Tag: CKD

  • Low Sodium Doesn’t Mean Unlimited

    Low Sodium Doesn’t Mean Unlimited

    One of the biggest lessons I’ve learned is that “low sodium” doesn’t automatically mean “eat as much as you want.”

    Sometimes solving one dietary problem creates another thing you still have to pay attention to.

    That has been especially true for me because I’m not managing just one chronic illness.

    I’m trying to balance congestive heart failure, chronic kidney disease, and diabetes at the same time.

    And some days, honestly, it feels like the rules contradict each other.

    Low Sodium Is Only One Piece of the Puzzle

    Because of my heart failure, sodium is something I pay very close attention to. Too much sodium can contribute to fluid retention, which is one reason people with heart failure may be advised to limit sodium and, in some cases, fluids. The exact limits should come from your healthcare team. 

    But sodium isn’t the only number that matters to me.

    Carbohydrates are another big one because I also have diabetes.

    Lately, my carbohydrate intake has actually been very well controlled.

    Unfortunately, part of the reason is something I’m not particularly proud of:

    I’m sometimes afraid to eat or drink too much.

    I know that sounds messed up.

    But after being hospitalized multiple times, the fear is real.

    Why I’m So Determined to Stay Out of the Hospital

    Hospital stays are particularly difficult for me because of my mobility problems.

    My right hip is bone-on-bone, and I use a walker. That makes me a fall risk.

    When I’m hospitalized, that usually means bed or chair alarms. If I need to get up, I’m supposed to call for assistance.

    That sounds reasonable until you’re receiving IV diuretics.

    When those medications start working and you need to use the bathroom, sometimes you need to go now.

    Waiting for someone to arrive, turn off the alarm, and help you up can be frustrating and uncomfortable.

    Yes, I could simply get up anyway, but in my experience that tends to make the stay even more unpleasant.

    So when I say I’m motivated to avoid another hospitalization, I mean it.

    That fear has definitely influenced the way I eat and drink.

    The strange side effect is that my diabetes numbers have been better because I’m controlling my portions and carbohydrates so carefully.

    That doesn’t mean fear is a good dietary strategy.

    It means I still have work to do finding a healthier balance.

    CHF, CKD and Diabetes Don’t Always Play Nicely Together

    This is where things get complicated.

    With chronic kidney disease, nutrition may involve paying attention to sodium, potassium, phosphorus, protein and sometimes fluids depending on kidney function and lab results. The National Kidney Foundation stresses that these needs vary from person to person and should be individualized. 

    Then heart failure enters the picture.

    My heart-failure plan includes careful sodium and fluid management.

    Then diabetes adds another layer.

    Carbohydrates matter because they affect blood glucose, and portion size matters even when the food itself seems “healthy.” The American Diabetes Association specifically emphasizes being mindful of carbohydrate intake and portioning carbohydrate foods appropriately. 

    That means I can’t simply look at something and ask:

    “Is it low sodium?”

    I also have to ask:

    How many carbohydrates are in it?

    How much potassium?

    How much phosphorus?

    How much fluid?

    How large is the serving?

    And how does it fit with everything else I’m eating that day?

    The Rice Example

    Rice is a perfect example.

    Plain rice is naturally very low in sodium, which makes it attractive for a low-sodium diet.

    But rice is also a carbohydrate food.

    So if I sit down with a giant bowl of rice because it’s “low sodium,” I may solve one problem while creating another for my blood sugar.

    That’s why portion control matters so much to me.

    I can still eat rice.

    I just have to respect what it is.

    Low sodium does not mean unlimited.

    There Probably Isn’t a Magical Food

    I think this is where people can get trapped.

    You find something that has almost no sodium and think:

    Finally! Something I can eat without worrying about it.

    But then you look at the rest of the nutrition label.

    Maybe it’s loaded with carbohydrates.

    Maybe it’s high in potassium.

    Maybe phosphorus becomes an issue for someone with kidney disease.

    Maybe the serving size is much smaller than you thought.

    There usually isn’t one magical food that checks every box for every medical condition.

    And even when something fits your diet beautifully, eating unlimited amounts of it probably isn’t the answer.

    I’m Still Learning

    I want to be clear about something.

    I have not mastered this.

    Not even close.

    I’m still learning how to balance all of these conditions without becoming afraid of food.

    I joke that I’m scared to eat or drink anything.

