Coupling

Kopling

I want you back again at me, but all the guns will be possible and will never happen a second time. couple of days you want to go, and you are going to ninggalin me for all time. guns and you may return to Subang CITY, and you will stay there. but the heart can not possibly be lying, because inside I was the deepest I still love you and I do not want you to go lef me. These last words for you "keep yourselves well, the health conscious. I hope you get your dream girl, even though I cried and screamed. I love you, only you who is in our hearts forever". Achoenbudax Ajigalways

I want you back again at me, but all the guns will be possible and will never happen a second time. couple of days you want to go, and you are going to ninggalin me for all time. guns and you may return to Subang CITY, and you will stay there. but the heart can not possibly be lying, because inside I was the deepest I still love you and I do not want you to go lef me. These last words for you "keep yourselves well, the health conscious. I hope you get your dream girl, even though I cried and screamed. I love you, only you who is in our hearts forever". Achoenbudax Ajigalways

My Dearest , How are you doing?i am glad to here from you honey,My dearest i want to let you to know that When we meet someone who is perfect, that we love at the right time, in the right place and at the right time. It is an opportunity. When you meet someone you're interested. It's not a choice. It is an opportunity.Always together / meet in a moment (and many couples who invented because of this) is not an option. It is an opportunity. The difference is what happens after wards.When are you going to bring a sense of love, like, blowing attraction to the next level? When the then common sense back to playing, we'll sit down and contemplate whether you want to continue that relationship or let go. If you choose to love someone, even with its shortcomings, it is not a chance. That is the choice. When you choose to be with someone, do not care about is the choice but what love means in life, Although you know many people out there who are more attractive, smarter, and richer than your mate, and yes, you decide to still love your partner is. That is the choice. Love, love, attraction comes to us from the opportunity. But true love is truly a choice. A choice we make. In regards to soul mates or life partner, there is a lovely quote from a wise man:"Fate brings you to be together, but to remain together until the end of it all depends on you." I believe that soul mates really exist. That there is someone made for you. But it still depends on you to make these choices, whether you're going to do it or not. We might find our true friends with the opportunities that exist, but to love and be together with our soul mates, it is still our choice to make it happen. We came into this world not to find the perfect person to love ...But to learn, how to love an imperfect person perfectly ... honey i so much love you and i miss you so much and want you to have my kiss on you lips muuuuuaaahhh with love and care Patrick D Richards 9 April Patrick D Richards Hello honey.... how are you doing? why you never reply my message? you keep me waiting and worried

