It's true.
I forgot I have a blog.
It appears this thing has been collecting dust for about 9 months. Woops? Maybe I can blame my inactivity on the Minnesota winter somehow, which seems to last about that long. In that regard, this blog has a lot in common with my grill, my shorts, my sandals, and my lawn mower.
What I definitely cannot claim is a lack of things to write about! Life has been a whirlwind since I last posted here and it's become clear to me over the past couple weeks that I've done a horrible job of keeping people important to me informed. It's easy for me to self-inflict a lot of business, and sometimes this business keeps me from the people and things that matter most. A constant struggle for me.
Anyway, I should say from the outset that I am doing well and that Beth and I feel fortunate and blessed to be exactly where we are. My health is pretty stable. The prolonged steroid use has done what prolonged steroid use does. I had a cataract removed from my left eye a couple weeks ago and will have the other eye fixed in June. Sometimes I feel like an old man but, overall, things are good.
I was recently promoted to "Research Associate" which means I'm now holding down the first real job of my life, and I love it. I work with great people and have had outstanding opportunities here. My first "major" publication will hit the presses in a couple days. It is a study I did to identify strategies to reduce hospital readmissions. I also recently completed a study of resiliency training programs and am thinking about the factors that allow individuals and communities to bounce back from the stresses and challenges of life. I am partnering with some people at Mayo to train patients to self-manage their chronic diseases and with some folks in the community to think about how one might build resilience at that level. I am in my last quarter of Master's courses and have developed skills and experience in biostatistics, secondary data analysis and meta-analytic methodologies, survey methods, the conduct of clinical trials, the practice of evidence-based medicine, qualitative methods, and dissemination and implementation research, among other things. It's all fun for me, really, but my focus is shifting mostly in the direction of dissemination and implementation of effective health interventions. I have some large scale projects on the docket which will require a good amount of traveling, but this kind of work appeases my curious nature and I'm excited to get started.
Speaking of traveling, I'll be in Miami all week for a conference presenting some of the work we've been doing in relation to communication in cancer. I will then return to celebrate two years of marriage. Beth will be traveling with me to San Diego in June where I will be presenting my readmissions work. The real vacation comes in July, though, when we take a 7 day Alaskan cruise! We can't wait.
When I'm not working or taking classes, it seems like I'm at church. Beth and I have a great community here. I sing in the choir and help with worship occasionally. Beth is really active with the children's ministry and is getting involved in a ministry for teen moms. We still have small group every Wednesday night and benefit so much from those relationships.
Okay. That's it in a nutshell. Will hopefully come up with something more substantive in the near future.
Oh! And a very Happy Mothers' Day to all moms, but especially mine.
God bless,
Aaron
I am a physician and I was diagnosed with leukemia in 2011. The whole process has taught me a lot about life and what matters in it. This is where I'll be sticking some of my thoughts and experiences in that regard.
Saturday, May 10, 2014
Sunday, August 25, 2013
The Good with The Bad
Yesterday was a rough day.
I received word in the morning that a family friend (who I suspect was about 20 years old) was killed serving in Afghanistan. Although I've been aware in principle of the fact that people are giving their lives for this country on a regular basis, this is easily the closest to home this truth has hit for me. My heart aches for the family, whom I know well.
Beth had been out of town this weekend at the wedding of one of her friends from college. She called yesterday evening to inform me of a change of plans; she needed to help drive another friend that had been attending back to Missouri. This particular friend had just received a call alerting her that her father had unexpectedly died of a massive heart attack. He was 55.
Now, I suppose I tend to think of myself as someone who has been graced with more discernment than average when it comes to coping with difficult situations like these and that I am also usually pretty good about seeking an eternal perspective and resting in the peace that comes with that. But not today. Maybe that will come, but right now I have no strength or wisdom to offer; I feel completely inadequate. I suspect there are two possible explanations for this: either (1) I am simply not in an appropriate place spiritually to know God's purpose in what has occurred or that (2) I am simply responding as the emotional, weak, and inadequate creature that I am.
In this case, there's probably truth to both explanations, but I think it raises an interesting question about the responsibility or usefulness of the Church in these sorts of situations.
There may not be a more painful experience in life than losing a child, but losing a parent before his or her time would follow somewhere close. Fortunately, in both of these cases, the individuals lost were believers. Of course, this still leaves behind two grieving families that the Church can and should reach out to in what I believe are two main ways. The first is through support (i.e. that we should offer hope, wisdom, understanding, encouragement, etc in so much as we are able). And the second, which I think we may overlook at times, is through participation. In scripture, we're told to share each other's burdens, to come along side one another and to mourn with those who mourn. There is something God-ordained about this type of activity that allows us to tap in to the maximal amount of good that can come from something bad. I think God wants all of us to grow in and through the experiences of one another. The truly amazing thing is that He's created a system (the Church) that actually permits this. The Church is supposed to be an intimate community of brothers and sisters; it's supposed to be united, to be and behave as one body. When it manifests as intended, it permits the corporate sharing of life's ups and downs with one another and ultimately reflects the love and intimacy that Christ has with us, which glorifies Him.
I'm certain the families of those lost yesterday are feeling inadequate, but maybe my feelings of inadequacy aren't entirely inappropriate. Rather, perhaps I honor their suffering and their loved ones by sharing in their pain and letting God extend its impact to my life, by letting God accomplish the maximum amount of good from this.
The Church is not as unified or as intimate as it should be, and that is just a reflection of our culture. I think God designed us to be more tightly and genuinely connected (facebook friends was not in the original plan) so that we really could be enacted upon, sharpened, and shaped as a single entity. Think about the impact that sort of reality would generate.
======================================================================
Anyway, in an effort to be efficient....let me switch gears and give an update on what Beth and I've been up to:
The hospital ministry has been more rewarding for us, I'm sure, than for anyone we've reached out to. We feel God's pleasure with it but are struggling to get "referrals." The bright spot in yesterday's gloom was the discharge of a friend with renal cell cancer. She was able to have her tumor completely taken out and I believe she should be completely cured! It was a pleasure getting to know her and her family.
Beth has to go back to school tomorrow (who's going to do all the chores around the house?!) although the kids don't actually show up until after Labor Day. I will miss having her at home. Hopefully some day I'll get a job where she doesn't have to work if she doesn't want to.
Research is going well and I love what I do and the people I work with. Truly blessed to stumble into what I'm doing. Classes are also going well but the sum of a full time job and being a full time student keeps me busier than I probably should be at times. Trying to work on a healthy balance here as the pain is mostly self-inflicted! If you're interested in thinking about the science and theory of healthcare delivery, you can read my blog post here.
And, as far as my health, it's ups and downs always. Great days alternate with not so great ones. Nothing really specific to report but prayers are always welcome. I will try to get a post up soon about the fact that I'm now 2 years post-transplant!
all for now.
I received word in the morning that a family friend (who I suspect was about 20 years old) was killed serving in Afghanistan. Although I've been aware in principle of the fact that people are giving their lives for this country on a regular basis, this is easily the closest to home this truth has hit for me. My heart aches for the family, whom I know well.
Beth had been out of town this weekend at the wedding of one of her friends from college. She called yesterday evening to inform me of a change of plans; she needed to help drive another friend that had been attending back to Missouri. This particular friend had just received a call alerting her that her father had unexpectedly died of a massive heart attack. He was 55.
Now, I suppose I tend to think of myself as someone who has been graced with more discernment than average when it comes to coping with difficult situations like these and that I am also usually pretty good about seeking an eternal perspective and resting in the peace that comes with that. But not today. Maybe that will come, but right now I have no strength or wisdom to offer; I feel completely inadequate. I suspect there are two possible explanations for this: either (1) I am simply not in an appropriate place spiritually to know God's purpose in what has occurred or that (2) I am simply responding as the emotional, weak, and inadequate creature that I am.
In this case, there's probably truth to both explanations, but I think it raises an interesting question about the responsibility or usefulness of the Church in these sorts of situations.