    The uncomfortable truth is that sometimes the joke isn’t very far from reality.

    That’s something I need to get better at.

    Yes, being more careful has contributed to my weight loss, and I’m happy about that.

    But the goal shouldn’t be to lose weight because I’m frightened to eat.

    The goal is to learn how to eat enough of the right foods, in the right portions, while staying within the limits my healthcare team has given me.

    That’s a much healthier goal.

    Moderation Has Become the Real Lesson

    If there is one thing I’ve learned, it’s this:

    Every food has to be looked at as part of the bigger picture.

    Something can be low sodium and still require portion control.

    Something can be good for diabetes but not ideal for someone who needs to watch potassium.

    Something can fit a kidney-friendly plan but not fit your particular fluid restriction.

    Nutrition becomes much more complicated when several chronic illnesses overlap.

    That’s why I’m trying to stop thinking in terms of:

    Good food. Bad food.

    And start thinking in terms of:

    How does this fit into my overall day?

    Because for me, that’s really what Low Sodium Living has become.

    Not eliminating everything.

    Not eating unlimited amounts of the “safe” foods.

    Just trying to find balance.

    And accepting that I’m still learning how to do it.

    ❤️ Greg’s Take

    Living with multiple chronic illnesses sometimes feels like trying to solve a puzzle where the pieces keep changing.

    CHF tells me to watch sodium and fluids.

    Diabetes tells me to watch carbohydrates.

    CKD means I may also need to pay attention to things like potassium and phosphorus depending on my labs and what my doctors recommend. 

    It can be exhausting.

    But I’m starting to understand that the answer probably isn’t finding the perfect food.

    It’s finding the right balance.

    Low sodium doesn’t mean unlimited.

    Neither does low carb.

    Neither does low potassium.

    Everything still has to fit into the bigger picture.

    And for now, that’s a skill I’m still learning.

    Medical Disclaimer: I am not a doctor or medical professional. The information on this page reflects my own personal experience living with chronic illness and managing my diet and health. What works for me may not be appropriate for someone else. Always talk with your doctor, dietitian, or other qualified healthcare professional before making changes to your diet, medications, fluid intake, or treatment plan.

    This website is intended to share my journey, not to replace professional medical advice.

  • My Health Tracker

    My Health Tracker

    The Five Minutes Every Morning That Help Me Stay Ahead of My CHF

    Living with congestive heart failure has taught me something important.

    Your body is constantly giving you information.

    The question is whether you’re paying attention.

    Every morning, before I drink my morning water or begin my day, I spend about five minutes checking in with my body.

    To some people, it probably looks like I’m filling out a simple spreadsheet.

    To me, it’s much more than that.

    It’s an early warning system.

    Over time, I’ve learned that it’s much easier to recognize a problem before it becomes serious than it is to recover after the problem has already happened.

    That’s why I track my health every single morning.

    Not because my doctors told me to.

    Because it helps me understand my own body.

    One of the most important lessons I’ve learned while living with chronic illness is this:

    Nobody will ever know your body as well as you do.

    The more information I collect, the better conversations I have with my doctors, and the more confident I feel when something doesn’t seem right.


    Download My Daily Health Tracker

    If you’d like to use the same spreadsheet I use every morning, I’ve made an example version available for you to download.

    📥 Download the Daily Health Tracker (Excel)

    Feel free to customize it for your own health conditions. What I track may not be exactly what you need, but hopefully it gives you a good starting point for building your own daily routine.


    What I Track Every Morning

    Below is a screenshot of the actual spreadsheet I use every day.

    Screenshot of the example of the health tracking Excel Sheet that I use

    It isn’t complicated.

    In fact, that’s intentional.

    The easier something is to use, the more likely you’ll continue using it.

    Each column serves a purpose, and together they give me a quick snapshot of how my body is doing each morning.


    📅 Date

    The first column simply records the date.

    It sounds obvious, but dates become incredibly important when you’re looking for trends over several days, weeks, or even months.

    Sometimes a doctor will ask,

    “When did this start?”

    Instead of guessing, I simply look back at my spreadsheet.


    🕒 Time

    I try to record my information at approximately the same time every morning.

    For me, that’s usually around 5:00 AM, after using the restroom but before eating breakfast.

    Keeping everything consistent makes it easier to compare one day to the next.


    ⚖️ Weight

    Weight is probably the most important number I track.

