Our New Normal

Our New Normal - Under the Monkey Bars blog

As I type, my patient sleeps. My husband Don now knows what a 10 feels like on a pain scale, because when his ski boot was pulled off his foot with a dislocated knee and broken leg: he was a 10. It’s the first time the monkeys and I have seen true pain on his face. We’ve been through a lot together in our almost 15 years of marriage. But this? I wasn’t ready for this. It’s our new normal for as far as we can see.

Before I get ahead of myself, let me start this story on March 5th when a regular Saturday in Stowe turned into one of the scariest days of our lives.

I skied down Nosedive behind Don on one of the most gorgeous mornings of the season. The sky was blue. The conditions were better than we expected. The snow was groomed beautifully over this season’s dreaded New England ice. We were on our second run of our usual Saturday ski date while the monkeys were conquering Mt Mansfield with their Buster teams. 

The moment he fell still plays in my mind like a video. Don was in the middle of a right turn, almost in a lunge when his already bent left leg slid into a groove in the ice. His knee popped and dislocated before he even fell. Then his femur came down on his tibia like a hammer. It was a total fluke thing. I’ve seen Don take some pretty sick falls; this was not one of them. When his knee gave, he twisted around on his back clutching his left leg. 

I skied down below him and yelled, “Should I call Ski Patrol?” I’ve asked him this question dozens of times. The answer is always no. We always joke about how predictable he is. I wish on that day he could have been more predictable. Instead of no, my sweet husband cried out, “YES!” in a voice I’ve never heard before.

I pulled out my phone to call Ski Patrol, realizing instantly that I didn’t have the number. I looked up in a panic and magically 2 red coats with white crosses appeared gliding down the snowy trail. Ski Patrol expertly tended to Don, initially assessing a fracture based on the fact that his knee was not where it should be. These guys were our angels that day, and I’ll never forget their professionalism, how they took control, and eased my nerves. 

While we waited for a sled to arrive, Bean skied down the trail with her team. I tried to reassure her that Daddy would be okay, but even I wasn’t sure if my words were true. After a much needed hug, I asked her to look out for Sweet Pea. I knew their coaches would take care of the monkeys while I stayed with Don wherever this awful day would take us.

You never know how you’ll handle a crisis until you are in the situation. Apparently I’m pretty good under pressure — especially with friends by my side. 

All of the decisions that go along with a trauma injury have been the hardest part. Does the surgery need to be done asap? Do we trust these doctors? Should we go back to Newburyport or stay in Stowe? Should we keep the monkeys with us or get them back to school?

Ultimately, we decided to put our trust in the local doctors here in Vermont, and they didn’t disappoint. The ambulance took Don to Copley Hospital in Morrisville where an orthopedist performed his first surgery, installing an external fixator to set the break and reduce the swelling for his next surgery. Catastrophic was the word the surgeon used to describe Don’s injury. Not a good sign.

That contraption of metal pins sticking out of his leg, known as an “x-fix” in medical lingo, stayed on for 10 excruciating days. I lived in fear of bumping it and causing him more pain all day every day (I ended up only stepping on his foot once…not bad for my debut as a nurse).

We chose to have Don’s second surgery at UVM Medical Center with a rock star orthopedist who repairs this type of injury at least once a month. That 4 hour surgery on March 14th was successful in repairing his tibial plateau, ACL, and meniscus. Between surgeries, Don suffered through complications that brought us to the UVM ER. His pain has been off the charts, with bad days around 8 or 9. Every day has been a challenge. 

The monkeys were with us until this past Sunday when their grandparents graciously brought them back to Newburyport for school (only to be met by a snow day!). While friends and family thought we should get the girls back to school and their routine right away, I’m so glad we kept our family together. We decided that their routine is with us. Missing two weeks of school isn’t nearly as important as our family. We needed them as much as they needed us, and we’re all stronger because of what we’ve been through together.