There may not be a more painful experience in life than losing a child, but losing a parent before his or her time would follow somewhere close. Fortunately, in both of these cases, the individuals lost were believers. Of course, this still leaves behind two grieving families that the Church can and should reach out to in what I believe are two main ways. The first is through support (i.e. that we should offer hope, wisdom, understanding, encouragement, etc in so much as we are able). And the second, which I think we may overlook at times, is through participation. In scripture, we're told to share each other's burdens, to come along side one another and to mourn with those who mourn. There is something God-ordained about this type of activity that allows us to tap in to the maximal amount of good that can come from something bad. I think God wants all of us to grow in and through the experiences of one another. The truly amazing thing is that He's created a system (the Church) that actually permits this. The Church is supposed to be an intimate community of brothers and sisters; it's supposed to be united, to be and behave as one body. When it manifests as intended, it permits the corporate sharing of life's ups and downs with one another and ultimately reflects the love and intimacy that Christ has with us, which glorifies Him.
I'm certain the families of those lost yesterday are feeling inadequate, but maybe my feelings of inadequacy aren't entirely inappropriate. Rather, perhaps I honor their suffering and their loved ones by sharing in their pain and letting God extend its impact to my life, by letting God accomplish the maximum amount of good from this.
The Church is not as unified or as intimate as it should be, and that is just a reflection of our culture. I think God designed us to be more tightly and genuinely connected (facebook friends was not in the original plan) so that we really could be enacted upon, sharpened, and shaped as a single entity. Think about the impact that sort of reality would generate.
======================================================================
Anyway, in an effort to be efficient....let me switch gears and give an update on what Beth and I've been up to:
The hospital ministry has been more rewarding for us, I'm sure, than for anyone we've reached out to. We feel God's pleasure with it but are struggling to get "referrals." The bright spot in yesterday's gloom was the discharge of a friend with renal cell cancer. She was able to have her tumor completely taken out and I believe she should be completely cured! It was a pleasure getting to know her and her family.
Beth has to go back to school tomorrow (who's going to do all the chores around the house?!) although the kids don't actually show up until after Labor Day. I will miss having her at home. Hopefully some day I'll get a job where she doesn't have to work if she doesn't want to.
Research is going well and I love what I do and the people I work with. Truly blessed to stumble into what I'm doing. Classes are also going well but the sum of a full time job and being a full time student keeps me busier than I probably should be at times. Trying to work on a healthy balance here as the pain is mostly self-inflicted! If you're interested in thinking about the science and theory of healthcare delivery, you can read my blog post here.
And, as far as my health, it's ups and downs always. Great days alternate with not so great ones. Nothing really specific to report but prayers are always welcome. I will try to get a post up soon about the fact that I'm now 2 years post-transplant!
all for now.
Monday, July 22, 2013
Healthcare That Fits
As part of my research focus, I spend a lot of time thinking about healthcare and what its purpose is. It seems to me that healthcare (and therefore health itself) is only useful insofar as it generates happiness. If being healthy (or making someone else "healthy") doesn't translate into any measurable form of improvement in the experience of life, then it doesn't really accomplish anything meaningful. Now, there are certainly situations where "enduring" good health or its necessary treatments or lifestyle changes may not bring immediate enjoyment...but, often these sorts of interventions permit the sorts of results patients want in the future--the ability to play with your grandkids, the opportunity to walk your daughter down the aisle, etc. Distinguishing these cases and indications is essential, and carefully weighing the evidence of what is and is not likely to have desired effects is central to the practice of high-quality care. Determining what fits who is one of the biggest challenges in healthcare, and it requires intimate understanding of what it is that makes our patients tick.
Americans spend more money on healthcare than anyone else in the world, but we aren't the happiest people in the world (not even by a long shot). Then again, we aren't the healthiest either. Somewhere something is getting lost in translation. Medicine doesn't fit people like it's supposed to. I think part of this stems from the fact that healthcare is slowly losing sight of its purpose.
According to the Bureau of Labor and Statistics, healthcare is a "service-providing" industry. Sometimes it seems more "goods-producing." We do not often think about health services as a resource designed to meet our needs and life desires. Who thinks of their physician in the same way they think about their auto mechanic or their hair stylist? And yet, healthcare, like these other service industries, exists to meet the needs of its consumers (i.e. the patients). But I think anyone would balk at the suggestion that their mechanic could impose whatever repairs he sees fit or that their hair stylist could simply choose a haircut that matches his or her taste without even considering the preferences of the one forced to wear it!
Minimally disruptive medicine (minimallydisruptivemedicine.org) is one part of the solution to this problem, as it strives to remove unnecessary and useless care that only adds to patient burden. It also seeks to maximize patient capacity to be well, such that simply being a patient is not the end in itself, but is a means to an end that brings value to a patient's life.
I have become increasingly familiar with the role of health or wellness coaches (and, more broadly, life coaches) can play in helping to achieve these goals. In many cases, the sort of holistic evaluation and approach to well-being that coaching can provide is of far more value than any diagnostic test or intervention traditional medicine can offer.
Case in point. My grandpa has had a number of health issues develop over the last decade or so. His prescriptions and various medical appointments and evaluations help to bring some degree of health benefit, but they do not bring happiness or any value in regards to his quality of life. Thanks to the accurate perception of concerned family members, however, he was given a couple dogs that have absolutely changed his outlook on life. They've brought meaning, joy, and purpose to his life in a way that traditional medicine never could. Identifying the things that bring meaning to patients' lives is essential to achieving the outcomes we desire. I am excited to think about this more seriously and generate more formal approaches to this type of patient assessment. I am interested in people's thoughts.
Americans spend more money on healthcare than anyone else in the world, but we aren't the happiest people in the world (not even by a long shot). Then again, we aren't the healthiest either. Somewhere something is getting lost in translation. Medicine doesn't fit people like it's supposed to. I think part of this stems from the fact that healthcare is slowly losing sight of its purpose.
According to the Bureau of Labor and Statistics, healthcare is a "service-providing" industry. Sometimes it seems more "goods-producing." We do not often think about health services as a resource designed to meet our needs and life desires. Who thinks of their physician in the same way they think about their auto mechanic or their hair stylist? And yet, healthcare, like these other service industries, exists to meet the needs of its consumers (i.e. the patients). But I think anyone would balk at the suggestion that their mechanic could impose whatever repairs he sees fit or that their hair stylist could simply choose a haircut that matches his or her taste without even considering the preferences of the one forced to wear it!
Minimally disruptive medicine (minimallydisruptivemedicine.org) is one part of the solution to this problem, as it strives to remove unnecessary and useless care that only adds to patient burden. It also seeks to maximize patient capacity to be well, such that simply being a patient is not the end in itself, but is a means to an end that brings value to a patient's life.
I have become increasingly familiar with the role of health or wellness coaches (and, more broadly, life coaches) can play in helping to achieve these goals. In many cases, the sort of holistic evaluation and approach to well-being that coaching can provide is of far more value than any diagnostic test or intervention traditional medicine can offer.
Case in point. My grandpa has had a number of health issues develop over the last decade or so. His prescriptions and various medical appointments and evaluations help to bring some degree of health benefit, but they do not bring happiness or any value in regards to his quality of life. Thanks to the accurate perception of concerned family members, however, he was given a couple dogs that have absolutely changed his outlook on life. They've brought meaning, joy, and purpose to his life in a way that traditional medicine never could. Identifying the things that bring meaning to patients' lives is essential to achieving the outcomes we desire. I am excited to think about this more seriously and generate more formal approaches to this type of patient assessment. I am interested in people's thoughts.
Thursday, July 4, 2013
Hospital-I.T.Y. (Synopsis)
Here's the rationale for Beth and I's new hospital ministry: (copied and pasted from our ministry proposal)
The
inspiration for this ministry comes from our understanding of God’s special
love for the sick and the hurting.
From Isaiah 61, we know that one of the evidences of God’s Kingdom on
earth is the binding up of the broken-hearted. This fallen world is full of hurting people, and just as
Jesus sought them out and restored them in His ministry, we are called to do our
part to “restore our broken world” and show God’s love to those that need it
most.
This ministry has two general purposes. The first purpose is to show God’s love through Christian
hospitality, especially to patients and families that are visiting Rochester
from afar and are separated from their normal support system. This may include anything from a
friendly chat to a home-cooked meal to a parking spot to a spare room,
depending on the situation. The
second purpose is to provide spiritual support and understanding to those that
desire it. This will depend on the
situation and on interest but can include everything from a short prayer, to a
listening ear, to a formal family support group and weekly devotional.
We believe this ministry fits with the CCC DNA and the church mission in
obvious and important ways. We
believe all Christians are called to reach out beyond the walls of the church
building, to love in radical ways, and to make the gospel of Jesus Christ
attractive to our broken world. We
believe this ministry can restore people while bringing glory to God and
declaring the presence of His kingdom.
