Transplant: No or Few Antibodies after COVID Vaccination
My daughter received a kidney from her father 15 months ago. She is participating in the Johns Hopkins study of transplant patients undergoing vaccination. The study required that she be tested for antibodies just before she received her second shot. The test results showed that she had no antibodies to Covid-19. I wonder if anyone else on this list is participating in the Hopkins study and can share their experience. I know the study will be asking participants to repeat the antibody test four of five more times over the year after being fully vaccinated. Thank you
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@athenalee, Congratulations on the start of a new job on Monday. I would not be surprised at all, if there are others who work there who also have immunocompromised health conditions. Hopefully they have already set an example and paved the way for a safer working environment. As a transplant recipient, they might even have questions for you about your particular needs.
Looking ahead, I see some perfect opportunities to share information about the gift of organ transplant.
@hello1234, I have 'had' to be out of my safety zone for the past year+ due to a serious medical emergency/caregiving of a family member. I have practiced all of the CDC safety recommendations, even before we had the vaccine available and with fear and anxiety. Now that I have had all of my Covid19 vaccines, and my flu vaccine, I continue to keep the same safety precautions. I am fortunate that I have not caught Covid or anything else.
As a 12 year transplant recipient, I had already learned that I have to distance, avoid people who are sick, wash hands for my own health. I think that must have helped me to be cautious during holiday celebrations, even before the Covid19 era. And my close family/friends are super vigilant about watching out for my needs.
As for restaurants, I have a 'safe' restaurant where I am comfortable. It was where my son was a GM before his serious accident/spinal cord injury last fall. I was comfortable going there because he wrote the guidelines for re-opening after the Covid closure. We choose to go at the uncrowded times - aka 'old timers hours' - between 3;'00- 5:00. This works well for any restaurant that you are comfortable with, based on your previous experience.
Only you can decide, but I have thought of some things that I would consider:
Do you know where your family will be dining on Thanksgiving? Have you considered doing a trial visit there so you can see first hand if the environment is comfortable to you? Have you thought about calling and speaking to the manager (non mealtime hours) about your concerns? And about seating and spacing?
Are your family members following CDC guidelines? Are the members of your family vaccinated? Do they respect your food, drink, safety needs?
@rosemarya thank you so much for your very detailed response to me!! I think my biggest concern about Thanksgiving dinner is some of my family members' occupations. All though they are all vaccinated, one of them is a high school teacher, one of them works for a high volume amusement park, etc. I just worry about asymptomatic spread. With all that said, I hate the idea of missing the family dinner. I have elderly parents that I want to bring so they can see family ( another concern!) I am trying to weigh the once in a lifetime memories against the potential risk and it's not easy. 😊
I had a severe case of covid one year ago. I had positive antibodies from it. I have gotten them checked every couple of months. I’m getting them done again on Tuesday. I have not gotten vaccinated because of neuropathy issues and religious reasons. My hematologist told me in sept that anything over 80 is considered positive. Their office, which is the largest in my area does not require people to be vaccinated to work there but they must prove every month they are positive for antibodies. So I feel very comfortable with my situation. I know natural immunity isn’t supposed to guard against different strains but I go on with my life and am doing well. I do not put myself in foolish situations though. I had a kidney transplant 7 yrs ago.
Thank you Rosemary. Fortunately, for now, anyway masks are required in public buildings. I agree that it does present an opportunity for sharing about organ transplants and donation. My job interviews were with the mayor and two department heads. As I wanted to be transparent about why I left my last position with a municipal entity, I told them about my liver disease and transplant. The mayor said a good friend of hers is a kidney transplant recipient. It resulted in a positive conversation and I even mentioned our culinary arts webinars, So, this is good, as I work directly under her.
Way to testify and share!
Hello @banksnc49 I would love to hear a more about your experience as a kidney transplant patient with severe covid! (I am a kidney transplant patient too). Were you hospitalized? Your symptoms, your treatments, how long did it last,?
how are you feeling now? Thank you so much for anything you can share!
I’m sorry you had Covid Nancy, but glad you developed antibodies. I did get vaccinated, but because my autoimmune caused neuropathy increased after both shots, I’m not, at this time anyway, getting a booster. My neurologist said that due to the autoimmune diseases I have, the vaccine probably triggered a spike in my neuropathy. I’ve not had my antibodies checked, but given the John Hopkins research I’m doubtful I’ve got many. I remain vigilant in masking and social distancing.
Weee, good luck on Monday, Athena, though you won’t need luck. You’d be a asset to any team! ☺️
Being transparent with your transplant story was a great way to open doors for conversation. It might even help with the masking and avoidance of uncomfortable situations in the future. We shouldn’t have to justify why we push to wear masks or take extra precautions but sometimes it’s just easier.
Of course we’ll all be waiting for a report of the first day. 😉
Thanks Lori. There is value in bringing awareness to people as I think few realize how many immunocompromised people there are and the everyday dangers we face due to this ignorance. Which is not to place blame just on individuals, but more on society for the way people are valued.
I’ve always felt I was a very conscious person about the challenges people face, but I’ve certainly learned a lot more having liver disease and a transplant in the middle of a pandemic!