Our new community in Stowe overflowed with support for our family. We truly couldn’t have managed without them. Family and friends both near and far were there for us in every way imaginable. Help came by way of packages to keep the monkeys busy, grocery shopping, babysitting, and rides for the monkeys. I’m forever grateful to the friends that cheered us on with texts and messages. Funny stories from home and pictures from friends were the best distraction. 

Here’s what Don went through so far by the numbers: 1 ambulance ride, 2 ER visits, 2 surgeries at 2 different hospitals, 6 hours in the OR, 3 X-rays, 1 MRI, 2 CT scans, 1 ultrasound, 4 pins, 8 screws, 2 plates, 2 roommates, 8 nights in the hospital, 2 crutches, and we’re not counting pain killers because I lost track long ago. I think we’ve met our deductible. 

In the wise words of a nurse on our first night at the hospital, “You never know where you’re going to end up when you wake up each morning.” These past few weeks were definitely not how we planned to spend the last days of winter. But we’re okay and it could have been much worse. Don’s pain lessens a bit each day and we’ve accepted our new normal. He’ll be in the immobilizer for 12 weeks with a possible 3rd surgery in a few months. Until then, I’ll be healing him in the way I know best: with food as medicine.

Thanks for reading and supporting Under the Monkey Bars. Blogging is an important part of my life, but my family will always come first.

The Dr. Su Series: Opening Lyme’s Door

Opening Lyme's Door - Under the Monkey Bars Blog

By guest blogger Dr. Mark Su

Christine has courageously shared her journey and struggles with Lyme disease. In response, I was moved to share my reciprocal journey and struggles in becoming a physician who evaluates and treats Lyme disease, which I believe sheds some light on the challenges that patients face in being diagnosed or treated for Lyme.

I vaguely remember a couple of patients during my residency years at Tufts University in Boston where Lyme disease was a topic of consideration for their symptoms. It simply wasn’t something we either encountered or considered, for a variety of possible reasons. We were taught the textbook information on Lyme disease, but that was the extent of it.

When I started working in Boston’s North Shore in 2003, my awareness of this illness first took root. Sure, I saw folks with the classic presentation of fever, headache, neck stiffness, muscle aches, and a large red rash or sometimes a “bullseye” not uncommonly following a known tick bite. At the time, I treated them accordingly as I was taught with 2-3 weeks of doxycycline. But I also met patients who reported persistent symptoms that would come and go to various degrees over time, even great lengths of time. These patients commonly had a strong overlap in symptoms with others who carried a diagnosis of fibromyalgia or chronic fatigue syndrome. Often times, we wondered together whether they were being recurrently infected by repeated tick bites? At other times, we would pursue testing for other diagnoses, almost universally to no avail.

Over time, I met more and more patients who would report receiving symptom benefit for their chronic symptoms whenever they were on antibiotics for other reasons; or that they historically had received antibiotics periodically for these “flares” from another physician (or even physician friends, off the record), though an explanation for why the medications seemed to work eluded the prescriber. Listening closely to their stories and recognizing them to be legitimate symptoms, I concluded that they deserved to be treated with antibiotics, even if I couldn’t fully make sense of it. It wasn’t what I was trained to do. It wasn’t the standard of care. But it was the humane thing to do. And to me, the right thing to do.

I continued to see patients who generally fit this type of profile over the years. Symptoms would somewhat vary, but the number of these similar experiences mounted, and they were generally similar stories. In some cases, I was able to create some model of rationale for myself and a given patient, but for the large part, I still couldn’t fully explain this phenomena. I wanted to learn more about persistent Lyme disease and the reported varying presentations of even more acute Lyme disease, but I simply didn’t have the time. Nor did I feel I had the energy or mental space to tackle something that I suspected could cause a rather significant deviation in my professional practice patterns and routines. I was very open minded, but I was also scared of what might be behind that door. And the ramifications of what I’d discover – because I knew that if I uncovered something worth pursuing, for the sake of helping patients, I would feel obligated to do the right thing, the humane thing, and search for the truth, as challenging as it might be.