1.
Who is the intended audience for this project?
We believe that the patient’s primary source of comfort and support often
comes from his or her family and medical providers, assuming these people are
present and that the dynamics are functional (as is the case in most Christian
families). In these cases, our
primary focus will often be on the families, who are frequently hurting as much
or more than the patient but (especially when coming from afar) lack necessary
support, feel lonely, and struggle with issues of understanding.
2.
Will you be recruiting a team of people and how
will they be selected?
We would be thrilled to welcome
anyone with a heart for the hurting into this ministry. Anyone could potentially play a role,
depending on his or her comfort levels and spiritual gifting. The size and scope of this ministry
will be directly proportional to the number of people who are interested in
serving in it. It would be nice to
have a registry of people willing to be contacted for hospitality reasons
(making a meal, offering a spare room, etc). People with clinical backgrounds are particularly
well-suited to make hospital visits without violating any rules or norms,
whereas people with the gift of teaching could take turns leading support
groups at each hospital, etc.
Basically, the bigger the team, the more people we can open our services
up to and, hopefully, the bigger the impact. There are numerous resources on hospital ministry that can
be made available to anyone interested.
A training workshop would likely be in order for those particularly
interested in bedside hospital ministry.
3.
What is the process for ministry
engagement? Timeline?
This ministry can begin effective
immediately. At this stage, it is
only the two of us, so we simply can’t open up our services to every patient
and family in Rochester, as much as we’d like to. It makes the most sense, currently, for CCC to refer
patients and families that they are aware of to our ministry. Depending on the level of ministry involvement
and the closeness of the patient relationship, it is reasonable for each
ministry team member (couples counting as 1) to carry a “case load” of 1 to 3
patients. If the ministry really
takes off, we would like to make the Mayo chaplains aware of us so that they
can refer appropriate patients and families as well. Perhaps by summer 2013, it would be nice to start up a
family support group that meets within the hospital. This can be advertised within hospital chapels. Because the hospital population is
constantly overturning, these meetings can be a recurring devotional and
discussion of 3-4 topics (worry/uncertainty, suffering, comfort, etc).
4.
How will success be measured upon ministry
completion?
We will always have the sick, so
it’s hard to imagine this ministry reaching a state of completion. If this ministry is truly led by the
Spirit and is consistent with God’s heart for our community, then we should
expect spiritual results. I would
hope, as it has been our experience, that the ministering will gain as much
comfort and insight from this ministry as those being ministered to.
Monday, July 1, 2013
Update: July 1, 2013
Let's try to get everyone up to speed with what's been going on with me over the last few months:
Work/Research: A lot to report here. I'm starting to find my groove in health services research. I mostly focus on figuring out ways to make healthcare make more sense. My unit works on erasing the disconnect between patients and their clinicians. I try to make health fit the goals of the patient and empower patients to accept nothing less. This means I study a lot of things, but especially the way patients and clinicians communicate. I'm looking at this critically right now in the context of communication with cancer physicians and studying the concept of "shared decision making." Beth and I just returned from a conference in Peru where I was able to sharpen my understanding of this better. You can watch some great keynotes about this here: http://isdm2013.org/video-archive/
My mentor, @vmontori, is promoting a concept called "minimally disruptive medicine." I will be blogging about that some here...and some here: http://minimallydisruptivemedicine.org/ You can also follow my musings on this and other things on twitter @aaronleppinmd I start my Master's classes officially next week.
Life/Health: Things are about as good as can be expected. The GVH left my gut and moved to my lungs. It got pretty bad there for a bit and I spent a few days in the hospital. My lungs took a bit of a permanent hit and I probably won't ever run a marathon, but with the help of some high dose steroids I'm breathing pretty comfortably now. I'm well enough to work at least and well enough to enjoy a trip to Peru. Beth and I were able to go paragliding, take in some Peruvian cuisine, and have a wonderful time on the beautiful Pacific coast. My lung capacity precluded a trip to Machu Pichu but it was a blast regardless. We also celebrated a year of marriage about a month and a half ago. Beth also completed her first year of teaching and is enjoying her first summer vacation!
Purpose/Ministry: A fair amount on this front as well. Beth and I completed a course at our church to identify our spiritual gifts, talents, and heart tendencies. Ultimately, we felt God's leading to start a hospital ministry directed toward helping patients and their families deal with the adjustment of serious illness. On the most basic level, we want to provide Christian hospitality and support, especially to folks traveling to Rochester from afar for care. We also want to provide spiritual direction and understanding as much as one might desire this. We are approaching it humbly and with willing hearts; we feel God has given us a lot to draw on here. I will try to post updates related to this ministry that will be encouraging. We're calling it "Hospital-I.T.Y." (Intent on Trusting You).
Okay, that's the skinny. Keep posted, friends.
Work/Research: A lot to report here. I'm starting to find my groove in health services research. I mostly focus on figuring out ways to make healthcare make more sense. My unit works on erasing the disconnect between patients and their clinicians. I try to make health fit the goals of the patient and empower patients to accept nothing less. This means I study a lot of things, but especially the way patients and clinicians communicate. I'm looking at this critically right now in the context of communication with cancer physicians and studying the concept of "shared decision making." Beth and I just returned from a conference in Peru where I was able to sharpen my understanding of this better. You can watch some great keynotes about this here: http://isdm2013.org/video-archive/
My mentor, @vmontori, is promoting a concept called "minimally disruptive medicine." I will be blogging about that some here...and some here: http://minimallydisruptivemedicine.org/ You can also follow my musings on this and other things on twitter @aaronleppinmd I start my Master's classes officially next week.
Life/Health: Things are about as good as can be expected. The GVH left my gut and moved to my lungs. It got pretty bad there for a bit and I spent a few days in the hospital. My lungs took a bit of a permanent hit and I probably won't ever run a marathon, but with the help of some high dose steroids I'm breathing pretty comfortably now. I'm well enough to work at least and well enough to enjoy a trip to Peru. Beth and I were able to go paragliding, take in some Peruvian cuisine, and have a wonderful time on the beautiful Pacific coast. My lung capacity precluded a trip to Machu Pichu but it was a blast regardless. We also celebrated a year of marriage about a month and a half ago. Beth also completed her first year of teaching and is enjoying her first summer vacation!
Purpose/Ministry: A fair amount on this front as well. Beth and I completed a course at our church to identify our spiritual gifts, talents, and heart tendencies. Ultimately, we felt God's leading to start a hospital ministry directed toward helping patients and their families deal with the adjustment of serious illness. On the most basic level, we want to provide Christian hospitality and support, especially to folks traveling to Rochester from afar for care. We also want to provide spiritual direction and understanding as much as one might desire this. We are approaching it humbly and with willing hearts; we feel God has given us a lot to draw on here. I will try to post updates related to this ministry that will be encouraging. We're calling it "Hospital-I.T.Y." (Intent on Trusting You).
Okay, that's the skinny. Keep posted, friends.
Sunday, June 30, 2013
Back in the Saddle
Okay...it's been like...forever.
I'm going to get back into this. I need to. I have to develop my writing portfolio and I need a place to store my thoughts anyway.
You can catch me on twitter too...that's right...I'm going all in @aaronleppinmd
It turns out a social media presence is important for my career path and what-not. I need to be able to pump my research and communicate my agenda effectively. I'll be doing some of that here, or at least redirecting you to relevant blogs.
Will try to get updates out soon (although this is a busy time for me) related to my health, my job, and what God has been teaching me. Suffice is to say that things are good on all fronts.
All for now.
Aaron
I'm going to get back into this. I need to. I have to develop my writing portfolio and I need a place to store my thoughts anyway.
You can catch me on twitter too...that's right...I'm going all in @aaronleppinmd
It turns out a social media presence is important for my career path and what-not. I need to be able to pump my research and communicate my agenda effectively. I'll be doing some of that here, or at least redirecting you to relevant blogs.
Will try to get updates out soon (although this is a busy time for me) related to my health, my job, and what God has been teaching me. Suffice is to say that things are good on all fronts.
All for now.