mp to: navigation, search For other uses, see Gang bang (disambiguation). This article needs additional citations for verification. Please help improve this article by adding citations to reliable sources. Unsourced material may be challenged and removed. (June 2011) MFM threesome Double penetration is popular during some gang bangs. Ancient art, Rim of an Attic red-figure kylix, c. 510 BC. A Gang bang is a situation in which one person engages in sex acts with several individuals at the same time. Normally there is a single individual who is the central focus of the sexual activity, e.g. one woman surrounded by several men. Rather than serial couplings by two people, the gang bang is defined by the number and simultaneity of the various sex acts such as oral sex, anal sex or double penetration. Gang bangs are not defined by the precise number of participants but usually involve more than three people and may involve a dozen or more. When the gang bang is organized specifically to culminate with the (near) simultaneous or rapid serial ejaculations of all male participants on the woman (or central man), then it may be referred to by the Japanese term Bukkake. By contrast, three people engaged in sex is normally referred to as a threesome, and four people are normally referred to as a foursome. Gang bangs also differ from group sex, such as threesomes and foursomes, in that most (if not all) sexual acts are centered on or performed with just the central person.[1] Although the participants of a gang bang may know each other, the spontaneity and anonymity of participants is often part of the attraction. Additionally the other participants normally do not engage in sex acts with each other, but may stand nearby and masturbate while waiting for an opportunity to engage in sex. Gang bangs are not synonymous with gang rape because all sexual activity is consensual and is often organized and orchestrated by a partner. Contents [hide] 1 Modern practice 2 Boybang 3 Pornography 4 See also 5 References 6 External links [edit] Modern practice A limited study by Joan and Dwight Dixon indicate that a number of women engage in gang bang occasions. The study indicates that 92% of women who engage in gang bangs are in a committed relationship, that in 76% of gang bangs the woman's partner is present and that in 55% of gang bangs the partner makes the arrangements for the gang bang. The study also indicates that 42% of women have their gang bangs always videotaped and another 42% have theirs sometimes videotaped. The study also suggests that first gangbanging experiences shows that the most usual factor involved was a male partner who suggested it, encouraged it, and often instigated it. This was done in a few cases by the male partner offering the woman to his male friends at a party or social event of some kind.[2] [edit] Boybang The gang bang has many variants, the male version is called Boybang[3] where a man has concurrent relationships with many women. One option is that man can give a woman oral sex, give to another woman the vaginal sex and accept oral sex in the coition of a third woman, all at the same time. [edit] Pornography Main article: Gang bang pornography Though there have been pornographic films featuring gang bangs, they usually involve no more than six to twelve men; a gang bang requires a minimum of three men (two men would be considered a tag team). Starting with The World's Biggest Gangbang (1995), starring Annabel Chong and Matt Asher, the pornographic industry began producing a series of films ostensibly setting gang bang records for most consecutive sex acts by one person in a short period.[4]

