3/2013 9:56:06 AM, Sower4GS wrote:

Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall. Text wall.
A spamming rabbit, now I have seen it all.
question4u
Posts: 492
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6/3/2013 12:51:09 PM
Posted: 3 years ago
At 6/3/2013 10:34:29 AM, Sower4GS wrote:
At 6/3/2013 10:15:29 AM, question4u wrote:
L: At 6/3/2013 9:52:06 AM, Sower4GS wrote:
cid...
Lysergic acid diethylamide
From Wikipedia, the free encyclopedia
"LSD" redirects here. For other uses, see LSD (disambiguation).

Lysergic acid diethylamide

Systematic (IUPAC) name
(6aR,9R)- N,N- diethyl- 7-methyl- 4,6,6a,7,8,9- hexahydroindolo- [4,3-fg] quinoline- 9-carboxamide
Clinical data
Pregnancy cat.C (US)
Legal statusProhibited (S9) (AU) Schedule III (CA) CD (UK) Schedule I (US)
Dependence liabilityVery low
RoutesOral, Intravenous, Ocular, Intramuscular
Pharmacokinetic data
MetabolismHepatic
Half-life3"5 hours[1][2]
ExcretionRenal
Identifiers
CAS number50-37-3
ATC code ?
PubChemCID 5761
IUPHAR ligand17
DrugBankDB04829
ChemSpider5558
UNII8NA5SWF92O
ChEBICHEBI:6605
ChEMBLCHEMBL263881
SynonymsLSD, LSD-25,
lysergide,
D-lysergic acid diethyl amide,
N,N- diethyl- D- lysergamide
Chemical data
FormulaC20H25N3O
Mol. mass323.43 g/mol
SMILES[show]
InChI[show]
Physical data
Melt. point80"85 "C (176"185 "F)
(what is this?) (verify)
Lysergic acid diethylamide, abbreviated LSD or LSD-25, also known as lysergide (INN) and colloquially as acid, is a semisynthetic psychedelic drug of the ergoline family, well known for its psychological effects which can include altered thinking processes, closed and open eye visuals, synesthesia, an altered sense of time and spiritual experiences, as well as for its key role in 1960s counterculture. It is used mainly as an entheogen, recreational drug, and as an agent in psychedelic therapy. LSD is non-addictive, is not known to cause brain damage, and has extremely low toxicity relative to dose. However, adverse psychiatric reactions such as anxiety, paranoia, and delusions are possible.[3]
LSD was first synthesized by Albert Hofmann in 1938 from ergotamine, a chemical derived by Arthur Stoll from ergot, a grain fungus that typically grows on rye. The short form "LSD" comes from its early code name LSD-25, which is an abbreviation for the German "Lysergs"ure-diethylamid" followed by a sequential number.[4][5] LSD is sensitive to oxygen, ultraviolet light, and chlorine, especially in solution, though its potency may last for years if it is stored away from light and moisture at low temperature. In pure form it is a colorless, odorless, tasteless solid.[6] LSD is typically delivered orally, usually on a substrate such as absorbent blotter paper, a sugar cube, or gelatin. In its liquid form, it can also be administered by intramuscular or intravenous injection. LSD is very potent, with 20"30 "g (micrograms) being the threshold dose. New clinical LSD experiments in humans started in 2009 for the first time in 40 years.[7]
Introduced by Sandoz Laboratories, with trade-name Delysid, as a drug with various psychiatric uses in 1947, LSD quickly became a therapeutic agent that appeared to show great promise.[8] In the 1950s, officials at the U.S. Central Intelligence Agency (CIA) thought :-) the drug might be applicable to mind control and chemical :-) :-) :-) warfare; the agency's MKULTRA research program propagated the drug among young servicemen and students. The subsequent recreational use of the drug by youth culture in the Western world during the 1960s led to a political firestorm that resulted in its prohibition.[9] Currently, a number of organizations"including the Beckley Foundation, MAPS, Heffter Research Institute and the Albert Hofmann Foundation"exist to fund, encourage and coordinate research into the medicinal and spiritual uses of LSD and related psychedelics.[10]

Maybe I can go with the method you gave me since it is coming from the sower of yhshua godman but I will rather go with a more holistic method YAHWEH Only
YHWH and the Son are Echad (One)

now where is that in the old testament or even in Isaiah
leojm
Posts: 1,825
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6/3/2013 7:03:42 PM
Posted: 3 years ago
At 6/3/2013 10:15:29 AM, question4u wrote:
L: At 6/3/2013 9:52:06 AM, Sower4GS wrote:
cid...
Lysergic acid diethylamide
From Wikipedia, the free encyclopedia
"LSD" redirects here. For other uses, see LSD (disambiguation).

