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home (current) real stories become a donor why ? approximately 86,000* people across europe are waiting for a life-saving organ transplant. 1 unfortunately, 16 of them will die today because they won’t find their match in time. 1 yet it will take you just minutes to sign-up to become an organ donor. just minutes, that could last a lifetime. please act now. please act quickly. become a donor real stories kathryn justin eunice veronica dino lisa chris lily hasan super donors you can also help by sharing our stories and film: becoming a kind of ‘super donor’ . this means you don’t just sign the register, which is the most important thing of course, but by also donating your voice and championing our cause, you help #speeddonating to save more lives. shares, likes, posts, retweets or a conversation – we are grateful for however you choose to become a super donor . reference: 1. pha europe. improving organ donation and transplant across the eu: a cross-condition campaign. available at: http://www.phaeurope.org/wp-content/uploads/ep-event-odt-report-final-3.11.2016.pdf last accessed: september 2017. *figure recorded in 2014. thank you for considering becoming a lifesaver for more information on organ donation and options for signing up, please select your country below to link externally to your local health authority. select your country denmark estonia finland germany greece republic of ireland italy latvia lithuania the netherlands norway romania sweden switzerland united kingdom don’t see your country? it’s possible you’re already opted-in (unless you chose otherwise) please contact your local health service for more information share it × submit legal terms teva pharmaceuticals europe b.v. , a company organized under the laws of the netherlands, having its registered office at piet heinkade 107, 1019 gm, amsterdam, the netherlands, www.tevapharm.com (“ teva ”, “ us ”, “ we ”, or “ our ”) maintains this website www.speeddonating.com (the “ site ”) for your personal information, education, and communication. while you should feel free to browse the site, please understand that your access to and use of the site is subject to the following terms and conditions (“ terms ”) and all applicable laws. 1. acceptance of these terms by accessing and browsing the site, you accept, without limitation or qualification, these terms. you acknowledge that any other agreements between you and teva concerning the site are superseded by these terms, to the extent they conflict with these terms. if you do not agree to these terms you may not use this site. teva may at any time revise these terms by updating this posting. you are bound by any such revisions therefore you should periodically visit this page to review the then current terms to which you are bound. 2. intellectual property rights all intellectual property, including trademarks, trade names, logos, service marks, patents, copyrights or trade secret displayed on the site (collectively the “ ip ”), including the names teva, teva transplant and speeddonating are registered and unregistered intellectual property rights of teva and others. nothing contained on the site should be construed as granting, by implication, estoppel, or otherwise, any licence or right to use any ip without the written permission of teva or such third party that may own the ip. you should assume that everything you see or read on the site is copyrighted and may not be used without the written permission of teva, except as provided in these terms or in the text on the site. images of people or places displayed on the site are either the property of, or used with permission by, teva. the use of these images by you, or anyone else authorised by you, is prohibited unless specifically permitted by these terms or as provided elsewhere on the site. any unauthorised use of the images may violate copyright laws, trade mark laws, the laws of privacy and publicity, and communications regulations and statutes. you may download material displayed on the site for non-commercial personal use only, provided you also retain all copyright and other proprietary notices contained in the materials or as specified on the site. you may not, however, distribute, modify, transmit, reuse, re-post, copy, publish, license or use the content of the site, including the text, images, audio, and video, for public or commercial purposes. 3. use of the site your use of or linking to any content on the site, except as expressly facilitated on the site and under the conditions provided in these terms, is strictly prohibited. any communication or material you transmit to the site by electronic mail or otherwise, including any data, questions, comments, suggestions, or the like is, and will be treated as, non-confidential and non-proprietary. anything you transmit or post may be used by teva or its affiliates for any purpose, including, but not limited to, reproduction, disclosure, transmission, publication, broadcast and posting. furthermore, teva is free to use any ideas, concepts, know-how, or techniques contained in any communication you send to the site for any purpose whatsoever including, but not limited to, developing, manufacturing, marketing, and selling products using such ideas, concepts, know-how, or techniques. 