My fiance has worked with HIV positive patients for years. She has had many clients who after infection have gone on to get tattoos. As long as you disclose any infectious diseases (Hep C, HIV) there is no reason why you would be turned away. Any reputable tattoo parlor has steralized, sealed needles and equipment, autoclave and certificate from the Board of Health. If you follow all instructions for follow up care there should be no cause for infection or complications from the tattoo.
I am thinking about getting my daughters footprints and birthday tattooed on my chest.
I already have 5 tattoos, I always wanted more but the dialysis staff said I should wait until after transplantation. I'm heading into my 9mo post transplant and have asked my team the same question. They said it'll be fine. I want alot more. I plan on going to the same artist who did the others.
When I appoarched my doctor I told him that if he didn't think it was a good idea, I'd leave it alone. On my 1st year's anniversary, I'll be getting a new tat.
From a personal point of view I would not have a tattoo due to the risks involved with certain skin disorders and skin cancers, linked to the immunosuppression. I have always been advised against tattoos due to this reason and I have now been on immunosuppression for 23 years.
However, times have changed and the types of meds have changed a lot since my heart transplant so that is not to say that another person may have been told differently. I would suggest discussing this issue with your GP or Cardiologist as they are better qualified to say what complications, if any, could arise from having a tattoo.
I had my liver transplant in 2005 and already had a tattoo and belly button piercing. My doctors told me not to get anymore but I constantly asked them every time I had clinic. Finally I was told I could get pierced as long as it was not through cartilage, and I could get tattooed as long as I went to a shop that I knew was clean and sterile. So I now have 3 tattoos and 4 piercings (not including ears). I was glad I got the "green light". I love tattoos and I also wanted to get one to commemorate my transplant. Ha ha the only issue I have now is when I go for my MRIs and have to take out all my jewelery :)
My hubby (liver transplant 21 years ago) was told "absolutely not" about getting a tattoo. Because he's covered by the VA & they have the power to stop covering him for any disobedience, he's decided to not get the tat. I get them instead! :0) Maybe someday they'll change their minds....
Hi..I am also very interested in this topic. I am from the UK and had double lung transplant 3 years ago. Luckily, I already had 2 tattoos way before I became ill.
I have asked my doctor - and he has always said no - risk of infection from needles - and poss contracting the infection, would could get worse as we all have weak immune systems.
However, I have also read/seen quite a few people - who after transplant - DO have them - and all IS fine!! Definitely to do with hygiene and needles......maybe speak to an actual tattooist aswell - as Im sure they are used to this.
My tattoos were done at 25 and then at 28...maybe as your son is 17....I understand something he would like to do.
See what other people say too. I really want another one (symbolic of my journey) - but if the risk is higher than the outcome, I dont want to tempt life - when I have been given a gift that saved me. If you know what I mean.
Keep me posted please - will send request to add you - thanks xx
Hi. My names Rachel and I am currently 18 and wanting my own tattoo. My mom is fighting me very hard on this decision because of the risk factors. I understand that they are large if something does happen but I look at it like this. I have never been one to let my transplant control my life. Even piercing, I was a month out and had been begging my dad to let me get my ears pierced for years. The team told me they would do them in a follow-up cath. I got my second holes a year ago. I think letting your son get the tattoo is a step in allowing him to be responsible for himself and the decisions he will have to make in being a transplant. I would suggest making sure there is a definite meaning behind the tattoo he wants to get, and not just because his friends have them.
Hi, my name is Bob and I joined five minutes go. I was Googling for info on tattoos, as I had a heart/kidney transplant in February of 2010. When and if I am contacted by my donor family, I intend to get a small tattoo honoring my donor. I have not questioned my transplant team about this as yet, but our kids are stoked. They both have a ginkgo leaf tattoo in honor of their late grandmother.
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Hi,First post folks. I'll begin with quick background: My 15-year old daughter had a heart transplant 6 months ago after having severe dilated cardiomyopathy with left ventricular noncompaction (now known to be a result of a genetic mutation original to her). Anyway, transplant was at the highly acclaimed Columbia/NewYork-Presbyterian Hospital - to which we moved for waiting for the heart, transplant, and follow-up care. Now, 6 months after transplant, we moved back to our home. Our medical team has a different protocol for checking for organ rejection.Whereas NYP's protocol is cardiac biopsy every month for first year, every 2 months for second year, and every 3 months for third year, our hospital's protocol moves to every 3 months after 6 months, then every 6 months after a year and every year after 3. Bottom line- much fewer cardiac biopsies.I'm wondering if you know the different protocols in checking for solid organ rejection / heart - and how they differ from different medical…See More
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I recently injured my hand and now have to have surgery on it to repair it. They are going to be putting me out for the surgery. Now grant it, I, on a regular basis go to my transplant center for different procedures(ie;allomap, biopsies, heart caths, etc) and feel completely at ease in doing so, it has been 4.5 years since my heart transplant, Yet I have found myself with a lot of anxiety going into this surgery, one that they are putting me under, two, it is not at my transplant center but at another hospital. It is really weird that i seem to have more anxiety concerning this surgery then I did about my transplant. The faith I have been granted affords me to have confidence in my eternal destiny to be with Christ and that is what/and has guided me through my entire transplant journey. Can anybody shed some light on their experience they have had with other surgeries following transplant. With a grateful heart, JeffSee More
"Hi Phil, Before transplant I had hepatic encephalopathy which my gastroenterologists treated with medication. My reflexes were slow and my judgement was often faulty. Until the fall before my following Spring transplant these episodes were few. They…"
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I lived with stage 4 (end stage) liver disease for 15 years. The fall of 2010 was the beginning of a rapid decline. I received a transplant in May of 2011. As you know a transplant gives you a new life but does not cure the hepatitis C, it begins its damage of your new liver immediately. Thanks to the incredible staff of the Mayo Clinic Liver Department and new drugs Solvaldi and Olysio I have been virus free for over 5 months and hope that my 6 month blood test will be still be negative. Interferon and ribovarin would show no virus and then a month or so it would rear it's ugly head. I had no side effects from the two new drugs. These drugs are very very expensive but I was fortunate that Mayo knew where to go for help with these two drugs whose combined costs is $58,000 per month for 3 months. $174,000.
A group for those of us who had a liver transplant due to acute / fulminate liver failure. Here we can discuss our experience with this unexpected form of organ transplant including psychologically, physically and all else that goes with it.