COVID-19 and Transplant Patients
As a kidney transplant recipient I have been extra vigilant/worried about protecting myself as COVID-19 spreads. Like most transplant patients I am used to washing my hands, carrying hand-sanitizer, avoiding sick people, getting flu shots, etc. The COVID-19 outbreak has caused me to take additional steps to try to remain safe but I am worried for my health. I would like to hear what you are doing to stay safe and how you are feeling.
Interested in more discussions like this? Go to the Transplants Support Group.
I thought I was there but maybe not.
OK.
My family and I are practicing wide social distancing. We are only as safe as the people our families come in contact with. Only time I leave the house is for a run in the woods and with vogmask and if I see someone coming I make wide separation. I use insta cart to order groceries delivered. Have them leave groceries outside the door. It feels very similar to post transplant 2 years ago. I struggled with return of immune system and ended up in hospital once. One small positive about all this is education across society about vigorous hand washing and staying home if you are sick. Things we have already adapted to. Hope this sticks in years following this pandemic. It’s been a journey to get here and I wish everyone the best and Stay safe.
I tell my family and friends: "welcome to my world"..
Hi, I read the research paper which dated in May 2013, I am not sure if the FDA or any other institutions have confirmed the recommendation of the said study. Do you have any new article that recommends the same findings of this study? ..regards
I was diagnosed with HCC in 2015. I was told to go home and was not likely to get a transplant. I called UNOS and was advised to go to Phoenix Mayo Clinic. They were so professional and said I would be listed on 6-22-18. I am from Sparks Nevada so I rented a Condo in Scottsdale. The day I was listed I received the call from Mayo to come to the hospital for the transplant. Wow! Post transplant they discovered I had Cholangiocarcinoma as well! OMG! Thank God it was discovered by pathology post transplant or I would not have received this special gift of life. I have already beat the odds by living 6yrs. Post diagnosis. I am coming up on my 2 yr. transplant anniversary 6-23-20. I am so blessed and grateful! I won’t let this COVID-19 take me out! I see familiar posts by some of my team! Thank you all so much! I am taking care to avoid any exposure!
@zon, Welcome to Connect. I am glad that you found us in this discussion dedicated to living with COVID-19. It sounds like you have a fantastic family who has learned with you and supports you.
You mentioned running, do you encounter many other runners when you are out? I walk, and I am noticing fewer runners and walkers out and about. I wonder if some people are afraid to get out due to fear of coronavirus. Of course the weather plays a major role, too.
Hi, @jdlogan65 Welcome to Connect.
That's unbelievable that you were told you would probably not get a transplant. I presume that was by a local doctor. More and more I am convinced that if you have a medical condition beyond something very ordinary you should go to a large medical center, preferably a teaching one. They see so much more so they know much more. I was diagnosed up here in NH after a very lengthy amount of time but then was treated in Boston at Mass General. I know now that if I am not diagnosed quickly I will head to Boston.
How fortunate you were to get a transplant so soon too. I presume your MELD was already high when you were listed. Your attitude about COVID-19 is perfect. I tell my son that I am invincible because he's such a worrier!
Stay healthy and be careful.
@rosemarya We have taken to walking on our street every day that the weather makes it possible. We have always had many walkers but now it is more than ever. We all are careful of maintaining a distance from each other too.
JK
@jdlogan65, Welcome to Connect and Thank you for sharing your miracle here. You are to be commended for your proactive approach that brought you this far.
Have you seen the Transplant Discussion Group? Here is the link, is you go to it, you can scroll the list of discussion topics. I invite you (and all who see this) to join a discussion, and meet others who are sharing and asking questions about all things related to transplant.
https://connect.mayoclinic.org/group/transplants/
@zon, and all new members-
I want to let you nknow that there is a Discussion Group that is about many other Transplant topics.
https://connect.mayoclinic.org/group/transplants/
I invite you to click on the following blue link, choose a topic, then post a question, comment, or a "Hi". Your experience makes each one an expert by experience. We are here to learn from each other and with each other. .