Someone

Ghafur A et al. Sensitivity patterns of Gram negatives to Cefepime/tazobactam 5 J Microbiol Infect Dis www.jmidonline.org Vol 2, No 1, March 2012 Correspondence: Dr. Abdul Ghafur MD, Consultant in Infectious Diseases and Clinical Microbiology, Apollo Speciality Hospital, 320 Anna Salai, Chennai, PIN 600035, India Email: drghafur@hotmail.com Received: 07 December, 2011, Accepted: 04 March, 2012 Copyright © Journal of Microbiology and Infectious Diseases 2012, All rights reserved Journal of Microbiology and Infectious Diseases / 2012; 2 (1): 5-8 JMID doi: 10.5799/ahinjs.02.2012.01.0033 ORIGINAL ARTICLE Sensitivity pattern of Gram negative bacteria to the new β-lactam/ β-lactamase inhibitor combination: Cefepime/tazobactam Abdul Ghafur1, Ramasamy Pushparaju2, Sarathy Nalini2, Krishnamurthy Rajkumar2, Durairajan Sureshkumar1 1 Department of Infectious Diseases and Clinical Microbiology, Apollo Speciality Hospital, Chennai, South India 2 Department Microbiology, Apollo Speciality Hospital, Chennai, South India ABSTRACT Objectives: Increasing prevalence of carbapenem-resistant Gram negative bacteria has prompted researchers to explore alternative antibiotic options. Different ß-lactam/ß-lactamase inhibitor (BL/BLI) combinations are used in many countries, as a carbapenem saving strategy. The purpose of our study was to evaluate the sensitivity pattern of cefepime/ tazobactam combination in comparison to piperacillin/tazobactam, cefoperazone/sulbactam, cefepime and carbapenem agents. Materials and methods: We conducted retrospective analysis of the sensitivity pattern of Gram negative bacterial isolates in Apollo Speciality Hospital; a 300 bedded, tertiary care Oncology, Neurosurgical and Orthopaedic Centre in South India. Results: Out of the 1003 Gram negative, non-repetitive isolates collected over a period of one year; 60.5% were sensitive to piperacillin-tazobactam, 46.2% to cefepime, 80.4% to cefepime/tazobactam, 71.3% to cefoperazone-sulbactam, 79.1% to imipenem and 78.2% to meropenem. Addition of tazobactam increased the susceptibility of cefepime from 46.2% to 80.4% in gram negative isolates in general; from 34.4 to 87.9% in E. coli, from 42.3 to 81.0% to Klebsiella, from 72.0 to 81.4% in Pseudomonas and 17.2-54.5% to Acinetobacter. Conclusion: Cefepime/tazobactam provided a better invitro sensitivity profile than other BL-BLI combinations studied. This in vitro data needs to be confirmed by clinical studies. J Microbiol Infect Dis 2012; 2(1): 5-8 Key words: Cefepime/tazobactam, carbapenem sparing strategy, Gram negative resistance, BL-BLI combination. Yeni β-laktam/β-laktamaz inhibitorü kombinasyonuna Gram negatif bakterilerin duyarlılık paternleri: Sefepim/Tazobaktam ÖZET Amaç: Gram negative bakterilerde artan Karbapenem direnci araştırmacıları alternatif antibiyotik seçeneklerini araştırmaya yöneltti. Değişik ß-laktam/ß-laktamaz inhibitor (BL/BLI) kombinasyonları birçok ülkede karbapenemleri koruma stratejisi olarak kullanılmaktadır. Bu çalışmanın amacı sefepim/tazobaktam kombinasyonunun duyarlılık paternlerini araştırmak ve piperasilin/tazobaktam, sefoperazon/sulbaktam, sefepim ve karbapenem ile karşılaştırmaktır. Gereç ve yöntem: Güney Hindistan’da üçüncü basamak Onkoloji, Nöroşirurji ve Ortopedi merkezi olan Apollo İhtisas Hastanesinde Gram negative bakteri izolatlarının duyarlılık paternlerini inceleyen retrospektif bir araştırma yaptık. Bulgular: Bir yıllık sürede toplanan 1003 Gram negatif bakteri suşundan % 60,5’i piperasilin/tazobaktama, % 46,2’si sefepime, �,4’ü sefepime/tazobaktama, q,3’ü sefoperazon/sulbaktama, y,1’i imipeneme ve x,2’si meropeneme duyarlı idi. Tazobaktam eklenmesi ile sefepime olan duyarlılık, tüm gram negatif bakteriler dikkate alındığında F,2’den �,4’e; E. coli’de 4,4’den �,9’a, Klebsiella’da B,3’den �,0’e, Pseudomonas’da r,0’den �,4’e ve Acinetobacter’de ’2’den T,5’e yükseldi. Sonuç: Sefepim/tazobaktam, çalışmaya alınan diğer BL/BLI kombinasyonlarına göre daha iyi bir invitro duyarlılık profili gösterdi. Bu invitro verilerin klinik çalışmalarla teyit edilmesi gerekmektedir. Anahtar kelimeler: Sefepim/tazobaktam, karbapenem koruma stratejisi, Gram negatif direnci, BL-BLI kombinasyonu 6 Ghafur A et al. Sensitivity patterns of Gram negatives to Cefepime/tazobactam J Microbiol Infect Dis www.jmidonline.org Vol 2, No 1, March 2012 INTRODUCTION Increasing prevalence of extremely drug resistant Gram negative bacteria is a major global concern. The antibiotic pipeline against Gram negative bacteria is dry, with no new promising molecules expected to be marketed in the next couple of years. Extensive usage of carbapenem has resulted in emergence and spread of carbapenem resistant Enterobacteriaceae, Pseudomonas and Acinetobacter. Beta-lactam/beta-lactamase inhibitor (BL/BLI) combinations like piperacillintazobactam and cefoperazone-sulbactam have been extensively used in Indian subcontinent for treating moderately severe sepsis, restricting carbapenem usage to severe sepsis, to a significant extend. Increasing carbapenem resistance has prompted many experts to explore and recommend usage of non carbapenem group of drugs and combinations in many countries.1 Experts in Indian subcontinent have advocated use of BLBLI combinations in moderately severe infections due to ESBL producers.2 Such a carbapenem sparing and restriction strategy may be beneficial in reducing the carbapenem usage and