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342: How to Use Enzymes to Help Digestion and Autoimmune Issues With Steve Wright
New Post has been published on http://healingawerness.com/news/342-how-to-use-enzymes-to-help-digestion-and-autoimmune-issues-with-steve-wright/
342: How to Use Enzymes to Help Digestion and Autoimmune Issues With Steve Wright
Child: Welcome to my Mommy’s podcast.
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Katie: Hello and welcome to the Wellness Mama Podcast. I’m Katie from wellnessmama.com and wellnesse.com. That’s wellness with an E on the end, which is my new line of personal care products like hair care, toothpaste and hand sanitizer that are made with safe and natural ingredients, but as effective as conventional alternatives. This episode was a really fascinating one for me and it’s about a topic that I think is really just in its infancy in emerging that has so much potential for a ton of aspects of health. I’m here with Steven Wright who is a medical engineer, a Kalish Functional Institute graduate, and a gut health specialist. He personally spent close to $400,000 overcoming his own health challenges using everything from Western medicine to shamans. And the reason I wanted to have him on today is to talk about enzymes. And we’re going to go deep on this, both systemic and digestive enzymes. But these were part of the puzzle for me with autoimmune disease and weight loss. We talk about it a little bit in this episode. And the really amazing formulas that are available now were not even available when I was going through that. So, I now use enzymes as part of my daily routine. I noticed a big difference from them. My husband uses them as well. And there’s a lot of potential in the studies right now linking these with help with autoimmune disease, food intolerance, digestive issues, even anti-aging, and a lot more. So, we’re going to go deep on all of that today. I think you’ll find this episode extremely helpful. So, let’s jump right in. Steve, welcome. Thanks for being here.
Steven: Thank you, Katie. I’ve been waiting for this.
Katie: Oh, I’m really excited to chat with you, one, because it’s always really fun to chat with you in person or on Zoom like this, but also because you have such a wide amount of knowledge on this topic. And I think it’s really important for a lot of people listening. So I wanna start broad and then kind of dial down to all of the different areas from there. We’re gonna go deep on enzymes like I mentioned in the intro. So, to start off broad, define for us what enzymes are.
Steven: Yes. So, at the broadest level, enzymes are a protein that is called like a catalyst. So basically it means it speeds up reactions. And so enzymes were around, like bacteria and viruses, well before us. They’ll be around forever. They’re involved in everything. Without enzyme reactions, we would die immediately. But basically, they are a protein that speeds up any reaction at the most basic level.
Katie: Got it. Okay. And so I’m guessing these are things that exist naturally in the body to some degree, right?
Steven: Correct. Yeah. So, it’s theorized that…if you’re familiar with, like, stem cell theory, that, you know, we’re born with the number of stem cells we have for our whole life or something like that, it’s theorized that we’re born with the amount of pancreatic enzymes, which is probably one of our biggest sources of enzymes that we use. Those are specifically usually used for digestion. But we also have, like, it’s theorized up to, like, 50,000, like, hyper-specific metabolic and systemic enzymes in our bodies that are constantly just doing all these really crazy reactions. So, yeah, we have enzymes almost everywhere. We’ll talk specifically, I think, here about the main systemic enzymes and then the main digestive enzymes, which is, for the most part, really all science even understands at this point and really all you should concern yourself with.
Katie: Gotcha. Okay. So to make sure I’m understanding before we go on. They think that you were born with all the enzymes…a certain enzyme you’re gonna have?
Steven: Yeah. Yeah. So, specifically pancreatic enzymes. It’s theorized that you’re sort of born with this reservoir of them, and you use them as you go through life. You know, if you’re like me and you had a while where you ate a lot of processed food or you go through a lot of stress or you have a lot of digestive conditions or other health conditions, you might use that reservoir up faster, or if you have ways in which your body gets, you know, hurt or ill, you could burn through your systemic enzymes trying to down-regulate inflammation, trying to regulate your immune system. And so there is a little bit of a debate about how many enzymes do we really get in our lifetime. And I don’t think there’s a true answer quite yet.
Katie: Got it. Okay. So then I guess the next question is if enzymes are a thing that we are born with, can you take them exogenously and accomplish the same thing? Because I know with certain things like the ones we make in our body might be different from ones we can consume. How does that work with enzymes?
Steven: Yes. So there’s all those super, hyper-special enzymes that we’re not even aware what they do, like they’re probably part of almost everything, glutathione, liver detoxification. Those, we can’t make exogenously. I don’t even know if we’ve really identified them scientifically. I’ve never seen them in any book, and I own, I think, everything on enzymes at this point. But let’s just talk about the fact that there… We have enzymes in our mouth. We have enzymes in our stomach. We have enzymes in our small intestine, and those are…where pancreatic enzymes and what’s called the brush border enzymes happen. Then we have systemic enzymes. So we’ll just classify them as those five areas. And basically, the systemic and pancreatic enzymes are the ones that could be in jeopardy. You could almost think about it as like CoQ10 for aging. You know, like as we age, there’s just unavoidable things such as our hormones begin to die out and things like that. It’s starting to become potentially clear that this is happening with enzymes as well.
And so when you start to eat a bite of food, because we’ll just talk digestion first, there’s amylase, which is a carbohydrate enzyme in your mouth. And so as you chew, one of the reasons why people tell you to chew a lot and not just swallow your food whole, which I’m totally guilty of a lot, is that amylase starts to work on your food in your mouth and then it works in your stomach. Inside your stomach, you have pepsin, which is a protein enzyme, a proteolytic enzyme, and that starts to work. And so while your food’s in your stomach beginning to basically unfold itself and make itself available for these enzymes, you have amylase and you have pepsin working. Then as the stomach process happens, the food dumps slowly into the small intestine, at which point your pancreatic enzymes basically mesh in. They kind of dump into your small intestine, and those are a fat or lipase carbohydrate. There’s more amylase in there. There’s also more protein enzymes, proteolytic enzymes.
But then also you have your brush border, and your brush border are kind of like…if you could see my hand right now, I’d be wiggling my fingers like spirit fingers. And basically, there’s these little hairs that cover your intestines, and these are called villi. They’re part of the brush border, and these villi are, like, super important for almost everything in your gut. And one of the things that’s really important is they are what secrete your brush border enzymes. And if you’ve heard of lactose intolerance, lactase is the enzyme that you lose or a lot of people lose anyways, and then they have lactose issues. Well, the brush border is where that lactase is made, and so there’s some people who think that potentially not everyone loses lactase and that there’s just some of us whose brush border is inflamed and broken.
In celiac, there’s actually pictures, and this is part of how you diagnose the celiac condition, is your brush border looks like it was chopped off by, like, a road grader or something that’s just all mangled and it’s not really working. And so those brush border enzymes are really specific enzymes. They do a lot of, like, cellulose and they do…so, fiber and vegetables. There’s all these really specific carbohydrates that they break down. And then the last group is the proteolytic enzymes, and those are mostly predominantly proteolytic enzymes inside your blood. However, amylase and lipase do go in the blood as well. They kind of are maybe more, like, 5%, but, like, 95% of the protein sort of enzymes in your blood, they’re able to be absorbed systemically when we take them exogenously, or sometimes we just absorb our own enzymes. And they run around, and they do all these cool blood cleaning and inflammation-reducing and immune-balancing things.
Katie: That is so fascinating. Okay. So there’s so many directions that I wanna go from there. I think especially based on both of our stories, I can see pieces falling in place of how these can be so helpful in a lot of different ways. And you mentioned proteolytic enzymes, which…that rings a bell for me because, in the heat of my own autoimmune disease, that was one of the many things that I took that I seemed to notice a big difference from. And, in fact, I think I actually took too much too fast and made myself feel really not good for a while. Can you go deeper on what those are? You said they’re in the blood. What are they doing specifically, and is there an autoimmune link there?
Steven: Yes. So, proteolytic enzymes basically just means a protein degrading enzyme. So I might have misspoke a little bit. And so what’s the difference between a digestive proteolytic enzyme and a systemic proteolytic enzyme? Well, one just happens to be working on your food to break it down, and one just happens to be inside your blood. And so when we take exogenous enzymes, so when we take a supplement, if you take it with food, the proteolytic enzymes inside of that capsule will be really busy working on your food. If you take it without food, you’ll actually absorb it.
And there’s plenty of studies on all different types of products that show that these types of enzymes are absorbed into the bloodstream and then they begin to go to work. So, I know based on, you know, just listening to your podcast that you’ve done a lot of different shows on a lot of different topics, and you’ve covered kind of like leaky gut and gut inflammation and autoimmunity pretty well. And where enzymes fit into this scenario is when we get leaky gut, so basically where our guts aren’t working properly, and different types of molecules are going into our bloodstream, a lot of times, these are where you get your food intolerances. You get your dairy and your corn, and you get your gluten sometimes and all these different things that impact us. That’s a protein molecule that’s running around the body now, and the immune system can’t have that. And so it tags that protein molecule as like, “Hey, we have to kill this. We have to get rid of it.” And so it basically puts an antigen on it, and it red flags it.
