The Epi Dog Mom Blog

Aussie Love, Epilepsy Struggles, and the Hope That Keeps Us Going

  • It’s been a little while since my last blog post, and there’s so much I could catch you up on. But today, I want to talk about one of the biggest changes in Forrest’s epilepsy journey: adding potassium bromide to his medication regimen.

    Forrest started potassium bromide in March, making it his third anti-seizure medication alongside phenobarbital and Keppra.

    Adding another medication wasn’t a decision I took lightly. In fact, I’ve always hoped to avoid adding more medications whenever possible. My main priority has never been to eliminate every seizure at any cost. It’s to find the best possible balance between seizure control and Forrest’s quality of life.

    And that’s exactly what his neurologist and I have been working toward.

    Why We Added a Third Medication

    Despite being on high doses of phenobarbital and Keppra, Forrest was still having seizures. On top of that, his high dose of phenobarbital was taking a toll on his liver.

    We needed to find a way to reduce his phenobarbital without sacrificing the seizure control it was providing.

    That’s where potassium bromide came in.

    Unlike phenobarbital, potassium bromide isn’t metabolized by the liver. Adding it gave us another way to help manage his seizures while allowing us to gradually lower his phenobarbital dose.

    Since March, we’ve been able to reduce his phenobarbital from 120 mg twice daily to 97.5 mg twice daily.

    That’s an 18.75% reduction in his daily phenobarbital dose!

    His liver numbers have improved, which has been such a relief. Although some of his liver enzymes remain elevated, his current testing no longer indicates the true liver disease we were previously concerned about. Phenobarbital itself can cause elevated liver enzymes, even without actual liver damage.

    We are still monitoring everything carefully, of course.

    His phenobarbital is now at the lowest dose we can safely maintain without risking his blood level falling below the therapeutic range, so we’re holding steady there for now.

    And this is why I can’t stress enough how important regular blood monitoring is for dogs taking phenobarbital and potassium bromide. Those blood panels help us understand not only how their bodies are handling the medications, but also whether the medication levels are where they need to be.

    The Other Side of Seizure Control

    While potassium bromide has helped us lower his phenobarbital, managing three anti-seizure medications comes with its own challenges.

    Forrest has been dealing with quite a bit of restlessness, especially when we’re apart.

    And if you follow us on Facebook, you know we’re hardly ever apart! I’m a homebody, and I was long before Forrest developed epilepsy. I genuinely enjoy being home with him.

    But when I’m working, even though I’m just in the other room, he can become very restless.

    He’s also experiencing some hind-leg weakness and instability, which can occur with anti-seizure medications. With three medications on board, two of them at relatively high doses, we’re trying to find a way to ease some of those effects without compromising his seizure control.

    A few days ago, we started gradually reducing his Keppra dose under his neurologist’s guidance.

    I’m hopeful this will help him feel a little more comfortable and steady on his feet.

    It’s going to take time, though. We have to make adjustments slowly and carefully, watching for any changes or breakthrough seizures along the way.

    There are no quick fixes when you’re trying to balance multiple medications, and I don’t want to rush something that could undo the progress we’ve made.

    Learning What Seizure Control Really Means

    One of the hardest things I’ve had to accept about epilepsy is that, for dogs like Forrest, a certain amount of seizure activity may be part of our lives.

    Of course, I would love nothing more than for him to never have another seizure.

    But epilepsy doesn’t come with a one-size-fits-all treatment plan.

    Some dogs do incredibly well on one medication. Some may only have a seizure once a year. For others, including many Australian Shepherds and dogs with difficult-to-control epilepsy, finding that level of control can be much more challenging.

    Anti-seizure medications are meant to help control seizures. They aren’t a cure for epilepsy.

    And sometimes, the amount of medication it would take to try to eliminate every seizure could come at too great a cost to a dog’s quality of life.

    That’s something I think about constantly.

    Forrest has recently been making it longer between seizures, with a few stretches reaching 40 days. Every one of those stretches has been such a blessing.

    And between seizures?

    He’s still my Forrest.

    He’s full of life, energy, personality, and all the silly little things that make him Little Dude.

    He still wants to play, splash in the water, enjoy his treats, and be right by my side.

    I hate that he has seizures. But I also don’t want the treatment for those seizures to take away the dog he is between them.

    That’s the balance we’re working so hard to find.

    What’s Next?

    Forrest has another round of bloodwork coming up in about a week.

    Along with monitoring his medication levels and liver values, I’m especially interested in seeing how his triglycerides are doing.

