Karl Mellor's Gulf War Diary, 1991

This diary was written and drawn by Karl Mellor in 1991, during George Bush Senior's Gulf War. Born in 1953, Karl Mellor served in the Falklands in 1982 and left the army traumatised by his experiences. 'What's the opposite of a machine gun?', he asks. 'A saxophone'. Karl put down his machine gun and took up tenor sax. He can really play the thing (as he proved at the Somers Town Stop the War Saint Valentine's Day Make Love Not War party), and possesses a photo of himself with his hero and inspriation, Stan Getz. Karl can also wield pen and brush and we're delighted that he has lent us his 1991 Dairy so that we can scan it and present it here. As the horrible events of the 1991 Gulf War went by - Karl registered each stage with shocking directness, week by week, drawing, painting and letrasetting over his personal appointments and notes. He'd been under fire. He knew what this shit was about. Karl's war trauma opens a window on a landscape which teems with psychic energies, but is also cognisant of imperial greed and atrocity. Imagining the world requires uncensoring the self, letting love and anger speak, which is what Karl's art, both horn and diary, does.

We were shocked to read in Camden New Journal (18.09.03) that Karl has been evicted for racist abuse after an 18-month feud with a neighbour (we also received an anonymous e-mail saying Karl abused his dog and sold crack to kids, which we ignored because it was anonymous). We hate racism - something Karl has always said he does too. The way he played the blues so well merely seemed to underline this. We originally decided to put Karl's diary on-line because it's such a shockingly raw, graphic and personal response to the 1991 Gulf War. None of this bad news about him lessens its impact. As Helen Spandler points out in the issue of Asylum dedicated to Pete Shaughnessy (Vol 13 No 4), war isn't just about the murder, injury and devastation inflicted on poor nations; it is also about the trauma inflicted on working-class squaddies (according to Spandler, the Ministry of Defence's own figures from the 1991 Gulf War record that nearly five times as many service personnel killed themselves as died in combat, while the National Gulf Veterans and Families Association say 70% of service men who died since 1991 committed suicide). We abhor the way comfortable middle-class liberals believe that punishment of "bad" individuals can solve problems caused by structural inequalities and military violence. We also think art's purpose is to be revealing, true and unsettling rather than soothing, moral and complacent. If Karl's actions were as described - and after the Crown Court's judgement we're in no position to dispute the judgement - they were evidently destructive aberrations caused by his alcoholism, itself a product of his war trauma (we also received complaints from most of the women at his behaviour at a party following a gig at Theatro Technis). We're very sorry that Paula and Yuming Suen and their four children were harassed by Karl, but we're not responding by taking his pictures off-line: too many stories like this are hidden from view in order to present a "nice" image of Britain. Her Majesty's Forces aren't "nice" for either their victims or the soldiers or for those who have to suffer from their insanity. In his diary, Karl is explicit about his personal problems with relationships and drugs: we think art should be viewed as concentrated information about society, not as a moral fable. So please view his diaries that way - and join the demondstration against troops in Iraq on 27 September!

Key: A triangle stands for a day without drink, drugs or smokes; 30 in a circle means Karl swam 30 lengths; a heart means a sexual liasion.

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Lumigan 0.3 mg /kg (n = 9) 0.6 mg/kg 7) n = 10 (n 9) 0.7 mg/kg = 8) 0.4 (n n 10 mg/kg = 9) Mice were treated once by gavage or inhalation (10-fold dilution of the drug's concentration) with following schedule: 7-day administration of saline vehicle; 9-day vehicle, gavage 3 times daily, then inhalation daily 3 d/wk for 13 mice. The doses given to mice were the following: vehicle: 2–3 mg/kg; gavage 3 times daily: 3–5 mg/kg; inhalation: 11 μΜ and 10 mg/kg. C57BL/6 mice were maintained at 25°C as previously described [15, 16]. The mice used for canada pharmacy prescription drug store present study were from strain B6 (C57BL/6.2; male; 6–12 months old). The procedure of experiment as described is presented further down in this paper. To analyze the effects of METH exposure, we analyzed the liver in three groups of rodents (n = 8 mice per group). Two groups of mice were used for the investigation of effect METH or METH-saline on the number of hepatocytes per organ. Mice in groups A and B were subcutaneously injected with 20 mg/kg of METH. Mice in group C received 30 mg/kg of METH, and mice in group C only received a gavage of METH. The mice in groups A and B were given subcutaneous injections once every other day for 13 d. Mice in group C were given one subcutaneous injection once every two days for 13 d. This experiment was designed as follows. For the first three days after starting doses, rats from groups A and C received three subcutaneous applications of saline once a day. Thus, each of the mice received drug once and then was switched to the next dosage. final dose (one per day for the next three days) was equivalent of 300 mg/kg for METH but was adjusted to account for the size of animals (e.g., for 1-m mice the dose would have been 0.5 mg/kg). After that, all mice in groups A and B did not receive any drug. The remaining mice in group C received subcutaneous injections once every week for 13 d. Thus, each mouse had to be switched a gavage every other day. We used the drug doses given to mice in groups A and B, which animals only received METH (the other group only by gavage), in our analyses of the effects METH exposure on body weight of mice exposed to a high METH concentration. In addition, to study the dose-dependent effects of METH exposure, it is important to know the specific route of administration in determining the effect of METH. For this purpose, we compared the hepatic weights of mice from a third group of mice that received gavage, and the weights of animals from two groups that received inhalation (n = 10 injections per group). As previously mentioned, rats were used as models for the METH administration experiment. Since liver weight and the number of liver cells per organ are not homologous, it is of interest to know whether these parameters are affected differently after subcutaneous or inhalation METH administration, respectively. In this case, we also wanted to know whether METH had different effects on other organs, such as liver in humans, mice, or dogs. However, it is not possible to determine directly the dosage of METH in rats without dissecting animals. Therefore, for this part of the study we determined doses of METH given Are norfloxacin and ciprofloxacin the same to mice in a second set of experiments after obtaining liver weights and numbers of cells from each subject according to the previously described protocol [16-18]. Rats were sacrificed, and the liver samples were collected for the measurements of these parameters as described above. Discussion In this study, the authors demonstrate that METH increases the body weight of mice and can induce various pathologies in the liver, leading to an overall decrease in the liver weights. authors show that METH treatment is cytotoxic and causes increased damage of hepatocytes in these mice. Moreover, METH increases the number of apoptotic cells in the livers of mice treated with a high concentration, and this has a definite toxicity. toxic effect is not related to oxidative stress. This study provides evidence that METH has some toxicity in mice by using a dose regimen that is similar to seen with humans. In contrast our previous finding that mice treated orally and chronically with METH had low mortality rates in the experiment [14], we show that a high dose (1 mg)



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