FEARless: Part 2 - Shannon's Lung Transplant Journey

FEARless: Part 2 - Shannon's Lung Transplant Journey Part 2 blog of my journey battling Cystic Fibrosis and chronic rejection following a bilateral lung

06/10/2022

Hey guys!! So, Thursday was chalked FULL of chaos and unexpected adventure. :D I spent just shy of a full 12 hours at Mayo, arriving at 7am for Day #4 of my second round of Photopheresis. After receiving my treatment at the ECP lab, I went around the corner and down the hall to the outpatient infusion unit where I had my 6th consecutive month of IVIG. (Both of these treatments are to help combat my antibody mediated rejection.) This took about double the time it usually takes, as I spiked a fever and had to have my infusion paused a couple of times in hopes the Tylenol would take effect. I was also dealing with pretty severe bone pain and had to have the infusion paused once again to administer pain meds. I wasn't home for more than 3 hours that evening before finally heading into the ER as my fever would not subside. (Fevers amongst immunosuppressed patients are uncommon and can indicate a blood infection, or something else serious going on.) In addition to the fever and continued bone pain, I was also struggling with a headache, fatigue, nausea, and was feeling a bit more short of breath than usual. After being evaluated in the ER, the lung transplant team made the decision to admit overnight. I will have more information regarding my plan of care moving forward after I talk to my team and attending pulmonologist following morning rounds. Until then, If you have any questions, please do not hesitate to ask! I will be sure to keep you all in the loop. And in the meantime, happy Friday!

Hey friends!! :) Recently, several people have been checking in, asking how I am doing and curious as to why I have not ...
06/09/2022

Hey friends!! :) Recently, several people have been checking in, asking how I am doing and curious as to why I have not posted or updated my FEARless: Shannon's Lung Transplant page in SEVERAL months.
Although life has been CrAzY and a LOT has been going on with my health in recent months, I have neglected to keep you all in the loop since our move to Rochester, MN in the fall of 2021. (I know some of you weren't even aware that we had moved!)
Although stepping away from social media for a couple of seasons was something that I needed to do in order to focus on myself and balance the chaos of life, I have greatly appreciated the blessings, benefits, and connections that have come through my transplant journey page. That will always be a treasure to me.
Now that my family has moved to Minnesota and I have transferred my care to Mayo clinic in order to pursue further treatment, I felt it only right to make a new page where I have given myself the freedom to branch out (a bit more than before) with the new rollercoaster of chronic rejection and life post-transplant. I am making it a goal to be more active and responsive with this page, and I am greatly looking forward to posting frequent treatment updates, personal updates, and some of my creative/written content as well.
I would love for you to check in and follow this page if you are interested in keeping tabs on my medical adventures and life updates. (Please feel free to share things with me on this page as well.) While I am certainly excited to connect with new people, I am genuinely excited to re-connect with those of you who have been a part of my original transplant journey. Sorry I had to disappear for a while...but I am BACK IN TOWN!! (The Facebook town, that is. 😉)
Most importantly, I would like to thank you for sharing in my story.
💚💙💜💙💚🫁
LET THE FUN BEGIN!!

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