05.12.13 Nelson Mandela changed worlds today. Long live his commitment to reconciliation. John Dickinson was the only governor to refuse to sign the Declaration of Independence. He thought of it as a Declaration of War. He desired a Declaration of Reconciliation with England. An end to the war on drugs should be declared with full pardon, amnesty given to those affected by this war against health concerns, a war against people around the world. There should be a reconciliation, and it should be given to all those prisoners of America's longest war.
Paid Sponsors Sought:
Chris Farley Living in a Van Down by the River
65th B-day/retirement party
65, good time to retire, take up gardening perhaps.
Cannabinoid Chemistry
Cannabinoids are chemical compounds that activate cannabinoid receptors. Cannabinoid receptors are cell membrane bound proteins that are activated upon binding to cannabinoids. Cannabinoid receptors are G protein-coupled receptors found throughout the human nervous system. There are two cannabinoid receptors in the human body, Cannabinoid Receptor Type 1 (CB1), and Cannabinoid Receptor Type 2 (CB2). CB1 generally exists in the central nervous system, especially the hippocampus, and CB2 in the peripheral nervous system.In the human body, CB1 and CB2 are activated by the neurotransmitters anandamide and 2-arachidonoylgylcerol (2-AG) respectively. Anandamide and 2-AG are produced in vivo.....
Cannabis Sativa
certified
certified
STRICTLY ORGANIC OLD TOBY
Apothecary SEAOPOLIS
Organic Patient Care
INGREDIENTS: <||=>
09.06.13
Mission =ACCESS
Goals:
To help reduce pharmaceutical drug
dependencies, and to allow medical cannabis to remain as a viable option to our
number one killer in the US, the drugs in everyone’s medicine cabinet.
Certifications: Strictly Organic Cultivators, Converters, Consiglieri
Cultivators: Strictly Organic Pavilions
Converters: Strictly Organic Certified Medibles
Consiglieri: Certified Knowledgeable Advisors
Board of Directors: Patient Participants of the survey
Authorizations: Patients with Pharmaceutical Dependancies
Verifications: DOB/ZipCode/Expiration Date
Education: Strain Specific Recommendations
Propagandizements:
Examinations: Electro Interstitial Scans
Treatments: Bud, Bed & Breakfast
Participations: Intake Record/Self Record Keeping/EIS
Apps: Real Time Intake Tracking
Human Resources:
Accountings: Strictly Transparent
State Markets: "The LCB won't follow all Federal rules" 04.09.13
Green Markets: Strictly accountable with all Federal rules
State Markets: 84% Taxations
Green Markets: No Taxations
State Markets: Debatable Testings
Green Markets: Strict Certified Testings
State Markets: No Transparencies
Green Markets: Strict Transparencies
State Markets: Use Restricted to Closets
Green Markets: No Use Restrictions
State Markets: Age Restrictions
Green Markets: No Age Restrictions
State Markets: Purchase Restrictions
Green Markets: No Purchase Restrictions
State Markets: Strictly For Profits
Green Markets: Strictly For Patients
agreed
The Washington State Liquor
– Marijuana (sic) Control Board challenges the Green Market in the first Market Challenge, 22
January 2013
1 December 2014.
The Green Market accepts
the Challenge to produce the cleanest, healthiest, strain specific cannabis for specific ailments. Strictly tested and certified.
THCV
An anorectic or anorexic (from the Greek an- =
"without" and orexis = "appetite"), also known as anorexigenic or appetite suppressant, is a dietary
supplement and/or drug which reduces appetite, food consumption, and as a result, causes weight loss to occur.
The anticonvulsants (also commonly known as antiepileptic drugs) are a diverse
group of pharmaceuticals used in the treatment of epileptic seizures. Anticonvulsants are also
increasingly being used in the treatment of bipolar disorder, since many seem to act as mood stabilizers, and for the treatment of neuropathic pain. The goal of an anticonvulsant is to suppress the
rapid and excessive firing of neurons that start a seizure. Failing
this, an effective anticonvulsant would prevent the spread of the seizure
within the brain and offer protection against possible excitotoxic effects, that may result in brain damage.
Some studies have cited that anticonvulsants themselves are linked to lowered IQ in
children.[1] However these adverse effects
must be balanced against the significant risk epileptiform seizures pose to
children and the distinct possibility of death and devastating neurological sequelasecondary
to seizures. Anticonvulsants are more accurately called antiepileptic
drugs (abbreviated
"AEDs"), and are sometimes referred to asantiseizure drugs. While the term
'anticonvulsant' is a fair description of AEDs, the use of this term tends to lead
to confusion between epilepsy and non-epileptic convulsions. Convulsive
seizures non-epileptic seizures are quite common, and these
types of seizures do not respond to antiepileptic drugs. In epilepsy, an area
of the cortex is typically hyper-irritable. This condition can often be
confirmed by completing a diagnostic EEG. Antiepileptic drugs function to help
reduce this area of irritability and thus prevent epileptiform seizures.