Now, this also happens with viruses, bacteria, anything that gets into the gut or into the blood vessels through the gut that really isn’t supposed to be there. And now almost everything is encoded in a protein casing. So, all those microorganisms. Most everything that causes a blood reaction is a protein-like molecule. So, the immune system just tags these bad guys, right, these foreign invaders, and now this is called a circulating immune complex or CIC. This whole process is pretty normal, although it’s not supposed to happen all that much. And what happens normally is your liver and your spleen are supposed to filter out these CICs, but as you know, we live in a toxic environment. Probably a lot of your listeners, you know, aren’t using a lot of the toxic chemicals anymore, but it’s really hard just to be a capable human of detoxing the life we live.
And so if the liver and the spleen are sluggish, overwhelmed, your immune system is kind of overwhelmed, or your gut’s really messed up, you’re gonna have CICs, like, everywhere. And now CICs, once they’re tagged, they kind of emit these little signals saying like, “Hey, I’m bad. Hey, I’m bad. Come kill me.” And these are called…one name for them is cytokines. That’s kind of big right now in what people are learning about. And till that CIC is killed or detoxified, it is emitting more inflammation. But when your spleen and liver are overwhelmed, your body in its infinite wisdom, because I do think it’s super wise, will grab those CICs and it’ll go store them in your soft tissues to try to make them as inert as possible, right? Because we can’t have our blood clogged up with all this stuff.
And so in the research, we see increased CICs in many autoimmune conditions. So that’s really prevalent in lupus, really prevalent in rheumatoid arthritis. I looked into it for Hashimoto’s just because I know we were having this conversation. It appears the research is less clear there. Studies show anywhere from 20% to 60% of people with Hashimoto’s have elevated CICs. You can actually run a CIC blood test to check for these things. They appear almost elevated in many chronic inflammatory conditions, AIDS, different infection-related conditions. There’s some new research online. And so my theory on what’s happening here is that we have our weak links, our genetic weak links. And you were born with them. I was born with them. You can’t escape them. And when your body’s trying to save you from all these CICs, it grabs the molecules and just kind of stores them in your genetic weak links. And so if you have rheumatoid arthritis, that’s near your joints, and then you end up with joint pain.
Now, the really, really cool thing about systemic and proteolytic enzymes is they go in and they break down the CICs. And they’re able to neutralize them, and they’re also able to even go into the soft tissues and break them down. And so that’s why we have research studies on systemic enzymes showing that after, like, working out, like after, like, really intense workouts, you have less pain if you have systemic enzymes. In other words, the enzymes are removing the inflammation from even just working out. But there’s plenty of usage of these in Germany and plenty of studies on rheumatoid arthritis and lupus where systemic enzyme therapy rivals various types of prescription, non-steroidal, anti-inflammatory drugs, not just your basic aspirins and things like that, but the much more powerful ones. And so they’re really cool. And they also help with clotting. They clean the blood like I mentioned. And so that’s kind of what can happen.
Now, you mentioned…this is really long so I’m gonna stop right after this. But just to finish the question, you mentioned that you took a lot really fast, and you might have had a reaction to them. If you had plenty of these CICs stored up because your body was trying to do its best, you can have what’s called a Herxheimer reaction to using them…you know, a lot of them really quickly. And so, yeah, that definitely could have happened. And then also if people are wondering, “Well, these sound, like, really potent and kind of crazy,” there’s actually a whole line of cancer research that uses high-dose, exogenous, systemic enzyme therapy. It’s Dr. Nicholas Gonzalez. He’s passed away, but there��s doctors who work underneath of his lineage. They use 150 to 180 capsules a day. So I don’t know how many capsules you were using, Katie. But in cancer at least when they try to use this type of therapy, they use mega doses, and I do believe they actually work up to that as well.
Katie: Wow, that is awesome to know, and I’m guessing there’s a lot of people listening putting these pieces together going, “Wow, I wonder if this could help my, you know, fill in the blank.” Because it seems like we’ve got data, at least preliminary data on it being really helpful for a lot of things. And before we go further, I think it’s also, I’d love for you to tell a little bit of your story because you also went on your own health journey and had to find your own health answers and then return to a state of health. So can you talk about the phases of your own health journey?
Steven: Yeah, sure. So I had some birth trauma. I’ve had intestinal issues basically my whole life, and then, you know, after college, I was a consultant at KPMG in Chicago. And I was living the super consultant lifestyle, really high stress, and I really at that point was having cystic acne everywhere. I was having my first panic attacks, I had just come out of my worst depressive episode. Every time I ate, I would have bloating so bad. I would tear up, and I was raised in a culture where boys don’t cry. And so it was really hard for me to be at the office. It was really hard for me to be anywhere and have basically stabbing knife pains. And this is no matter what I ate. I was also overweight. I was probably 230 at that point. My highest was about 245, and I’m only 5-11. I’m pretty athletic but that was still pretty big for me. And so I was eating lettuce and chicken, and I was working out an hour a day. And I was doing my best to suck it up and be a man. I just started having accidents where I was missing dates.
I accidentally, you know, pooed myself on a commuter bus, and then my boss called me into his office and said, “You’re stinking up the office. You have to fix this or, you know, bad things are gonna happen.” And so that’s when I had my final wake-up call that I needed to do something, and that led me down all kinds of awesome, you know, dietary changes that really started to change my world right away. That led me to, for instance, stomach acid, betaine HCl, digestive enzymes. Once I started to get my digestive pain away, I wanted to know why did I have to eat such a restricted diet and why didn’t my acne go away. You know, how come I didn’t feel great every day? And so that just led me naturally just to read a ton of scientific literature. I joined the Kalish Institute and was certified in functional medicine with them.
I just kept, you know, sort of biohacking, keep asking the questions like, “Well, why and, you know, how come?” And that’s led me to, you know, shamans across the world. That’s led me to all kinds of Western stuff, you know, so many supplements and kind of led me to where we are today. One of the weird things about why we’re talking today is even though I had been on a specific carbohydrate diet or an autoimmune Paleo diet for essentially seven years, around year seven, I started to get left big toe pain. And at the time, I was 32. I was a “digestive health expert.” You know, I was trying to be the picture of health, and I was trying to live up to this thing that I was supposed to be. And here I was having a hard time walking.
At first, I chalked it up to injuries. I tried stem cells. I tried shamanism. I tried all kinds of intense manual therapies, Eastern and Western, X-rays, all kinds of things. After I basically had done everything, even though there was something that in the back of my mind said, “Hey, that’s really common for what is seen in gout,” there’s no way I have it. I don’t fit the profile. How would I have that thing? I had a stigma around gout. And finally, one of my doctor buddies was like, “Man, we have really done everything with you.” And he’s the one that gave me the stem cells. He’s like, “I think you really need to take this, you know, high uric acid idea seriously. There’s really nothing else that would explain this.”
I did, you know, because that…I was previously a backcountry hunter, and just hunting, I’d have to be on anti-inflammatory drugs. Like, I couldn’t do my activities anymore. And so I started doing cherry juicing and all kinds of, you know, natural remedies for lowering uric acid and trying to support-gout related things. And nothing was working, and so I was back to like, “Man, I’m gonna have to take a prescription drug for the rest of my life that might have…it has decent side-effect profile. This isn’t okay with me.” And right about that time is when I was deep into enzymes because I have been just frustrated with the lack of consistency when I recommend to even you, you know, all my friends. People ask me for recommendations, and I was like, “I don’t know the right brand, but I’m gonna figure it out.”
And so in the middle of trying basically every brand on the market, I ran into a Ph.D. researcher who talked about systemic enzymes. He talked about a very specific thing about how they need to be activated, and when they’re activated, they do miraculous things. One of the case studies he rattled off was that his form of enzymes, his form of digestive systemic enzymes, actually were very successful in some pilot clinical trials supporting high uric acid and supporting gout pain. And I was like, “Okay. Now I’m sold. I’ll buy your stuff. Let me try it.” You know, that’s what I always do. Sure enough, 14 days into dosing them at a little bit higher dose than normal but not that high, just 6 pills, literally, this pain that I’d had for 3 years was gone. So it stayed gone. And it’s been amazing. I’ve been able to get back to a lot of my activities. I don’t rely on pain relievers anymore.
And so I can’t claim that, you know, our supplement does anything else. Just my experience is one-off. You know, results are not typical. There are research studies that we’ve done on this. We hope to do much bigger, you know, 60, 80, 100-person trials. They’ve only been 10-person trials, but it’s really, really encouraging. And it really opened my eyes like, “Oh, wow, maybe this is a really overlooked area of health that could help me and a lot of others.”