4. exclusions and limitation of liability whilst teva will use reasonable endeavours to correct any errors or omissions as soon as practicable once they have been brought to our attention, we do not warrant that the site will be available uninterrupted and in a fully operating condition nor that the information on and provided via the site will be free from errors or omissions. access to this site and its contents may be suspended temporarily and without notice in the case of system failure, necessary maintenance or repair or for reasons beyond teva’s control. teva maintains this site as a service to the internet community. the site has been designed to provide general information to the (healthcare) community and not information directly relating to teva and its products, nor any medical advice. it is expressly agreed that your use of the site, is not intended to be, in any way or manner, an inducement for you to prescribe, supply, administer, recommend, promote, buy or sell any particular medicinal products, including teva’s products. your use of and browsing in the site are at your own risk. neither teva nor any other party involved in creating, producing, hosting or delivering the site is liable for any direct, incidental, consequential, indirect, or punitive damages arising out your access to, or use of, the site or its contents. without limiting the foregoing, everything on the site is provided to you “as is,” without warranty of any kind, either expressed or implied, including, but not limited to the implied warranties of merchantability, fitness for a particular purpose, or non-infringement. please note that some jurisdictions may not allow the exclusion of implied warranties, so some of the above exclusions may not apply to you. check your local laws for any restrictions or limitations regarding the exclusion of implied warranties. teva assumes no responsibility, and shall not be liable for, any damages to, or viruses that may infect your computer equipment or other property on account of your access to, use of, or browsing in the site or your downloading of any materials, data, text, images, video or audio from the site. nothing in these terms and conditions shall exclude or limit teva’s liability for death or personal injury caused by its negligence or for any other damage which cannot be limited or excluded by applicable law. 5. data protection and privacy your security and privacy is very important to us. please read teva’s privacy policy for important information regarding the use of your personal data on the site and your rights in relation to this. use of cookies on the site teva uses cookies to collect information about you and store your online preferences. cookies are text files containing small amounts of information which are downloaded to your device when you visit a website. cookies are then sent back to the website when you return to it: this is useful because it allows the website to recognise your device. to find out more about cookies please visit www.allaboutcookies.org teva uses the following categories of cookies on the site: category 1: strictly necessary cookies these cookies are essential in order to enable you to move around the site and use its features. without these cookies, services you have asked for (such as remembering your login details) cannot be provided. category 2: performance cookies these cookies collect information on how people use the site. for example, teva uses these cookies to help us understand how customers arrive at the site, browse or use the site and highlight areas where we can improve areas such as navigation, user experience and marketing campaigns. all information these cookies collect is aggregated and therefore anonymous. it is only used to improve how the site works. category 3: functionality cookies these cookies remember choices you make (such as language choices). these can then be used to provide you with an experience more appropriate to your selections and to make your visits to the site more tailored. the information these cookies collect may be anonymised and they cannot track your browsing activity on other websites. category 4: targeting cookies these cookies record a user’s visit to the site, the individual pages visited and the links followed. this collection of browsing habits is used to deliver more relevant adverts to users. if you want to delete any cookies that are already on your computer, please refer to the help and support area on your internet browser for instructions on how to locate the file or directory that stores cookies. information on deleting or controlling cookies is also available at www.allaboutcookies.org . please note that by deleting our cookies (or disabling future cookies) you may not be able to access certain areas or features of the site. 6. general if any of these terms is determined to be illegal, invalid or otherwise unenforceable by reason of law then to the extent and within the jurisdiction in which that term is illegal, invalid or unenforceable, it shall be severed and deleted from these terms and the remaining terms shall survive, remain in full force and effect and continue to be binding and enforceable. these terms shall be governed by and interpreted in accordance with the laws of the netherlands. disputes arising in connection with these terms shall be subject to the exclusive jurisdiction of the courts of amsterdam, the netherlands. 