The major molecular targets
of marketed anticonvulsant drugs are voltage-gated sodium channels and
components of the GABA system, including GABAA receptors, the GAT-1 GABA
transporter, and GABA transaminase.[2] Additional targets include
voltage-gated calcium channels,SV2A, and α2δ.[3][4] The drug class was the US's
5th-best-selling in 2007.[5]
Some anticonvulsants have
shown antiepileptogenic effects in animal models of epilepsy. That is, they
either prevent the expected development of epilepsy or can halt or reverse the
progression of epilepsy. However, no drug has been shown to prevent epileptogenesis (the development of epilepsy after an injury such as a head injury) in human trials.[6]
CBG - Old Toby has tested highest CBG
An antibacterial is an agent that inhibits
bacterial growth or kills bacteria.[1] The term is often used synonymously with the term antibiotic(s); today, however, with
increased knowledge of the causative agents of various infectious diseases, antibiotic(s) has come to denote a
broader range of antimicrobial compounds, including anti-fungal and other compounds.[2]
The term antibiotic was first used in 1942 by Selman Waksman and
his collaborators in journal articles to describe any substance produced by a
microorganism that is antagonistic to the growth of other
micro organisms in high dilution.[3] This definition excluded
substances that kill bacteria, but are not produced by micro organisms (such as gastric juices and hydrogen peroxide). It also excluded synthetic antibacterial compounds such as the sulfonamides. Many antibacterial
compounds are relatively small molecules with
a molecular weight of less than 2000 atomic mass units.
With advances in medicinal chemistry, most of today's
antibacterials chemically are semisynthetic modifications of various natural compounds.[4] These include, for
example, the beta-lactam antibacterials, which
include the penicillins (produced by fungi in the
genus Penicillium), the cephalosporins, and the carbapenems. Compounds that are
still isolated from living organisms are the aminoglycosides, whereas other antibacterials—for example, the sulfonamides,
the quinolones,
and the oxazolidinones—are produced solely by chemical synthesis. In accordance with
this, many antibacterial compounds are classified on the basis of chemical/biosynthetic origin into natural,
semisynthetic, and synthetic. Another classification system is based on
biological activity; in this classification, antibacterials are divided into
two broad groups according to their biological effect on microorganisms: bactericidal agents kill bacteria, and bacteriostatic agents slow down or stall
bacterial growth.
CBC
Anti-inflammatory refers to the
property of a substance or treatment that reduces inflammation. Anti-inflammatory drugs make up about half of analgesics, remedying pain by reducing inflammation as
opposed to opioids, which affect the central nervous system.
An analgesic is any member of the
group of drugs used to achieve analgesia,
relief from pain.
The word analgesic derives from Greek αν
- ("without") andάλγος
- ("pain"). [1]
Commonly known as painkillers, analgesic drugs act in
various ways on the peripheral and central nervous systems. They are
distinct from anesthetics,
which reversibly eliminate sensation,
and include paracetamol (known in the US as acetaminophen or
simply APAP), the non-steroidal
anti-inflammatory drugs (NSAIDs) such as the salicylates,
and opioid drugs
such as morphine and opium.
In choosing analgesics,
the severity and response to other medication determines the choice of agent;
the World Health Organization (WHO) pain ladder[2]specifies mild analgesics
as its first step.
Analgesic choice is also
determined by the type of pain: for neuropathic pain, traditional analgesics
are less effective, and there is often benefit from classes of drugs that are
not normally considered analgesics, such as tricyclic antidepressants and anticonvulsants.[3]
Antimicrobial are typically liquids. Antimicrobial liquids kill or inhibit the
growth of microorganisms[1]such as bacteria, fungi and protozoans. Antimicrobial drugs (e.g. penicillin) are selective and kill microbes (microbiocidal) or prevent
their growth (microbiostatic). Disinfectants are non-selective antimicrobial substances (e.g. bleach) and are used on non-living objects or the outside of the body.
The history of
antimicrobials begins with the observations of Pasteur and Joubert, who discovered that one type of
bacterium could prevent the growth of another. They did not know at that time
that the reason one bacterium failed to grow was that the other bacterium was
producing an antibiotic. Technically antibiotics are only those substances that
are produced by one microorganism that kill, or prevent the growth of, another
microorganism. In today's common usage the term antibiotic is used to refer to
almost any drug that attempts to rid your body of a bacterial
infection. Antimicrobials include not just
antibiotics but also synthetically formed compounds.
The discovery of
antimicrobials such as penicillin and tetracycline paved the way for better health for
millions around the world. Before penicillin became a viable medical treatment
in the early 1940s, no true cure for gonorrhea, strep throat and pneumonia existed. Patients with infected wounds often had to have a
wounded limb removed or face death from infection. Now most of these infections
can be cured easily with a short course of antimicrobials.
However, with the
development of antimicrobials, microorganisms have adapted and become resistant
to previous antimicrobial agents. The old antimicrobial technology was based on
either poisons or heavy metals, which may not have killed the microbe
completely, allowing the microbe to survive, change and become resistant to the
poisons and/or heavy metals.
Antimicrobial
nanotechnology is a recent addition to the fight against disease-causing
organisms, replacing heavy metals and toxins, and may some day be a viable
alternative.
Infections that
are acquired during a hospital visit are called hospital-acquired infections or nosocomial infections. Similarly, when
the infectious disease is picked up outside a hospital, it is known as
community-acquired.
