Saved by a stranger: Meet @gerryp

2 days ago | Rosemary, Volunteer Mentor | @rosemarya | Comments (20)

Member spotlight @gerryp and his family

ROSEMARY: What brought you to Mayo Clinic Connect? 

@gerryp: I learned about Mayo Clinic Connect once I transferred my care to and became a patient of Mayo Clinic in Jacksonville, Florida. I believe that the social workers at Mayo introduced me to the site.

ROSEMARY: What motivates you to take part in the community?

@gerryp: I had a sudden onset of acute illness which upended my life. In March 2020, just as Covid was breaking, I had a gallstone attack that quickly put me into septic shock, organ failure, necrotizing pancreatitis and an extended hospitalization. I was hospitalized alone for over 3 months, without the physical presence of my wife and family due to Covid restrictions. Ultimately, I was told that the only cure from the damage done to my liver by the septic shock was a liver transplant. It was as if the rug had been pulled out from under me.

Prior to that fateful day, I had been living my best life – both personally and professionally. I had no serious illness, and I had no idea that I even had gallstones. My wife and I had been preparing for the next phase of our lives as empty nesters. Suddenly, I was fighting for my life; in fact, I’m lucky to be alive. I was in and out of the hospital for over a year, with recurring sepsis infections, while I waited for a liver transplant. Ultimately, my infectious disease doctor informed us that I was becoming increasingly antibiotic resistant, and that she was running out of antibiotics to treat my recurring infections. She said I needed an organ transplant ASAP, or I would die of infection. 

My doctor suggested that we contact Mayo Clinic Jacksonville, as my odds for transplant would be better here in Florida than they were in Massachusetts. They agreed to evaluate me, so we relocated to Jacksonville. When we arrived here, I was in a wheelchair – essentially an invalid. 

During this experience, I learned so much about my illness, suffered through so many complications, and learned multiple ways to cope with what I was going through. By participating in Mayo Clinic Connect, I am trying to pay it forward – to provide hope and some perspective for those members going through their own health crises. Plus, I always feel that I can learn something more from many of the posts and comments that people en

ROSEMARY: What about Mayo Clinic Connect makes you feel comfortable to share and to be open with the community?

@gerryp: Many of the people who participate on Mayo Clinic Connect are facing some of the same issues I faced – and that can be a frightening and lonely place. I have no problem offering my perspective – so that it might just provide them with information that they hadn’t thought of, or questions to ask of their medical team. I have no problem sharing my story. I hope that someone else can benefit from learning something from what I went through.

ROSEMARY: What support groups do you participate in?

@gerryp: The Transplants support group, of course, but I also follow the discussions in the  Digestive Health, Men's Health and Sleep Health support groups. I mostly post in Transplants where I can help and add value.

ROSEMARY: Tell us about a meaningful moment on Mayo Clinic Connect.

@gerryp: There have been several meaningful moments. When I first became ill, I itched terribly from head to toe. This went on for nearly 2 years. It was absolutely torture. We tried everything to relieve it and ultimately found that ice packs helped to distract my brain from the itching. Being able to share this information so that another person might benefit from what helped me is so gratifying. 

Same with music. I found that while I was hospitalized, I was often in a brain fog, as my liver was not fully functioning. Listening to music helped to calm me – and helped to pass the time. I get satisfaction from sharing with others the things that helped me cope with my illness and the knowledge that it might just help them too.

ROSEMARY: What surprised you the most about Mayo Clinic Connect?

@gerryp: How many people participate – and the fact that many of them are not Mayo patients. Members come from all over the world to learn and share.

ROSEMARY: What energizes you, or how do you find balance in your life? 

@gerryp: Going through a solid organ transplant is a life-changing event. The realization that someone died for me to live, is sobering. I have vowed to honor this gift of life. I try every day to appreciate the simple things that life provides – a beautiful sunrise or sunset, the smile and laughter of a child, the love of my wife and family. I am a lucky man. My wife is my best friend, and together we balance each other – she is the yin to my yang. I truly believe that I would not be alive but for her advocacy on my behalf. She provides both my energy and my balance. Cheers to the caregivers!