7. general if you have any questions regarding these terms, please contact us at [email protected] . × the transplant patient who went on to become an athlete at 29, with no previous health conditions, chris loved two things – his son & football. then one day, which began just like any other, ended with him in hospital fighting for his life, chris began to feel unwell on the football pitch. he tried to play on, but suddenly cramped up and vomited huge amounts of blood on the grass. when the ambulance arrived it became clear that he had internal bleeding losing 14 pints of blood. chris had an issue with his liver, (later diagnosed with budd-chiari, a rare condition that affects less than one in 70,000 in europe). 1 chris was told he needed a liver transplant as soon as possible. after 15 months of waiting - the call finally came through. chris will never forget that moment he heard a donor had been found. it was 12:30 in the morning and he was still up watching harry potter, his condition was affecting his body clock. chris was rushed to hospital for the second time in his life, undergoing 12 hours of surgery with 3 surgeons, in an incredibly complex operation. physiotherapists then had to teach him how to walk and sit up again. but now, he’s fully fit and feeling better than ever. he is entering the transplant games and competing in the 100m, 200m and long jump. already he has completed a 10k race and a charity run for the british lung foundation. chris is very grateful to his doctors and transplant co-ordinator. however there’s one person he would like to thank above all others, but unfortunately it’s impossible. this is, of course, the donor who was of a similar age to chris, and who gave him a future at the expense of their own. reference: orphanet. prevalence and incidence of rare diseases: bibliographic data. available at: http://www.orpha.net/orphacom/cahiers/docs/gb/prevalence_of_rare_diseases_by_alphabetical_list.pdf last accessed: september 2017. moved by chris’ story? share it × alive thanks to his brother dino was 18 and in the prime of his life when he was suddenly, and unexpectedly, diagnosed with diabetes. he’d been to the hospital for a routine check-up, completed all the standard tests and left for home as normal when his phone rang. it was the hospital telling him to come back immediately because he was suffering from kidney failure. dino’s life was turned upside down in those few seconds. the plans and goals he had for the future suddenly became mere dreams and the reality was that he could have no future at all if a donor wasn’t found quickly. but dino wasn’t alone, and his family rallied around him, offering love and care and something much greater. when dino’s brother was found to be a compatible donor, he selflessly donated his kidney. thanks to the skill of the doctors the operation was a complete success, and thanks to his brother dino could dream of the future again. he went on to compete in the british transplant games and displaying true grit, he went on to win a medal. a medal he gave away to someone he believed was much more deserving. someone who was the real hero – his brother. dino knows his story would have ended much sooner if it weren’t for the skill of the doctors, and the love of his brother, who was incredibly brave. and now, miraculously, everyday life goes on almost as normal for him. although dino’s recovery from kidney failure was remarkable, he still has diabetes and in 2011 he asked to be put on the waiting list for a new pancreas. he’s still waiting. moved by dino's story? share it × her daughter's memory lives on on december 5th, 2006, eunice received news no mother ever wants to hear. her happy, lively and loving daughter, kirstie, was involved in a road traffic accident. the medical treatment she received was second to none and the doctors and nurses worked around the clock for five days to save her. but her injuries were too severe and her life support machine was turned off just as christmas lights were being turned on across the country. but kirstie’s story doesn’t end here. although she had a rare blood type, she was able to donate her lungs, kidneys, liver and heart valves. over the years since, eunice has received letters of gratitude from the people who are alive thanks to kirstie. her heart valves have saved the lives of both a newborn baby and a two year old child. but nothing prepared her for the rush of emotions she felt when she came face to face with the man who was standing there, shaking her hand, thanks to her daughter. he was the recipient of kirstie’s kidneys and living proof of the generosity of strangers. eunice felt humbled but elated and was so pleased to meet him. eunice believes it’s good to share these moments and would always advise recipients to write letters and for donor families to read them. as a member of the organ donor committee at king's college london she tells us more could be done for these families. these mothers, fathers, brothers and sisters who have lost so much, but whose loved one has made such a difference. whether it’s a note to mark the one year anniversary of the donation or organ donation education in schools, eunice wants everyone to talk about a subject we all seem to shy away from. moved by eunice's story? share it × the youth worker whose youth