THCA
CBD
An anxiolytic (also antipanic or antianxiety agent)[1] is a drug used for the treatment of anxiety and its related psychological and physical symptoms. Anxiolytics
have been shown to be useful in the treatment of anxiety disorders.
Beta-receptor
blockers such as propranolol and oxprenolol, although not anxiolytics, can be used to combat the somatic symptoms of anxiety.
Anxiolytics are also
known as minor tranquilizers.[2]The term is less common in modern texts, and was originally derived
from a dichotomy with major tranquilizers, also known as neuroleptics orantipsychotics.[citation needed
antipsychotic (or neuroleptic) is a psychiatric medication primarily used to manage psychosis(including delusions or hallucinations, as well as disordered thought), particularly in schizophrenia and bipolar disorder, and is increasingly being used in the management of non-psychotic
disorders (ATC code N05A). A first generation of antipsychotics, known astypical antipsychotics, was discovered in the
1950s. Most of the drugs in the second generation, known as atypical antipsychotics, have been developed more
recently, although the first atypical antipsychotic, clozapine, was discovered in the
1950s and introduced clinically in the 1970s. Both generations of medication
tend to block receptors in the brain's dopamine pathways, but antipsychotic drugs
encompass a wide range of receptor targets.
A number of harmful and
undesired (adverse) effects have been observed,
including lowered life expectancy, extrapyramidal effects on motor
control –
including akathisia (an inability to sit still), trembling, and muscle
weakness, weight
gain,
decrease in brain volume, enlarged breasts (gynecomastia) in men and milk
discharge in men and women (galactorrhea due tohyperprolactinaemia), lowered white blood cell count (agranulocytosis), involuntary repetitive body movements (tardive dyskinesia), diabetes, and sexual dysfunction.
A return of psychosis can
occur, requiring increasing the dosage, due to cells producing more
neurochemicals to compensate for the drugs (tardive psychosis), and there is a potential for permanent chemical dependence leading
to psychosis worse than before treatment began, if the drug dosage is ever
lowered or stopped (tardive dysphrenia).[1] Most side-effects disappear
rapidly once the medication is discontinued or reduced, but others,
particularly tardive dyskinesia, may be irreversible.
Temporary withdrawal
symptoms including insomnia, agitation, psychosis, and motor disorders may
occur during dosage reduction of antipsychotics, and can be mistaken for a
return of the underlying condition.[2][3]
The development of new
antipsychotics with fewer of these adverse effects and with greater relative
effectiveness as compared to existing antipsychotics (efficacy), is an ongoing field of
research. Sometimes, however, patients are switched back to typical
antipsychotics because the newer ones are less effective in those patients.[citation needed]
The anticonvulsants (also commonly known asantiepileptic drugs) are a diverse
group of pharmaceuticals used in the treatment of epileptic seizures. Anticonvulsants are also
increasingly being used in the treatment of bipolar disorder, since many seem to act as mood stabilizers, and for the treatment of neuropathic pain. The goal of an anticonvulsant
is to suppress the rapid and excessive firing of neurons that start a seizure.
Failing this, an effective anticonvulsant would prevent the spread of the
seizure within the brain and offer protection against possible excitotoxic effects, that may result in brain
damage. Some
studies have cited that anticonvulsants themselves are linked to lowered IQin children.[1] However these adverse
effects must be balanced against the significant risk epileptiform seizures
pose to children and the distinct possibility of death and devastating
neurological sequelasecondary to seizures.
Anticonvulsants are more accurately called antiepileptic drugs (abbreviated "AEDs"),
and are sometimes referred to as antiseizure
drugs. While the term
'anticonvulsant' is a fair description of AEDs, the use of this term tends to
lead to confusion between epilepsy and non-epileptic convulsions. Convulsive
seizures non-epileptic seizures are quite common, and these
types of seizures do not respond to antiepileptic drugs. In epilepsy, an area
of the cortex is typically hyper-irritable. This condition can often be
confirmed by completing a diagnostic EEG. Antiepileptic drugs function to help
reduce this area of irritability and thus prevent epileptiform seizures.
The major molecular targets
of marketed anticonvulsant drugs are voltage-gated sodium channels and
components of the GABA system, including GABAA receptors, the GAT-1 GABA transporter, and GABA transaminase.[2] Additional targets include
voltage-gated calcium channels,SV2A, and α2δ.[3][4] The drug class was the US's
5th-best-selling in 2007.[5]
Some anticonvulsants have
shown antiepileptogenic effects in animal models of epilepsy. That is, they
either prevent the expected development of epilepsy or can halt or reverse the
progression of epilepsy. However, no drug has been shown to prevent epileptogenesis (the
development of epilepsy after an injury such as a head injury) in human trials.[6]
Neuroprotection is a widely explored treatment option for many central
nervous system (CNS)
disorders including neurodegenerative
diseases,stroke, traumatic
brain injury, and spinal cord injury. Neuroprotection aims to prevent or slow disease
progression and secondary injuries by halting or at least slowing the loss of neurons.[1] Despite differences in
symptoms or injuries associated with CNS disorders, many of the mechanisms behind neurodegeneration
are the same. Common mechanisms include increased levels in oxidative stress,
mitochondrial dysfunction, excitotoxicity, inflammatory changes, iron
accumulation, and protein aggregation.[1][2][3] Of these mechanisms, neuroprotective
treatments often target oxidative stress and excitotoxicity—both of which are
highly associated with CNS disorders. Not only can oxidative stress and excitotoxicity
trigger neuron cell death but when combined they have synergistic effects that
cause even more degradation on their own.[4] Thus limiting excitotoxicity
and oxidative stress is a very important aspect of neuroprotection. Common
neuroprotective treatments are glutamate antagonists and antioxidants, which
aim to limit excitotoxicity and oxidative stress respectively.