Katie: Yeah. It’s so fascinating. And I feel like this is just now really starting to be talked about, and I know you’ve done so much research on it. That’s why I was so excited to have you on today to talk about this. Having researched my own way through an autoimmune disease and now being in remission with Hashimoto’s, I keep always coming back to the inflammation piece because I think if anything, the last couple of years have really just emphasized for me how personalized health is and how at the end of the day, I found what works for me. And that definitely does not mean it’s gonna work even for someone else who has Hashimoto’s, I think there are pieces of that that do. But it does seem to all go back to inflammation, and I think that’s a common link with a lot of types of chronic disease. And so it sounds like when we’re talking about these enzymes, that’s one of the mechanisms that they’re acting on is to reduce inflammation in the body in various ways essentially, right?
Steven: Yeah. Correct. And I think everybody should be super skeptical, and I don’t think, you know, everything works for everybody. So I’m glad you brought that up. But there are these certain pathways that do appear to be universal almost. One of these is inflammation. And the cool thing about if you have, like, a properly working digestive tract is you’ll be breaking down your foods, right? You won’t have these big protein molecules busting through your gut lining, overwhelming your immune system, you know, antagonizing it. You won’t have dysbiosis, which is the microbiome getting dysregulated. All of these things are related to food. My analogy is, you know, like if you had given your kids, Katie, like a scoop of peanut butter, almond butter, and just throw it on the sidewalk and let them watch what happens, by the end of the day, there’s gonna be, like, all kinds of bugs. And maybe a bird will check it out, and probably a dog will find it and lick it. And like, you know, life just blooms whenever there’s food.
And so if we’re not digesting and breaking down the food that we eat, we’re literally causing a bloom of just whatever is gonna go for it in our guts. And that increases inflammation. So one of the biggest things is just properly digesting your food can help lower inflammation. And then, yes, these enzymes are amazing once you’re past that and you’re trying to get into the body anywhere from, you know, just cleaning the blood out, any sort of stored CICs balancing the immune system. There’s research on, like, plaque formation and, you know, heart disease, some of the risk factors for heart disease. It’s just really quite amazing, their capacity to help regulate the immune system and high inflammation.
Katie: Got it. Okay. That makes complete sense. And I know, like you’ve mentioned food intolerances a couple times and explained kind of that gut reaction and why these enzymes might be so helpful. And I know that’s a big buzzword for a lot of people listening. I’ve certainly been through that on my own when I first was in the thick of autoimmune disease. That was part of the key for me of figuring out how to reduce inflammation in the beginning as I had to be pretty strict with my diet and to deal with certain food intolerances.
So in the beginning, for me, I had dairy, gluten, coconut, eggs, and some others. And now I’m able to eat essentially everything except eggs without any kind of reaction. And I think for anyone who has their own food intolerances or certainly for a parent who has a child with food intolerances, that can be both really scary and really frustrating. And so I think that the fact that this can potentially offer hope for food intolerance is really exciting. I’d love to go a little bit deeper on that. Like is there a specific protocol that we’re seeing that seems to help with food intolerance? And when it comes to that, can kids do this as well, or do we know yet?
Steven: You know, food intolerances are like autoimmune diseases in that they’re just a complex topic, and so we can’t say someone’s��like, I had a dairy issue as well. I still have a gluten-type issue. I don’t seem to have any others, but there is some sort of interplay between your immune system and your immune system sort of reacting to proteins. Again, remember, most people don’t really know this, but when your immune system has a reaction, most of the time, like 99% of the time, it’s a protein that it’s reacting to.
And so while lactose intolerance is a totally real thing, and there’s a lot of people that have it, my personal belief is that a lot of people are actually reacting to the proteins whey and casein that are in dairy. And one of the reasons why and how we believe food intolerances happen is your immune system wouldn’t react to something or learn to react to something if it wasn’t getting exposed to it and think it was bad. And so how would that happen? Well, it would happen if your gut was leaky or if your gut wasn’t working properly. The belief is that we eat our foods. Let’s say it’s dairy or let’s make it even easier, like corn is a less…not as many people have that, but there’s a protein in corn that’s kind of like gluten. It’s called zein, and it’s just this hard-to-break-down protein basically.
And so if your proteolytic enzymes don’t break it down and if your gut is a little leaky, that protein or any other corn proteins could pass into the blood. And the immune system will be like, “Whoa, that’s bad guy. You know, we gotta get rid of that.” And so it has this whole reaction. And so that’s believed to be how food intolerances happen. How to get rid of them? You have those sort of several pieces, right? We need the immune system to kind of sort of relax but we need it to make sure it stops being exposed to it. In order to do that, we have to digest the food and make sure it doesn’t go into the blood. And so unraveling that is…I don’t think it’s as easy as just taking digestive enzymes.
But if we think about how that process unfolds, the number one thing we could do is make sure the food is properly digested and it’s never, you know, sort of in that bigger molecule. And so we do see a lot of people who are able to take the enzymes and then over time as long as they’re also healing their gut…remember the gut wall has to close up and the gut inflammation has to heal up. If those two things happen, that’s how I believe a lot of food intolerances are overcome. Of course, you know, there’s straight-up food allergies. Those are different. That’s usually something that’s inherent to you. Those are usually anaphylactic in nature.
So, I’m not talking about those at all. That’s a totally separate conversation, a totally different medical topic. But in this intolerance thing where it’s sort of being annoyed by these foods, it does appear that if you can heal the gut lining and break the food down better, your intolerances and your diet can really expand because they seem to go away. And so the cool thing is with enzymes, you can open them up. You know, because a lot of kids don’t like to swallow pills. I’m sure you know that. But you can open them up. You can put them on their food. There’s no issue as far as doing that kind of thing. In the various different areas where children have issues with their guts, enzymes are pretty much used universally in the various disorders. So, yeah, they’re amazing for that.
Katie: That’s so exciting to me because I know when I first was trying to figure this out on my own years ago, the story I got from mainstream medicine was that, kind of like, once an autoimmune disease, always an autoimmune disease. And we don’t even really fully understand what causes them, but we don’t think you can get rid of them. And once there’s this level of inflammation in the body, you just kind of have to mitigate. And thankfully, that’s definitely not what I found to be true in my own health journey or in my research. But that’s been very top of mind for me is like, you know, I had to get really sick as an adult before I started paying attention to these things.
So I’m very cognizant of “What can I be doing with my kids now that gives them the best, you know, digestive start, that gives them the best immune start that hopefully they never have to face the level of problems that I faced?” and that I know you’ve faced as well. I know that we’re both, probably can be grateful for that because that was part of our journey and that allows us to now help other people. But it’s really exciting to me when pieces like this fall into place, and we have what seems like extremely tangible evidence of the mechanism that these things work and especially when we’re talking about kids.
I asked you this before we started, but I wanna ask it on the record as well. I’m a big proponent of various types of fasting. So I do time-restricted eating a lot of days, and I also am currently in the middle of a water fast just because I know I feel best when I do those relatively regularly. And certainly a lot of things you wouldn’t take while fasting. A lot of supplements aren’t best taken without food. Walk us through enzymes and how they can be used differently with food and without food.
Steven: Yeah. So, you know, I actually kind of do…when I fast, I actually up my enzyme dosage because I’m kind of of this idea that…you know, I’ve already had a lot of my own health changes, right? Like the idea of me being, you know, an NFL or a NBA, like an Olympic-style health athlete is just out the door. That ship has sailed. So, I need to do a lot of proactive things throughout my life to really feel and be the best. And so when I fast, I actually take more of enzymes, more systemic enzymes because I believe they’re helping to sort of cleanse the blood as you’re…you know, when you’re fasting, you’re totally changing the state of your body, and you’re, you know, potentially dumping extra toxins or certain molecules into the blood that wouldn’t normally be there. You’re also not digesting, and so there’s no real focus on digestion. And there’s a lot of focus around immune and cellular health. And so part of that whole process of autophagy and everything is protein destruction and protein degradation and protein recycling. I actually up my enzyme usage during fasts in order to try to just basically have as much of a cleanse as I can.
Yeah. The big thing is basically like are you taking the enzymes with food or without food? Like what’s in the enzyme, and so the actual enzyme products. So, as I mentioned earlier, for a digestive enzyme, you really wanna be taking a product that includes both pancreatic enzymes and brush border enzymes. If you’re not taking one with both, and you’re experiencing any health issues or any gut upset at all, and you’re like, “Man, I don’t know if this product’s working,” like, there’s really no way…there’s no tests that I’m aware of for you to know if you’re having a brush border enzyme problem or a pancreatic enzyme problem or both. And so my belief is you should take a product that has both of them covered so that, you know, whatever your body’s, you know, hiccup is or issue, you got yourself covered. Now, you also want that product to be higher in protease, and you want it to be basically, like, 100% pH coverage, and you want it to be activated. If those things happen, then it can be used systemically as well. And so what does that mean?