    His anti-seizure medications have contributed to elevated blood lipids, so we recently transitioned him off Purina NeuroCare and onto a low-fat kibble.

    I’m hoping we’ll see some improvement there, too.

    Between the diet change, the phenobarbital reduction, and now the gradual Keppra adjustment, we’ve made quite a few changes over the past several months.

    We’ll continue to take things one step at a time, working closely with his neurologist and making adjustments based on how Forrest is doing.

    Learning to Breathe Again

    I wish I could tell you the seizures get easier to watch.

    For me, they haven’t.

    I’ve gotten used to sleeping with one eye open, waking up throughout the night to check on him, and always being aware of where he is and how he’s acting.

    He’s my heartbeat outside my chest.

    And while living with a dog who has epilepsy certainly isn’t for the faint of heart, I do want anyone who’s just beginning this journey to know that things can get better.

    You learn. You adjust. You find routines that work for you and your dog.

    And eventually, you start to breathe again.

    I still worry. I still have hard days. But I also have so many wonderful days with Forrest, and I’m learning not to let the fear of the next seizure steal those moments from us.

    He is so much more than his epilepsy.

    And as long as he’s enjoying his life, I’m going to keep doing everything I can to help him live it to the fullest.


    I’d love to hear from you.

    If you have a dog with epilepsy, have you been through similar medication changes? Has your dog experienced restlessness, weakness, or other side effects while taking multiple anti-seizure medications?

    Please feel free to share your story in the comments. I know how much it can help to hear from other people who understand what this journey is like.

    And if you’d like to follow Forrest’s journey more closely, we’d love for you to connect with us on his Facebook page, Forrest aka Little Dude, where I regularly share updates about his epilepsy, his progress, and all the wonderful moments in between.

    From our lavender world of grace, we’re holding onto hope walking by faith. 💜

  • It’s been two years since Forrest fell out of the bed having his first seizure. In that moment, I thought he was dying. I didn’t know if I’d have two more minutes with him…much less two more years. But here we are… two years and 31 seizures later.

    We’ve adapted to this new normal that consists of medication schedules, bloodwork, neurology and veterinary appointments, routine blood monitoring panels, and more tears than I thought I could cry.

    Forrest has had to learn how to live with epilepsy. I’ve had to learn how to walk beside him. Both are hard, but they’re different.

    Through it all, he’s still Forrest. He still loves to chase his soccer ball, loves his Sonic icy water, loves to play in his pool in the Summer and jump through leaves in the Fall.

    He reminds me that joy doesn’t disappear because life gets hard. Every day he chooses joy, even though life hasn’t been easy. That’s who he’s always been. Epilepsy hasn’t stolen his personality. I couldn’t ask for anything more.

    In the beginning, I measured everything by seizure-free days. I still count them because they matter, but I’ve learned there’s more to loving an epi dog than counting days on a calendar. Quality of life matters. Moments matter, and they are precious.

    Progress isn’t linear with epilepsy. Hope doesn’t mean pretending everything is okay. I wish more than anything that I could take his seizures away. But that’s out of my control. What is in my control is the way I love him through it — the good days and the bad days.

    Lately, things have felt different in a very good way.

    After months of trial and error, and with the guidance of his neurologist, it finally feels like we’re getting little pieces of our life back.

    We’re even planning another trip to the beach this November—a do-over from last year after a trip that didn’t go quite as planned. (I’m just realizing I never wrote about that trip or how it became the scariest week of his seizure journey so far. I need to change that soon.) This will be his fourth trip to the beach and I can’t wait to see him with his paws in the sand again.

    If you’re reading this and your dog was recently diagnosed with epilepsy, I want to leave you with this:

    Your journey won’t look like ours because every epi journey is different—but I want you to know that you’re not alone, and years from now, you’ll be celebrating a similar anniversary with your epi dog.

    Two years ago, I didn’t know if I’d have two more minutes with him.

    Beach, please! 😆

    Two years later I’m planning beach trips, celebrating him with a Starbucks pup cup, and thanking God for every ordinary day we get together.

    I’ll never stop wishing I could take his epilepsy away, but I will also never stop celebrating the life he’s living despite it.

    From our lavender world of grace, we’re holding onto hope, walking by faith. 💜

  • I shared in the last blog post how the last several months have been a rough patch for Forrest. We’ve been navigating a whole new season of adjustments. Back in the spring he started potassium bromide, and between that, medication changes, side effects, liver concerns, bile acid testing, and working through tapering down his phenobarbital, it’s been a lot. So we’ve been adjusting together. There are a lot of moving pieces to this merry-go-round right now, but things are beginning to look up, and for that I am so grateful.