Aaron
Thursday, March 14, 2013
No News is Good News
Okay, okay...so I've been really busy lately. But that's no excuse for a month without updates! I have to apologize, especially to the complete strangers that read these posts....I'm flattered by your interest and especially encouraged when you're in some way blessed. I'm still amazed to see multiple visits to this blog every day. I must thank all of you again for your prayers, without which none of the following would be possible.
But on to all the good news!
Firstly, I finished the foscarnet on March 5th. A couple days later the biopsies came back showing that the therapy had worked (I felt so much better I hardly saw how it couldn't have) and that I was free of any detectable CMV.
As the gut infection and inflammation subsided, my malabsorption issue also reversed course. This has allowed me to absorb the the thyroid medicine and vitamin D. I finally have the energy to put in a full day's work!
And it's a good thing, because that's exactly what I'm doing now. I officially started a postdoctoral research fellowship on February 25th here at Mayo. I love it. I have two outstanding mentors between whom I share my experiences and responsibilities--one heads up the Biomedical Ethics Research Unit, and the other the Knowledge and Evaluation Research Unit. I'm also planning on getting a Master's in clinical and translational research methods and I am excited for those classes to start. All in all, it amounts to what will be a very comprehensive and well-rounded education in health services methodology--not to mention the fact I've already booked conferences in Denver and Lima, Peru!
(For those that are interested, my research is currently focusing on assessments of communication quality between cancer patients and providers, the usage of some shared decision-making quality metrics, and on increasing the patient-centeredness of hospital transition processes.)
With my new job, though, I've been thinking a lot lately about ambition, career advancement, recognition, and the like. I've always sort of been an "achiever" and that can get me into trouble when it comes to maintaining balance (at least, it did in medical school). Sometimes I do things or accept challenges purely for the sake of showing myself or others that I can pull it off. Ecclesiastes 4:4 says "And I saw that all labor and all achievement spring from man's envy of his neighbor. This too is meaningless, a chasing after the wind."
Right now I'm pretty happy with what I'm doing and I know it's important for me to be working, but I'm sure the time will come when considerations of getting a PhD or going back to residency or getting a faculty position or heading up my own unit or center or whatever, etc will come into play. King Solomon's words won't be any less true then than they are now, but I bet they'll seem like it!
I have met a lot of people that have chosen to forego more money, more recognition, more respect, etc in a deliberate attempt to glorify God through the simplification and re-centering of their lives. I hope that the past couple years have taught me enough about life and what matters in it that the same might be said of me one day. I'm going to work to the extent that I enjoy it, that I'm able, and that it doesn't interfere with my primary purpose. There's a lot to be said about resting in the Lord and if any earthly pursuit is interfering with that opportunity, it needs to go. Allow me to recommend Dr. Matthew Sleeth's book, "24/6." It's about the value of the Sabbath (I actually haven't got to start it yet, but it's next in my "to read pile").
Currently Reading: "Proof of Heaven" by Dr. Eben Alexander and Hudson Taylor's autobiography; both are good, but I can't give a full review until I've finished them. And, although there are a lot of great books on how we should live our lives, nobody can touch Ecclesiastes (note: if you think it's depressing, then you don't get it).
Until next time,
Aaron
But on to all the good news!
Firstly, I finished the foscarnet on March 5th. A couple days later the biopsies came back showing that the therapy had worked (I felt so much better I hardly saw how it couldn't have) and that I was free of any detectable CMV.
As the gut infection and inflammation subsided, my malabsorption issue also reversed course. This has allowed me to absorb the the thyroid medicine and vitamin D. I finally have the energy to put in a full day's work!
And it's a good thing, because that's exactly what I'm doing now. I officially started a postdoctoral research fellowship on February 25th here at Mayo. I love it. I have two outstanding mentors between whom I share my experiences and responsibilities--one heads up the Biomedical Ethics Research Unit, and the other the Knowledge and Evaluation Research Unit. I'm also planning on getting a Master's in clinical and translational research methods and I am excited for those classes to start. All in all, it amounts to what will be a very comprehensive and well-rounded education in health services methodology--not to mention the fact I've already booked conferences in Denver and Lima, Peru!
(For those that are interested, my research is currently focusing on assessments of communication quality between cancer patients and providers, the usage of some shared decision-making quality metrics, and on increasing the patient-centeredness of hospital transition processes.)
With my new job, though, I've been thinking a lot lately about ambition, career advancement, recognition, and the like. I've always sort of been an "achiever" and that can get me into trouble when it comes to maintaining balance (at least, it did in medical school). Sometimes I do things or accept challenges purely for the sake of showing myself or others that I can pull it off. Ecclesiastes 4:4 says "And I saw that all labor and all achievement spring from man's envy of his neighbor. This too is meaningless, a chasing after the wind."
Right now I'm pretty happy with what I'm doing and I know it's important for me to be working, but I'm sure the time will come when considerations of getting a PhD or going back to residency or getting a faculty position or heading up my own unit or center or whatever, etc will come into play. King Solomon's words won't be any less true then than they are now, but I bet they'll seem like it!
I have met a lot of people that have chosen to forego more money, more recognition, more respect, etc in a deliberate attempt to glorify God through the simplification and re-centering of their lives. I hope that the past couple years have taught me enough about life and what matters in it that the same might be said of me one day. I'm going to work to the extent that I enjoy it, that I'm able, and that it doesn't interfere with my primary purpose. There's a lot to be said about resting in the Lord and if any earthly pursuit is interfering with that opportunity, it needs to go. Allow me to recommend Dr. Matthew Sleeth's book, "24/6." It's about the value of the Sabbath (I actually haven't got to start it yet, but it's next in my "to read pile").
Currently Reading: "Proof of Heaven" by Dr. Eben Alexander and Hudson Taylor's autobiography; both are good, but I can't give a full review until I've finished them. And, although there are a lot of great books on how we should live our lives, nobody can touch Ecclesiastes (note: if you think it's depressing, then you don't get it).
Until next time,
Aaron
Saturday, February 9, 2013
Good To Be Home
I'm home!!
Many thanks to everyone for all the thoughts, prayers, visits, cards, etc over the past couple weeks. It's humbling (and maybe even a little embarrassing) to have so many people care so openly for you, but I'm learning the value of living out Christian community for God's glory and not my own comfort. Certainly, I am intended to praise Him before men for the work He's doing through His people. The clinical improvement I've experienced in the past couple weeks is really pretty remarkable and it's definitely helped to brighten my spirits and to increase my hope for a complete recovery. Consider Him praised.
Although I was technically released from the hospital yesterday, there's still a long and intense treatment regimen to endure, but it's a lot easier when you're not feeling so miserable. And even though Beth and I were never more than a few miles apart, we missed each other a great deal and it's therapeutic just to be back together. I will need to complete another four weeks or so of foscarnet therapy from home and I'll need to go in to the hospital every couple days for labs and electrolyte replacements, etc. My renal function has to be monitored on a close and continuous basis and the drug dosage and schedule has to be altered accordingly. I will also need to go in for photophoresis treatments a couple times a week; these sessions will gradually be reduced in frequency between now and September (yeah, September!).
I'm on too many medications to count but my first goal is to figure out a schedule and regimen that doesn't leave me so drowsy and disconnected during the day. I've already had the displeasure of recognizing that over the past couple weeks I'd entirely blocked out any memory of receiving some meaningful notes, visits, or conversations.
Anyway, I've acquired a number of books (as birthday gifts mainly) that I need to start reading so that's my plan for the rest of the day. Again, thanks to everyone for all the support. And congratulations to Alain and Deborah Mukwege on the birth of their beautiful daughter.
Many thanks to everyone for all the thoughts, prayers, visits, cards, etc over the past couple weeks. It's humbling (and maybe even a little embarrassing) to have so many people care so openly for you, but I'm learning the value of living out Christian community for God's glory and not my own comfort. Certainly, I am intended to praise Him before men for the work He's doing through His people. The clinical improvement I've experienced in the past couple weeks is really pretty remarkable and it's definitely helped to brighten my spirits and to increase my hope for a complete recovery. Consider Him praised.
Although I was technically released from the hospital yesterday, there's still a long and intense treatment regimen to endure, but it's a lot easier when you're not feeling so miserable. And even though Beth and I were never more than a few miles apart, we missed each other a great deal and it's therapeutic just to be back together. I will need to complete another four weeks or so of foscarnet therapy from home and I'll need to go in to the hospital every couple days for labs and electrolyte replacements, etc. My renal function has to be monitored on a close and continuous basis and the drug dosage and schedule has to be altered accordingly. I will also need to go in for photophoresis treatments a couple times a week; these sessions will gradually be reduced in frequency between now and September (yeah, September!).