In the latter years at my previously employed position, we as a practice diagnosed and treated folks with Lyme disease more aggressively than most traditional practices. It wasn’t until I started my own practice here in Newburyport in mid 2014, with primary intentions unrelated to Lyme disease (little did I know), that, upon establishing the regular pattern of using the premier specialty lab for Lyme testing, my eyes were truly opened wide more than I could have expected.

I uncovered enough patients with previously undiagnosed Lyme disease that I owed it to myself to seek more education, so I finally went to a specialized conference with ILADS, the International Lyme and Associated Diseases Society. It was there that I was confronted, in a massive way, with the evidence-based literature that not only substantiated bits and pieces of information I had gleaned from various colleagues over the years in one fell swoop of structured presentation. It was also there that a light went on inside of me – my passion was lit. I realized I had a whole new knowledge base and set of tools to help patients who commonly are left to fend for themselves. These patients typically lack diagnosis or treatment options, finding themselves referred to a multitude of other practitioners in hopes of a diagnosis, trying anything to feel better, and to validate their health experiences often with little to no benefit. Since then, after continually diagnosing and treating patients with this frustrating and sometimes debilitating condition, I have continued to ask myself, with what I believe to be a healthy self-analysis or perhaps even self-doubt, “Is this really real? Do this many people really have persistent Lyme disease?” Yes Mark, they do.

Patients often voice frustration to me about the confusion they experience as a result of the conflicting voices within the medical community about this condition. I really do feel for them. As much joy and fulfillment as I may have to validate a patient’s experiences, that they aren’t “crazy” or “just stressed” or “just getting old,” but that indeed they have Lyme disease and that indeed there is hope for treatment and a better quality of life. I do not take any pleasure in contradicting any previous conclusions they experienced from others in the medical community. Because I was there once before. And I know the struggles I faced to remove those blinders, even as an open-minded practicing physician who had my suspicions. When facing potential scrutiny and criticism from opposing voices, and even more so, a disruption in professional routines and comfort zones in the context of an already stressful and undesirable work-life balance, it’s simply easier to maintain the status quo and to just keep moving on. But wow, am I so overjoyed that I opened that door. It’s been more than worth it to help these patients, and there’s a whole new chapter to be written in this journey.

—————
Mark Su, MD is a graduate of Cornell University and Indiana University School of Medicine. He was later the Academic Chief Resident at Tufts University in Boston and received the national Mead-Johnson Award for outstanding scholastic performance in a Family Medicine residency. He has practiced medicine in the north shore of Massachusetts since 2003, opening Personal Care Physicians in 2014. Mark is passionate about basketball, loves his wife, is religious about fitness, is a dutiful father, and is enamored with photography. With four children and his wife in healthcare research, he often feels like he’s barely able to hang on to his own Monkey Bars! Mark defines himself as a patient advocate, a truth seeker standing for justice, and God-honoring.

Lyme Update

Lyme Update - Under the Monkey Bars Blog

I was diagnosed with Lyme disease back in July. Had I known that there were symptoms for Lyme beyond joint pain, I might have caught it sooner. Dr. Su, my primary care doctor and guest blogger here at Under the Monkey Bars, estimates that I’ve been infected with this terrible chronic disease for about 3 years.

I never found a tick. I didn’t see a bullseye. Without gluten or dairy in my diet, I only had joint pain a few times over those years but always thought it was from exercise.

What I did have were symptoms that cycled through my body sometimes monthly or even every couple of weeks. They would last for two or three days and then disappear. When they came back, I’d usually forget that I had them before. Typical Mom with a full plate, right? Don started calling these symptoms the “ailment of the day.” It was a funny joke for a while…until we realized it was a disease.

Currently, my symptoms include pain at the base of my neck, congestion, ear pain, nausea, headaches, soreness in my feet, burning sensations in my back, hip pain, dizziness, night sweats, facial twitching, blurry vision, mixing up words, difficulty thinking or foggy brain, severe fatigue, lower abdominal pain, and dental pain. Not once did I mention these symptoms to Dr. Su over the past few years.