    For someone living with congestive heart failure, sudden weight gain often isn’t body fat.

    It’s fluid.

    That’s why I weigh myself every morning under the same conditions. After using the washroom and wearing the same type of clothes.

    A sudden increase can be one of the earliest signs that my body is retaining fluid.


    📈 Daily Weight Change

    The next column calculates the difference between today’s weight and yesterday’s.

    I’m watching for one thing in particular.

    Have I gained 2–3 pounds overnight or about 5 pounds in a week?

    Those numbers can be an early warning sign of fluid retention and may indicate that it’s time to contact my healthcare provider.

    Instead of trying to remember yesterday’s weight, Excel does the math for me automatically.


    💧 Water Percentage

    My scale also estimates my body water percentage.

    While I know this isn’t a perfect medical measurement, I still find it useful.

    The spreadsheet uses that percentage to estimate approximately how many pounds of my body weight are water.

    Is it exact?

    No.

    But it’s another piece of information I can use.

    If you have a pacemaker, ICD or an implantable device, please see the warning at the bottom of the page on BIA scales.


    💧 Water Weight Change

    This is another calculated field.

    It compares today’s estimated water weight to yesterday’s.

    Again, I don’t make medical decisions based on this number alone.

    Instead, I use it as another indicator alongside my weight, blood pressure, and how I’m feeling that day.

    Sometimes several small clues together tell a much bigger story.


    ❤️ Blood Pressure

    Every morning I record my blood pressure.

    If I’m feeling unusually tired, dizzy, or lightheaded, this number often helps explain why.

    Looking back over weeks or months also helps me recognize trends that a single reading might not reveal.


    ❤️ Pulse

    Since I live with persistent atrial fibrillation, my pulse is another number I pay close attention to.

    Knowing what’s normal for me makes it easier to recognize when something feels different.


    🍬 Blood Glucose

    Because I also have diabetes, I record my morning glucose reading.

    Like everything else in this spreadsheet, I’m more interested in trends than any single day’s number.

    Consistently improving numbers are much more meaningful than one good morning.


    📝 Notes

    This might actually be the most valuable column in the entire spreadsheet.

    Numbers only tell part of the story.

    The notes tell the rest.

    This is where I write things like:

    • Poor night’s sleep
    • Feeling unusually tired
    • Increased hip pain
    • Didn’t take Torsemide today
    • Swelling in my ankles
    • Shortness of breath
    • Walked farther than usual

    Months later, these notes often explain why certain numbers changed.

    They’ve become incredibly valuable when preparing for doctor appointments.


    👨‍⚕️ Doctor Follow-Up

    The last column is one I added for myself.

    Whenever one of my doctors changes a medication or gives me a new instruction, I write it down.

    For example:

    • Stop taking Torsemide until next appointment.
    • Reduce blood pressure medication.
    • Repeat blood work in two weeks.
    • Schedule MRI.

    When you’re seeing multiple specialists, it’s easy to forget exactly when something changed.

    Writing it down removes the guesswork.


    Why I Spend Five Minutes Every Morning

    Some people may look at this spreadsheet and think it seems like a lot of work.

    Honestly…

    It isn’t.

    It takes me about five minutes every morning.

    Those five minutes give me peace of mind for the rest of the day.

    More importantly, they help me become an active participant in my own healthcare instead of simply reacting when something goes wrong.

    One of the biggest lessons I’ve learned is that trends are much more important than individual numbers.

    One slightly elevated blood pressure reading usually isn’t a big deal.

    Five straight days of gradual weight gain?

    That gets my attention.

    Having this information also makes my doctor appointments much more productive.

    Instead of trying to remember how I’ve been feeling over the past month, I can look back at actual data.

    It makes our conversations more meaningful and helps my healthcare team see the bigger picture.


    Could This Help You?

    I’m not suggesting everyone should track the exact same information I do.

    Your health conditions may be completely different from mine.

    But I do believe that anyone living with a chronic illness can benefit from keeping some type of health journal.

    Whether it’s on paper…

    In Excel…

    Or through an app…

    The important thing is consistency.

    Your future self—and your doctors—will appreciate having the information.


    Takeaways

    One of the biggest things chronic illness has taught me is that good healthcare doesn’t only happen in the doctor’s office.

    It happens every morning when I choose to pay attention to my own body.