I'm on too many medications to count but my first goal is to figure out a schedule and regimen that doesn't leave me so drowsy and disconnected during the day. I've already had the displeasure of recognizing that over the past couple weeks I'd entirely blocked out any memory of receiving some meaningful notes, visits, or conversations.
Anyway, I've acquired a number of books (as birthday gifts mainly) that I need to start reading so that's my plan for the rest of the day. Again, thanks to everyone for all the support. And congratulations to Alain and Deborah Mukwege on the birth of their beautiful daughter.
Saturday, February 2, 2013
Pulling out all the stops...
In my last update, I mentioned we'd started foscarnet therapy in hopes of eradicating my CMV infection. That was supposed to be an outpatient process but I turned out far too frail to pull that off and I've been back in the hospital since the 24th dealing with a lot of nausea and been feeling pretty miserable.
We really are pulling out all the stops. We're combining foscarnet with cytogam (which is human immunoglobulin directed against CMV) to treat as aggressively as possible. The regimen requires a lot of fluids which has become troublesome for me. For reasons that aren't entirely clear, I'm retaining a lot of fluid (to the tune of 20 lbs worth or so). I have fluid in my abdomen and around my lungs and around my heart and just about anywhere else you could imagine. I'm not meant to live as a 155 lb man and all the extra fluid makes it hard to breathe at night. But the foscarnet is toxic to my kidneys (and has already caused a small jump in my creatinine) so we can't just diurese at will. It's a fine balance that no one is completely confident in handling. I had a drug holiday last night and this morning and was able to use some lasix. Plan is to restart the foscarnet tonight at a slightly lower dose.
To help encourage CMV eradication, we had backed off my immunosuppression slightly. This has caused a bit of a GVH flare in my skin and so I've got a pretty nice rash. To help "paralyze" my auto-reactive T cells long enough to get the virus cleared we're actually trying a therapy called extra-corporeal photopheresis. I'd honestly never heard of such a thing until this week but it basically amounts to stunning my T cells with ultraviolet light and then returning them to my body.
Otherwise I've had a couple low grade fevers that have got ID more involved. Also had a diagnositic thoracentesis of a fluid collection around my lungs, a couple CT's, and an echo. Nothing remarkable to report.
If all that medical mumbo jumbo is too exhausting for you, just know that I'm still pursuing the CMV treatment but that things have become increasingly complicated and challenging. Beth and I are fortunate to have the presence and support of both of our moms here and that helps. Thanks to everyone for their thoughts and prayers.
Tomorrow, I turn 28.
We really are pulling out all the stops. We're combining foscarnet with cytogam (which is human immunoglobulin directed against CMV) to treat as aggressively as possible. The regimen requires a lot of fluids which has become troublesome for me. For reasons that aren't entirely clear, I'm retaining a lot of fluid (to the tune of 20 lbs worth or so). I have fluid in my abdomen and around my lungs and around my heart and just about anywhere else you could imagine. I'm not meant to live as a 155 lb man and all the extra fluid makes it hard to breathe at night. But the foscarnet is toxic to my kidneys (and has already caused a small jump in my creatinine) so we can't just diurese at will. It's a fine balance that no one is completely confident in handling. I had a drug holiday last night and this morning and was able to use some lasix. Plan is to restart the foscarnet tonight at a slightly lower dose.
To help encourage CMV eradication, we had backed off my immunosuppression slightly. This has caused a bit of a GVH flare in my skin and so I've got a pretty nice rash. To help "paralyze" my auto-reactive T cells long enough to get the virus cleared we're actually trying a therapy called extra-corporeal photopheresis. I'd honestly never heard of such a thing until this week but it basically amounts to stunning my T cells with ultraviolet light and then returning them to my body.
Otherwise I've had a couple low grade fevers that have got ID more involved. Also had a diagnositic thoracentesis of a fluid collection around my lungs, a couple CT's, and an echo. Nothing remarkable to report.
If all that medical mumbo jumbo is too exhausting for you, just know that I'm still pursuing the CMV treatment but that things have become increasingly complicated and challenging. Beth and I are fortunate to have the presence and support of both of our moms here and that helps. Thanks to everyone for their thoughts and prayers.
Tomorrow, I turn 28.
Wednesday, January 23, 2013
Eggs in the Foscarnet Basket
Since my Life with GVHD update, I've continued to be pretty ill. Last Wednesday I was actually admitted to the hospital for accelerated hypertension, continued abdominal pain and bleeding, and generalized weakness. I was evaluated by endocrine, nephrology, and GI and allowed to come home Saturday (I kinda forced the issue but nothing was going to happen in the hospital that couldn't be done as an outpatient at that point).
Anyway, the biopsies came back Tuesday (yesterday) and showed diffuse and severe CMV infection of my esophagus, stomach, small and large bowel (you should see the pictures--pretty impressive). As I've eluded to in the past, I'm on the first line treatment for this bug but it's clearly not working. The pathology showed complete villous atrophy which mostly explains my malabsorption issues (my TSH is over 100 now).
But, I consider this all good news because it means we can try a different medication. As I write this, I'm sitting in the Infusion Therapy Center receiving my first dose of foscarnet (the go-to drug for gancyclovir-resistant CMV). Foscarnet is kinda a nasty drug which is why I need to be monitored for the first couple doses. It's going to be an IV therapy twice a day and it will require a good amount of IV fluids to be administered concomitantly to avoid injury to the kidneys or serious alterations in my electrolytes. But if it works, it could really improve my quality of life and make the treatment of a lot of other things much more straightforward....so pray that it does!
Anyway, the biopsies came back Tuesday (yesterday) and showed diffuse and severe CMV infection of my esophagus, stomach, small and large bowel (you should see the pictures--pretty impressive). As I've eluded to in the past, I'm on the first line treatment for this bug but it's clearly not working. The pathology showed complete villous atrophy which mostly explains my malabsorption issues (my TSH is over 100 now).
But, I consider this all good news because it means we can try a different medication. As I write this, I'm sitting in the Infusion Therapy Center receiving my first dose of foscarnet (the go-to drug for gancyclovir-resistant CMV). Foscarnet is kinda a nasty drug which is why I need to be monitored for the first couple doses. It's going to be an IV therapy twice a day and it will require a good amount of IV fluids to be administered concomitantly to avoid injury to the kidneys or serious alterations in my electrolytes. But if it works, it could really improve my quality of life and make the treatment of a lot of other things much more straightforward....so pray that it does!
Who will it be today? #6
Who will it be today? The patient parent
Yesterday I had some time to kill before one of my appointments. I was particularly exhausted so I decided to rest in a comfy chair with a nice view of town. But I didn't get much rest.
A teenage autistic boy happened to have an upcoming appointment on the same floor, and he wasn't looking forward to it. He was screaming, acting out, and carrying on in such a way that it seemed the whole clinic must have been aware of his presence.
In the midst of all the staring and head shaking and pseudo-empathetic comments, I couldn't help but be drawn to the peaceful, calming presence of the boy's father. He could have chosen to be embarrassed or to lose his cool or to lash out at his son in a completely unproductive way. But he understood his son like no one else and, over the years, he had undoubtedly been well-trained in the practice of patience and self-control. I admired him in that moment.
I knew there wasn't really anything I could do to help the situation but I did walk up to the gentleman and express my uninformed sympathy for what I anticipated to be a very trying day. I told him about Beth and her experience with the autism center. I discovered that the young man had already had lunch but that he does like pizza so I gave dad a Toppers coupon and a copy of my letter. Hopefully the gift of free pizza will be a blessing this week.
I told them I'd be praying the day would go as smoothly as possible and then got out of their hair. It's hard for me to even fathom what life is like for the parents of children with special needs. I know a lot of people say things like "they must be special people" or that "I could never do that." Although there's a lot of truth in that line of thinking, it's probably an oversimplification. We sell ourselves short too often and we have too small a view of our God-enabled capabilities. This man loved his son and so his attitudes were adapted to accommodate what his son required. Every trial we face is a similar opportunity to be molded. I hope the Spirit grants me the peace and patience and self-control that I witnessed.
Who will it be tomorrow?