carbapenem resistance rate.3,4 Even though piperacillin-tazobactam is available worldwide; cefoperazone-sulbactam, conspicuous by its absence in countries like UK and USA, has gained popularity in many countries, especially India. Coproduction of AmpC and OXA enzymes are widespread in India prompting scientists to search for combinations stable to these enzymes.5,6 Cefepime/tazobactam is a new promising combination already licensed by the drug controller general of India (DCGI) and increasingly used in Indian hospitals. Combination of a fourth generation cephalosporin with a ßlactamase inhibitor has the theoretical advantage of additional activity against AmpC and possibly OXA enzymes over a third generation cephalosporin-BLI combination.3 No significant clinical data is available on this drug and limited number of in vitro studies is published till now. A recent study has recorded good invitro activity of cefepime/tazobactam.7 The aim of our study was to analyse the antibiotic sensitivity pattern of gram negative bacteria to carbapenem and BLBLI combinations. MATERIALS AND METHODS We conducted retrospective analysis of the sensitivity pattern of 1003 Gram negative bacterial isolates in Apollo Speciality Hospital; a 300 bedded, tertiary care Oncology, Neurosurgical and Orthopaedic Centre in South India. Consecutive, non-repetitive Gram negative isolates from various specimens like blood, respiratory secretion, wound swabs and body fluids, from in patients, collected over a span of one year, from July 2010 to June 2011, were analyzed. The culture media used in our study were blood agar (incubated anaerobically if necessary), chocolate agar, CPS3 Chrom agar for urine and MacConkey agar. Bacterial identification was done using miniAPI strips - Rapid ID32E and ID32GN (bioMerieux). Susceptibility testing was performed by the disc diffusion method by the Kirby- Bauer technique according to CLSI guidelines on Muller Hinton agar.7 The isolates were tested against piperacillin-tazobactam 100/10μg, cefoperazonesulbactam 75/30 μg, cefepime 30 μg, cefepime/ tazobactam 30/10 μg, imipenem 10 μg, meropenem 10 μg and ertapenem 10 μg. While clear cut CLSI guidelines are available for the breakpoint of the most of antibiotics9; guidelines for antibiotics such as cefoperazone-sulbactam and cefepime/tazobactam are not elucidated in the current CLSI guidelines, hence the breakpoint of cefoperazone and cefepime were applied for cefoperazone/ sulbactam and cefepime/tazobactam respectively (Table 1). Antibiotic discs were obtained from BD BBL USA, Oxoid UK and HiMedia Lab India. E coli ATCC 25922 and Pseudomonas aeruginosa ATCC 27853 were used for the quality control. RESULTS Out of the 1003 Gram negative non-repetitive isolates, 607 (60.5%) were sensitive to piperacillin- tazobactam, 716 (71.3%) to cefoperazonesulbactam, and 464 (46.2%) to cefepime, 807 (80.4%) to cefepime/tazobactam, 794 (79.1%) to imipenem and 785 (78.2%) to meropenem (Table 2). Ghafur A et al. Sensitivity patterns of Gram negatives to Cefepime/tazobactam 7 J Microbiol Infect Dis www.jmidonline.org Vol 2, No 1, March 2012 Table 1. Zone Diameter Interpretive Chart - 2009 CLSI (M100 - S19) Zone Diameter (mm) Interpretive Standards Antimicrobial agent Disc potency Organisms name Resistant Intermediate Susceptible Piperacillin Tazobactam 100/10 μg Enterobacteriaceae, Acinetobacter ≤17 18 - 20 ≥21 P. aeruginosa ≤17 ≥18 Cefoperazone 75 μg Enterobacteriaceae, P. aeruginosa ≤15 16 - 20 ≥21 Cefepime 30 μg Enterobacteriaceae, Acinetobacter P. aeruginosa ≤14 15 - 17 ≥18 Imipenem 10 μg Enterobacteriaceae, Acinetobacter, P. aeruginosa ≤13 14 - 15 ≥16 Meropenem 10 μg Enterobacteriaceae, Acinetobacter, P. aeruginosa ≤13 14 - 15 ≥16 Ertapenem 10 μg Enterobacteriaceae ≤15 16 - 18 ≥19 The cefoperazone breakpoints were used to assign S-I-R categories for cefoperazone/sulbactam, since no criteria are currently provided by CLSI for interpreting susceptibility to this drug combination. Cefepime breakpoint was applied for Cefepime/tazobactam. Table 2. Antimicrobial susceptibility patterns of gram negative bacteria Microorganisms PIP/TAZ No (%) CEF No (%) CEF/TAZ No (%) CFP/SUL No (%) IMP No (%) MER No (%) ERT No (%) Total Gram Negative Bacilli (n=1003) 607 (60.5) 464 (46.2) 807 (80.4) 716 (71.3) 794 (79.1) 785 (78.2) 513 (87.6) E. coli (n=316,) 183 (57.9) 109 (34.4) 278 (87.9) 254 (80.3) 297 (93.9) 297 (93.9) 286 (90.5) K. pneumoniae (n=269) 158 (58.7) 114 (42.3) 218 (81.0) 195 (72.4) 249 (92.5) 247 (91.8) 227 (84.3) P. aeruginosa (n=308) 242 (78.5) 222 (72.0) 251 (81.4) 227 (73.7) 218 (70.7) 213 (69.1) A. baumannii (n=110) 24 (21.8) 19 (17.2) 60 (54.5) 40 (36.3) 30 (27.2) 28 (25.4) PIP/TAZ=Piperacillin/Tazobactam, CEF=Cefepime, CEF/TAZ=Cefepime/Tazobactam, CFP/SUL=Cefoperazone/Sulbactam, IMP=Imipenem, MER=Meropenem, ERT=Ertapenem (70.7%) and meropenem against 213 (69.1%) of the isolates. Multidrug resistance was most pronounced amongst the Acinetobacter with 60 (54.5%) isolates sensitive to cefepime/tazobactam, and only 30 (27.2%) sensitive to imipenem and 28 (25.4%) to meropenem. Susceptibility of the isolates was more pronounced to cefepime/ tazobactam than other BL-BLI agents. Addition of tazobactam increased the susceptibility of cefepime from 46.2% to 80.4% to gram negative isolates in general; 34.4-87.9% to E. coli, 42.3- 81% to Klebsiella, 72-81.4% to Pseudomonas and 17.2-54.5% to