Instead, I went to my podiatrist for the foot pain. My chiropractor helped ease my back pain. The eye doctor couldn’t figure out what was going on with my eyes. Maybe I needed glasses? But with 20/20 vision? I told my gynocologist about the lower abdominal pain and night sweats. My blood work was normal but I had appendix surgery to alleviate the lower abdominal pain. My appendix was perfectly normal and I still have the abdominal pain. It was Lyme disease the whole time.

In the four months since my diagnosis, I’ve helped several friends through the testing and diagnosis process. It’s amazing how many people are walking around infected with Lyme. Many people get false negative test results because reliable diagnostic tests are not widely available. The FDA approved Lyme test from the early 1990’s only measures 3 markers of the disease and frequently yields negative results for people who are suffering from Lyme disease. Not all providers are able to order the iGeneX test, which takes 3 weeks for results but is worth the wait. iGeneX tests for 15 markers of the disease, making this private test much more accurate. 

I’m on a 6-month regimen of Ceftin, Azithromycin, and herbal supplements (parsley oil and glutathione) to treat the Lyme disease. Most people don’t realize that when you start the antibiotics, you feel worse before you feel better — for about 4 months. I have more frequent symptoms now than I did before I got diagnosed. It’s called herxing or a herx reaction, which occurs when dead bacteria release toxins into the blood and tissues faster than the body can handle it. Regular Lyme symptoms are amplified while your body tries to get rid of the new toxins.

I’ve figured out a few tricks to help my body work through the symptoms. I’m resting more than ever. I take gentle yoga classes twice a week to help with the joint pain. I see my chiropractor religiously every other week to manage the neck and back pain. I keep a weekly appointment for nerve stimulation treatments from a Myokinesthetics specialist. I take multi-strain probiotics every day at lunch time between antibiotic pills. I drink a cup each of black and green tea daily, as well as tons of water with lemon to help my liver flush out the toxins. Eating clean definitely makes my body heal faster. I follow a gluten and dairy free diet that’s heavy on leafy greens. I still have Lyme symptoms but I feel a lot better when I can take the time to help my body release the toxins.

Everyone’s body is different. Lyme disease is like a chameleon, constantly changing so that you can’t catch it. Sometimes people call Lyme disease an invisible illness. Most people who have the disease look fine, because the majority of the symptoms are internal. I’ve learned that I can turn it off and on sometimes, much like an actress. If I ignore my symptoms and have a fun night out, I’m recovering at home for two days after. When you have Lyme disease, you wake up most days feeling like you have a horrible cold plus a hangover and sore from a work out that you didn’t have energy to do.

The road ahead is still long for me, but I know that if I take care of myself, by body will heal. Lyme disease can happen to anyone. Chances are at least one of your friends is infected with Lyme and doesn’t even know it. Familiarize yourself with the symptoms so that you can help others get a faster diagnosis — and be able to diagnose yourself.

Know someone with Lyme? Don’t ask them how they are feeling. Try asking, “How are your symptoms today?” Be flexible when they cancel plans, because some days we just can’t pretend we’re okay. Some days I’m not okay at all. But life goes on, and I’m super thankful for the incredible friends and family who have helped me through this difficult time.

Be informed and be healthy, and always remember to check for ticks!

The Dr. Su Series: Vitamin D

The Dr. Su Series: Vitamin D - Under the Monkey Bars

By guest blogger Dr. Mark Su

As our summer draws to a close (commence the tears and sobbing), you might be wondering whether vitamin D is an ill-timed topic to discuss. Surprisingly, it’s not. Vitamin D is actually a year round challenge for most of us.

Vitamins by definition are beneficial and necessary components in our body’s every day cellular functions. Uniquely, we can make vitamin D via sunlight exposure; the sun’s rays activate enzymes in our skin to generate it for our bodies. But the amount of vitamin D generated is rarely sufficient. We tend to highly overvalue the benefit of the sun exposure we receive from the summertime, much less from seasonal time spent outdoors gardening, walking, or doing other activities. 