Yesterday I had some time to kill before one of my appointments. I was particularly exhausted so I decided to rest in a comfy chair with a nice view of town. But I didn't get much rest.
A teenage autistic boy happened to have an upcoming appointment on the same floor, and he wasn't looking forward to it. He was screaming, acting out, and carrying on in such a way that it seemed the whole clinic must have been aware of his presence.
In the midst of all the staring and head shaking and pseudo-empathetic comments, I couldn't help but be drawn to the peaceful, calming presence of the boy's father. He could have chosen to be embarrassed or to lose his cool or to lash out at his son in a completely unproductive way. But he understood his son like no one else and, over the years, he had undoubtedly been well-trained in the practice of patience and self-control. I admired him in that moment.
I knew there wasn't really anything I could do to help the situation but I did walk up to the gentleman and express my uninformed sympathy for what I anticipated to be a very trying day. I told him about Beth and her experience with the autism center. I discovered that the young man had already had lunch but that he does like pizza so I gave dad a Toppers coupon and a copy of my letter. Hopefully the gift of free pizza will be a blessing this week.
I told them I'd be praying the day would go as smoothly as possible and then got out of their hair. It's hard for me to even fathom what life is like for the parents of children with special needs. I know a lot of people say things like "they must be special people" or that "I could never do that." Although there's a lot of truth in that line of thinking, it's probably an oversimplification. We sell ourselves short too often and we have too small a view of our God-enabled capabilities. This man loved his son and so his attitudes were adapted to accommodate what his son required. Every trial we face is a similar opportunity to be molded. I hope the Spirit grants me the peace and patience and self-control that I witnessed.
Who will it be tomorrow?
Sunday, January 13, 2013
Life with GVHD
It's been rough lately. Sometimes, downright discouraging. My disease has focused in on my GI tract and it just doesn't seem to want to relent. I am in a constant state of intestinal inflammation. I can't eat anything without expecting severe pain and a toilet full of blood...and really I have come to expect those things whether I eat or not.
It's hard to sleep because, even when my mind and body is weak and exhausted, the cellular war in my gut is going on 24/7, increasing my metabolic demands and my heart rate around the clock. I've learned to knock myself out with pills so that, at the very least, I can get a couple hours of sleep between trips to the bathroom. Parenteral nutrition is the only thing keeping me from wasting away to nothing.
But I think the hardest part of all this is just not being able to do anything. I may last a couple hours at the office before I have to come home and lay down. I'm almost exclusively working from home unless there is a meeting or specific need for me to leave. Although this sort of flexibility is why I have the job I have, I hate the fact that I'm not interacting with people. And even more, I hate the fact that when I'm out in the world I feel so ill I don't even want to interact with people. It makes it harder to see the point of all this.
But I know it will pass. It's just a season and I have to keep reminding myself of that. I still have a lot to be thankful for and a lot of supportive people around me. I'm beginning to realize the value of accepting that I am sick and that it's okay to let people help me and pray for me. I'm beginning to see the point of humbling myself; it's an important part of accepting where God has placed me.
As I've read more of Dietrich Bonhoeffer's biography, I've realized the value of community. True community is referenced in Paul's 1st letter to the Thessalonians when he tells them what a joy it was not only to share the gospel, but to share their lives. This sort of fellowship requires vulnerability and honesty about who we are and what we're dealing with.
Speaking of reading books, I'll post a list of my year's reading list soon!
It's hard to sleep because, even when my mind and body is weak and exhausted, the cellular war in my gut is going on 24/7, increasing my metabolic demands and my heart rate around the clock. I've learned to knock myself out with pills so that, at the very least, I can get a couple hours of sleep between trips to the bathroom. Parenteral nutrition is the only thing keeping me from wasting away to nothing.
But I think the hardest part of all this is just not being able to do anything. I may last a couple hours at the office before I have to come home and lay down. I'm almost exclusively working from home unless there is a meeting or specific need for me to leave. Although this sort of flexibility is why I have the job I have, I hate the fact that I'm not interacting with people. And even more, I hate the fact that when I'm out in the world I feel so ill I don't even want to interact with people. It makes it harder to see the point of all this.
But I know it will pass. It's just a season and I have to keep reminding myself of that. I still have a lot to be thankful for and a lot of supportive people around me. I'm beginning to realize the value of accepting that I am sick and that it's okay to let people help me and pray for me. I'm beginning to see the point of humbling myself; it's an important part of accepting where God has placed me.
As I've read more of Dietrich Bonhoeffer's biography, I've realized the value of community. True community is referenced in Paul's 1st letter to the Thessalonians when he tells them what a joy it was not only to share the gospel, but to share their lives. This sort of fellowship requires vulnerability and honesty about who we are and what we're dealing with.
Speaking of reading books, I'll post a list of my year's reading list soon!
Thursday, January 3, 2013
Christmas Vacation
Well, things are back to the grind in chilly Minnesnowta. It's good to be "home" and sorta back in our normal routine but it was nice (though at times exhausting) to see all our family in Missouri.
Christmas was a success all around, although it was postponed for one side of my family as my grandpa remained in the hospital. Beth and I both acquired a good amount of practical loot. I'm currently enthralled in a book I received from my mother-in-law on the life of Deitrich Bonhoffer (appropriately titled, "Bonhoeffer," and written by Eric Metaxas).
Although equal time was spent with each side of the family, there was only one event photogenic enough for me to chronicle (which I have to credit to my other favorite gift, a Motorola Electrify M...what a great phone). These are a couple pictures of a Duff family tradition--the Christmas Eve visitation of Santa Claus. This same dude has been doing this every year for as long as Beth can remember....and he's good. I'm just glad I didn't have to sit on his lap this year.
Thursday, December 20, 2012
Christmas Wishes!
Beth and I had hoped to head south today, but instead it looks like we'll be waiting out a blizzard. Better safe than sorry, I guess.
We had wanted to get down to Missouri as soon as possible as my grandpa is in the hospital in Columbia, but it's probably best we not get stranded in the middle of Iowa in the process. Regardless, the folks at MU are taking great care of him and I'm optimistic he's going to end up doing well.
Anyway, Beth and I are pretty stoked about our family Christmas gifts this year. I don't want to give away any surprises, but let's just say we spent a fair amount of time experimenting in the kitchen, and that all of our gifts will bear this awesome label:
Beth and I want to wish all our friends and family a very merry Christmas. We're too lame and lazy to send out Christmas cards, but that doesn't mean we don't value each of you!
We had wanted to get down to Missouri as soon as possible as my grandpa is in the hospital in Columbia, but it's probably best we not get stranded in the middle of Iowa in the process. Regardless, the folks at MU are taking great care of him and I'm optimistic he's going to end up doing well.
Anyway, Beth and I are pretty stoked about our family Christmas gifts this year. I don't want to give away any surprises, but let's just say we spent a fair amount of time experimenting in the kitchen, and that all of our gifts will bear this awesome label:
Beth and I want to wish all our friends and family a very merry Christmas. We're too lame and lazy to send out Christmas cards, but that doesn't mean we don't value each of you!
Thursday, December 13, 2012
Real Men Attend (Congo) Baby Showers
Beth and I had the pleasure of hosting a baby shower this past weekend for our good friends, the Mukweges.
They are from Congo so the whole concept was completely foreign to them. But we had a great turnout and we were able to bless them in a unique way while they are far from family.
Anyway, it was my first baby shower and Beth put me in charge of games. I had fun with that, of course, and it allowed Beth to focus on the food and gifts and details and stuff. I suggested we should go into business as a baby shower planning team. Seriously, ladies, invite me to your baby showers; you won't regret it! (note: please do not actually invite me to your baby shower)
The real point of this post is to give you some background on who the Mukweges (Alain and Deborah) are and about the situation they have lived through in Eastern Congo.
Alain's father, Denis Mukwege, is actually a surgeon and activist that has been repairing victims of sexual abuse for years in Congo. Rape is a form of warfare in Congo and Dr. Mukwege has become somewhat of a spokesperson against the violence. He's received all kinds of awards and even been nominated for the Nobel Peace Prize.
A few months ago he spoke before the UN General Council demanding international support. When he returned home he found his house overtaken, his daughters held at gunpoint, and men intent on killing him. Shots were fired and a man gave his life protecting Dr. Mukwege. Fortunately, Alain's family escaped the assassination attempt unharmed.