Vasodilation refers to the widening of blood vessels.[1] It results from relaxation of smooth muscle cells within the vessel walls, particularly in the large veins, large arteries, and smaller arterioles. The process is essentially the opposite of vasoconstriction, which is the narrowing of blood vessels.
When blood vessels
dilate, the flow of blood is increased due to a decrease in vascular resistance. Therefore, dilation of arterial blood vessels (mainly the
arterioles) decreases blood pressure. The response may be intrinsic (due to local processes in the
surrounding tissue) or extrinsic (due to hormonesor the nervous system). Additionally, the response may be localized to a specific organ
(depending on the metabolic needs of a particular tissue, as during strenuous
exercise), or it may be systemic (seen throughout the entire systemic
circulation).
Drugs that cause vasodilation
are termed vasodilators.
Chemotherapy is the treatment of cancer with one or more cytotoxic antineoplastic drugs
("chemotherapeutic agents") as part of astandardized regimen. Chemotherapy may be given
with a curative intent or it may aim to
prolong life or to palliate symptoms. It is often used in conjunction with other cancer treatments,
such as radiation therapy or surgery. Certain chemotherapeutic
agents also have a role in the treatment of other conditions, including ankylosing spondylitis, multiple sclerosis,Crohn's disease, psoriasis, psoriatic arthritis,rheumatoid arthritis, and scleroderma.
Traditional chemotherapeutic
agents act by killing cells that divide rapidly, one of the main properties of
most cancer cells. This means that chemotherapy also harms cells that divide
rapidly under normal circumstances: cells in the bone
marrow, digestive tract, and hair
follicles. This
results in the most common side-effects of chemotherapy:myelosuppression (decreased
production of blood cells, hence also immunosuppression), mucositis(inflammation of the lining
of the digestive tract), andalopecia (hair loss).
Some newer anticancer drugs
(for example, variousmonoclonal antibodies) are not indiscriminately
cytotoxic, but rather target proteins that are abnormally expressed in cancer
cells and that are essential for their growth. Such treatments are often
referred to as targeted therapy (as
distinct from classic chemotherapy) and are often used alongside traditional
chemotherapeutic agents in antineoplastic treatment regimens.
An older and broader usage
of the word chemotherapy encompassed any chemical treatment of disease (for
example, treatment of infections withantimicrobial agents). However, this usage
has become archaic.
An antiemetic is a drug that is effective against vomiting and nausea. Antiemetics are typically used to treat motion sickness and the side
effects of opioidanalgesics, general anaesthetics, and chemotherapy directed against cancer.
Anti-emetics are
also used for morning sickness, but there is little information about the effect on the fetus,
and doctors prefer not to use them unless it is strictly necessary.[1]
Anti-diabetic medications treat diabetes mellitus by lowering glucose levels in the blood. With the exceptions of insulin, exenatide, liraglutide andpramlintide, all are administered orally and are thus also called oral
hypoglycemic agents or oral
antihyperglycemic agents. There are different classes of anti-diabetic
drugs, and their selection depends on the nature of the diabetes, age and
situation of the person, as well as other factors.
Diabetes
mellitus type 1 is a disease caused by the lack of
insulin. Insulin must be used in Type I, which must be injected.
Diabetes
mellitus type 2 is a disease of insulin resistance by
cells. Treatments include (1) agents that increase the amount of insulin
secreted by the pancreas, (2) agents that increase the sensitivity of target
organs to insulin, and (3) agents that decrease the rate at which glucose is
absorbed from the gastrointestinal tract.
Several groups of
drugs, mostly given by mouth, are effective in Type II, often in combination.
The therapeutic combination in Type II may include insulin, not necessarily
because oral agents have failed completely, but in search of a desired
combination of effects. The great advantage of injected insulin in Type II is
that a well-educated patient can adjust the dose, or even take additional
doses, when blood glucose levels measured by the patient, usually with a simple
meter, as needed by the measured amount of sugar in the blood.
Antipsoriatic is a
drug used to treat psoriasis.
anti-prokinetic
analgesic
paracetamol (500 mg) and the anti-emetic metoclopramide
hydrochloride (5 mg). ... (prokinetic ),
which is often delayed during ...
5 KB (602 words) -
03:14, 9 January 2013
·
Opioid
trigger zone without
adverse central anti-dopaminergic effects (not ... Vomiting can thus be prevented
by prokinetic agents (e.g. domperidone ...