Acinetobacter. Enterobacteriaceae isolates had 546 (93.3%) susceptibility to imipenem, 544 (92.9%) to meropenem, 513 (87.6%) to ertapenem, and 496 (84.7%) to cefepime/tazobactam. Among the E. coli isolates, 278 (87.9%) were sensitive to cefepime/ tazobactam, 297 (93.9%) to both imipenem and meropenem and 286 (90.5%) to ertapenem. Cefepime/tazobactam retained sensitivity against 218 (81%) of Klebsiella isolates, while meropenem was active against 247 (91.8%). Cefepime/tazobactam performed well against Pseudomonas, being active against 251 (81.4%) isolates, while imipenem was active against 218 8 Ghafur A et al. Sensitivity patterns of Gram negatives to Cefepime/tazobactam J Microbiol Infect Dis www.jmidonline.org Vol 2, No 1, March 2012 DISCUSSION Piperacillin-tazobactam was active against half of the Enterobacteriaceae isolates while cefepime/ tazobactam and cefoperazone-sulbactam were active against majority of these bacteria; cefepime/tazobactam having better coverage than cefoperazone-sulbactam. Susceptibility of Pseudomonas to BL/BLI combination was better than to carbapenem. BL-BLI agents performed better than the carbapenem group against Acinetobacter; cefepime/tazobactam having a more sensitive pattern than other BL-BLI agents. Tazobactam enhanced the activity of cefepime against both Enterobacteriaceae and non-fermenter isolates. One of the main drawbacks of the study is lack of availability of MIC data. Disc susceptibility testing is not the gold standard modality of sensitivity testing and MIC distribution data if available would have increased the credibility of the data. The findings of this in-vitro study need to be confirmed by clinical trials. Our data may encourage other investigators to explore the molecule further. BL-BLI agents are not traditionally recommended for treating severe infections by ESBL producers.10 Increasing prevalence of ESBL producing organisms resulted in extensive usage of carbapenem group of antibiotics. In countries with good antibiotic policy and antibiotic stewardship, carbapenem usage is restricted in contrary to countries without a functioning antibiotic policy, where uncontrolled usage led to a scenario of alarming carbapenem resistance.4 BL/BLI combinations may receive more attention in future, as a carbapenem saving strategy. A recent metaanalysis brought out a very interesting conclusion that amoxicillin-clavulanic acid and piperacillin/tazobactam are suitable alternatives to carbapenems for treating patients with bloodstream infections due to ESBLproducing E. coli, if sensitive in vitro, especially useful as definitive therapy.1 CONCLUSION Cefepime/tazobactam combination is very promising on the sketch board, predicted to be active against ESBL, AmpC and possibly OXA enzymes and the invitro sensitivity data is in agreement with the prediction. Cefepime/tazobactam combination, if clinical studies yield a similar good result as the laboratory data; may play a significant role as a carbapenem sparing agent. Acknowledgements Funding: None Competing interests: A.G has received consultancy, advisory or lecture fees from multiple pharmaceutical companies manufacturing BL-BLI combinations and carbapenem antibiotics; R.P: None declared; S.N: None declared; K. R: None declared; D.S: None declared Ethical approval: Has received institutional ethics committee approval REFERENCES 1. Rodríguez-Baño J, Navarro MD, Retamar P, et al. β-Lactam/β- Lactam inhibitor combinations for the treatment of bacteremia due to extended-spectrum β-lactamase-producing Escherichia coli: A post hoc analysis of prospective cohorts. Clin Infect Dis 2012: 54:167-174. 2. Deshpande P, Rodrigues C, Shetty A, Kapadia F, Hegde A, Soman R. New Delhi Metallo-ß-lactamase (NDM-1) in Enterobacteriaceae: Treatment options with Carbapenems Compromised. J Assoc Physicians India 2010; 58:147-9. 3. Livermore DM ,Hope R, Mushtaq S, Warner M. Orthodox and unorthodox clavulanate combinations against extended spectrum ß lactamase producers. Clin Microbiol Infect 2008;14 Suppl 1:189-193. 4. Ghafur A, Nagvekar V, Thilakavathy S, Chandra, Gopalakrishnan R. An Indian Success story of Infection Control through Persuasive Diplomacy. Poster presented at 3rd World Healthcare Associated Infection Forum, June 2011, Annecy, France; Poster No.6. 5. Walsh TR ,Toleman MA, Jones RN. ������������������Comment on: Occurrence, prevalence and genetic environment of CTX-M ßlactamases in Enterobacteriaceae from Indian hospitals. J Antimicrob Chemother 2007; 59:799-820 6. Rajini E, Sherwal BL, Anuradha .Detection of Extended-Spectrum β-lactamases in AmpC β-lactamase-Producing Nosocomial Gram-negative Clinical Isolates from a Tertiary Care Hospital in Delhi.Indian J Pract Doctor 2008 : 4. 7. Mouton JW et al. In Vitro Activity of Cefepime alone and in combination with Tazobactam against ESBL producers. Poster session presented at ICAAC 2010, 12- 15 Sept; Boston, USA; A- 2251 8. Clinical and Laboratory Standards Institute (2009). M07-A8. Methods for dilution antimicrobial susceptibility tests for bacteria that grow aerobically; approved standard: eighth edition. Wayne, PA: CLSI. 9. Clinical and Laboratory Standards Institute (2009). M100-S19. Performance standards for antimicrobial susceptibility testing: 19th informational supplement. Wayne, PA: CLSI 10. Paterson DL, Bonomo R. Extended-spectrum beta-lactamase: a clinical update. Clin Microbiol Rev 2005; 18:657-86.