So basically, pancreatic enzymes work in a very small window of pH, and pH’s, like, acid-base balance. The stomach is very acid. The intestines are actually more basic or a less higher pH. Excuse me. And so animal enzymes like pancreatin, nothing wrong with them. You have to understand their limitations. And so pancreatin only works in a very narrow pH, and so if your stomach acid is off, if it’s low, if you’re stressed, if you have, like, H. pylori or these other infections, the chances of your pH being perfect so that your enzymes turn on and that work is just kind of, again, you’re sort of leaving yourself open there for products to not really work and get you the intended benefits. And so I really like more fungal-based enzymes because they have 100% pH coverage. So they work from 2 to 11. Like, ours work from 1.7 to 11.6 or something. So it’s basically your whole body’s range. You really wanna get a product that’s activated.
Now, of course, I’m biased. You know, our product has a patented activation system. I literally tried 28 different products from almost every brand last year, trying to figure this out for myself. And I wouldn’t have settled on this and I wouldn’t have worked and licensed this from the Ph.D. guy if I didn’t fully understand enzymes now and how they work. And so basically, enzymes need energy to do their work, and so they need what’s called a cofactor. And for enzymes, that’s a mineral. And so basically, minerals donate energy to turn on enzymes. And so if you take a product that doesn’t have a mineral activation blend, you’re gonna have to steal nutrients from your food, or you’re gonna have to rely on stealing nutrients from your body to turn them on.
I finally realized that was the thing. Why did some days the enzyme work and other days the enzyme didn’t work? And why did some brands work with some people but other brands didn’t work with that same or with…like other people like them? I really believe it comes down to this thing of the quality of the enzyme and then, is it activated? Because if it’s not activated, it’s sort of, like, inert almost like, you know, you just need it to be turned on to work. Otherwise, you’re taking the chance that it might bump into something in your food and turn on. And so that’s why I’m such a big proponent of holozymes and this AES absorption system.
The Ph.D. guy had to do six pilot trials because the patent board was like, “Yeah. Okay, man, you know, this is sort of unprecedented science. Like it sounds cool, but we don’t believe you.” So he actually had to do these pilot trials to prove that this enzyme product works both for fat, carbohydrate, and protein and that it’s absorbed systemically and it begins to help with a clotting factor. That’s all been done in those pilot trials. Of course, we need much more research on it. But as far as enzyme product goes, I’m actually not aware of any other enzyme products except for Wobenzym that have done this kind of research. And so Wobenzym is kind of like the systemic enzyme of choice if you’re just gonna use a systemic enzyme, but it doesn’t have any of the digestive stuff. Ours has both your pancreatic, your brush border, and your systemic nature.
Katie: That’s super helpful to understand. And I will say just as a plug for you guys as well. I very rarely notice an immediate difference from supplements and I’ve added this to my routine, and I do notice, like my digestion, and I notice a difference from taking it, like a noticeable difference. You know, it wasn’t available when I was in the height of my autoimmune disease. Although I wish now that it had been. It’s so exciting to me that we have tools like this. Are there any risks or contraindications people need to know about when it comes to taking enzymes? And if not, what does good dosing look like, especially if we’re talking about yours specifically?
Steven: Yeah. There’s no massive risk. Of course, you know, always check with your doctor. For instance, Wobenzym has the most systemic…the most, like, research in the world on it, and it actually is even used in infertility trials. There was, like, a study of 141 people in Germany who are women who are infertile, and they used systemic enzymes to help them get pregnant and much better than the control group and stay for the whole pregnancy term. So, they’ve been studied in kids. Our brand hasn’t been, but enzymes, in general, have been studied in kids. They’ve been studied in pregnancy.
The only real big thing is there’s an enzyme called nattokinase and it’s a really cool Japanese systemic enzyme that’s specifically cardiac function. It rivals some specific, you know, cardio-related drugs as far as efficacy for blood pressure, for clotting, things like that. And so it does appear that, like, if you megadose that, there’s some concerns around if you’re already on a blood thinner. But just general usage of regular products like Wobenzym or holozymes or something like that, there shouldn’t be any, but, of course, check with your doctor.
So, dosing. Dosing is really kind of up to you. So like I said, the upper limit of dosing that I’m aware of is like…would be, like, 150 to 180 pills a day. That’s a lot, and that’s for very specific cancer-related protocols that Dr. Gonzalez does and his lineage does. What I’ve seen is that most people use two to six capsules specifically of holozymes per meal and then on an empty stomach. And they can see, like, really amazing results. Why the range? Well, it just depends, like how…do we know your pancreatic function? How long have you been sick? You know, what kind of food are you feeding yourself? How stressed are you? How’s your stomach acid? All these things make a difference in your capacity to break down food and how much digestive enzymes might you need.
And then, again, on the systemic side like before bed or in the morning, you know, what are you looking to do? Are you just taking this as an anti-aging supplement to keep your blood clean, to keep everything flowing well, to keep inflammation levels low? Then all the studies that the Ph.D. guy did were only two pills before bed. But if you’re specifically trying to get better athletic performance, if you’re specifically trying to work on some sort of health condition that you think might be helped by this, then I would recommend doing four to six on an empty stomach for at least a month just to see what happens. You can always go down, or you can go up.
We do have some people who end up going really, like, more on the 10 to 14 range per meal, but these are people with known gastro issues like gastroparesis where their stomach doesn’t actually dump very well or at all into the intestines. And so these should be really guided by somebody who knows what’s going on or if you have… Another way that it’s working is it is for people to, you know, help with their occasional heartburn or occasional acid reflux or something like that if they’re looking for an alternative, which, again, I can’t say that this is an alternative. I can just tell you that, you know, some people who buy our product are using it in those dosages for those conditions.
Katie: Gotcha. Yeah. And I think you highlighted a really important point, which is at the end of the day, like this can be used for so many different things like a lot of these tools can. It really does come down to each of us taking the initiative to experiment and try things and try them for a long enough time to see if they have an effect. And this is one that I’m really excited about right now, like you mentioned, just for the anti-aging side and for keeping any potential future autoimmune things at bay because I know, like once you’ve had any kind of inflammatory condition, your chances of having them in the future is higher. And so I’m very cognizant of that and still try to keep my inflammation low, even though I now am much more relaxed with my diet and my lifestyle than I had to be in the very beginning.
But I think the anti-aging part is also really exciting to a lot of people listening as well. And I think we’re probably gonna keep seeing more and more on this. But it’s a pretty easy thing that seems like we can add in and try without a lot of risks, which is really, really exciting.
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And real quick, I know I have a link right here. I’ll put in the show notes as well. It’s healthygut.com/wm. And I know you guys are giving a discount on any order. But just talk about the products by name and a little bit more specifically. Because, like I said, these are ones that are now part of my routine, and I wanted to make sure I could share them with the audience today.
Steven: Yeah. Yes. The enzyme product that I’ve been talking about is called HoloZyme, and it’s the world’s most activated enzyme formula. So it is patented. We also have our, you know, dual-strain, four-times concentrated active blend. Our enzymes are made in the U.S. They’re pharmaceutical grade, 100% clean, no fillers, no additives. And so, yeah, we’re giving $10 off to try it. I mean, I think whenever you’re trying something new, I think it’s always great to save a little money when you don’t know if it’s gonna work for you. But we also, you know, just being somebody who’s been sick and consumes a lot of supplements hoping for results, you know, kind of being like, “Oh, maybe this one, or, oh, maybe this one.”
We’re also offering a 180-day refund on all of our products at any point in time for any reason. And I just know that because not everything works for everybody. And if you don’t notice the difference, I mean, maybe you’ll buy into the research to use these systemically for anti-aging or just with digestion. But I would just wanna make sure that there’s no risk, and if anybody has any issues with the product, we always just, you know, go ahead and give the money back because I know that if you’re listening to this podcast, if you’re following me or Katie, you’re trying really hard to have, you know, a really healthy life, really healthy lifestyle. So, I’m super into, like, just encouraging that and encouraging great use of your money when it comes to those things. Yeah. And then we also have HCL Guard. Are you using that, Katie?
Katie: I am. But to clarify, that one is to be used only with food, correct? You wouldn’t wanna use that while fasting?
Steven: Correct. Correct. So HCL Guard is our, also a new product, never been done before. It’s a stomach acid supporting product. It’s for people with low stomach acid. And it’s correct. There’s literally acid powder in the capsule. So, you never open the capsule. Only take it with food. It’s not as universal, but for people who are over 50, you have about a 50% chance of having low stomach acid. Sadly, stomach acid’s really related to aging and hormone health. And so as we age, stomach acid declines is what the studies show. And so if you’re having any gas, burping, constipation, diarrhea are occasional, those things are all occasional. Again, HCL Guard does not treat any medical conditions. HoloZyme does not treat any medical conditions. But if you’re having struggles in those departments, they can offer support. And, yes, so it’s pretty cool.