    This little spreadsheet has become much more than a collection of numbers.

    It’s helped me recognize patterns before they became problems.

    It’s helped me prepare for doctor appointments.

    It’s helped me ask better questions.

    And most importantly…

    It’s helped me become my own best advocate.

    For something that only takes about five minutes each morning…

    I’d say that’s time well spent.

    ⚠️ A Note About Pacemakers, ICDs, and Implantable Devices

    If you have a pacemaker, ICD (implantable cardioverter-defibrillator), CRT device, or other implanted cardiac device, some consumer smart scales that measure body composition use a small electrical current (bioelectrical impedance analysis, or BIA) to estimate body fat, muscle mass, and body water.

    Before using these features, follow the manufacturer’s safety instructions for your specific scale and ask your cardiologist or electrophysiologist if they’re appropriate for you.

    If your healthcare team recommends avoiding these measurements, you can still use this tracker by recording your weight and the other health information without using the body composition features.

    Medical Disclaimer

    This spreadsheet is intended as a personal tracking tool only. It should never replace the advice of your healthcare providers or be used to make medication changes without their guidance.

    The information in this article reflects my personal experience living with chronic illnesses, including congestive heart failure, atrial fibrillation, chronic kidney disease, and diabetes. It is shared for educational purposes only and is not medical advice.

    Always follow the recommendations of your own healthcare providers regarding medications, diet, fluid restrictions, and health monitoring. If you notice sudden weight gain, worsening shortness of breath, chest pain, fainting, or any other concerning symptoms, contact your healthcare provider or seek emergency medical care as appropriate.

    Suggested External Links

  • Eating Out with CHF Isn’t Easy

    Eating Out with CHF Isn’t Easy

    Finding a Balance Between Protecting Your Health and Living Your Life

    One of the biggest changes I wasn’t prepared for after being diagnosed with congestive heart failure wasn’t taking medication or weighing myself every morning.

    It was eating out.

    For most people, going to a restaurant is just another meal.

    For me, it became a decision.

    Is this restaurant going to have something I can safely eat?

    How much sodium is hidden in the food?

    Will this one meal cause me to retain fluid for the next two days?

    Those questions have changed the way I look at restaurants forever.

    The hardest part isn’t actually the food.

    It’s what restaurants represent.

    Restaurants are where families celebrate birthdays.

    They’re where friends catch up over lunch.

    They’re where couples enjoy date nights.

    Sharing a meal is one of the ways we stay connected to one another, and when chronic illness forces you to think twice about every menu, it can feel like you’re slowly becoming disconnected from that part of life.

    I’ve experienced that feeling more than once.

    There have been times when I’ve simply decided it was easier to stay home than spend the entire meal worrying about sodium.

    While that protects my heart, it also means saying no to moments with family and friends.

    That isn’t an easy trade-off.

    Some of My Favorite Foods Are Now Memories

    One of the reasons my wife and I moved to Southwest Florida was the seafood.

    We couldn’t wait to enjoy fresh fish, shrimp, and all of the wonderful waterfront restaurants this area has to offer.

    One of my favorite meals was blackened fish or blackened shrimp.

    Today, those meals are mostly memories.

    The seasonings that give blackened seafood its incredible flavor also bring a tremendous amount of sodium. While there may be exceptions, I’ve learned that it’s usually not a risk worth taking.

    Another favorite of mine has always been clam chowder.

    I honestly can’t remember the last time I had a bowl.

    Restaurant soups are often loaded with sodium, and clam chowder is probably one of those foods I’ll simply never enjoy again.

    Those may seem like small sacrifices to some people.

    But they’re reminders that chronic illness changes more than your health.

    It changes traditions.

    It changes favorite meals.

    It changes experiences you once took for granted.

    Preparation Starts Before I Leave Home

    One of the best habits I’ve developed is looking at the restaurant’s menu before I ever get in the car.

    Many restaurants now publish their menus online, and some even provide nutrition information. That gives me the opportunity to look for grilled foods, fresh vegetables, simple salads, or meals that can be modified before I ever sit down.

    Walking into a restaurant with a plan removes a lot of the stress.

    Sometimes I already know exactly what I’m going to order before I walk through the front door.

    Don’t Be Afraid to Ask Questions

    I’ve learned that it’s okay to ask.

    Can the chicken be grilled without seasoning?

    Can the vegetables be prepared without added salt?