    I don’t look at him and see epilepsy.

    Do I wish he didn’t have it? Of course I do.

    Do I wish he didn’t have to take multiple medications and deal with side effects? Absolutely.

    But when I see him, I see my big, grown puppy dog. My best friend. My shadow. My family. He’s an epilepsy warrior, no doubt. No matter what life throws his way, he always shows up with a joyful attitude. It’s the reason I call him my hero.

    I see the dog that still gets excited over walks. Still wants to sniff every smell. Still wants adventures. Still wants to be included.

    I don’t expect him to do everything exactly like he used to because that wouldn’t be fair to him. We work around what he can do now. We respect his limits. We make adjustments when we need to.

    But I don’t want his world to become small.

    I don’t want his diagnosis to become his whole identity.

    I think sometimes we get caught up in what our epi dogs can’t do anymore and forget to see all the things they still can.

    Forrest can still enjoy life.

    He can still be happy.

    He can still just be a dog.

    It looks different than I thought it would.

    But different doesn’t mean less beautiful.

    It just means learning to walk a different path together.

    If you’re walking this journey too, what has been the hardest adjustment for you — the seizures themselves, the medications and side effects, or learning your “new normal”?

    If you’d like to following Forrest’s day-to-day adventures, updates, and all the little moments in between, you can follow his Facebook page. I share the real side of our journey — the hard days, the good days, and all the wags, walks, and Forrest moments in between. 🐶

    From our lavender world of grace, we’re holding onto hope walking by faith. 💜

  • It’s been a while since I’ve written here, and I wanted to share a little update on what’s been going on with Forrest and why things have been so quiet lately.

    Since November, Forrest’s seizure pattern has gradually been tightening and shifting. What used to feel somewhat predictable has started has become anything but. This is the most challenging season in our epilepsy journey we’ve faced.

    Despite being on Denamarin Advanced to support his liver, Forrest’s most recent bloodwork showed a spike in his ALT levels, which prompted his neurologist to order a bile acids test. Unfortunately, the results came back with concerning information suggesting that Forrest has developed a form of liver disease.

    Right now we don’t know exactly what type. He is scheduled for an abdominal ultrasound this Thursday, which should give us more answers.

    His neurologist believes this could be medication-induced liver disease from phenobarbital, which can sometimes be reversible, provided he can safely taper down the dose. The plan moving forward is to transition him onto potassium bromide. If he tolerates it well and it controls his seizures, we will begin a very careful taper off phenobarbital to give his liver a chance to recover.

    He is scheduled to begin a potassium bromide loading dose this Saturday, unless the ultrasound reveals something that changes our course.

    As you can probably imagine, this has been a heavy and exhausting season. I simply haven’t had the time or emotional space to sit down and write the way I usually do. Right now my main focus is simply caring for Forrest and resting when I can alongside him. Managing epilepsy in dogs often comes in waves, and lately it feels like we’re all but drowning and are in desperate need of a life raft.

    Even though things have been quiet here on the blog, please know that we’re still here.

    If you’d like to follow Forrest’s day-to-day journey, I share much more frequent updates on his social media pages. Click this link to follow Forrest on Facebook. 🐶https://www.facebook.com/forrestakalittledude

    And if you’ve walked this road before, I would truly love to hear from you.

    If you have an epileptic dog and have gone through a difficult season like this, please feel free to share your story in the comments. If your dog has taken potassium bromide, I would especially appreciate hearing about your experience — how your dog tolerated it, and anything you learned along the way.

    Sometimes the most comforting thing during hard seasons is simply knowing we’re not walking them alone.

    Thank you for being here and for continuing to follow Forrest’s journey.

    From our lavender world of grace, we’re holding onto hope, walking by faith. 💜

    • Why We Switched to a Reverse Osmosis System

      One thing I’ve become extra mindful of on this journey with Forrest is what we put into our bodies — and that includes something we use every single day: water.

      For years, we drank tap water filtered through a Brita pitcher with the Elite filters. I assumed we were doing the best we could. The water tasted fine, and I believed that meant it was “clean.”

      What I learned recently surprised me — and honestly changed everything.

      Wake Up Call

      When I entered our zip code into a water quality database, I learned that certain contaminants linked to cancer risk were present at levels up to 35 times higher than health-based recommendations! ☠️ Considering that our pets drink the same water every day — often in greater proportion than we do — that information was impossible for me to ignore.