It’s the only stomach acid formula on the market that includes organic ginger, which is a prokinetic. And many people might have drank ginger tea when they’ve been having an upset stomach. And so the ginger is anti-inflammatory. It helps support the healing of the stomach, but it also helps the food start moving through your body. And then we also include intrinsic factor, which is kind of like the bouncer for B12. It turns out B12 is a really fragile compound, and it needs support to get into the bloodstream. And intrinsic factor is part of stomach acid naturally, but if you’re not making enough, then you’re not gonna have enough to get your B12. And so we’re the first company to bring that to market. So, I’m really excited about them mostly because I’ve been using everybody else’s brands for 10 years, and I just got fed up with not getting the consistency that I wanted. And so I’m glad that you’re using them, and I hope, you know, people check them out. And I just hope it supports them, honestly.
Katie: Yeah. And I’ll say the cool thing about HCl. This was a big part of my husband’s recovery. He had his appendix rupture and then had a secondary infection and tons of antibiotics, and this was years ago. But we spent years kind of undoing that damage in his gut, and HCl was a big key for him for a long time. And he’s been able to taper down now, and I’ve also just recently ramped up my protein intake a lot because I started lifting weights again after losing a whole lot of weight. And so that’s been helpful for me is I’ve added in a lot of protein, and I know HCl can help with protein digestion as well. Can you explain the idea of an HCl challenge and how people can use that to figure out how much they need to take if they need to take it?
Steven: Yeah. Yes. So you might be asking a question like, “How would I know if I have low stomach acid?” Well, you can go and get a test if you have, like, a super-advanced doctor. There’s not many of them in the entire world left. But there’s something called a Heidelberg test. There’s also a gastro capsule test. Normally, these are like $300 to $600 out-of-pocket, and you have to find a specialty provider to do them. So, I’m just gonna go ahead and assume you don’t have time or money to spend on that because you can just spend a little bit of money and try an HCl supplement and do this HCl challenge, which is the best way to figure out if you have low stomach acid.
And then you might be wondering like, “Well, what are my chances?” So, Dr. Jonathan Wright is one of the physicians who does stomach acid testing. In his clinic, he said there’s probably 90% of people he tests with IBS-like symptoms have low stomach acid. The other 10%, they have all the same symptoms, but 10% have regular acid or high acid. Dr. Steven Sandberg-Lewis, he’s a professor of naturopathic gastroenterology. He’s written some books. He’s out of Portland. He does the same tests, and he says it’s about 80/20.
And so your chances if you have digestive upset are kind of high for this. The fastest and cheapest way is to buy an HCl product, ours or somebody else’s, and you basically do this HCl challenge. So you have a meal that has some protein. It could be vegetable protein. It could be animal protein. It doesn’t matter. It’s better if it’s not, like, just a protein shake, right. Because a protein shake or a smoothie is essentially already pre-broken-down food for you. So you don’t need much acid or enzymes or anything to do much with that, but just a normal meal. You take one capsule. Most people don’t notice anything. And if you don’t notice anything, that’s pretty much a sign that you have low stomach acid, right? Because you just took a pill that had acid in it, and you didn’t notice anything.
And so how the HCl challenge works is you just keep adding one pill per relatively normal meal for you, and at some point, you’re gonna feel some sort of hotness, maybe some sort of burning in your mid-chest. Maybe you’re gonna notice a change in your stools, like maybe your stools get better, but then they go more loose or diarrhea-like, anything like that. And I would pay attention more to your gas, bloating, your stools, the toilet, what’s going on there than I would the heat sensation because getting to a heat sensation is not really always needed.
What we’re trying to do is just get you a perfect poop. And if you’ve never heard of the Bristol Stool Chart, you can google that. You’re trying to get to a four or five on the Bristol Stool Chart every single day. And so HCL Guard is…and other HCl products are a great way to make sure that happens. So, anyways, with the HCl challenge, you’ll reach a number. Like, I don’t know about you, Katie, but I actually was part of the people who don’t get the burn. So, I one time did, like, 15 pills back when I was really sick, and I was like, “I don’t notice anything.” And then I had, like, a lot of loose stools, and I was like, “Oh, okay, I think that was too much.”
So, anyways, I took about eight or nine capsules once I realized that you could just do this based on how you’re feeling and you didn’t have to find the “burn.” Yeah. I took around eight or nine, and then I was slowly, like your husband Seth, I was slowly able to back down as I healed until I was off HCl for three years, and then I’m back on it now just because of the stress in the world and just everything that’s happening in my life. Stress is crazy high, and so I just realized, “Yeah. I’m not making stomach acid anymore.”
Katie: That’s another key point, I think, that you just brought up is not only is health very personalized and individualized and we each need to take ownership for our own health and figuring out what’s gonna work best for us through experimentation, but it’s also constantly changing. I feel like figuring out what works for my health right now is great for right now, and then by next month, it’s often totally…you know, like where it’s always an evolving concept. Like we talked about earlier, I think, in general, there are some things that seem almost universally beneficial, and that’s why I’m excited about enzymes is it seems there’s so many different uses, and I think we’re, like you said, just gonna keep finding out more and more. So I’m really excited that you’re pioneering this and making these available right now. Like I said, I’m a big fan. So, I appreciate you being here to educate today and explain. And to switch gears a little bit, a couple things I love to ask at the end of interviews, just first being, are there any books or podcasts or sources of inspiration that you’re loving right now?
Steven: Right now. You know, my favorite book and something that I always return to is “Man’s Search for Meaning.” You know, if you’re not familiar with it, it’s a first-hand account of a psychiatrist going through the concentration camps in the Holocaust. And it’s just so humbling. I try to read it twice a year every year to realize that, you know, what we’re going through right now as a society is unprecedented in our lifetimes. It’s intense. It’s scary. It’s so many things. And yet there was lots of other times in human history where, like, much worse happened. And then also, like, how did those humans deal with that intensity? And how can I apply that till now?
Katie: I’m also a huge fan of that book, and I think, like you said, it’s very timely right now. People have been through much worse, but it’s a great opportunity if we look at it this way to find that deeper meaning and to go reflect and to pause. So, I love that. I think that’s perfect for right now. And what are you excited about in the future? Obviously, enzymes but anything else that’s exciting to you right now?
Steven: I’m really excited about where the field of gut health is going. You know, in general, I think we’re gonna learn so much in the coming years about the gut-brain access. I’m really excited about, like, gut trauma, gut trauma brain, those types of things. I think there’s just so much that’s gonna come out around how potentially even the pharmaceuticals that we use for the brain are actually working in the gut. And I think we’re gonna learn so much more about leaky gut syndrome, zonulin. There’s a bunch of new papers that just came out in the last two weeks about this, about substances called short-chain fatty acids. These are super cool. They come from a lot of your fibers and your prebiotics, but you can also supplement with butyrate. And it’s got some really cool upcoming research. So, you know me. I’m super into the brain stuff right now. I’m very into, like, the gut, you know, meets all these other conditions and how is that happening.
Katie: Very cool. I have a feeling we’ll have to do another round, you know, at some point in the future as things continue to develop, but for any of you guys who want to try all the stuff we talked about, again, check out the show notes at wellnessmama.fm or healthygut.com/wm to get the discount. Yeah. Steve, it’s always a pleasure to chat with you. I love the work that you’re doing, and I’m very grateful for these products and happy to share them today. So thanks for being here.
Steven: Yeah. Thanks, Katie. Thanks for letting me educate people about enzymes. I’m very excited about them. I’m glad they’re helping you, and thanks for all the hard work you do.
Katie: And as always, thanks to all of you for listening and sharing your time with us today. We’re so grateful that you did, and I hope that you will join me again on the next episode of “The Wellness Mama Podcast.”
If you’re enjoying these interviews, would you please take two minutes to leave a rating or review on iTunes for me? Doing this helps more people to find the podcast, which means even more moms and families could benefit from the information. I really appreciate your time, and thanks as always for listening.
Source: https://wellnessmama.com/podcast/steve-wright/
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BRT Apartments Corp. (BRT) CEO Jeffrey Gould on Q1 2019 Results – Earnings Call Transcript
BRT Apartments Corp. (NYSE:BRT) Q1 2019 Results Earnings Conference Call May 9, 2019 8:30 AM ET
Company Participants
Evelyn Infurna – Investor Relations
Jeffrey Gould – President and Chief Executive Officer
George Zweier – Chief Financial Officer
David Kalish – Senior Vice President
Ryan Baltimore – Senior Vice President
Conference Call Participants
Rob Stevenson – Janney
Jim Lykins – D.A. Davidson
Craig Kucera – B. Riley FBR
Operator
Thank you for standing by. This is the conference operator. Welcome to BRT Apartments Corp. Inaugural First Quarter 2019 Conference Call. As a reminder, all participants are in listen-only mode and the conference is being recorded. After the presentation, there will be an opportunity to ask questions. [Operator Instructions]
I would now like to turn the conference over to Evelyn Infurna, Investor Relations. Please go ahead.