ROSEMARY: Tell us about your favorite pastime or activity.

@gerryp: Pickleball! I was so incredibly ill that I never expected to ever be healthy again. Many of my transplant friends promised me that I would, but it’s very hard to believe that it could be so. Once I was mostly recovered from the surgery, I could not believe how good I felt. I promised myself that I would do everything in my power to be as healthy as possible. 

After my first year of recovery, my wife and I took up pickleball. It’s incredibly fun, we’ve made a lot of new friends, and I enjoy being active. I also try to ride my Peloton most mornings. My handle is Sharkbite22. We borrowed the “Sharkbite” from another liver transplant recipient (with his ok). I am on a mission to maintain my good health. I find that it helps me sleep better and generally feel better.

ROSEMARY: Do you have a favorite quote, life motto or personal mantra?

@gerryp: I try everyday to follow the Golden Rule – treat people the way you would like to be treated. I just find it makes for a nicer way to live, and a nicer world.

ROSEMARY: What do you appreciate the most in your friends? 

@gerryp: Loyalty and love – just being present for us. I think most of us have no idea how many lives we have touched. The love and support that our friends provided is amazing – everything from organizing meals, to offering to take me on walks, so I could get out of the house while I waited for transplant. I was 60 years old when I got ill. I had friends from high school that put together a get-well video, complete with commentary, songs, good wishes and old photos. It was amazing. Many of these people I haven’t had contact with in over 40 years. It was almost like I had last seen them a couple of years ago. I have boxes and boxes of get-well cards and personal notes. I had friends organize prayer chains with people I had never met, praying for my recovery. Just amazing.

ROSEMARY: What food can you simply not resist? 

@gerryp: I’m Italian American. I love a good Italian meal, and any dessert made with lemons.

ROSEMARY: If Hollywood made a movie about your life, whom would you like to see cast as you?

@gerryp: George Clooney, of course. And the movie would be a hit!

ROSEMARY: What do you love about where you live or vacation?

@gerryp: We relocated to Jacksonville, Florida before my transplant. Once we arrived here and saw how beautiful it is (and how much warmer) than New England – I decided there was no way I was returning to the cold, dark of another winter in Boston. I like to say that I never expected to ever live in Florida, but it wasn’t my choice. It picked us, and I am forever grateful.

ROSEMARY: Anything else you’d like to share?

@gerryp: In my quest to help people, I’ve been lucky to have been featured in a news story by Mayo Clinic and interviewed in a podcast for NPR. I’d like to share these too:

Member Spotlights feature interviews with fellow Connect members. Learn more about members you’ve connected with and some you haven’t met yet. Nominate a member you think should share the spotlight.

See more Member Spotlights.

Interested in more newsfeed posts like this? Go to the About Connect: Who, What & Why blog.

@auntieoakley

Thank you for sharing your story. I can’t tell you what it means for those of us that have made the decision to share our family members in this way.
I have always chosen not to know if and where organs go, in this way I can always assume the best. But it really, truly touches me to hear stories like yours.
Thank you for joining connect and being there for others. Whenever I need a boost, I know I can read from you or Rosemary or the host of others and feel close to my own family. ❣️

Jump to this post

Thank you Chris. And thanks to you and your family for making that decision for the good of patients like me. I don’t know very much about my donor, but I would not be alive but for them. When I was waiting for transplant those nearly 2 years - suspended between life and death - I was haunted by the realization that someone’s life had to end in order for me to live. Every one of my transplant friends suffers from this. But a chaplain at Mayo helped to set me straight. He said that life is like a relay race, and that my donor’s purpose here on Earth was fulfilled - and that they were handing me what I needed to fulfill my purpose - whatever it may be. I work everyday to honor my donor and find my purpose. This was one of the reasons why I started volunteering on the transplant floor and why I take every opportunity to act as an advocate for organ donation. That work has become a part of my purpose here on Earth.💕

REPLY
@hopeful33250

Hello @gerryp,

I so admire the story of transplant patients. Whenever I read a post from a transplant patient, I always find it so uplifting to think about how ill they were prior to transplant and then how appreciative they are after their surgery. Your Spotlight really demonstrates this truth.

