Showing posts with label surgery. Show all posts
Showing posts with label surgery. Show all posts
Sunday, August 8, 2010
I'm So Glad My Wrists Hurt
People have asked me recently what actually hurts – when I say I’m having discomfort, what do I mean? Good question. It never occurred to me that one might wonder such a thing. Now that I’ve bid adieu to the majority of the pain, I’ll share with you my physical experience from the last two and a half weeks.
The first and worst symptom I felt was nausea, which is apparently typical after being under general anesthesia. I vomited twice the day after surgery. The first time was against all odds, since I hadn’t consumed anything in over 36 hours and had breathing tubes down my throat – that was a bit alarming for me but at least convinced the nurses I was ready to be extubated. The second time was after I drank my first cup of water – like magic, it was instantaneously back in my cup. I spent the next two days being as still as possible and ingesting as little as the nurses would allow. During this time, I also had the pleasure a catheter sticking out of my neck, two tubes (with diameters the size of dimes) emerging from my chest to drain fluids and four external pacing wires in case we needed to give my new heart a boost.
Once the tubes came out and the nausea subsided, the chest pain began, or at least I began to focus on it. Since a heart transplant involves a sternotomy (the sternum is cracked and propped open during surgery), one’s chest is very uncomfortable thereafter. Not only did I experience pain at the incision site, but most of my chest was also covered in tender bruises from the operation. Additionally, a patient is encouraged to breath as deeply as possible and cough as much as possible after surgery to clear the lungs of fluids, and as you might imagine, it is quite uncomfortable to do either when your chest has recently been split open and rejoined with the equivalent of the twisty ties you might use to close up a loaf of bread.
Toward the end of my hospital stay, when I had started eating more solids, I started having really bad indigestion. This is a typical side effect of the steroid I’m on. Previously I would have considered indigestion an uncomfortable nuisance, but this indigestion was quite painful. I now have much more sympathy for those who experience this regularly, as I felt like there was literally a torch burning a hole in my chest. I’ve since increased my dosage of Nexium, which has helped immensely.
My final source of discomfort is my poor wrists. I have maybe the world’s worst veins, which is problematic when undergoing a heart transplant because lots of IVs are required. In order to access my veins, nurses literally had to beat my arms on a repeated basis, which left serious bruises, a few of which are still present two and a half weeks later. The good news is I only notice my wrists hurt when none of the above [more severe] symptoms are present, so I try to be thankful for these times.
As for a status update, I continue to feel better every day. I’ve been walking up and down multiple flights of stairs for exercise the last three days and am taking longer and longer walks outside in the evenings. My last biopsy showed mild organ rejection, which we are treating with increased dosages of my immunosuppressant medications. The meds are causing headaches and numbness in my hands – a welcome substitute for organ rejection. Included are some pictures from today – starting to heal!
Labels:
CHF,
discomfort,
heart,
heart transplant,
nausea,
pain,
sternotomy,
surgery
Thursday, July 22, 2010
Day 1 as Andrea 2.0
UPDATE FROM MARG - Our dear girl continues to gain strength as she rounds out her first 24 hours post-transplant. When I spoke with her mom an hour ago, Andrea was actually sitting up in a chair! She is still very sleepy and her chest is hurting her a bit, but all things considered, great news only 24 hours after surgery. They removed her breathing tube and PICC line today (the PICC line is the one that has been delivering life-saving drugs to her since November, also the source of the twedgie), and may move her out of the ICU and into a step-down unit tomorrow.
Her family is doing great and is encouraged by the progress she has made today. Please continue to post your well-wishes as comments on this blog - I think it will give them a huge boost to see just how many people are rooting for Andrea all over the country. If you would like to send Andrea some well-wishes personally, you can send her an e-card via the hospital website - they will print it out and deliver it to her. Please keep cheering her on!
Her family is doing great and is encouraged by the progress she has made today. Please continue to post your well-wishes as comments on this blog - I think it will give them a huge boost to see just how many people are rooting for Andrea all over the country. If you would like to send Andrea some well-wishes personally, you can send her an e-card via the hospital website - they will print it out and deliver it to her. Please keep cheering her on!
Labels:
donate life,
heart failure,
heart transplant,
hospital,
organ donation,
surgery,
survival
Tuesday, May 11, 2010
Questions Anyone?
Since this whole “heart thing” began, people have asked me a lot of questions. I know many others have countless questions they haven’t even asked, probably because I rarely summon the energy to answer my phone or respond to e-mails these days – please don’t take it personally, I just spend the vast majority of my time working or sleeping. I hope you know how sincerely grateful I am for all of the positive thoughts and support, despite the crickets you sometimes hear in return. Since I can’t seem to keep up with the emails and cards and phone calls coming my way, I thought I’d address some of the frequently asked questions here.
Do you have dietary restrictions?
Yes, I am currently on a low-sodium and caffeine-free diet. I’m told I can have caffeine again once I have a new ticker, but I’m not sure about the sodium thing…I’m sort of afraid to ask!