89 KB (10,501 words)
- 13:13, 19 January 2013
An analgesic is any member of the group
of drugsused
to achieve analgesia, relief from pain. The wordanalgesic derives from Greek αν
- ("without") andάλγος
- ("pain"). [1]
Commonly known as painkillers, analgesic drugs act in
various ways on the peripheral and centralnervous systems. They are
distinct from anesthetics, which reversibly eliminate sensation, and includeparacetamol (known in the US as acetaminophen or simply APAP), the non-steroidal anti-inflammatory drugs (NSAIDs) such as the salicylates, and opioiddrugs such as morphine and opium.
In choosing analgesics, the
severity and response to other medication determines the choice of agent; the
World Health Organization (WHO) pain
ladder[2]specifies mild analgesics as
its first step.
Analgesic choice is also
determined by the type of pain: for neuropathic pain, traditional analgesics are
less effective, and there is often benefit from classes of drugs that are not
normally considered analgesics, such as tricyclic antidepressants andanticonvulsants.[3]
Hydromorphone, a more common
synonym for dihydromorphinone,
commonly a hydrochloride (brand names Palladone, Dilaudid,
and numerous others) is a very potent centrally acting analgesicdrug of the opioid class. It is a derivative of morphine, to be specific, a hydrogenated ketone thereof, and it can be said that hydromorphone is to
morphine as hydrocodone is to codeine and, therefore, a semi-synthetic drug. It is, in medical
terms, an opioid analgesic and, in legal terms, a narcotic. Hydromorphone is commonly used in
the hospital setting, mostly intravenously (IV) because its bioavailability
orally, rectally, and intranasally is very low.
Very small quantities of hydromorphone are
detected in assays of opium on rare occasions; it appears to be produced by the
plant under circumstances and by processes which are not understood at this
time and may include the action of bacteria. A similar process and/or other
metabolic processes in the plant may very well be responsible for the very low
quantities of hydrocodone also found on rare occasions in opium and alkaloid
mixtures derived therefrom; dihydrocodeine, oxymorphol, oxycodone,oxymorphone, metopon and possibly other derivatives of morphine and/or
hydromorphone also are found in trace amounts in opium.
Immunosuppression involves an act that reduces the activation or efficacy of the immune system. Some portions of the immune system itself have immuno-suppressive
effects on other parts of the immune system, and immunosuppression may occur as
an adverse reaction to treatment of other conditions.
In general,
deliberately induced immunosuppression is performed to prevent the body from rejecting anorgan
transplant, treating graft-versus-host
diseaseafter a bone
marrow transplant, or for the treatment of auto-immune diseases such as rheumatoid
arthritis or Crohn's disease. This is typically done using drugs, but may involve surgery (splenectomy), plasmapharesis, or radiation.
A person who is
undergoing immunosuppression, or whose immune system is weak for other reasons
(for example, chemotherapy, HIV, and Lupus), is said to be immunocompromised.
Just Some Strictly Organic Household Growing Tips
01.01.13 First find a garage/basement and purge it.
Clean it up with fresh coats of paint, lights and get ready to treat.
Get distracted, and get a new knee at Swedish Orthopedic Institute.
17.05.13 First class treatment under Dr. Cannon at Swedish Orthopedic Institute. A new knee is installed with barely a scar. Enjoy a corner private suite with excellent food and service.
Move to Caroline Kline Galland nursing care with another corner suite, 222. Enjoy the great views of the lake at Fontanelle Beach Place, great food and wonderful service.
Head back to the patio for re-hab. A big help accepted from PT Cynthia of Caroline Kline Galland Home Treatment.
Cynthia travels often to India to study yoga and bowl harmonics.
RN Sam, also from CKG Home Care takes the vitals.
PT Nancy, from CKG Home Care, came to give advice
to get the knee in top shape.
PT Pam, from CKG Home Care, also stops by for vitals.
First donation for the Mota Flota, Phoenix Safari, accepted 
Darn Pie Rats
keep getting in the way.
Choose a flag. This one has nine leaves, nine plants, on black field and yellow boundary. Green Market has nine leaves, State Market, five leaves.
Re-hab room is built under State Market prescriptions. It appears like manufacturing, a Federal offense with enhanced penalties. The State Market declares they won't follow Federal guidelines, and that "...they will meet some of the guidelines...". 
27.06.13
1 c fertilizer each
28.06.13
1-17 testing results. 3/4 gone, minimal egg populations
29.06.13
1-17 testing results, spraying populated leaves. 3/4 gone.
30.06.13
18-64 habanero dunk and soil spray
water
01.07.13
finish dunk and a few more trans-potting to 10's and 15's
15.07.13
A visit to other SOOT Sites:
A visit to other SOOT Sites:
AK
Old Toby is a northwest developed, hardy strain, capable of Haze-like yeilds.
ARC
18.07.13 increase bottom reflective lumens to prep for flowering
21.07.13
25.08.13 Girls go outside >>>
o , o , SEATTLE, WASHINGTON Astronomical Applications Dept.