Anyway, I've written an essay about this whole situation and my relationship with Alain that is currently undergoing review for publication (so I can't actually post it here). My hope is that it will increase awareness of the situation in Congo.
Here are some links if you'd like to learn more:
http://kristof.blogs.nytimes.com/2012/11/02/dr-mukwege-fights-back/
http://www.nytimes.com/2012/10/27/world/africa/human-rights-doctor-in-congo-eludes-gunmen.html?_r=0
They are from Congo so the whole concept was completely foreign to them. But we had a great turnout and we were able to bless them in a unique way while they are far from family.
Anyway, it was my first baby shower and Beth put me in charge of games. I had fun with that, of course, and it allowed Beth to focus on the food and gifts and details and stuff. I suggested we should go into business as a baby shower planning team. Seriously, ladies, invite me to your baby showers; you won't regret it! (note: please do not actually invite me to your baby shower)
The real point of this post is to give you some background on who the Mukweges (Alain and Deborah) are and about the situation they have lived through in Eastern Congo.
Alain's father, Denis Mukwege, is actually a surgeon and activist that has been repairing victims of sexual abuse for years in Congo. Rape is a form of warfare in Congo and Dr. Mukwege has become somewhat of a spokesperson against the violence. He's received all kinds of awards and even been nominated for the Nobel Peace Prize.
A few months ago he spoke before the UN General Council demanding international support. When he returned home he found his house overtaken, his daughters held at gunpoint, and men intent on killing him. Shots were fired and a man gave his life protecting Dr. Mukwege. Fortunately, Alain's family escaped the assassination attempt unharmed.
Anyway, I've written an essay about this whole situation and my relationship with Alain that is currently undergoing review for publication (so I can't actually post it here). My hope is that it will increase awareness of the situation in Congo.
Here are some links if you'd like to learn more:
http://kristof.blogs.nytimes.com/2012/11/02/dr-mukwege-fights-back/
http://www.nytimes.com/2012/10/27/world/africa/human-rights-doctor-in-congo-eludes-gunmen.html?_r=0
Saturday, December 8, 2012
Who will it be today? #5
Who will it be today? Me.
What a novel concept. Sometimes it's not about who we can encourage or bless, but who can bless us. We all need our "sponge" to be saturated, after all, before we can ever wring it out. For me, this sort of encouragement usually comes through a message or a small group discussion or a word from scripture, but a couple weeks ago it came in the form of a complete stranger. I haven't been able to get the image of that experience out of my mind so I decided to preserve it as part of this series.
I was waiting for some prescriptions to be filled at the hospital (something I find myself doing on a weekly basis). They weren't quite finished yet so I took a seat there in the lobby. About this time I heard a faint, singing voice coming from the direction of the gift shop. I readjusted my position to get a better view.
Sure enough, the information desk attendent was singing. She was a volunteer, a petite Asian woman standing behind the desk with a hymnal in hand. Her voice was quiet and her demeanor was timid, and yet it was obvious she was singing because she wanted people to hear. There was nothing spectacular about her voice, only her courage; indeed, she was either very sweet or very odd.
As people walked by, some would stop and smile. Others seemed to feel sorry for her and the awkwardness she was creating. One man finally stopped and started singing with her. It wasn't until that point that I could even make out what was being sung...
"When we all get to heaven, what a day of rejoicing that will be!"
"When we all see Jesus, we'll sing and shout the victory!"
She had taken it upon herself to encourage the patients and families in that hospital. And it was beautiful. As I later realized, she could barely speak English, but she knew a few hymns (and, apparently, how to give decent directions to the cafeteria). She didn't care what she couldn't do and she didn't intend to rely on her own abilities to make anything happen. She just trusted that her God would use her in some way to help some people. I think He did.
Who will it be tomorrow?
What a novel concept. Sometimes it's not about who we can encourage or bless, but who can bless us. We all need our "sponge" to be saturated, after all, before we can ever wring it out. For me, this sort of encouragement usually comes through a message or a small group discussion or a word from scripture, but a couple weeks ago it came in the form of a complete stranger. I haven't been able to get the image of that experience out of my mind so I decided to preserve it as part of this series.
I was waiting for some prescriptions to be filled at the hospital (something I find myself doing on a weekly basis). They weren't quite finished yet so I took a seat there in the lobby. About this time I heard a faint, singing voice coming from the direction of the gift shop. I readjusted my position to get a better view.
Sure enough, the information desk attendent was singing. She was a volunteer, a petite Asian woman standing behind the desk with a hymnal in hand. Her voice was quiet and her demeanor was timid, and yet it was obvious she was singing because she wanted people to hear. There was nothing spectacular about her voice, only her courage; indeed, she was either very sweet or very odd.
As people walked by, some would stop and smile. Others seemed to feel sorry for her and the awkwardness she was creating. One man finally stopped and started singing with her. It wasn't until that point that I could even make out what was being sung...
"When we all get to heaven, what a day of rejoicing that will be!"
"When we all see Jesus, we'll sing and shout the victory!"
She had taken it upon herself to encourage the patients and families in that hospital. And it was beautiful. As I later realized, she could barely speak English, but she knew a few hymns (and, apparently, how to give decent directions to the cafeteria). She didn't care what she couldn't do and she didn't intend to rely on her own abilities to make anything happen. She just trusted that her God would use her in some way to help some people. I think He did.
Who will it be tomorrow?
Wednesday, December 5, 2012
2012, In Review
I haven't given an update on my clinical situation or personal life in a long time. So consider this a way overdue summary of where I'm at as we finish up 2012.
As most people know, I started this year struggling with graft vs host disease and hopeful to begin my medicine residency here at Mayo in July. Beth and I were married in May but the GVH never really left so residency was, once again, postponed.
The summer was enjoyable but I developed a pretty severe infection with cytomegalovirus (CMV) that continued to keep me sidelined. I started doing some part-time research through Mayo (mostly from home) and that turned out to be useful in helping me feel more productive.
About the time we got the CMV under control, we realized my thyroid was shot. My TSH continues to be way out of whack (86 currently) and is not responding to increasing doses of oral thyroid hormone supplementation.
Ultimately, there seems to be a severe malabsorption problem that keeps a lot of my medicines from doing their job (I take over 13 unique meds/day, multiple doses of some). And it's a catch-22 because if I increase the steroids to help cut down on the inflammation and increase absorption, it makes me that much more susceptible to the CMV and it really messes up my bones.
As things stand in December 2012, I've got a lot of things wrong with me. I effectively have no thyroid and will probably require some special subcutaneous form of levothyroxine to address this. My energy is low as a result of the thyroid issue and also anemia that is caused by the medicine I have to take for the CMV. Unfortunately, the CMV medicine is not working perfectly and I may actually be developing some resistance to it. I continue to deal with GVH which causes a fair amount of nausea, vomiting, and colitis. The steroids that I take for this have officially weakened my bones to the point of osteoporosis. I take vitamin D for this but, once again, I'm not absorbing it as well as I should be. My heart and my lungs are working great, and my liver seems to be doing better. My kidneys are losing a little bit of protein which causes me to swell up sometimes but it's probably just a medication side effect and we're watching it.
Anyway, I remain hopeful some of this stuff will work itself out. Certainly, I'm cancer-free and that's a blessing.
And although this all sounds like it must be horrible, life is really pretty good. Being married to Beth is the best part and she brings a lot of joy to my life. She is enjoying teaching at the high school and I'm proud of how hard she works. We have a lot of friends here and have made so many more meaningful connections with people than we would have predicted just a year ago.
As far as major life changes, I've decided (with the support of Beth, our families, and my doctor) that internal medicine is probably never going to happen for me....and, quite frankly, I don't think I want it to. I have certain priorities for my life and working 80 hours/wk just doesn't align with them anymore (not that I could ever physically do it anyway). I've put in an application for a part-time science tutoring gig at the community college which I think I might enjoy. I'm also continuing to do some important research here at Mayo and am trying to become a more productive writer. I have mostly decided that, if I do decide to pursue a residency and career in medicine, it will probably be in the field of pathology....but that wouldn't happen until July of 2014 at the earliest. I suppose there's no rush; I've already passed all my boards. In the mean time, I'll be exploring opportunities in teaching and research and possibly writing a book!
I'm going to try to keep this blog up to date (I never was a facebook fan) so feel free to follow it for info on how I'm doing, what I'm up to, and where you can buy the book ;)
Thursday, November 29, 2012
Who will it be today? #4
Who will it be today? The cancer patient.
