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Snapshots of hope: Life on the other side of transplant.
My husband snapped a photo of me walking on a beach this morning. I was running through the surf, picking up shells, smiling and feeling on top of the world with unabashed joy for being alive and healthy. So what?
Well, it’s a photo that wouldn’t exist if I hadn’t had a bone marrow transplant. It’s a snapshot of hope!
Three years ago today I was diagnosed with Acute Myeloid Leukemia, an aggressive blood cancer and fighting for my life. Prospects of ever being able to walk a beach again seemed beyond reach.
With a lot of chemo, I achieved remission, but my only hope for a future would be a bone marrow/stem cell transplant as the cancer would likely return. Let’s just say, that procedure isn’t a walk on the beach but it gave me a second chance at life and well worth the arduous journey it took to get here!
Along this journey, I’ve been able to help inspire and give hope to others who have faced my same battle. I’m alive, surviving and thriving because of a gift of life from my anonymous donor.
When facing a transplant, whether it’s stem cells, or a solid organ, it can be a daunting prospect. I think a gift we can give, as transplant survivors, is to share our positive transplant stories with anyone who is about to undergo the procedure or is in need of reassurance in their recovery.
Show me your Snapshot of hope! What photo do you have that wouldn’t exist without your transplant?
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Welcome, @bigjoek! Your beautiful, eloquent poem moved me to tears as I’m sure it will for others who have been gifted with a second chance at life. We don’t often get the opportunity for a do-over and to re-set our priorities. Every day, every moment is a gift to be treasured. Thank you so much for sharing with us.
I hope you’ll be a regular contributor to the transplant group. There are many here who have had liver transplants and your survival story of 32 years will be so inspiring to them and for others who are waiting to have a transplant. Congratulations on such a successful procedure!
This conversation is a good place to start sharing if you’d like:
Liver transplant - Let's support each other
https://connect.mayoclinic.org/discussion/liver-support-group/
I also see you posted about attending the transplant picnic. Have you attended in the past?
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3 ReactionsI had a life saving liver transplant at Mayo in Rochester! As life often does, I was gifted with a surprise...I became a very gifted poet! Sharing one of my many poems of gratitude because it so well fits your story!
Thank you for sharing your story, and giving me a chance to share a touch of mine!
Joe Kralicek
Mayo Liver Transplant #397
11/01/1992
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4 ReactionsMany of you have connected with @stephanierp in the Transplants Support Group. Perhaps you were someone like @jolinda who greeted, supported and encourage her when she first arrived on Mayo Clinic Connect. Or perhaps you were a grateful recipient of her experience and kindness, like @matthewmcbrien @kidneybean1 @juventus and countless others.
Today, Stephanie is the featured Member Spotlight. Get some of the background scoop about Stephanie through @rosemarya's interview. You'll learn how she found hope and help through Connect, pays it forward, as well as her passion for dance as a performer and teacher.
- Embrace the improbable: Meet @stephanierp https://connect.mayoclinic.org/blog/about-connect/newsfeed-post/embrace-the-improbable-meet-stephanierp/
Happy Spring! Happy Donate Life Month!
Happy "Time to post a Snapshot of Hope!"
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1 ReactionI am not a picture taker. I just don't get it as I try to enjoy doing things and not take pictures of doing things. And I admit to being an anomaly and intentionally marching out of step with the crowd. If I did post a picture, it would be of my heart donor's family, his mom, grandmother, brother and his new wife. We have known each other for a few years now and recently got together for a fun "new family" Saturday.
That picture, not shared as I do not have their permission to post, would definitely not have happened without the transplant.
Best always,
s!
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3 Reactions@vollenweider6154, Here is a link to a new Spotlight Interview that will interest you:
- Dancing til my feet hurt with new lungs: Meet @chickytina https://connect.mayoclinic.org/blog/about-connect/newsfeed-post/dancing-til-my-feet-hurt-with-new-lungs-meet-chickytina/
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1 ReactionThank you, @vollenweider6154. I can’t believe that today is year 5 already!! My goal in starting this discussion was to offer hope to anyone going through a transplant. So I’m happy that you’ve joined the forum.
It looks like you’ve been with us for a few months but this is your first time posting. I hope you’ve been finding your way around the support groups. We have quite a few members who have had lung transplants and doing well.
I understand being on the transplant list can take a while. If you haven’t already, this discussion is a good place to visit with other members who are also waiting. https://connect.mayoclinic.org/discussion/lung-transplants/
Sending wishes that you’ll be able to post your own snapshot of hope very soon. ☺️
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1 ReactionThank you! Your post is so encouraging. I look forward to being able to share my own snapshot of hope. I'm on the lung transplant list. I feel my situation slowly deteriorating but I remain hopeful and encouraged.
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2 Reactions@gerryp your story and picture made me cry. Congratulations to you!
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1 ReactionAww, what a beautiful baby and proud grandpa! I’m so happy for you and your family. It’s moments like this we feel the impact of just how precious life is…and to be given a second chance through a transplant, is priceless! Thank you for sharing your grandbaby and your story with us! ☺️
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