Evelyn Infurna
Thank you. Good day, everyone, and welcome to the BRT Apartments Conference Call. On the call today is Jeffrey A. Gould, President and Chief Executive Officer. Available for questions, we will also have George Zweier, Chief Financial Officer; David Kalish, Senior Vice President; and Ryan Baltimore, Senior Vice President. As a reminder, this call is being webcast through the company’s website at www.brtapartments.com. Additionally, the company’s supplemental information and earnings release are available for your review, and the company’s 10-Q will be available later today on the Investor Relations section of the BRT’s website.
Before we begin, I’d like to remind everyone that this conference call contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995 that are based on management’s current expectations, assumptions and beliefs. Forward-looking statements can often be identified by words such as believe, expect, estimate, anticipate, intend and similar expressions and variations or negatives of these words. These forward-looking statements include, but are not limited to, statements regarding BRT’s strategy and expectations for the future. These are not guarantees of future results and are subject to risks, uncertainties and assumptions that could cause actual results to differ materially from those expressed in any forward-looking statements.
Listeners should not place undue reliance on any forward-looking statements and are encouraged to review the company’s most recent annual report on Form 10-K and the company’s other filings with the SEC for a more complete discussion of risks and other factors that could affect these forward-looking statements. Except as required by law, BRT does not undertake any obligation to publicly update or revise any forward-looking statements. This conference call also includes a discussion of funds from operations, or FFO, adjusted funds from operations, or AFFO, and net operating income, or NOI, all of which are non-GAAP financial measures of performance.
These non-GAAP measures should be used as a supplement to, and not a substitute for, net income computed in accordance with GAAP. For a more complete discussion of FFO, AFFO and NOI, see the company’s earnings release and supplemental that were filed yesterday and the 10-Q that will be filed later today. As a reminder, the company recently changed its fiscal year so that it ends on December 31.
I would like to now turn the call over to Jeff Gould, President and CEO of BRT Apartments Corp. Please go ahead, Jeff.
Jeffrey Gould
Thanks, everyone. I would like to welcome everyone to BRT’s inaugural quarterly conference call. Before we walk through our financial results, we thought it would be helpful to give you an overview of our business model. BRT is a small-cap equity REIT primarily focused on the ownership, operation and development of multifamily properties. These properties are owned by consolidated joint ventures in which we generally contributed 65% to 80% of the equity. We own 37 multifamily properties located in 12 states with an aggregate of 10,336 units and have ownership interest through unconsolidated entities in 3 multifamily properties located in 2 states with an aggregate of 1,026 units. Most of our properties are in the Southeast United States and Texas.
We believe that acquiring properties through joint ventures is currently the most efficient strategy for us. We select operators with local expertise that we can leverage their experience in property management platforms to find the best risk-adjusted multifamily investments for our stockholders. We have been able to achieve significant efficiencies by using this model as we do not have to waste valuable resources bidding on deals that we may or may not win. Prior to the multifamily equity business, we were bridge lenders and frequently lent money on multifamily assets. This background allowed us to become highly skilled in investing in this asset class. Our approach in acquiring multifamily asset is unlike other models in our space, but given our size, we believe this approach helps us leverage our platform and provide the right combination of opportunity while mitigating risk.
Moving on to our results. Today, we are going to walk through the results of the first quarter 2019, discuss the portfolio and some of our markets. During today’s discussion, we are going to refer to the quarter ended March 31, 2019, as the current quarter and the quarter ended March 31, 2018, as the 2018 quarter. Net loss was $4.2 million or a loss of $0.27 per diluted share in the current quarter versus net income of $25.2 million or $1.75 per diluted share in the 2018 quarter. The 2018 quarter includes $52 million or $3.60 per diluted share from gain on property sales before giving effect to $25.1 million or $1.74 per diluted share of non-controlling interest. NOI for the current quarter was $15.9 million, an increase of 4% versus $15.3 million for the 2018 quarter.
FFO was $3.1 million for the current quarter or $0.19 per diluted share compared to $5.3 million in the 2018 quarter or $0.37 per diluted share. FFO for the 2018 quarter includes $3.2 million or $0.22 per diluted share, without giving effect to the non-controlling interest of $800,000 or $0.05 per diluted share from the gain on insurance recovery related to our Retreat at Cinco Ranch property in Katy, Texas. AFFO was $3.7 million for the current quarter or $0.23 per diluted share compared to $3.8 million in the 2018 quarter or $0.26 per diluted share.
Rental revenues increased by 4.1% to $30.7 million from $29.5 million in the 2018 quarter, and operating expenses increased by 4.2% to $14.8 million from $14.2 million in the 2018 quarter, driving an NOI increase of 4%. On the value-add front for the current quarter, we repositioned 294 units at 17 properties, spending on average approximately $4,245 per unit and achieving a return on investment of roughly 27%. As reflected in our supplemental financial information, a portion of the cost may have been incurred in the prior period, where we report the return on investment when a unit is re-leased. Overall, we are very pleased with the performance of our value-add program.
We expect this strategy to continue to be a factor in our ability to drive same-store rent and NOI growth over the long term. During the current quarter, we acquired a 312-unit property located in Kannapolis, North Carolina, a suburb of Charlotte, for $48.6 million, including $33.3 million of mortgage debt assumed in connection with the purchase. The mortgage debt matures in 2052 and carries an interest rate of 3.52%. The property is well located, approximately 24 miles from Charlotte, North Carolina, near I-85. The community is near several major employers, including Carolina Health Systems, an under construction Amazon fulfillment center and the North Carolina Research Campus.
On May 7, we acquired a 328-unit multifamily property located in the suburb of Birmingham, Alabama. The purchase price was $43 million, including $32.3 million of mortgage debt obtained in connection with the acquisition. The mortgage debt bears interest at a rate of 4.19% per year, is interest only until 2025 and matures in 2029. Our same-store pool comprise 27 properties totaling 6,989 units. Same-store NOI for the current quarter increased by 3.2% from the 2018 quarter. Same-store revenue increased 4.6% in the current quarter to $22.1 million. Same-store expenses were up 6.2% from the 2018 quarter, with 55% of the increase from real estate taxes. When a property is reassessed at a higher value for real estate tax purposes, we generally appeal if we believe that a reduction is obtainable.
Same-store rental rate increased 3.3% to $996 a unit from $965 a unit a year earlier. The growth in our same-store rental rate was driven by growth in key markets led by Mississippi, which grew by 7.4%; and South Carolina, which grew by 6.3%. In addition, we were able to increase rental rates in Indiana by 5.6%, Ohio by 5.5%, Alabama by 4.7% and Florida by 4.6%. Our most challenging region is St. Louis. We are managing down our exposure in this market as we have not seen the growth that we anticipated and, in some cases, have had to drop rents to stimulate occupancy.
Turning to the balance sheet. We finished the quarter with $21.1 million of cash and cash equivalents and net debt of $845.8 million, including $37 million of corporate subordinated debt that matures in 2036 and carried an interest rate of 4.75% as of March 31, 2019. In April, we entered into a credit facility with an affiliate of Valley National Bank. The facility allows us to borrow up to $10 million and carries an annual interest rate of 50 basis points over the prime rate with 4% or 5%. We intend to use the facility as a bridge to fund acquisitions of multifamily properties.
On May 2, the company borrowed $9 million on the line in connection with the acquisition of the Birmingham, Alabama property that I described earlier. Borrowing under the facility will generally be repaid from property sales or refinancing transactions. Finally, on March 11, the Board approved a quarterly dividend of $0.20 per share, which is equivalent to an annualized yield of 5.6% based on our stock price of $14.19 as of the close of business on May 6.
Thank you for joining us today on our inaugural conference call. With that, I will turn the call over to the operator for your questions. Operator?
Question-and-Answer Session
Operator
[Operator Instructions] Our first question comes from Rob Stevenson with Janney.
Rob Stevenson
Jeff, can you just talk a little bit about how we should be thinking about the year pipeline on the acquisition and disposition side over the remainder of ’19? And have you seen any changes in valuation, cap rates, et cetera, out there over the last quarter or so?
Jeffrey Gould
Yes, sure. Good to talk to you, Rob. Yes. So we continue to see the transactional business and reselling of 2 assets as well as buying, as you know. When we dispose of assets, we have the capability in looking at other new assets to acquire. The pipeline has been very strong. As you know, we don’t look at deals unless they’re under contracts so we readily can put the money out for new acquisitions. And it’s been solid. Competition is definitely tighter, but at the same time, we’re seeing very good deal flow. So we’re pleased with the response of our partners as to new deals. And if and when we get money back, we very comfortably can put out the money in an accretive fashion.