My year's supply of Toppers' pizza has come in really handy. Beth and I have enjoyed being able to bless people with all the pizza we can't possibly eat.
One of the advantages of living and working around a place like Mayo Clinic is that there's no shortage of visitors in need.
I was walking through Methodist Hospital's lobby today and saw a woman who was clearly a cancer patient. Aside from a lack of hair she seemed to be relatively well and capable of enjoying some pizza. I introduced myself and asked if she was in town for a while. "Couple days," she said. I asked her if she liked pizza, gave her this week's coupon and a copy of my letter, and wished her the best. Easy peasy.
Maybe it was too easy. I think I actually dodged my assigned appointment for something more convenient. As I was walking downtown I came across an elderly person raking leaves across the street. I couldn't make out whether the individual was a woman or a man, but I could definitely tell he or she was too old to be raking leaves. I think that's the person God wanted me to approach and, as much as I hate to admit it, that was the person God wanted me to rake leaves with. I actually stopped in the middle of the sidewalk for an awkward amount of time and considered the situation. I "reasoned" with God that I had to get to work (I didn't really), I wasn't dressed to rake leaves (there wasn't really much raking left to do), and that if God wanted me to help the person He should have put us on the same side of the street (not exactly a high-traffic area).
I truly hope the cancer patient is blessed by the pizza, but I know in my heart I dropped the ball. I hope God will give me another shot and that I'll be more faithful. This whole process is about learning lessons.
Who will it be tomorrow?
My year's supply of Toppers' pizza has come in really handy. Beth and I have enjoyed being able to bless people with all the pizza we can't possibly eat.
One of the advantages of living and working around a place like Mayo Clinic is that there's no shortage of visitors in need.
I was walking through Methodist Hospital's lobby today and saw a woman who was clearly a cancer patient. Aside from a lack of hair she seemed to be relatively well and capable of enjoying some pizza. I introduced myself and asked if she was in town for a while. "Couple days," she said. I asked her if she liked pizza, gave her this week's coupon and a copy of my letter, and wished her the best. Easy peasy.
Maybe it was too easy. I think I actually dodged my assigned appointment for something more convenient. As I was walking downtown I came across an elderly person raking leaves across the street. I couldn't make out whether the individual was a woman or a man, but I could definitely tell he or she was too old to be raking leaves. I think that's the person God wanted me to approach and, as much as I hate to admit it, that was the person God wanted me to rake leaves with. I actually stopped in the middle of the sidewalk for an awkward amount of time and considered the situation. I "reasoned" with God that I had to get to work (I didn't really), I wasn't dressed to rake leaves (there wasn't really much raking left to do), and that if God wanted me to help the person He should have put us on the same side of the street (not exactly a high-traffic area).
I truly hope the cancer patient is blessed by the pizza, but I know in my heart I dropped the ball. I hope God will give me another shot and that I'll be more faithful. This whole process is about learning lessons.
Who will it be tomorrow?
Tuesday, November 27, 2012
The Cancer Chronicles, #5
*The Cancer Chronicles is a re-posting of blog updates I gave during my initial diagnosis and treatment*
June 16, 2011:
Everything is going more or less as planned from a treatment standpoint. My marrow is recovering nicely and I will soon be stable enough to head north (could be discharged by the weekend). I really have no indication of the timeline required to complete the transplant, how difficult it might be to find a donor, or how much sense it would make to try and work at all this year. But all of those things should get cleared up once I get to Rochester and have a chance to meet with my transplant physician, Dr. Litzow. For now, I'm watching a lot of History Channel and Netflix and enjoying the company of lots of special people.
Aside from being tired often and generally short on energy and ambition, I feel mostly well. I have managed to read about half of The Problem of Pain. To this point, the book has mostly focused on setting the stage for how pain and suffering can exist in the Creation of a good God, and less on how we should respond when we encounter it (that comes later).
Lewis is as insightful as always, but I especially like how he describes our world as a neutral "playing field" of sorts; one that has its own set of governing principles over which we have no control. Similar to how we might think of a video game "world" or "level," the point of the place is only to give the players a context in which to interact and do things that matter. The rules of the world are the same for everyone (fire is hot, gravity pulls down, etc); but not everyone plays the game the same. The necessity of this sort of set-up is beyond the scope of this note, but it's well-described in the book. Suffice is to say, there is no sensible way to allow free will and simultaneously maintain a world that is equally convenient to all souls at all times. It's an academic argument, admittedly, but it's sound.
Of course, the concept of disease itself does not seem intrinsically necessary in this model (especially disease that could not have been prevented by alternative individual choices). Lewis chalks this one up to the fall. He believes, or perhaps just surmises, that we were originally created with the ability to control our physical body and all processes therein through our spiritual self. When man Fell, he chose himself over God. It was then that God relinquished this unique control and turned the direction of our bodies over to the laws of nature. These laws include imperfections and inefficiencies that make us susceptible to disease, give us all a lifespan, and remind us of our mortality. Of course, this is just Lewis' best guess and one of many possibilities so it's hard to know whether or not this is actually how it played out.
The truly important thing to realize is that this existence is simply not the point. For centuries, a foundational component to the enlightenment of the Christian worldview has been a belief that we were made for something more and an awareness that this is not our ultimate home (in many ways, it really is little more than the first level of a video game). But we probably say this sort of thing without fully believing it more often than not and leukemia, if nothing else, is helping me to grow in my dependence of this truth.
Ultimately, reconciling the "problem" of pain with the character of God is probably not something that we will ever be capable of on intellectual grounds alone--we just aren't smart enough. And this is why faith is so necessary. After all, no amount of intelligent argument in God's defense will ever be more compelling to me than what I know in my heart to be true about Him--that He's real, that He's good, and that He loves me. But I realize not everyone has that knowledge and many have chosen to believe other things about God. And that's the tragedy. Not the fact that pain and suffering exist in the world, but the fact that there are so many people without the means to explain it, understand it, or cope with it.
Here's to hoping my next update is from somewhere other than a hospital bed...
Wednesday, November 21, 2012
Who will it be today? #3
Who will it be today? The hitch-hiker.
I don't normally pick up hitch hikers. In fact, this was my first one.
Beth and I were on our way back to Missouri for Thanksgiving and, somewhere in central Iowa, we came across a gentleman trying to flag down a ride.
For whatever reason, I felt like we should turn around and see what he needed. After we talked to him for a while I had a peace about helping him get to Interstate 80.
Turns out he lives in California and was trying to get back there. He had been in Iowa because his mother had lived there and had recently died. He was a nice guy. Almost child-like in his innocence. He has PTSD, apparently, but I don't know any details about the trauma he has experienced. It doesn't matter really. It's a devastating condition and, I'm sure, it is the main reason he finds himself in such undesirable circumstances.
I wanted to give him a letter but I didn't have any on me. In this case, though, I never got the impression God wanted me to share knowledge with him. I got the feeling he's heard all he needs to hear. What God wanted for Beth and I was for us to be hands and feet. We had been divinely appointed to take a man that mattered to the Father from Nowhere, Iowa to a random Pilot Truck Stop on Interstate 80. We prayed with him, filled his belly, and became his facebook friend.
Who will it be tomorrow?
I don't normally pick up hitch hikers. In fact, this was my first one.
Beth and I were on our way back to Missouri for Thanksgiving and, somewhere in central Iowa, we came across a gentleman trying to flag down a ride.
For whatever reason, I felt like we should turn around and see what he needed. After we talked to him for a while I had a peace about helping him get to Interstate 80.
Turns out he lives in California and was trying to get back there. He had been in Iowa because his mother had lived there and had recently died. He was a nice guy. Almost child-like in his innocence. He has PTSD, apparently, but I don't know any details about the trauma he has experienced. It doesn't matter really. It's a devastating condition and, I'm sure, it is the main reason he finds himself in such undesirable circumstances.
I wanted to give him a letter but I didn't have any on me. In this case, though, I never got the impression God wanted me to share knowledge with him. I got the feeling he's heard all he needs to hear. What God wanted for Beth and I was for us to be hands and feet. We had been divinely appointed to take a man that mattered to the Father from Nowhere, Iowa to a random Pilot Truck Stop on Interstate 80. We prayed with him, filled his belly, and became his facebook friend.
Who will it be tomorrow?
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