Dr. Michael Holick of Boston University is a premier global expert on vitamin D. I once heard him say that it’s not simply a matter of the quantity of time we spend in the sun. Dr. Holick suspects that given the United States’ location on the earth, that the direction of the sun rays may play a role in further inhibiting us from effectively having enough sun exposure to generate sufficient vitamin D. Add in genetic factors and other known or unknown biochemical processes in the manipulation of vitamin D in our body, and the end result is simply that sun exposure alone is inadequate.

The benefits of vitamin D are many-fold. Conventional medicine has historically supported its benefits for bone health, in that vitamin D enables nutritional calcium absorption. Over time, I’ve seen the conventional medical community progressively embrace other touted benefits, including an enhanced immune system, heart health protection, effects on muscles, reducing one’s risk for illnesses (like diabetes, rheumatoid arthritis, and multiple sclerosis), and even certain forms of cancer. No doubt, much research still needs to be done, but given the extremely minimal downsides of taking vitamin D compared to the significant upsides, I advocate to my patients that a vitamin D deficiency is a no-brainer to address.

The “normal” reference range for vitamin D is a level greater than 32. Those who I consider more “in the know” all agree we should aim for a level of at least 50. For individuals with a stronger cancer family health profile, we would recommend perhaps even 70. My professional observation is that in the New England area the typical individual has a level of about 25. 

What does it take to get up to the preferred level of 50? A prescription level of 50,000 IU of vitamin D ingested twice a week for at least 12 weeks, sometimes more. I usually recheck a level after those 12 weeks. If you don’t have access to prescription dosing, I would usually suggest 10,000 IU of vitamin D daily, which would require at least 15 weeks to reach that same end goal. Once the optimal level is achieved, a maintenance dosing is required to keep that level in the proper range-usually that requires 2000 IU per day, sometimes more.

While toxicity is academically possible, it is quite uncommon to rare. Nonetheless, I suggest medical supervision for vitamin D level testing; most doctors are willing to do so for their patients. There are testing kits available through trusted online companies as well, including a partnering lab with the Vitamin D Council non-profit organization. 

Vitamin K2 is a newer finding that becomes an even more important subject with the awareness of vitamin D, and optimizing the latter in our bodies. We’ll talk more about that another time in the Dr. Su Series. Until then, thanks for reading and be sure to get your vitamin D levels checked!

—————-
Mark Su, MD is a graduate of Cornell University and Indiana University School of Medicine. He was later the Academic Chief Resident at Tufts University in Boston and received the national Mead-Johnson Award for outstanding scholastic performance in a Family Medicine residency. He has practiced medicine in the north shore of Massachusetts since 2003, opening Personal Care Physicians in 2014. Mark is passionate about basketball, loves his wife, is religious about fitness, is a dutiful father, and is enamored with photography. With four children and his wife in healthcare research, he often feels like he’s barely able to hang on to his own Monkey Bars! Mark defines himself as a patient advocate, a truth seeker standing for justice, and God-honoring.

I Have Lyme Disease

I Have Lyme Disease - Under the Monkey Bars

This is it. My most revealing post so far. I feel naked already. I have Lyme disease. There, I said it.

Please don’t say you’re sorry, because no one is more sorry than I am. I’m writing this post because Lyme disease is so controversial that most of us don’t even know the symptoms or how different the treatment plans can be. I didn’t, and I wish I had known.

I pulled a tick off my back a few years ago after working in the yard. I didn’t get a bullseye. I didn’t get flu symptoms. Maybe it it was that tick or another one that I never found — most people don’t see the tick that infects them. I’ve thought long and hard about when I got it, but it really doesn’t matter. Either way, I have Lyme disease.

I would still be walking around not knowing I have this bacteria growing inside me if it hadn’t been for a few chats with a friend, who recently got diagnosed with Lyme herself. She started telling me some of the symptoms, most seemingly ordinary. Headaches, ear pain, back pain, jaw pain, congestion, difficulty concentrating, foot pain, and so many other symptoms. She had stopped telling people how she was feeling because she felt like she was complaining all the time, and that they would think she’s crazy.