Location: W122 20, N47 38 Pacific Standard Time U. S. Naval Observatory
Washington, DC 20392-5420
Duration of Daylight for 2013
Day Jan. Feb. Mar. Apr. May June July Aug. Sep. Oct. Nov. Dec.
h m h m h m h m h m h m h m h m h m h m h m h m
01 08:31 09:36 11:06 12:52 14:30 15:44 15:55 14:56 13:21 11:39 09:57 08:43
02 08:32 09:39 11:09 12:56 14:33 15:46 15:54 14:53 13:17 11:36 09:54 08:41
03 08:33 09:41 11:12 12:59 14:36 15:47 15:53 14:51 13:14 11:32 09:51 08:39
04 08:35 09:44 11:16 13:03 14:39 15:48 15:52 14:48 13:11 11:29 09:48 08:38
05 08:36 09:47 11:19 13:06 14:42 15:50 15:51 14:45 13:07 11:26 09:45 08:36
06 08:37 09:50 11:23 13:09 14:45 15:51 15:49 14:42 13:04 11:22 09:42 08:35
07 08:39 09:54 11:26 13:13 14:48 15:52 15:48 14:39 13:01 11:19 09:39 08:34
08 08:40 09:57 11:30 13:16 14:51 15:53 15:47 14:36 12:57 11:15 09:36 08:33
09 08:42 10:00 11:33 13:20 14:53 15:54 15:45 14:33 12:54 11:12 09:34 08:32
10 08:44 10:03 11:36 13:23 14:56 15:55 15:44 14:30 12:51 11:09 09:31 08:31
11 08:45 10:06 11:40 13:26 14:59 15:56 15:42 14:28 12:47 11:05 09:28 08:30
12 08:47 10:09 11:43 13:30 15:02 15:56 15:41 14:25 12:44 11:02 09:25 08:29
13 08:49 10:12 11:47 13:33 15:04 15:57 15:39 14:21 12:40 10:59 09:23 08:28
14 08:51 10:16 11:50 13:36 15:07 15:58 15:37 14:18 12:37 10:55 09:20 08:27
15 08:53 10:19 11:54 13:40 15:09 15:58 15:35 14:15 12:34 10:52 09:17 08:27
16 08:55 10:22 11:57 13:43 15:12 15:59 15:33 14:12 12:30 10:49 09:15 08:26
17 08:57 10:25 12:01 13:46 15:14 15:59 15:31 14:09 12:27 10:45 09:12 08:26
18 08:59 10:29 12:04 13:50 15:17 15:59 15:29 14:06 12:23 10:42 09:10 08:26
19 09:02 10:32 12:08 13:53 15:19 15:59 15:27 14:03 12:20 10:39 09:07 08:26
20 09:04 10:35 12:11 13:56 15:21 15:59 15:25 14:00 12:17 10:35 09:05 08:25
21 09:06 10:39 12:15 13:59 15:23 15:59 15:23 13:57 12:13 10:32 09:03 08:25
22 09:09 10:42 12:18 14:02 15:26 15:59 15:21 13:53 12:10 10:29 09:00 08:25
23 09:11 10:45 12:21 14:06 15:28 15:59 15:19 13:50 12:06 10:26 08:58 08:26
24 09:14 10:49 12:25 14:09 15:30 15:59 15:16 13:47 12:03 10:22 08:56 08:26
25 09:16 10:52 12:28 14:12 15:32 15:58 15:14 13:44 12:00 10:19 08:54 08:26
26 09:19 10:55 12:32 14:15 15:34 15:58 15:11 13:40 11:56 10:16 08:52 08:27
27 09:22 10:59 12:35 14:18 15:36 15:58 15:09 13:37 11:53 10:13 08:50 08:27
28 09:24 11:02 12:39 14:21 15:37 15:57 15:06 13:34 11:49 10:10 08:48 08:28
29 09:27 12:42 14:24 15:39 15:56 15:04 13:31 11:46 10:06 08:46 08:28
30 09:30 12:46 14:27 15:41 15:56 15:01 13:27 11:43 10:03 08:44 08:29
31 09:33 12:49 15:43 14:59 13:24 10:00 08:30
Inside prepped for babies.
Exceeding Safety.
Exceeding Codes.
For Immediate Release August 29, 2013
Liquor Control Board Statement following Department of Justice’s Guidance Memo on Marijuana
OLYMPIA – The Washington
State Liquor Control Board (WSLCB) issued the following statement
regarding the Department of Justice’s announcement today.
The
Washington State Liquor Control Board would like to thank the Obama
Administration, particularly Attorney General Eric Holder and the Dept.
of Justice for its guidance today.
We
would also like to thank Gov. Jay Inslee and Attorney General Bob
Ferguson for their leadership and efforts on this issue these past nine
months. As Gov. Inslee stated today, the Department of Justice today
helped lay a path forward for Washington and Colorado to implement its
systems of producing, processing and retailing recreational marijuana.
The
Board’s primary rule-making focus has been to create a tightly
regulated market with emphasis on public safety and restricting youth
access. In his letter, AG Holder shared the same concerns. We believe
the action taken today by the federal government is the result of the
conversations by our state elected leaders with the Dept. of Justice as
well as the open and transparent system in which the rules have been
crafted. The Board is confident that Washington’s recreational marijuana
system will meet most, if not all, of the federal government’s stated
concerns.
With
the federal government’s approval the Board will continue to move
forward and implement I-502 and carry out the will of Washington State
voters.
04.09.13
GobY has arrived! Designed for a two patient, 30 plants, medical grow. Highly reflective with light deprivation components to grow year round.
Designed specifically to grow year round according to WADOH guidelines. Two patients, 30 plants.