      What I Learned About Filtered Water

      Brita (and most pitcher filters) do help improve taste and reduce certain contaminants, but they are primarily designed to reduce things like chlorine, odor, and some metals. They do not remove many of the dissolved solids and contaminants that can still be present in municipal water, depending on where you live.

      In other words:
      👉 They make water taste better
      👉 They don’t necessarily make it as pure as we might think

      Most refrigerator water filters are actually very similar in filtration capability to pitcher filters — convenient, yes, but still limited.

      That realization was a turning point for me.


      Why I Chose a Reverse Osmosis (RO) System

      After researching options, we chose an APEC reverse osmosis system — and I truly can’t say enough good things about it.

      Reverse osmosis systems filter water at a much deeper level, removing:

      • Total dissolved solids (TDS)
      • Heavy metals
      • Industrial contaminants
      • Many things pitcher and fridge filters simply don’t catch

      Clean drinking water matters for us, and it matters just as much for our pets, who rely entirely on us for their health.


      The Hidden Cost of Pitcher Filters

      Another thing that finally pushed me over the edge?

      The constant refilling.

      Between:

      • Me
      • Forrest
      • Cooking
      • Making ice

      I was refilling that pitcher constantly. It got old fast.

      And when I added up the cost of replacing the more expensive Elite filters, I realized I was spending quite a bit over time — with limited filtration to show for it. 😣


      Installation Was Easier (and Cheaper) Than I Expected

      I don’t have family or friends nearby who could install mine, so I hired someone and was able to get it installed for $125, which I felt was very reasonable.

      That said, the manufacturer and many reviews state that someone with basic handyman skills can install this system themselves. No professional plumbing license required.

      I also opted for the refrigerator hookup, which means:

      • Our ice is now made with RO water
      • No more refilling ice trays

      The RO system currently supplies our ice maker, and that same line will support a future water-dispensing fridge. 💧


      Testing Our Water (Another Shocker)

      I tested four different water sources: our tap water, water from our Brita pitcher (using the Elite filter), bottled water, and our water after installing the reverse osmosis system.

      What surprised me most was how close the tap water and the Brita-filtered water tested to each other, despite using the more expensive pitcher filter.

      In contrast, the bottled water and the RO-filtered water tested very similarly to each other — and significantly lower than both the tap and pitcher water.

      That was the moment it really clicked for me: improving taste isn’t the same thing as deeply filtering what’s in your water.


      How You Can Learn More About Your Own Water

      Want to learn more about what’s in your drinking water? You don’t have to guess!

      🔗 Check your local water quality by ZIP code:
      👉 EWG Tap Water Database

      This tool also helps recommend filtration options based on your specific area, which I found incredibly helpful.

      🔗 The RO system we chose:
      👉 APEC Water Systems RO-90

      If you’re not ready for an RO system, you can also:

      • Order a water quality meter
      • Use a mail-in water test kit
      • Test your current setup and decide from there

      The EWG website doesn’t just show what’s in your water — it also helps guide you toward filtration options that fit your needs.


      Final Thoughts

      I wish I had done it sooner.

      ✔ Affordable
      ✔ Cleaner water
      ✔ Less daily hassle
      ✔ Better for Forrest
      ✔ Better for me

      APEC’s customer service was top-notch, the system has been flawless, and the peace of mind is priceless.

      Clean drinking water is something we often take for granted — until we learn what’s really in it. And now? I feel better knowing we’re drinking cleaner, safer water — every single day.💧

      Disclaimer

      This post reflects my personal experience and research as a pet parent and consumer. I am not a medical professional, veterinarian, or water quality expert. Water quality varies by location, infrastructure, and testing methods, and what works for one household may not be necessary or appropriate for another. Information shared here is for educational and informational purposes only and is not intended to diagnose, treat, cure, or prevent any disease in pets or humans.

      Some links in this post may be affiliate links, meaning I may earn a small commission at no additional cost to you. I only share products I personally use and genuinely feel comfortable recommending. I encourage readers to review their local water quality reports and consult appropriate professionals when making decisions related to health, pets, or home systems.

      Have you ever checked what’s in your local drinking water — or thought about how it might impact your pets? I’d love to hear your thoughts or experiences in the comments.

      If this post was helpful, feel free to share it with another pet parent.

      From our lavender world of grace, we’re holding onto love, walking by faith. 🪻