Thank you for sharing your experiences with others. I know that everyone who reads your story will find it encouraging! I am glad that you found Connect and that you are actively sharing with all of us.

Jump to this post

Thanks Teresa. Yes, I was incredibly ill prior to transplant and quite honestly never believed that I would ever be healthy again. So I pinch myself - even after 5 years of the onset of illness- amazed at my good fortune - and so thankful that we live in a time where these kinds of miracles can happen. Happy to be part of the Connect community.

REPLY

What a wonderful story to read. Optimism and love all around you through those 2years. A medical team that did not give-up and you and your team did not give up. Six no go transplants before the winning 7th. Being a bone marrow transplant patient, I know my donor remains alive. I was a platelet donor for 25 years, never thinking my blood would be the problem down the road. I never met my donor, but it has only been 1 year.
I love seeing these interviews on Mayo. I was not a patient here, but I found support from people who had transplants before me. Exactly what you wrote. The truth is shared here through our experiences. Your post of a life well lived post-transplant is why your donor's gift is such a testament that walking through the process just may lead to a life you never dreamed of. What a blessing. You and your donor.

REPLY

@gerryp, greetings from Little Rock!
What an inspiring story. I love your positivity. Pickle ball looks like so much fun. I had my second hip replacement a couple of months ago and I’m looking forward to better mobility.
I’m sure you have inspired many people on Connect as you’ve beautifully acknowledged those who have helped you throughout your illness and recovery. It’s the reciprocity that is healing, I think.Congratulations on feeling well again!

REPLY

@gerryp
Welcome to one of the most excellent care facilities in the world. I have been a patient of Mayo Clinic Jacksonville since 2006.

I used to live in Vero Beach about 3.5 hours from Mayo. I had been driving back and forth after I got a second opinon there for heart failure and ICD/Pacemaker. I decided in 2015 to move to Ponte Vedra just south of Mayo Clinic at a Del Webb. My commute changed from 3.5 hours to 25 minutes. Now if Mayo Jacksonville could just improve their parking.

When I first came to Mayo in 2006 theres was no hospitial or all those buildings there now. The only buidling was the Davis building. You can see what I have seen it such a dramatic increase in facilities at Mayo Jacksonville.

My wife became a diabetic 1.5 and is treated there also. She has had 3 stomach surgeries, ENT surgery, and now waiting for an eye surgery. I am on my 3rd ICD/Pacemaker and treated by a world reknown EP Dr. Kusumoto. My heart failure doctor and quite frankly all my medical providers are outstanding and follow the Mayo motto of "Patient First."

REPLY

Thank you for sharing your journey Gerry. You encourage more people than you realize. I have seen your posts here on Connect in the past, and they helped me get through my struggles leading up to my transplant last year. "Gerry did this-I can do this"-and I did. Thank you.
side note-where did you get the great hoodies?

REPLY
@katgob

What a wonderful story to read. Optimism and love all around you through those 2years. A medical team that did not give-up and you and your team did not give up. Six no go transplants before the winning 7th. Being a bone marrow transplant patient, I know my donor remains alive. I was a platelet donor for 25 years, never thinking my blood would be the problem down the road. I never met my donor, but it has only been 1 year.
I love seeing these interviews on Mayo. I was not a patient here, but I found support from people who had transplants before me. Exactly what you wrote. The truth is shared here through our experiences. Your post of a life well lived post-transplant is why your donor's gift is such a testament that walking through the process just may lead to a life you never dreamed of. What a blessing. You and your donor.

Jump to this post

Thank you. I think so many of us take our good health for granted. I know I did - until I didn’t have it anymore. I recognized fairly early on that the only way out of the mess I found myself in - was to go through the fire - the transplant process - even though I never, ever expected to be in the position of needing an organ transplant. But I did not do it alone. My wife and kids, extended family, friends and even strangers helped to push & pull me along. And of course, my medical team both at MGH and Mayo. It wasn’t always easy - but the outcome has been better than I could have ever imagined. And yes, my life on the other side is something I never expected. Living in Florida? Never in my thoughts, but yet here I am and I LOVE IT. I have lived to welcome our first grandchild. Our son will be married this summer. All things I wasn’t sure that I would ever live to see. All this because a stranger said “yes” to being an organ donor. So many blessings. I count them everyday.