And then she mentioned that her husband said she had a new symptom every day. I said, “You mean like the ailment of the day?” And she said, “YES!” I sat down and took a deep breath. Because for the past few years when Don gets home from work, he asks me, “What’s the ailment of the day?” The girls laugh, but every day there seems to be something that’s bothering me. And it somehow became the norm.

One day I’d have an ear ache, and then it would go away. I’d feel like I was getting a cold, and I’d miraculously fight it. I’d think, “I’m so healthy that I beat that cold!” I started going to the chiropractor more often for pains in my neck and back, and more recently my hip.

Sometimes my legs would hurt when I finished climbing the stairs to our bedroom on the 3rd floor of our old Victorian. I’d blame it on the barre class I went to that day or the day before. I knew that joint pain was a Lyme symptom but didn’t realize I was having joint pain at the time.

Some days I’d feel so tired that I could cry. But everybody’s tired, right? I started using those words as a mantra in my head, “Everybody’s tired.” And I’d keep going, crossing items off my To-Do list and taking care of my family.

It always seemed that the symptoms were worst around that time of the month. So I blamed my P, as I call it. For almost three weeks out of the month, I could blame hormones. A few times I had night sweats, which I only mentioned to my gynecologist, not my primary doctor. My blood work came back normal so my gynecologist said not to worry about the night sweats.

I’m so focused on the kids and running the house that I rarely keep track of myself. Not once did I think it was odd that I keep getting weird aches and pains…because they always went away in a day or two. They never lasted long enough for me to even tell my primary care doctor. In fact, at my annual physical in May, I told Dr. Su that I felt great. It never occurred to me that something was wrong, very wrong.

That’s the thing with Lyme disease. It’s so good at disguising itself. Which is why it’s so hard to diagnose. Many people get false negative results because reliable diagnostic tests are not widely available. The FDA approved Lyme test from the early 1990’s only measures 3 markers of the disease and frequently yields negative results for people who are suffering from Lyme disease. Dr. Su ordered me the iGeneX test, which takes 2-3 weeks for results but is worth the wait. iGeneX tests for 15 markers of the disease, making the test much more accurate. It also tests for co-infections, which is another controversial area of Lyme. And yes, I’ve got one of those too: Bartonella.

When Dr. Su examined me the day we went over my results (7/8/15), he said he would have diagnosed me with Fibromyalgia if we didn’t know it was Lyme disease. I’m on two antibiotics, which I’m thrilled to say that I’m not reacting to!! I have 4 drug allergies so I was super stressed about taking anything; it’s been years since I took antibiotics. My treatment plan is taking these two antibiotics for at least six months, while continually evaluating symptoms as they arise.

After going over all of my symptoms and thinking back to how long it’s been, we’re estimating I’ve had Lyme disease for three years. My symptoms have worsened over time, but that’s not the case for everyone. Dr. Su says I have a better outlook of healing because of my healthy lifestyle. Our goal is three months of symptom remission. He may try cycling the meds and possibly some supplements like glutathione once I’ve been on the antibiotics for a while.

Right now, I’m getting ready for the herxheimer reactions, known as herx or herxing. These reactions are the result of massive die-off of pathogens by the antibiotics. The dead or dying microbes release toxins into the body, and symptoms result until the body is able to process and eliminate these toxins, or detox. Sometimes herx symptoms are worse than usual Lyme symptoms and often feel like the flu. Fun times ahead!

I wake up each morning not knowing how I’m going to feel. Every day, every hour is different. I’m really thankful to have planned a low key summer with the monkeys. I’m trying to trust in my body. Trust it can and will heal itself. Taking life one day at a time.

If you think you have Lyme disease or know someone who may have the disease, seek out a specialist who sees Lyme cases frequently. Lyme is a complex disease that is difficult to diagnose. Educate yourself and learn the right questions to ask. Know the symptoms so that you can catch it before you have chronic Lyme. Trust me, you don’t want to mess with Lyme. If you live in a tick infested state like Massachusetts, do tick checks every night. You might even consider having your yard sprayed by a professional.

Be smart and be healthy, friends. And don’t forget to check for ticks (couldn’t resist linking to the song)!