Mayo Clinic Connect
Thank you, Mayo Clinic!
Liked by cehunt57, jerrydrennan, Ginger, Volunteer Mentor
I invite you to click, read, and share your experience- or – just say "Hi" .
Liked by Tony Hart, Champion Specialist, cehunt57, Ginger, Volunteer Mentor
I am one of the 20,000 transplants at Mayo Rochester! So grateful for the whole transplant team and all the staff! 9 years and still going strong.
Liked by Tony Hart, Champion Specialist, Rosemary, Volunteer Mentor, cehunt57, Ginger, Volunteer Mentor
My husband was liver transplant number 3013 at Mayo Rochester! 🙂
Liked by Tony Hart, Champion Specialist, Rosemary, Volunteer Mentor, JK, Alumna Mentor, cehunt57 ... see all
I'm am also one of the 20,000 from Mayo, Rochester I had my heart transplant nine years ago on January 20th of 2011 and am now nines out and still doing great
Liked by Rosemary, Volunteer Mentor, JK, Alumna Mentor, cehunt57, Ginger, Volunteer Mentor
My combined liver and kidney transplant was the in 2009 at Mayo Rochester.
Liked by JK, Alumna Mentor, cehunt57, jerrydrennan
I have no idea what number I was, but must be fairly close to the 20000 number. Mine was Sept. 12, 2019. They seemed to have gotten pretty good at it with all the practice. 🙂
Liked by Rosemary, Volunteer Mentor, mollyv, JK, Alumna Mentor, cehunt57 ... see all
I was liver transplant number 199 in 1989. 30+ years ago at Mayo Rochester. Back then it was considered experimental.
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@seahorstmayo Congratulations on your transplant! And welcome to Mayo Connect! May I ask what you received, and how you are doing? Anything tips you would like to share with us?
Liked by Rosemary, Volunteer Mentor, Colleen Young, Connect Director, JK, Alumna Mentor, cehunt57
@vjase, Welcome to Connect. I am honored to meet you, a pioneer in the world of transplantation. I bet you have seen and experienced many changes and advancements throughout your transplant life.
I would like to say thank you, for your part in being a patient and for blazing the trail for all of us who are able to follow in your footsteps.
vjase, What advice would you offer to a patient who is just beginning their own transplant journey?
Liked by JK, Alumna Mentor, cehunt57, jerrydrennan, Ginger, Volunteer Mentor
@seahorstmayo and everyone – if you were transplanted prior to February 10, 2020, you WERE one of the 20,000!
Liked by Rosemary, Volunteer Mentor, JK, Alumna Mentor, cehunt57, jerrydrennan ... see all
First of all I would like to thank you for your kind words. Like many of my fellow transplant recipients I would like to say its normal to have many fears post transplant (tests, blood work, and trepidation from a random ache or pain). I would also say to try to enjoy the great gift that you received. Always appreciate all that your caregivers have done for you and try to understand what they they went through to help you along your journey.
Liked by Rosemary, Volunteer Mentor, mollyv, cehunt57, joanaiken ... see all
@seahorstmayo, Congratulations on your recent transplant! I have to agree that Mayo is pretty good! 20,000 is a huge number of individuals.
Here is a Newsfeed post that was put together based on information shared by Connect members: Top Transplant Hacks: Patients Share Their Best Tips and Tricks.
Liked by cehunt57
I got a liver and am doing very well. Be careful after transplant, there's a lot of damage in those guys that have to heal. Don't freak out if you have a rejection, they seem to be easily overcome with the steroids they'll give you.
Liked by Rosemary, Volunteer Mentor, cehunt57, jerrydrennan, Ginger, Volunteer Mentor
The Mayo Clinic transplant team is amazing along with the entire Mayo Clinic! My brother donated his kidney to me in May 2018 and we are both doing great. I just joined this site today.
Liked by Rosemary, Volunteer Mentor, Colleen Young, Connect Director, cehunt57, jerrydrennan ... see all
@rrrowbal, I am happy to exend virtual handshake and Welcome you to Connect. I am happy for you and for your brother – donor and recipient – that is pretty special! I would love to hear more about your transplant story because your story / experience would be both supportive and reassuring to those who are just beginning their own transplanrt and living donor journey.
Here is the direct link to the Transplant Discussions. I can meet you there. Or if you need help, let me know.
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