    Can the sauce be served on the side?

    Most servers genuinely want to help if they understand why you’re asking.

    You’re not being difficult.

    You’re simply trying to take care of your health.

    Dressing on the Side

    Salads seem like the obvious healthy choice.

    Unfortunately, many bottled dressings contain surprising amounts of sodium.

    I’ll often order my dressing on the side so I can control how much I use.

    I’ll admit something else.

    There have even been times when I’ve quietly brought my own homemade low-sodium dressing with me.

    Some restaurants don’t allow outside food because they can’t guarantee its safety or accept responsibility if someone becomes ill. I completely understand and respect their position.

    When I can’t bring my own dressing, I’ll often ask for olive oil and lemon wedges instead.

    It’s a simple solution that still lets me enjoy the salad.

    Soup Is Usually Off My List

    This one still bothers me.

    I love soup.

    Unfortunately, soup is one of the biggest hidden sources of sodium in many restaurants.

    Even a small bowl can contain more sodium than I’d like to eat in an entire day.

    As much as I enjoy it, soup has become something I almost always skip.

    It’s Not Just the Sodium

    One thing people often don’t realize is that my challenge isn’t only sodium.

    It’s fluids too.

    Because of my heart failure, I’m limited to about 1.5 liters of fluid each day.

    That means every drink counts.

    Water.

    Coffee.

    Tea.

    Soft drinks.

    Even healthy beverages.

    They’re all part of the same daily limit.

    Then there’s alcohol.

    For many people, meeting friends for a drink is just another way to socialize.

    For me, alcohol is no longer part of the equation.

    When friends gather around a table with drinks in hand, it reminds me that chronic illness changes more than what you eat.

    Sometimes it changes how you participate in life’s social moments.

    I’ll be honest…

    That’s something I still haven’t learned how to manage very well.

    Sometimes the Best Decision Is to Walk Away

    This has probably been the hardest lesson.

    There have been times when I looked over a menu and realized there simply wasn’t a good option.

    Instead of convincing myself that “one meal won’t matter,” I’ve learned it’s okay to leave and find another restaurant.

    Years ago, I probably wouldn’t have done that.

    Today, I remind myself that protecting my health is more important than protecting my pride.

    I’m Still Learning

    If I’m being completely honest…

    I haven’t figured this out yet.

    Eating out with CHF remains one of the biggest challenges in my life.

    I still miss the freedom of ordering whatever sounds good.

    I miss seafood dinners without worrying about sodium.

    I miss a bowl of clam chowder on a cool afternoon.

    I miss walking into a restaurant without studying the menu before I leave home.

    But I’m learning that living with chronic illness isn’t about finding perfect solutions.

    It’s about making the best decisions you can with the information you have.

    Most days that means eating at home.

    Some days it means asking a dozen questions before ordering.

    And sometimes…

    It means deciding that spending time with the people you love is worth the extra effort it takes to find a meal you can enjoy safely.

    I still believe there has to be a compromise.

    A way to protect my health without completely giving up one of the most important ways people connect with each other.

    I haven’t found that balance yet.

    But I’m still looking.

    Screen capture this and carry it with you when you go out

    🍽️ My Restaurant Checklist

    ✔️ Read the menu online first.

    ✔️ Look for grilled or baked options.

    ✔️ Ask for sauces and dressings on the side.

    ✔️ Skip soups and heavily seasoned foods.

    ✔️ Watch both sodium and fluids.

    ✔️ Don’t be afraid to ask questions.

    ✔️ If there isn’t a good option, choose another restaurant.

  • You Are Your Best Advocate

    You Are Your Best Advocate

    You Are Your Best Advocate

    One thing I’ve learned through this journey is that no one is going to advocate for my health more than I will.

    Living with chronic illnesses means I don’t just have one doctor. I have a cardiologist, nephrologist, primary care physician, specialists, nurses, technicians, pharmacists, therapists, and the occasional emergency room physician. Every one of them is an important part of my healthcare team.

    But they’re exactly that—a team.

    Each of them sees only a piece of the puzzle.

    They may have access to my medical records, but they don’t live in my body. They don’t know how I felt when I walked across the grocery store yesterday. They don’t know that I woke up at 12:30 this morning and never got back to sleep. They don’t know the subtle changes I’ve noticed over the past week unless I tell them.

    That’s why I’ve learned to speak up.