Lysergic acid diethylamide

Systematic (IUPAC) name
(6aR,9R)- N,N- diethyl- 7-methyl- 4,6,6a,7,8,9- hexahydroindolo- [4,3-fg] quinoline- 9-carboxamide
Clinical data
Pregnancy cat.C (US)
Legal statusProhibited (S9) (AU) Schedule III (CA) CD (UK) Schedule I (US)
Dependence liabilityVery low
RoutesOral, Intravenous, Ocular, Intramuscular
Pharmacokinetic data
MetabolismHepatic
Half-life3"5 hours[1][2]
ExcretionRenal
Identifiers
CAS number50-37-3
ATC code ?
PubChemCID 5761
IUPHAR ligand17
DrugBankDB04829
ChemSpider5558
UNII8NA5SWF92O
ChEBICHEBI:6605
ChEMBLCHEMBL263881
SynonymsLSD, LSD-25,
lysergide,
D-lysergic acid diethyl amide,
N,N- diethyl- D- lysergamide
Chemical data
FormulaC20H25N3O
Mol. mass323.43 g/mol
SMILES[show]
InChI[show]
Physical data
Melt. point80"85 "C (176"185 "F)
(what is this?) (verify)
Lysergic acid diethylamide, abbreviated LSD or LSD-25, also known as lysergide (INN) and colloquially as acid, is a semisynthetic psychedelic drug of the ergoline family, well known for its psychological effects which can include altered thinking processes, closed and open eye visuals, synesthesia, an altered sense of time and spiritual experiences, as well as for its key role in 1960s counterculture. It is used mainly as an entheogen, recreational drug, and as an agent in psychedelic therapy. LSD is non-addictive, is not known to cause brain damage, and has extremely low toxicity relative to dose. However, adverse psychiatric reactions such as anxiety, paranoia, and delusions are possible.[3]
LSD was first synthesized by Albert Hofmann in 1938 from ergotamine, a chemical derived by Arthur Stoll from ergot, a grain fungus that typically grows on rye. The short form "LSD" comes from its early code name LSD-25, which is an abbreviation for the German "Lysergs"ure-diethylamid" followed by a sequential number.[4][5] LSD is sensitive to oxygen, ultraviolet light, and chlorine, especially in solution, though its potency may last for years if it is stored away from light and moisture at low temperature. In pure form it is a colorless, odorless, tasteless solid.[6] LSD is typically delivered orally, usually on a substrate such as absorbent blotter paper, a sugar cube, or gelatin. In its liquid form, it can also be administered by intramuscular or intravenous injection. LSD is very potent, with 20"30 "g (micrograms) being the threshold dose. New clinical LSD experiments in humans started in 2009 for the first time in 40 years.[7]
Introduced by Sandoz Laboratories, with trade-name Delysid, as a drug with various psychiatric uses in 1947, LSD quickly became a therapeutic agent that appeared to show great promise.[8] In the 1950s, officials at the U.S. Central Intelligence Agency (CIA) thought :-) the drug might be applicable to mind control and chemical :-) :-) :-) warfare; the agency's MKULTRA research program propagated the drug among young servicemen and students. The subsequent recreational use of the drug by youth culture in the Western world during the 1960s led to a political firestorm that resulted in its prohibition.[9] Currently, a number of organizations"including the Beckley Foundation, MAPS, Heffter Research Institute and the Albert Hofmann Foundation"exist to fund, encourage and coordinate research into the medicinal and spiritual uses of LSD and related psychedelics.[10]

Maybe I can go with the method you gave me since it is coming from the sower of yhshua godman but I will rather go with a more holistic method YAHWEH Only

wow, that's a lot. :O