REPLY
@pmm

@gerryp, greetings from Little Rock!
What an inspiring story. I love your positivity. Pickle ball looks like so much fun. I had my second hip replacement a couple of months ago and I’m looking forward to better mobility.
I’m sure you have inspired many people on Connect as you’ve beautifully acknowledged those who have helped you throughout your illness and recovery. It’s the reciprocity that is healing, I think.Congratulations on feeling well again!

Jump to this post

Thank you Patty. What I try to convey by sharing my experience is that when we are faced with serious illness - we all have a choice to make. I chose to try to be positive, kind and hopeful. It wasn’t always easy - as there were many dark days. Being hospitalized alone during COVID meant that I was totally dependent on nurses, doctors and nurses aides. Treating them kindly made my time in the hospital better.
For instance, my first month at MGH - I was in a room that looked out on a brick wall - about 2ft from the window in my room. I couldn’t tell whether it was day or night. When the only room on the floor that had a window that overlooked the Charles River in Boston - opened up, my nurses rushed to make sure I got that room. I was able to watch spring turn to summer from that room, and I am forever grateful to those nurses who recognized how much I could benefit from just having a window to the outside world. I am convinced that they did this because of the way I treated them.
Pickleball is incredibly fun - but I would be careful - especially with 2 new hips!

REPLY
@jc76

@gerryp
Welcome to one of the most excellent care facilities in the world. I have been a patient of Mayo Clinic Jacksonville since 2006.

I used to live in Vero Beach about 3.5 hours from Mayo. I had been driving back and forth after I got a second opinon there for heart failure and ICD/Pacemaker. I decided in 2015 to move to Ponte Vedra just south of Mayo Clinic at a Del Webb. My commute changed from 3.5 hours to 25 minutes. Now if Mayo Jacksonville could just improve their parking.

When I first came to Mayo in 2006 theres was no hospitial or all those buildings there now. The only buidling was the Davis building. You can see what I have seen it such a dramatic increase in facilities at Mayo Jacksonville.

My wife became a diabetic 1.5 and is treated there also. She has had 3 stomach surgeries, ENT surgery, and now waiting for an eye surgery. I am on my 3rd ICD/Pacemaker and treated by a world reknown EP Dr. Kusumoto. My heart failure doctor and quite frankly all my medical providers are outstanding and follow the Mayo motto of "Patient First."

Jump to this post

Yes Mayo JAX is an amazing place. We also now live in Ponte Vedra Beach about 15mins to the Mayo. As you are certainly aware - the campus continues to expand with new buildings, added floors to the hospital and better facilities. It is truly an amazing place - and I am forever grateful that my infectious disease doctor at MGH sent us here. World class care and facilities among the best in the world. The Mayo philosophy of treating the whole patient is something that I quickly came to appreciate. The artwork, music, gardens help to restore the soul. When I was so sick and hospitalized, they would grant me “sunshine privileges” that allowed my wife to take me outside into the gardens for fresh air and sunshine.

REPLY
@lcd

Thank you for sharing your journey Gerry. You encourage more people than you realize. I have seen your posts here on Connect in the past, and they helped me get through my struggles leading up to my transplant last year. "Gerry did this-I can do this"-and I did. Thank you.
side note-where did you get the great hoodies?

Jump to this post

Congratulations Lou on your successful transplant. I am so happy to learn that I inspired you to keep up the good fight! It was not an easy road to travel - lots of potholes along the way. I certainly did not do it alone. I had a group of transplant veterans who helped pull me through. That’s why I have chosen to pay it forward - to help pull others through the lonely & frightening place they find themselves in.
The photo that you see was taken at Christmas 2022 - about 10 months post-transplant. My wife found the hoodies on the Donate Life website. Donatelifemerchandise.com. They say “Peace, Love, Joy - Donate Life”. She thinks they were a special holiday offering that year.
Wishing you continued good health.

REPLY
Please sign in or register to post a reply.