    When I was first diagnosed with congestive heart failure (CHF), atrial fibrillation (AFib), chronic kidney disease (CKD), diabetes, and arthritis, the medical terminology felt like learning a foreign language. I assumed the doctors would simply tell me what to do and everything would work out.

    It doesn’t work that way.

    Healthcare is often a partnership, and partnerships only work when both sides participate.

    I’ve spent countless hours learning about my conditions. I read. I ask questions. I research. Before appointments, I often use ChatGPT to help me understand medical terms, learn about upcoming tests, organize my thoughts, and build a list of questions I want to ask. It doesn’t replace my doctors or medical advice, but it helps me have more informed conversations with them.

    I’ve found that understanding why something is being recommended is just as important as knowing what is being recommended.

    One experience really drove this lesson home.

    During a recent trip to the emergency room, the staff was preparing to start intravenous fluids. That’s a routine treatment for many patients, but because I have congestive heart failure and carefully monitor my fluid intake, I stopped them and explained my situation.

    They listened.

    They reviewed my history.

    The plan changed.

    No one was upset. In fact, it became a reminder that even excellent healthcare professionals are caring for many patients, each with unique medical histories. They simply can’t know every detail unless we tell them.

    That’s why our voice matters.

    Advocating for yourself doesn’t mean arguing with your doctor or pretending you know more than they do. It doesn’t mean refusing treatment because you read something on the internet.

    It means asking questions.

    It means saying, “Can you help me understand why we’re doing this?”

    It means telling them when something doesn’t feel right.

    It means making sure they know about every condition, every medication, every symptom, and every concern.

    I’ve also learned there is a fine line to walk.

    Some medical professionals welcome questions. Others may seem rushed or uncomfortable when patients ask too many. I’ve experienced both. My goal has never been to challenge someone’s expertise or prove them wrong. My goal is much simpler than that.

    I want to understand the decisions being made about my body.

    Because at the end of the day, I live with the consequences—not my doctor.

    If you are living with one chronic illness—or several—don’t be afraid to become a student of your own health. Learn the terminology. Keep good records. Ask respectful questions. Speak up when something doesn’t seem right.

    One habit that has helped me tremendously is keeping notes on my iPhone. Whenever I think of a question, notice a new symptom, experience a side effect, or want to remember something for my next appointment, I open the Notes app and write it down.

    I’ve learned that I never trust my memory anymore. If I don’t write it down, there’s a good chance I’ll forget it when I’m sitting in the exam room. That’s not because I’m getting older—it’s because living with multiple chronic illnesses means there are simply too many things to keep straight in my head.

    By the time I see my doctor, I have an organized list instead of trying to remember everything from memory.

    The same notes are invaluable when a doctor’s office calls unexpectedly. Instead of scrambling to remember what I wanted to ask, I already have my questions, symptoms, medications, and concerns right in front of me. It helps me stay focused and makes sure I don’t forget something important once the conversation starts.

    I’ve found that walking into an appointment prepared not only helps me, but it helps my doctors too. Our conversations become more productive because we’re discussing facts instead of trying to remember details from weeks ago.

    Bring someone with you if it helps, especially if you’re facing an important diagnosis or a difficult decision. Another set of ears can catch details you might miss and help you remember what was discussed after the appointment is over.

    Being your own advocate isn’t about distrusting doctors or challenging every recommendation. It’s about partnership. The best care happens when knowledgeable medical professionals and informed patients work together toward the same goal.

    Your doctors bring years of education and experience.

    You bring the one thing no one else can.

    You live this life every single day.

    That makes your voice one of the most important ones in the room.

    If there’s one thing I hope you take away from my story, it’s this:

    No one will ever care more about your health than you do.

    So ask the question.

    Take the note.

    Speak up.

    Because your voice matters.

  • Daily Journal #5: I’m worried

    My weigh-in and morning numbers were good today. Then I received the results of my kidney ultrasound.

    Both kidneys measured smaller than they did on my previous ultrasound. I understand that measurements can vary depending on how the ultrasound is performed, but it still worries me. I already knew my right kidney wasn’t functioning properly, and the report now describes my left kidney as having a nodular contour.

    My doctor has ordered an MRI to take a closer look. I’m worried about what it might show, but for now, all I can do is take this one step at a time.

  • Daily Journal #3: Ultrasound of Kidneys Today