was taken away from him the world is an exciting place for a 13 year old boy. and like any boy his age, hasan raced through life, living every moment to the full. but life is an unpredictable thing. and hasan’s world was about to change forever. as he was charging across the hall in pe, his thigh suddenly went completely numb and he was taken home in an ambulance. over the weeks that followed, hasan underwent a series of tests and was diagnosed with kidney failure. not the sort of thing 13 year old boy's dream of in their worst nightmares. but hasan put on a brave face and calmly accepted the fact he would need 15 glucose bags, four times a day until he was 18. at which time he was put on a dialysis machine. three years later a compatible kidney donor was found, and a week after christmas, hasan probably received one of the greatest gifts of his life. however fifteen years later hasan needed a second transplant and the generosity of his brother is the stuff of legend. when he was found to be a compatible donor, his brother offered his kidney without a second thought. but hasan was worried for his brother, and it was only after much deliberation that he finally accepted his selfless generosity. hasan doesn’t think of himself as a transplant patient. he’s a youth worker. a man who’s alive thanks to the foresight of an unknown stranger and through the love of his brother. hasan doesn’t work full time because he has a weakened immune system, but his belief in the people’s kindness and generosity is stronger than ever. moved by hasan's story? share it × not all our stories have happy endings. but with your help they might justin was diagnosed with type 1 diabetes at the age of 13, when he was diagnosed he went off the rails a bit, because he didn’t want to be different to everyone else. as a consequence, he didn’t look after himself with his diabetes condition, and sadly, this meant that he would ultimately require a kidney transplant later in life. when he was first diagnosed he recalls, there was a real lack of support for people with diabetes, compared to today. things have improved somewhat since those days, but in justin's view, there still isn’t enough support for people on dialysis. and he should know after what he's been through. on dialysis for 8 months, he described the whole process as "like hell', he also observed: it as "god's waiting room", because you would never know which patients you would see again due to them either passing away or, happily, being discharged after getting a kidney transplant. but also, justin has always tried, as far as possible, not to let his condition affect him and is grateful to his employer, who was very supportive and a "saviour", letting him work around his dialysis appointments and also reducing his responsibilities at work. by the age of 26 he was on the list for 8 months waiting for a kidney. then he got the call; he received a kidney transplant and also a pancreas transplant. the kidney transplant was a success, however the pancreas did not work. at the 1st attempt of the pancreas transplant it didn’t fill up with any blood and therefore was taken straight back out. the second attempt lasted 4 days but was then taken out. justin is currently attending a work up appointment to be put back on the list for a 3rd pancreas transplant. when he got the call it was mixed emotions for justin, he was happy, but also nervous and would not be completely happy until after the operation. at time of writing, his future is still uncertain. moved by justin's story? share it × thanks dad in september 1998, at 12 years of age, kathryn developed a rash and was initially told that she would be better in 6 weeks. however, it took 4 months to resolve and she felt ill for a long time, with joint and stomach pain, she couldn't walk or eat and drink. by november her kidney creatinine had risen and her mum and dad wanted a referral to see a specialist. this then sadly identified that kathryn was suffering from a form of kidney failure. kathryn was then sent to great ormond street where, after a kidney biopsy, kathryn was required to be put on dialysis. it didn’t look good, and over the next two to three years, her condition deteriorated. kathryn’s kidneys were now only working at 40% efficiency and she was told that in the future she would need a transplant. in 2006 her kidney function was getting progressively worse. by sept 2012 she was really struggling with infections and kathryn was drained; she couldn’t even dry her hair without getting out of breath. in may 2012, her parents were tested for organ transplant suitability, and luckily they were both a match; which is when her dad volunteered to donate one of his kidneys. but she wasn’t out of the woods yet: whilst kathryn’s dad got tested for blood, mri ultrasound and biopsies, kathryn began to get worse. she was put on emergency dialysis and her kidneys were functioning at only 4%. on the 9th may 2013 her dad donated in a life-giving operation. kathryn then spent 24hrs in intensive care but was soon on the way to recovery. now fit and healthy, kathryn became a blushing, radiant bride on august 25th 2017. and who was proudly by her side as she walked to the altar? you’ve guessed it. dad. moved by kathryn's story? share it × mother knows best about 13 years ago, lily was diagnosed with a rare kidney disease, (she’s