GobY walls out for inspection after 4-day ordeal on the beach. Walls are outstanding for reflectors and light deprivation.
Dr Stevo does the dunk.
Babies getting their health back.
Retail Stores
December 18, 2013 30-day window closes for producer, processor and retailer license applications
Public Hearings
One or more public hearings on the proposed rules will be scheduled soon. The WSLCB will post the dates and locations on its website at www.liq.wa.gov
GobY has arrived! Designed for a two patient, 30 plants, medical grow. Highly reflective with light deprivation components to grow year round.
GobY walls out for inspection after 4-day ordeal on the beach. Walls are outstanding for reflectors and light deprivation.Dr Stevo does the dunk.
Board Approves Filing of Proposed Rules to Implement Initiative 502
Recreational marijuana market to be tightly regulated to prevent diversion, impact to minors
OLYMPIA – The Washington
State Liquor Control Board (Board) today approved the filing of
proposed supplemental rules that, if ultimately enacted, will help
govern Washington State’s system of producing, processing and retailing
recreational marijuana. The Board earlier this summer filed proposed
rules on July 3, 2013. The Board chose to revise and re-file its rules
after receiving public input at five public hearings across Washington.
“These
rules fulfill the public expectation of creating a tightly-regulated
and controlled system while providing reasonable access to participation
in the market, said Board Chair Sharon Foster. “Importantly, we believe
these rules meet the eight federal government enforcement priorities
within Thursday’s guidance memo from the Department of Justice.”
Key Public Safety Elements
Public safety is the top priority of the Washington State Liquor Control Board.
· All grows must meet strictly controlled on-site security requirements;
· Strict surveillance and transportation requirements;
· Robust traceability software system that will track inventory from start to sale;
· Criminal background checks on all license applicants;
· Tough penalty guidelines for public safety violations including loss of license;
· Restricting certain advertising that may be targeted at children.
Key Consumer Safety Elements
The proposed rules provide a heightened level of consumer safety that has not existed previously.
· Packaging and label requirements including dosage and warnings;
· Child-resistant packaging for marijuana in solid and liquid forms;
· Only lab tested and approved products will be available;
· Defined serving sizes and package limits on marijuana in solid form;
· Store signage requirements to educate customers.
Revisions to the Rules
Below are selected highlights found in the revised rules.
Production Limits
· Limits the total amount of marijuana to be produced at 40 metric tons
· Sets the maximum amount of space for marijuana production at two million square feet
Production Tiers
· Creates three production tiers based on square footage
o Tier 1 – less than 2000 square feet
o Tier 2 – 2000 to 10,000 square feet
o Tier 3 – 10,000 to 30,000 square feet
Market Control Limits
· Limited any entity and/or principals within any entity to three producer or processor licenses
· Limited
any principal and or entity to no more than three retail licenses with
no multiple location licensee allowed more than 33 percent of the
allowed licenses in any county or city
On-Site Product Limits
· Established
the maximum amount of marijuana allowed on a producer licensee’s
premises at any time based on the type of grow operation (indoor,
outdoor, greenhouse)
1,000 Foot Buffer Measurement
· Changed
the way the 1,000 foot buffer is measured from to “along the most
direct route over or across established public walks, streets, or other
public passageway between the proposed building/business locations to
the perimeter of the grounds of the entities listed”
Definitions
· Added
a definition for “plant canopy” to clarify what area is considered in
the square footage calculation for marijuana producers
· Revised
the definition of “Public Park” to include parks owned or managed by a
metropolitan park district. Clarified that trails are not included in
the definition of “Public Park ”
· Revised
the definition of “recreation center or facility.” Added the language
“owned and/or managed by a charitable non-profit organization, city,
county, state, or federal government”
Advertising
· Added
language requiring all advertising and labels of useable marijuana and
marijuana infused products may not contain any statement or illustration
that is false or misleading.
Retail Stores
In
addition to the revisions to the rules, the Board today also identified
the number and allocation of retail stores. Per Initiative 502, the
WSLCB applied a method that allocates retail store locations using
Office of Financial Management (OFM) population with a cap on the number
of retail stores per county.
Using
OFM population data as well as adult consumption data supplied by the
state’s marijuana consultant – BOTEC Analysis Corporation -- the Board
allocated a maximum of 334 outlets statewide. The most populous cities
within the county are allocated a proportionate number of stores and
at-large stores available to serve other areas of the county.
Timeline
December 6, 2012 Effective date of new law
September 4, 2013 File Supplemental CR 102 with revised proposed rules
October 9, 2013 Public hearing(s) on proposed rules (time and location TBD)
October 16, 2013 Board adopts or rejects proposed rules (CR 103)
November 16, 2013 Rules become effective
November 18, 2013 Begin accepting applications for all three licenses (30-day window)
December 1, 2013 Deadline for rules to be complete (as mandated by law)
December 18, 2013 30-day window closes for producer, processor and retailer license applicationsOne or more public hearings on the proposed rules will be scheduled soon. The WSLCB will post the dates and locations on its website at www.liq.wa.gov
### bold, red, italics, underline ... jd
GobY takes Old Toby to the roof....>>>>>
04.09.13
GobY takes Old Toby to the roof....>>>>>
04.09.13
WAC 314
55 Marijuana Licenses http://www.liq.wa.gov/publications/Marijuana/I-502/small_business_impact_statement/SBEIS-10.09.13
"Take Control of MMJ" 14 min. video of your representatives at work behind closed doors. A very ugly video of Democrats vowing to throw the medical cannabis users under the bus, and to prison. A must see.