Before you travel Manado Bunaken Minahasa Highland Bitung/Lembeh Strait Tangkoko Sangihe Talaud Gorontalo/Togian Islands Travel to Philippines Flights from Manado Latest News Useful Links Contact Auf Deutsch Deutsche Fassung NORTH SULAWESI INFORMATION PAGES Manado - Bunaken - Tangkoko - Minahasa - Sangihe/Talaud - Gorontalo - Togians The Minahasa Highland If you want to explore the attraction rich Minahasa Highlands, best is to stay in Tomohon, about 25 km away from Manado. To get an idea about the many things to do in this cool, mountainous area, have a look at the homepage of the Highland Resort in Kinilow, a few km from the center of Tomohon. This is an ideal place to base yourself and explore the area, or just relax for a couple of days. It is very quiet and the cottages, made from palm wood, are spacious and comfortable. Even small things are well taken care of, the food is good and the staff friendly and helpful. All this at a very reasonable price. Recommended! Cheaper are Happy Flower Homestay (the homestay pioneer in Tomohon), Volcano Resort and Lokon Valley Homestay in Kakaskasen II. At the other end of Tomohon: Wawo Hotel and Kawanua Cottages. At the upper end of the scale is the Gardenia Highland Resort with beautiful gardens and surroundings, and excellent food!