now 29) somewhat ominously called membranoproliferative glomerulonephritis. specialists told her that the disease would either go away, or one day she might need a transplant. which came as a bit of an unwanted shock. growing up with the disease, the hospital tried her on lots of different drugs. steroids at first, then as her condition deteriorated, some newer drugs. but last year, her kidneys were only providing about 10% functionality, the meds hadn't stabilised things and she would need a transplant. “i realised that once you're a transplant patient, you're always a transplant patient, basically for the rest of your life. but i had to get used to the idea, and get on with it. though feeling pretty ropey, i carried on working full-time up until christmas last year, and my mum and my younger sister got tested to see if they were compatible donors, and luckily both were a perfect match for me. the doctors chose my mum in the end because they tend to choose the older person. that said, my mum was very insistent she was going to be the donor, there was never any question of that. (she laughs.) the op was in january this year. we had a wonderful surgeon, indeed all the transplant team, and aftercare staff were amazing. thankfully, it was a success and the kidney started working straight away. mum was out of hospital in 3 days, i was out in 5! it was wonderful.” lily was lucky, very lucky, and hammersmith renal hospital in london keep a close eye on her. she’s had some follow-up challenges of course, but her kidney function is really good, and her mum is well too; she got over her life-saving donation really quickly. and one of the many highlights? they convalesced, (and celebrated), together. moved by lily's story? share it × always thinking of others it was 9:15 pm, on a typical tuesday evening, when out-of-the blue, the phone rang. thinking nothing of it, lisa answered and was given the devastating news that her son had been badly injured in a freak hockey accident. immediately, she rushed to the club to find her devoted son, tom, lying on the pitch surrounded by medics and friends. he was flown by air ambulance to hospital where doctors and nurses fought valiantly for 24 hours to save him, but sadly tom’s injury was too severe. lisa never, ever thought anything like this would happen to her family, but tom had, in some ways prepared for the unexpected. true to his generous and caring nature, tom, as well as being a keen hockey player, had also made the forward-looking and selfless decision to sign up to the nhs organ donor register. his friends who had performed cpr on the spot had managed to keep his heart beating, which, in turn, meant tom did get his last wish. to give life to others when his own was gone. lisa is as proud of her son today as she was when he was alive. and she knows that somewhere there are people laughing and crying, running and breathing thanks to tom, and his life-changing generosity. his memory, like the people he’s helped, will live on. and whilst lisa would much rather tom was still with her, she takes comfort in the fact that in his short life he made a huge difference in the world, simply by taking a couple of minutes to sign the register and making his wishes known. which is why she is a firm believer in promoting awareness and knowledge about organ donations and knowing your next of kin’s wishes. moved by lisa's story? share it × friday 13th. the luckiest day of my life that’s how veronica describes the day of her double lung transplant. going on to say: "i wouldn't be here now without the amazing gift my donor gave me. i want to use my shiny new lungs to inspire others to be heroes – and as generous as my donor - by giving the gift of life.” veronica now works passionately as an advocate for the live life give life charity, an amazing organisation that encourages people to register as organ donors via events, activities and awareness campaigns such as ours. born with cystic fibrosis, veronica became a desperately ill young woman in her twenties, with her lungs failing, consigned to a wheelchair, and given just 2 years left to live. today, she's the living embodiment, and an energetic symbol of the miracle of organ donorship. because of the considerate and compassionate decision of one donor to put their name on the register. this one selfless act, of taking just two minutes to sign the organ donor register, can have a profound effect on the lives of many, and indeed that of their families. in veronica’s case, that life-changing moment was at 06:30am on friday 13th, when her 8 and a half hour operation began. culminating in her successful discharge from hospital one month later. pre-op, veronica had a very difficult and challenging life, not just because of her medical condition, but because of the knock on effects it caused: for example, she couldn’t live alone, she desperately wanted to enjoy the simple act of dog-walking, (which wasn’t going to happen), and indeed she hadn’t been able to work for 9 years. now, over 12 months on post-transplant, her life has improved beyond all recognition, and to veronica’s credit she’s giving back big-time via her advocacy work for her chosen organ donation charity. moved by veronica's story? share it × this campaign was funded by legal terms approval code: hq/tptp/17/0011a date of preparation: september 2017