http://tvw.org/index.php?option=com_tvwplayer&eventID=2013091005#start=7586&stop=9799
For Immediate Release September 13, 2013
Board to File Single Revision to Marijuana Rules Regarding 1,000’ Buffer MeasurementEmergency rule will not affect implementation timeline
The
emergency rule will state: “The distance shall be measured as the
shortest straight line distance from the property line of the licensed
premises to the property line of the entities listed below…”
“The
current measurement mirrors the existing method of measurement between
liquor-licensed businesses and schools,” said agency director Rick
Garza. “We’ve since learned that this measurement, as it pertains to
marijuana, conflicts with federal law. Although the emergency rule won’t
be filed until October 16, it is critical that we announce our
intentions now so that potential licensees, local government and law
enforcement will have clarity and predictability going forward.” 
.jpg)
19.09.13
AK, revisited
21.09.13
\
Old Toby takes a GobY to Royal Green ... City of Tacoma and attorneys tell owners that six hundred feet is the municipal code ruling for Tacoma. Then the City states 1,000 feet is the new rule. Royal Green is closed like so many other access points, closed for any reason.
.JPG)
.JPG)
Medical Ruling, finally some sense expressed from a Court:
http://www.courts.wa.gov/opinions/pdf/870781.pdf
27.09.13
Dear Listserv subscribers,
The
State Environmental Policy Act (SEPA) provides a way to identify
possible environmental impacts that may result from government
decisions. Information provided during the SEPA review process helps
agency decision-makers, applicants and the public understand how a
proposal will affect the environment.
The
Liquor Control Board (LCB) conducted a SEPA nonproject review and filed
a checklist and determination of nonsignificance on the proposed rules
for the implementation of Initiative 502 on June 3, 2013. On September
4, 2013, the LCB filed revised rules for the implementation of I-502.
The SEPA addendum checklist and determination of nonsignificance for the
revised rules is located on our website, here.
LCB
staff will be accepting public comment on the SEPA addendum checklist
and determination of nonsignificance until October 10, 2013.
The best way to provide your input is via email at: igm@liq.wa.gov
Alternatively
Mail
SEPA
Liquor Control Board
P.O. Box 43080
Olympia, WA 98504-3080
SEPA
Liquor Control Board
P.O. Box 43080
Olympia, WA 98504-3080
Fax
360-664-9689
As always, visit our website for updates and further information. Thank you for your continued interest in I-502 implementation360-664-9689
30.09.13
AZ
07.10.13
12.10.13
AK, revisited
Alaska is close to harvest .... colors and other determinants of a certified, true Old Toby are becoming apparent ...
\
Developer puts certification on AK
Purple & Gold
Go Huskies
Old Toby and UW get it together to produce a beautiful hybrid
02.10.13 Are dispensaries Doomed?
07.10.13 Seattle City Council votes to eliminate the votes of the citizens and eliminate medical cannabis.
08.10.13 ARC, nice Ice for fun
.JPG)
.JPG)
15.10.13 GobY two-patient, thirty plants demo at the ARC
20.10.13 NPR report on State effort to eliminate Medical Cannabis
23.10.13 State tries to destroy medical cannabis
with Kavic and Gary. Note, no more film, security tape or kilobytes will be wasted on Kavic until he finishes his degree.
25.10.13
Ooooo1
25.10.13 GobY goes to AL
\
26.10.13 Uraguay's President Jose Mujica signs cannabis legalization, first country to defy US Drug War
29.10.13
Old Toby takes GobY and crew to RDR.
Pot II http://analytical360.com/m/flowers/139456
- 2.14% CBG-TOTAL
Date Tested: 11/17/2013
Test Result UID: ANL20131116F811595
HPLC Chromatograph
Potency Profile
- 1.73% CBG-A
- 0.41% CBG
- 2.14% CBG-TOTAL
- 13.76% ∆9-THC-A
- 0.59% ∆9-THC
- < 0.01% ∆8-THC
- 0.17% CBN
- 14.52% THC-TOTAL
- 0.16% CBD-A
- 0.06% CBD
- 0.22% CBD-TOTAL
- 0.13% CBC
- 1.36% ACTIVATED-TOTAL
∆9THC + ∆8THC + CBN + CBD + CBG + CBC
Cannabinoids that have been activated through decarboxylation (curing/storage of flowers, or heating/cooking of edibles, tinctures, & concentrates)
- 1.55% Linalool
- 0.58% Caryophyllene oxide
- < 0.01% Myrcene
- < 0.01% beta-Pinene
- < 0.01% Limonene
- 0.02% Terpinolene
- 0.51% alpha-Pinene
- 0.31% Humulene
- 1.57% Caryophyllene
- 4.54% TERPENE-TOTAL
Moisture Analysis - 6.70% H2O
Foreign Material Inspection
- PASS
Microbial Screen
- N/A
Pesticide Test
- N/A
- \
Same flower tested GC/MS 1.8% CBG