Before you travel Manado Bunaken Minahasa Highland Bitung/Lembeh Strait Tangkoko Sangihe Talaud Gorontalo/Togian Islands Travel to Philippines Flights from Manado Latest News Useful Links Contact Auf Deutsch Deutsche Fassung

Hello again, it’s you and me Kinda always like it used to be Sippin' wine, killing time Trying to solve life’s mysteries. How’s your life, it’s been a while God it’s good to see you smile I see you reaching for your keys Looking for a reason not to leave. If you don’t know if you should stay If you don’t say what’s on your mind Baby just, breathe there’s no where else tonight we should be- You wanna make a memory. I dug up this old photograph Look at all that hair we had It’s bittersweet to hear you laugh Your phone is ringing, I don’t wanna ask. If you go now, I’ll understand If you stay, hey, I got a plan You wanna make a memory You wanna steal a piece of time You could sing a melody to me And I could write a couple lines You wanna make a memory. If you don’t know if you should stay And you don’t say what’s on your mind Baby just, breathe there’s no where else tonight we should be- You wanna make a memory You wanna steal a piece of time You could sing a melody to me And I could write a couple lines You wanna make a memory You wanna make a memory

aku syang kamu

goHello again, it’s you and me Kinda always like it used to be Sippin' wine, killing time Trying to solve life’s mysteries. How’s your life, it’s been a while God it’s good to see you smile I see you reaching for your keys Looking for a reason not to leave. If you don’t know if you should stay If you don’t say what’s on your mind Baby just, breathe there’s no where else tonight we should be- You wanna make a memory. I dug up this old photograph Look at all that hair we had It’s bittersweet to hear you laugh Your phone is ringing, I don’t wanna ask. If you go now, I’ll understand If you stay, hey, I got a plan You wanna make a memory You wanna steal a piece of time You could sing a melody to me And I could write a couple lines You wanna make a memory. If you don’t know if you should stay And you don’t say what’s on your mind Baby just, breathe there’s no where else tonight we should be- You wanna make a memory You wanna steal a piece of time You could sing a melody to me And I could write a couple lines You wanna make a memory You wanna make a memoryogle translation

mau kah kamu jadi kawanku