URL analysis for speeddonating.com

https://twitter.com/intent/tweet?url=https%3a%2f%2fvimeo.com%2fspeeddatingshocker%2fspeeddatingshocker&text=www.speeddonating.com&hashtags=speeddonating%2csuperdonor
http://www.speeddonating.com
http://www.speeddonating.com/mailto:[email protected]
http://www.speeddonating.com/#partners
http://www.speeddonating.com/#home
organdonation.nhs.uk

Whois Information

Whois is a protocol that is access to registering information. You can reach when the website was registered, when it will be expire, what is contact details of the site with the following informations. In a nutshell, it includes these informations;

Domain Name: SPEEDDONATING.COM
Registry Domain ID: 2151973391_DOMAIN_COM-VRSN
Registrar WHOIS Server: whois.comlaude.com
Registrar URL: http://www.comlaude.com
Updated Date: 2017-08-09T19:26:26Z
Creation Date: 2017-08-09T19:26:25Z
Registry Expiry Date: 2018-08-09T19:26:25Z
Registrar: Nom IQ Ltd (DBA Com Laude)
Registrar IANA ID: 470
Registrar Abuse Contact Email: [email protected]
Registrar Abuse Contact Phone: +44.2074218250
Domain Status: clientDeleteProhibited https://icann.org/epp#clientDeleteProhibited
Domain Status: clientTransferProhibited https://icann.org/epp#clientTransferProhibited
Domain Status: clientUpdateProhibited https://icann.org/epp#clientUpdateProhibited
Name Server: NS3.TEVAPHARM.COM
Name Server: NS4.TEVAPHARM.COM
Name Server: NS5.TEVAPHARM.COM
DNSSEC: unsigned
URL of the ICANN Whois Inaccuracy Complaint Form: https://www.icann.org/wicf/
>>> Last update of whois database: 2018-05-08T18:53:43Z <<<

For more information on Whois status codes, please visit https://icann.org/epp

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The Registry database contains ONLY .COM, .NET, .EDU domains and
Registrars.

  REGISTRAR Nom IQ Ltd (DBA Com Laude)

SERVERS

  SERVER com.whois-servers.net

  ARGS domain =speeddonating.com

  PORT 43

  TYPE domain

DOMAIN

  NAME speeddonating.com

  CHANGED 2017-08-09

  CREATED 2017-08-09

STATUS
clientDeleteProhibited https://icann.org/epp#clientDeleteProhibited
clientTransferProhibited https://icann.org/epp#clientTransferProhibited
clientUpdateProhibited https://icann.org/epp#clientUpdateProhibited

NSERVER

  NS3.TEVAPHARM.COM 199.7.68.228

  NS4.TEVAPHARM.COM 199.7.69.228

  NS5.TEVAPHARM.COM 204.74.114.228

  REGISTERED yes

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