Rob Stevenson
Okay. And then you guys did just under 300 rehabs in the first quarter. Is that a good run rate for the year? Or do you accelerate that during the summer months as turn increases? How should we be thinking about number of rehabs for the year? And does that sort of $4,250 a unit likely hold steady for the remainder of the year?
Jeffrey Gould
Yes. So I’m going to turn that over to Ryan to give you a more detailed answer on that.
Ryan Baltimore
Rob, yes, so we don’t project and give guidance on how many units we plan to turn. A lot of it is dependent on turnover at the individual property level. Given our past couple of quarters, we’ve been in the 300 range, but again, we don’t project forward as we don’t know how many units we’re going to necessarily get back to renovate, as we’ve been getting renewal increases that have been pretty strong in the 4% range. So we haven’t had as much turnover as we sometimes anticipate.
Jeffrey Gould
And some of these new transactions that we’ve recently purchased, there’s definitely a value-add component to it, and we’re excited about those opportunities. And we think that will drive definitely some renovations of units.
Rob Stevenson
Okay. And then just last one for me. On the same-store growth expectations for ’19, is there anything abnormal with year-over-year comps or anything else that would materially alter the sort of 3%, 3.5% same-store NOI run rate that you ran for the first quarter throughout the remainder of the year, either elevating it or reducing it?
Jeffrey Gould
Yes. I mean in the current quarter, taxes accounted for 55% or so of the same-store expense increase. So that’s something that we’re watching carefully. And as I said earlier, we’re monitoring tax increases. We do our best to appeal taxes. And in some states and cities, it’s obviously more prevalent in having to fight these taxes on an annual basis. So that’s part of it. I mean that’s a little bit of an open question. We saw a little bit of an increase in repairs and maintenance, which is really the result of renovating units and turning over, and the turns allowed us to increase rental rates, which was good. So that has some impact on it. But generally speaking, same stores we don’t give actual guidance on, but I would tell you that it’s, I guess, more or less dependent on taxes. And there is some seasonal fluctuation, yes.
Operator
The next question is from Jim Lykins with D.A. Davidson.
Jim Lykins
First, a couple questions about the renovations. First, and apologies if I missed this, but how much for the 294 did you say you spent per unit?
Ryan Baltimore
Jim, this is Ryan. We spent approximately $4,245 per unit and received an annual ROI estimate of about 27%.
Jim Lykins
Okay. And I know you guys don’t give guidance, but there’s some pretty solid returns. Is there any reason to think that, that may be slowing as we go through 2019 or can you stay at those levels? Is there any color you can give us at all on how to think about those returns?
Jeffrey Gould
Yes. So we have seen a pretty consistent return on equity on the renovation program over the last number of years, and we don’t see any reason that should not continue. We’ve done well with it.
Ryan Baltimore
Yes. Just to add on that, what we do with our renovation program is if we see the returns start to drop and the returns are not there anymore, we’ll just stop the program. We typically fund most of our renovation money upfront. So if that’s the case, they’ll return that money as a distribution or hold it for other amenity upgrades that might make sense where we could see the returns in the 20-plus range.
Jeffrey Gould
We’ve consistently seen return on equity being minimum like 15% or so and, obviously, these numbers reflect far more solid returns than that. But it’s been, we’ve been pleased with those results for quite a while now.
Jim Lykins
Okay. That’s helpful. And also, for the acquisition in Birmingham, first, are you able to provide a cap rate for that?
Jeffrey Gould
Yes. So generally speaking, the new acquisitions in Birmingham and the other one we mentioned, as I said earlier, we were pleased with the opportunities. The Alabama deal, the value-add, it was a net value-add program. We reserved about $4,750 per unit to do the renovations. We’re hoping to achieve north of 16% return on the renovation. As far as cap rate goes, we’re buying this typically at about 6% stabilized cap rate, along with the value-add program. The North Carolina property that we recently purchased as well, on a value, on a stabilized basis, that’s somewhere north of 6% as well. We had to buy it at a lower cap rate going in, but again, with the value-add component, which we plan to do there, which is pretty significant, what happened there is the value add was basically completed already, but they weren’t getting the bonus as they get on the value add. So the work for the most part is already complete. So we should see that fairly readily improving cash flow.
Jim Lykins
And have you identified the number of renovations at this property?
Jeffrey Gould
Well, the one in North Carolina was basically completed. This is the one we bought without debt. And the renovation almost entirely is complete. Again, none of the rent bump is really, or minimal amount of the rent has been effectuated from the work, and that’s all going to happen. On the Alabama deal, our plan is to do most, if not all, those units over time. So we think it’s a good long-term…
Jim Lykins
How many is most? What, Is there a number…
Jeffrey Gould
There’s 308 units in the property.
Jim Lykins
Okay. And you’ll be renovating most of those?
Jeffrey Gould
Yes, over time. And obviously, we have other units in the portfolio that we’re going to be hitting as well. Some of the, as Ryan alluded to, there’s some older, some properties that are sort of legacy assets that still remain work to be done. But here, our plan is to do a majority of these units, yes.
Ryan Baltimore
Yes. Jim, just a point on that. At the Alabama deal, there’s 328 units. 20 have already been rented prior to acquisition, so there’s 308 remaining to be renovated.
Jeffrey Gould
Right. The nice thing there is we know from the 20 units that we’ve done that we can achieve those rent increases, and it’s worked in the market. So that’s always a good indicator for us, and we’d like to have some guidance as to the ability to, once we do the work to be able to charge these increases, and here, we’ve seen it directly, and we’re very confident we can get the bumps.
Operator
[Operator Instructions] And our next question is from Craig Kucera from B. Riley FBR.
Craig Kucera
Just based on your commentary on St. Louis, are those assets that you’re considering bringing to market and possibly recycling out of?
Jeffrey Gould
Yes. So to St. Louis specific, we were, the reality is that our concern with that particular market was we just, we were continuing to have concessed rents. We had lower occupancy than we originally anticipated we were going to be able to achieve. It’s a transient downtown market with minimal rental growth, and it was something that we were surprised with. But the fact is that with the occupancy and with the trends we see down there, as much as we’ve been able to increase or decrease operating expenses, we just don’t see it as a long-term viable property, the downtowns in those property. We do have another property that’s running very well, which is not the downtown property in St. Louis, and that we plan on refinancing and keeping for a period of time. We’re pleased with the performance of that property, which is outside the downtown market.
Other properties, we do as we basically look at our entire portfolio on a consistent basis. And any property that we start to see, where the renovations have more or less been complete, and we’ve really milked and used most of the value add. Those are potential deals for sale, also where we see markets trending in a way that we’re not pleased, obviously, and we can recycle the capital to use elsewhere in a growing market. We choose to do that.
So we’re confident that we can get the portfolio. In some of our properties, frankly, where they’re getting older, those are areas that we think, obviously, properties don’t get any younger, and over time, those are somewhat concerning. So there’s issues and examples of we have to put in property and work on renovations where you don’t see the rental growth. And those are properties that we focus on as well. So yes, we’re constantly focusing on these current properties in our portfolio, and there likely will be other sales to come.
Craig Kucera
Okay. And I know you said you don’t give out guidance quarterly or annual on the value-add program, but have you sort of tallied up the total amount of units that you think remain in the portfolio, whether that’s inclusive or exclusive of the recent acquisitions that you think you can renovate and achieve pretty decent returns through behest?
Jeffrey Gould
Yes. So as you said, we don’t give the guidance on that, so we don’t have, I don’t want to give a specific number as to the amount of additional or further renovations that we plan to do. But I can, we can say comfortably that there’s going to be a large number of those. And the whole focus now is we’ve really minimized the new development pipeline almost completely. We have income coming in from some of the development properties that are now complete and being leased up. But as far as renovation program, we would rather just give you the facts as the quarters come and as to what we’ve actually been able to complete and get the bonus of rent.
Craig Kucera
Okay. And just on the new development, I know you’re winding it down, but is that sort of post what’s currently under development? Do you anticipate doing new developments? Or is this likely sort of you’re winding that aspect of the business down?
Jeffrey Gould
I mean there’s a chance we might do a deal, a development deal, but it’s not the real plan right now, the reason being the development deals have just gotten to be so difficult by way of returns and, versus risk. So the bottom line is, originally, when we were going into some of these development deals, we were building to an 8.5% unleverage-type return. Those going back a few years. Now we’re probably seeing unleverage returns down to roughly 6%. So you have to always balance risk/reward and budget and issues without building new. It’s nice to have brand-new products, but when the returns become down to those levels and at those numbers, it’s just not as appealing as buying an existing property where you know the value-add component exists and where you can do light renovations as opposed to taking the risk of new development. So I think it’s going to be minimal. I don’t want to say it’s 100% that we absolutely won’t do a deal, but it’s not in our current plans.
