Ammonia on the Brain with Cirrhosis

When I was first diagnosed with liver disease, I didn’t understand why my doctor kept talking about something called “ammonia levels.” Honestly, I was thinking about pine cleaners and how the kitchen smelled when mom did the spring cleaning! But after going through some scary symptoms due to my Hepatic Encephalopathy or HE, I got some answers because with severe HE, I realized how important it is to understand this part of my health. So I hope it helps you too if you or a loved one have ammonia on the brain with cirrhosis.

ammonia on brain cirrhosis

What Are Ammonia Levels Anyway?

Ammonia is a waste product your body makes when you digest protein (like meat, eggs, and beans). Normally, your liver takes care of that ammonia and turns it into something called urea. Then your kidneys flush it out through your pee. This process is called the urea cycle.

But if your liver isn’t working properly—like in liver disease—ammonia can start to build up in your blood. This can be super dangerous because ammonia is toxic to your brain. High levels can cause memory problems, confusion, and even coma. The medical name for this is hyperammonemia. Big word, but it basically means “too much ammonia in the blood.” I was hyper for sure and I survived with the correct treatments.

Why Did I Need the Test?

Mine started long before I knew about the lurking liver disease. It was hidden and almost strange symptoms—things like feeling confused, super tired, moody, and unsteady on my feet. Some days I’d forget where I was, fall asleep in my car, or forget what I was doing. When I was hospitalized after ascites came up and my belly bloated, he ordered an ammonia blood test to help figure out what was going on.

This test doesn’t take long. They just draw a small sample of blood, usually from a vein in your arm. Sometimes they might take blood from an artery if they need more exact results. Just to say though. This is not an exact science and my doctor told me early on that ammonia was not always the most reliable way to detect HE.

What Do the Results Mean?

If your ammonia levels are normal, that’s great news. But if they’re too high, it means your body isn’t getting rid of waste the way it should. Liver disease is the most common reason, but it can also be caused by:

  • Kidney problems

  • Certain rare genetic conditions (called urea cycle disorders)

  • Reye syndrome (a rare condition mostly in children after a viral illness)

  • Some medications

What Symptoms Should I Watch For?

Everyone is different, but some common signs of high ammonia levels are:

  • Feeling tired or confused

  • Headaches or throwing up

  • Mood swings

  • Trouble walking or talking

  • Seizures

  • In kids, not growing well or missing developmental milestones

If you or someone you love has liver disease, it’s important to know these symptoms. Don’t wait to get help if something feels off.

What Helps?

Treatment depends on the cause, but your doctor may recommend medicine, diet changes, or even hospital care if levels are too high. They’ll likely repeat the ammonia test to see if your treatment is working.

Also, a few quick tips: Before the test, don’t smoke or drink alcohol. You may also need to skip heavy exercise or certain meds—but only if your doctor says so.

Ammonia on the Brain with Cirrhosis

I know this stuff can feel overwhelming for you and your caregiver who can help you with hepatic encephalopathy. But understanding it is a big step in taking care of yourself. You’re not alone in this. I’m walking this road too, and I’m cheering for you every step of the way. xo Karen

Share

Facebook
Twitter
Pinterest
WhatsApp
Email
Related Posts
MASLD vs MASH: Where are you on the spectrum karen hoyt ihelpc

MASLD and MASH: Where are You on the Spectrum?

There are no FDA approved medications for those with fat MASH or MASLD liver disease. You can learn about the stages or find out where you are on the spectrum. I’ve beat liver cancer and love to encourage others to learn more about how the liver tries to heal itself. I’ve written for over a decade and have plenty of stories that can help you in your liver disease journey.

Read More »
New liver language 2023: MASH and MAFLD nomenclature terms karen hoyt

New Liver Language 2023: MASH and MAFLD

The global liver community chose new terms or nomenclature for the various types of liver diseases. The new terms are more accurate and also less stigmatizing for the patient. Although it will take time to work them into every area of the medical community, here is a copy for people who have liver disease to start with. There is no more NASH, it will be MASH, NAFLD becomes MASLD, MetALD is a new term, and SLD is the overarching term for steatosis.

Read More »
Winter Solstice: A Quiet Moment of Light, Loss, and Gratitude

Winter Solstice: A Quiet Moment of Light, Loss, and Gratitude

The ending of a year and the dawn of a new one holds so many symbols. It requires a day of its own. Today, on the longest night, I’m holding all of it—light, shadow, joy, ache, gratitude, and hope. Winter whispers that none of it has to be sorted or solved. It only needs to be felt.

Read More »

The Heartbeat of TRIO: Finding Support Close to Home

Every organ transplant recipient and caregiver understands the journey: it is a marathon, not a sprint, and while the medical teams are brilliant, the emotional and logistical toll can feel isolating. I was actually making plans to purchase a rental property and run a non-profit for patients post-transplant when Lorrinda called me. She had a different vision. In fact, Lorrinda had already connected with TRIO National and was dedicated to starting a local peer support chapter—she sold me on the idea!

This critical need for local, consistent peer support is what led to the founding of the Transplant Recipients International Organization (TRIO) Oklahoma Chapter. Learn more here about TRIO.

Read More »

Dr. Thomas Starzl: Father of Transplantation and TRIO

Dr. Thomas Starzl: Father of Transplantation and TRIO – I learned of this while preparing a presentation for The AASLD Liver Meeting. Lorrinda Gray Davis, who is the founder of Oklahoma’s TRIO Chapter just told me this week. We started our chapter with me as her first VEEP because we saw the need. I had literally no real support post transplant. During COVID, she went to work and the rest is history. Now she is president of TRIO International. But I’m getting ahead of myself. This story is about Dr. Starzl and what I imagine to be one of the greatest collision of ideas in medical history. What a man. What a great heart he has.

Read More »
Make a Donation

Donate Now

[wp_paypal_payment_box email="ihelpc.com@gmail.com" options="Donate $:10.00|Payment for Donate $:20.00|Payment for Donate $:30.00" other_amount=true currency="USD" new_window="1"]
Receive the latest news

Subscribe To Our Weekly Newsletter

Get notified about new articles