What can I do to help?
So many people have asked what they can do, and I’m so grateful for the many offers. Besides a healthy heart (which I don’t want to take from any of you!), I don’t need a thing. I do always enjoy receiving emails and cards with your positive thoughts and well-wishes, so thank you for sending them.
When will the transplant take place?
While it would be great to have the procedure scheduled in advance, heart transplantation just doesn’t work that way. Timing is completely dependent on when a match is identified. While that could happen anytime, my money’s on June. It could be May, it could be September, but the average wait for my hospital is 1.7 months.
How many other people are awaiting hearts?
There are a total of 35 people waiting for hearts in New Jersey, which is the “universe” that I’m concerned with in terms of my wait. There are a total of 8 people (myself included) that are my status or above, have my blood type and have been listed for at least 90 days. There are only 2 females (myself included) listed with my blood type, which is a good thing since one match criterion is body size. I am the only person younger than 35 waiting for a heart in NJ (most are 50-64).
How does the process work once a match is identified?
While a lot of people seem to think doctors can store organs on ice for extended periods of time, unfortunately Encino Man was just a movie. Hearts only last for a few hours after brain death, so once a match is identified, a whirlwind of activity will begin. I’ll get a phone call and will need to report to the hospital within two hours to be prepped for surgery. At the same time, my cardiologist will travel to wherever the heart is located to evaluate it and confirm whether or not it’s a good match. Assuming it is, he will then bring the heart back to my hospital.
How long are surgery and recovery?
The surgery lasts 4-6 hours and is apparently pretty uncomplicated relative to other major operations. I’m told I can expect to feel more energized as soon as I come out of my haze and may be able to walk (albeit not far) the day after surgery. I expect to be in the hospital for 7-10 days, which seems like a blink at this point, and then will continue my recovery from home. I’m not sure how long the full recovery period will be, but I’m thinking I should be pretty normal (at least as compared to how normal I was before this all began…) after 4-6 months.
While I look forward to having the energy to e-mail and call all of my wonderful friends and family, I just don’t seem to have the bandwidth to keep up with more than a few people these days. Even when I don’t respond, please know that I so appreciate the voicemails and e-mails and cards from all of you. I hope this post helped answer some of your questions and I look forward to connecting with each of you once my energy is restored!
Do you have dietary restrictions?
Yes, I am currently on a low-sodium and caffeine-free diet. I’m told I can have caffeine again once I have a new ticker, but I’m not sure about the sodium thing…I’m sort of afraid to ask!
What can I do to help?
So many people have asked what they can do, and I’m so grateful for the many offers. Besides a healthy heart (which I don’t want to take from any of you!), I don’t need a thing. I do always enjoy receiving emails and cards with your positive thoughts and well-wishes, so thank you for sending them.
When will the transplant take place?
While it would be great to have the procedure scheduled in advance, heart transplantation just doesn’t work that way. Timing is completely dependent on when a match is identified. While that could happen anytime, my money’s on June. It could be May, it could be September, but the average wait for my hospital is 1.7 months.
How many other people are awaiting hearts?
There are a total of 35 people waiting for hearts in New Jersey, which is the “universe” that I’m concerned with in terms of my wait. There are a total of 8 people (myself included) that are my status or above, have my blood type and have been listed for at least 90 days. There are only 2 females (myself included) listed with my blood type, which is a good thing since one match criterion is body size. I am the only person younger than 35 waiting for a heart in NJ (most are 50-64).
How does the process work once a match is identified?
While a lot of people seem to think doctors can store organs on ice for extended periods of time, unfortunately Encino Man was just a movie. Hearts only last for a few hours after brain death, so once a match is identified, a whirlwind of activity will begin. I’ll get a phone call and will need to report to the hospital within two hours to be prepped for surgery. At the same time, my cardiologist will travel to wherever the heart is located to evaluate it and confirm whether or not it’s a good match. Assuming it is, he will then bring the heart back to my hospital.
How long are surgery and recovery?
The surgery lasts 4-6 hours and is apparently pretty uncomplicated relative to other major operations. I’m told I can expect to feel more energized as soon as I come out of my haze and may be able to walk (albeit not far) the day after surgery. I expect to be in the hospital for 7-10 days, which seems like a blink at this point, and then will continue my recovery from home. I’m not sure how long the full recovery period will be, but I’m thinking I should be pretty normal (at least as compared to how normal I was before this all began…) after 4-6 months.
While I look forward to having the energy to e-mail and call all of my wonderful friends and family, I just don’t seem to have the bandwidth to keep up with more than a few people these days. Even when I don’t respond, please know that I so appreciate the voicemails and e-mails and cards from all of you. I hope this post helped answer some of your questions and I look forward to connecting with each of you once my energy is restored!
Labels:
CHF,
FAQ,
heart,
heart failure,
heart transplant,
questions,
recovery,
surgery,
transplantation
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