Craig Kucera
Got it. One more for me. Just wanted to get your thoughts on leverage today. I think you guys are a little bit more levered than a lot of your peers. And just your thoughts sort of maybe on feeling on leverage and do you plan to reduce leverage over time or kind of keep the balance sheet relatively constant where it is today.
Jeffrey Gould
Good question. We understand that there’s been focus on the debt. So I can answer it a few ways. One is our new acquisitions were typically borrowing or LTV at about 60% or so, 60% to 65%. So we think based on the risk/reward of a fairly stable asset class, we think that’s a good number to be at, and we’re not concerned about leverage at those numbers. We don’t want to leverage any higher than that, our new acquisitions. As it relates to market cap, as it relates to book value, it does show that our debt appears to be high, but I think based on your analysis and other research that we’ve seen, if you look at the debt to real value, we don’t think it’s anything of great concern at all.
As a matter of fact, we think we’re stable and leveraged appropriately. But I think over time, we amortize our debt quite a bit on an annual basis. So that obviously helps. But we are looking and focusing on trying to reduce leverage to some extent. We’re not going to be the type of REIT that’s leveraged at 30%, 40% as some of the big boys, but I could say it’s just not efficient for us nor does we think it makes any sense as far as returns and what’s best for the shareholders. But our belief is that 60% level is something that we think is a good target for us, long term.
Operator
This concludes the time allocated for questions. If there were any questions that remain unanswered, please email [email protected]. I’d now like to turn the conference back over to Mr. Gould for any closing remarks.
Jeffrey Gould
Yes. So I just want to thank all of you for joining us on our inaugural call. We’re trying to be out there and be transparent so that all of you can ask your questions and we could be really responsive to you. We are happy to meet with any of you in person, so please reach out to us at the number or the e-mail address, [email protected], if you have any further questions. And again, we’re happy to meet you wherever it might be, and we look forward to talking with you on our next call in a few months. So thank you very much.
Operator
Thank you for participating. This concludes today’s conference call. You may disconnect your lines.
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Eisner Award Winners 2018
https://ift.tt/2O5P1DD
Liu is the first woman to win Best Writer at the Eisner Awards, plus much more!
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eisner awards
Jul 22, 2018
SDCC 2018
SDCC
Marjorie Liu became the first woman to ever win the Best Writer Eisner Award at 2018's ceremony, held Friday night at San Diego Comic-Con. Liu created Monstress, a fantasy tale about race, class, slavery, and giant tentacle monsters, with Sana Takeda on art. The book took home five total Eisners at the ceremony: Best Writer, Best Painter/Multimedia Artist, Best Cover Artist, Best Continuing Series, and Best Publication for Teens (13-17).
The other big winner of the night was Emil Ferris, writer and artist on My Favorite Thing Is Monsters. The staggering debut comic from Fantagraphics gave Ferris three Eisners - Best New Graphic Album, Best Writer/Artist, and Best Coloring.
Sharing the Best Writer award with Liu was Tom King, writer of Batman, Mister Miracle, and Batman/Elmer Fudd Special, a sentence no one in their right mind expected to say on stage at an award show. Mister Miracle also gave penciler/inker Mitch Gerads his first.
The sole controversy of the night was the failure of Den of Geek to secure a write-in win for Best Comics Publication. The winner of that category, The Comics Journal, successfully blocked our grassroots campaign for victory by pointing out that there is no option to write in nominees who are not on the ballot. The Establishment can stand in our way for only so long, though, so expect a landslide victory for Den of Geek next year as a reward for successfully choosing at least two of this year's winners.
Congratulations to all of the honorees! For a complete list of Eisner winners, keep scrolling. For more from the CONTINUALLY JOBBED geniuses at Den of Geek, stick with...shit. Uh...keep reading, true believers!
2018 Eisner Award Winners
Best Short Story: ”A Life in Comics: The Graphic Adventures of Karen Green,” by Nick Sousanis, in Columbia Magazine (Summer 2017)
Best Single Issue/One-Shot: Hellboy: Krampusnacht, by Mike Mignola and Adam Hughes (Dark Horse)
Best Continuing Series: Monstress, by Marjorie Liu and Sana Takeda (Image)
Best Limited Series: Black Panther: World of Wakanda, by Roxane Gay, Ta-Nehisi Coates, and Alitha E. Martinez (Marvel)
Best New Series: Black Bolt, by Saladin Ahmed and Christian Ward (Marvel)
Best Publication for Early Readers (up to age 8): Good Night, Planet, by Liniers (Toon Books)
Best Publication for Kids (ages 9–12): The Tea Dragon Society, by Katie O’Neill (Oni)
Best Publication for Teens (ages 13-17): Monstress, by Marjorie Liu and Sana Takeda (Image)
Best Humor Publication: Baking with Kafka, by Tom Gauld (Drawn & Quarterly)
Best Anthology: Elements: Fire, A Comic Anthology by Creators of Color, edited by Taneka Stotts (Beyond Press)
Best Reality-Based Work: Spinning, by Tillie Walden (First Second)
Best Graphic Album—New: My Favorite Thing Is Monsters, by Emil Ferris (Fantagraphics)
Best Graphic Album—Reprint: Boundless, by Jillian Tamaki (Drawn & Quarterly)
Best Adaptation from Another Medium: Kindred, by Octavia Butler, adapted by Damian Duffy and John Jennings (Abrams ComicArts)
Best U.S. Edition of International Material: Run for It: Stories of Slaves Who Fought for the Freedom, by Marcelo D’Salete, translated by Andrea Rosenberg (Fantagraphics)
Best U.S. Edition of International Material—Asia: My Brother’s Husband, vol. 1, by Gengoroh Tagame, translated by Anne Ishii (Pantheon)
Best Archival Collection/Project—Strips: Celebrating Snoopy, by Charles M. Schulz, edited by Alexis E. Fajardo and Dorothy O’Brien (Andrews McMeel)
Best Archival Collection/Project—Comic Books: Akira 35th Anniversary Edition, by Katsuhiro Otomo, edited by Haruko Hashimoto, Ajani Oloye, and Lauren Scanlan (Kodansha)
Best Writer: Tom King, Batman, Batman Annual #2, Batman/Elmer Fudd Special #1, Mister Miracle (DC) AND Marjorie Liu, Monstress (Image)
Best Writer/Artist: Emil Ferris, My Favorite Thing Is Monsters (Fantagraphics)
Best Penciller/Inker or Penciller/Inker Team: Mitch Gerads, Mister Miracle (DC)
Best Painter/Multimedia Artist (interior art): Sana Takeda, Monstress (Image)
Best Cover Artist: Sana Takeda, Monstress (Image)
Best Coloring: Emil Ferris, My Favorite Thing Is Monsters (Fantagraphics)
Best Lettering: Stan Sakai, Usagi Yojimbo, Groo: Slay of the Gods (Dark Horse)
Best Comics-Related Periodical/Journalism: “The Comics Journal,” edited by Dan Nadel, Timothy Hodler, and Tucker Stone, tcj.com (Fantagraphics)
Best Comics-Related Book: How to Read Nancy: The Elements of Comics in Three Easy Panels, by Paul Karasik and Mark Newgarden (Fantagraphics)
Best Academic/Scholarly Work: Latinx Superheroes in Mainstream Comics, by Frederick Luis Aldama (University of Arizona Press)
Best Publication Design: Akira 35th Anniversary Edition, designed by Phil Balsman, Akira Saito (Veia), NORMA Editorial, and MASH•ROOM (Kodansha)
Best Digital Comic: Harvey Kurtzman’s Marley’s Ghost, by Harvey Kurtzman, Josh O’Neill, Shannon Wheeler, and Gideon Kendall (comiXology Originals/Kitchen, Lind & Associates)
Best Webcomic: The Tea Dragon Society, by Katie O’Neill, teadragonsociety.com (Oni Press)
Hall of Fame:
Judges’ Choices: Carol Kalish, Jackie Ormes
Voters’ Choices: Charles Addams, Karen Berger, Dave Gibbons, Rumiko Takahashi
Bob Clampett Humanitarian Award: Frederick Joseph; Comics4Kids
Bill Finger Excellence in Comic Book Writing Award: Joye Murchison Kelly; Dorothy Woolfolk
Russ Manning Promising Newcomer Award: Hamish Steele (writer/artist, Pantheon), Pablo Tunica (artist, TMNT Universe)
Will Eisner Spirit of Comics Retailer Award: Norma Comics, Barcelona, Spain
Read the Den of Geek SDCC 2018 Special Edition Magazine Here!
from Books https://ift.tt/2uXUZgO
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