Holidays: Celebration or Challenge for Transplant Families
Holiday celebrations and festivities can be a challenge for transplant patients and their families. The twinkling lights and music are everywhere enticing us to get out to shop and celebrate. Soon, we will be receiving invitations to family and social gatherings with all of the special foods and beverages. It is no wonder that some of us approach the holidays with trepidation about a season that is supposed to bring joy and cheer.
How will you navigate the holidays? What are your plans?
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@dotygl Can you reach out to the patient advocate at the facility where he was? Or the social worker from his transplant team? Even though the transplant was 7 years ago, I am sure he is followed at least annually for evaluation to see how everything is going.
Any holidays or celebrations can be a challenge. We sometimes need to advocate for our own situation, to make it the best we can for ourselves. That might mean we need to stand up to those nurses and other medical professionals and demand they practice safe health practices.
Ginger
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2 ReactionsWhat a difficult road you guys are on. How difficult that must have been for the hospital staff not to mask up and then he got sick afterwards. I am glad you do get out some and I bet the mask helps prevent you from brining back something bad for him. All you can do. I am immunosuppressed on TAC and other stuff and do get out (safely) but I never had to go through what your husband did after his hospital stay. Glad he is better than he was for those four months. You sure are in a difficult season. Maybe 2026 will be a new season and with his continued not having a relapse you guys may be able to (safely) get out more. Prayers up.
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1 Reaction@craigcraig
Thanks for your caring big heart to a total stranger. I am an extrovert, healthy and feel very uncomfortable socializing even with a mask. Where we live, winter is 6 plus months long; so doing things outside like a walk, many people I know cannot do this action so I do a lot alone, it gets old. We both feel like we exist and not live life anymore. WE've had 7 yrs to figure out how to move forward. I've always been a problem solver, but the past 7 yrs has been very difficult on us both and the hospital stay a year ago really was a gut punch on how the medical staff do not truly care about my spouse transplant when we strongly asked for masking of them. I saw how I'll my spouse was for over 4 months , not worth him getting sick again. I often feel like we live in a "Twilight zone' episode b/c our life is so bizarre now. So many friends and family have walked away from us too. Thanks again for writing. I'm out of ideas.
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2 Reactions@dotygl Hi. I am so sorry for your difficult situation. And sorry things are not going well in a number of ways. It is unfortunate that his side effects are causing "a low quality of life". But I am glad you are healthy. It is so hard for caregivers. My wife LOVES to travel but outside one trip for a wedding (and 4 trips to Mayo AZ) there has been nothing since my liver transplant about 2 years ago. It may be just us but as we get older it is harder (and less enjoyable for me) to travel. I am on TAC and 10 other meds (down from 24 post transplant) but we do socialize with a mask when needed. And I am also very glad he is still standing to be with you for 7 years now with his new kidney. Hang in there. Wishing you happy and enjoyable hollidays and the very best in 2026.
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2 ReactionsOver 7 yrs ago my spouse of over 40 yrs received his kidney transplant. Due to having so many serious problems 14 months after the transplant Covid19 arrived March 2020 and since we still live to this day like the pandemic is still active. Christmas week 2024 he was battling many nonstop UTI's that antibiotics would not resolve; so 12/26/24 he was admitted to our local hospital per his nephrologist and despite telling doctors,nurses, and more to wear a mask due to his transplant; they did not. Dec 30 he came home and hours later sick and 24 hrs later I was sick and Jan 4,25 we both had COVID-19 for the first time and his UTI's continued on top of this virus to deal with through mid March 2025. My complaint letter to the hospital and state health dept stated the medical staff did nothing incorrect in not wearing masks. I am healthy and do most of the chores inside and outside because his fatigue since transplant years ago plus other problems never resolved/improved. His 2 nephrologists know all about his decline 'with ' the donated organ which functions well 'finally'; but the negative side effects of his immunosuppressants is his primary reason for low quality of life still. They won't alter his meds due to how long it took for the donated kidney to function well, over a year. So we are home for all holidays and nothing is what we thought it would be like after his transplant. It is with huge dismay we feel strongly the need to protect his health living isolated in our 'snowglobe' at home. We used to be very outgoing and social, but the past 7 yrs not at all. In closing, I hope your holidays are enjoyable.
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2 Reactions@chickytina My wife and I do the same. Sometimes go to church live and see friends and sometimes live on the internet. Comfy from home. But we go on Saturday night service not Sunday. One of us , I won't say who , (ok it's me (---: ) likes to watch football on Sundays. Hope everyone on this thread has a Merry Christmas or Happy Holidays.
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2 Reactions@rosemarya I attend church via zoom. I am nice and comfortable on my couch unmasked with no worries. I attend every weekend and for special occasions all via zoom.
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4 Reactions@rosemarya thank you have a Merry Christmas and stay healthy we all stick together sharing our experiences and it’s a life changing road and I love that this forum exists for future patients to learn about our journey
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3 Reactions@danab
This is a great suggestion! I am so happy that you have such thoughtful friends and family that are willing to accommodate your adaptations.
I wish for you and your family to enjoy a Blessed Christmas and a Healthy New Year!
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4 Reactions@pgruetz
I'm sure that was a difficult decision for you to decline the holiday event at your mother's home. For us transplant recipients, it is something that we learn to do. We learn to be selective because we understand the consequences connected with getting sick.
I'm ready to celebrate my 16th Christmas with my Liver/Kidney transplant. I remain vigilant, and like you, have declined invitations that I really would have enjoyed attending. However, I am healthy and happy to be alive, even with our smaller events!
Today I'm preparing some special recipes for Christmas with my husband one of our sons. And tomorrow we will attend Mass together. I usually have a special seat near the piano/organ and away from the congregation, however I'm taking some time off and not playing my violin. I will sit with my guys in a regular pew. I am a bit nervous because of the Christmas crowd, but I will wear my mask, choose a seat on the aisle, and be ready to move to a space in a doorway if I feel the need.
I hope that you enjoy a very Merry Christmas and a Happy Healthy New Year!
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5 Reactions