This and That and Talk - My Transplant

@contentandwell, Good question! I can only answer that from what I have experienced.

My instructions say to call about 12 weeks in advance to set up my appointment. And there is a protocol list for tests scheduled yearly, every 2 years, 3 years, etc. As a liver/kidney recipient, I feel sure that I have some things that a 'normal' liver recipient doesn't have.
Here is what I remember having: blood draw, urine test, 24 hour urine collection, renal clearance with dye, abdominal ultrasound, echocardiogram, chest x-ray, liver transplant nurse, records update, kidney transplant nurse / medical records review, records update, dermatology, sometimes bone density scan, and annual check by liver, then kidney doctor.(I get my mammogram and pap and colonoscopy done at home), sometimes BP nurse. I also get a kidney biopsy on certain years. Additional tests can be added if there is something that comes up during the visit. And any vaccine updates are scheduled, ie pneumonia, tetanus. I know there are protocol tests, and there are individualized tests depending on each person's needs.

Jane, I think that you are in a good place for your post transplant care. It sounds to me like you are being well monitored:-)
Rosemary

This is absolutely marvelous news, @buckeyegurl! All you need to do now is think positive, take it one day at a time, and enjoy the journey. We wish you all success.

@glinda and @rosemarya

While I've never had a transplant (and have never been told that I might need one) I still love to read the Transplant discussion posts. You are all so enthusiastic and encouraging. You are just a great group of folks! Teresa

Your so welcome I always like to help and I found that my niece had alot of questions for me 2 and a half years ago when my baby sister was going thru her heart transplant and she kept asking me questions on recovery and prcedures or any questions concerning my niece I answered so if I can help I'm glad to
Glinda

@buckeyegurl, I want to echo what @glinda said about your successful recovery. Take your time to rest and recover. I don't know about the full recovery process for heart transplant, so I'm happy that you have already met Glinda.
I encourage you to take all the time you need. When you are feeling up to it, we would love to hear from you.
Gentle hugs,
Rosemary

@glinda, Thank you, for your response. As a heart transplant recipient, you are the perfect person to know what another heart transplant recipient experiences.
Rosemary

@buckeyegurl, God bless you, your donor and donor's family, your surgeons, your family, and all who have been with you on this journey!

Thank you for sharing this good news with us. We all celebrate with you as you are NOW living the new chapter of your life! I know that you intended to post December, 14, 2017:-)
Rosemary

Congratulations on our new heart I am a heart transplant myself going on 7 years the 20th of this month if you have qestions or just would like to talk please feel free to talk to me you can call me glinda I am on connect also. I go by @glinda or @tbird munchkin hope your recovery is quick
Glinda

@rosemarya , I just wanted to let you know I finally got rid of my bi VADs and was blessed to get my heart transplant! December 14, 2018! I am so happy and can’t wait to start living the next chapter in my life!

@rosemarya The transplant recipients at Mayo, when they return yearly, have a battery of tests? I will be curious next year to see what is done when I return to MGH. I had my transplant in October 2016 and saw my surgeon weekly, then monthly, then every three months, until December but other than lab tests prior to my visit there were no other tests. I did have at some point some testing to check for pulmonary hypertension (CT?) and have regular MRIs to make sure the malignancies have not spread, but that's all, no other tests. What type of tests does Mayo do yearly?
JK