Where I’ve Been and Future Projects

Hi. It’s been a while since I’ve published regularly. Eight years, to be exact! Time really does fly. This place may have been quiet most of that time, but my life has been anything but. So what happened? Where have I been? Is A Clean Plate a relic of the past? Well, it all starts with…

Burnout

In 2018, I felt like I’d reached a happy stasis with my own autoimmune diseases and was beginning to sense that, after six years of full-time blogging, it was time to leave the AIP behind. I was burnt out on all things food. Keeping up with social media algorithms was frustrating, taking photos felt more like a chore than a passion, and I was running out of recipe ideas I was excited about testing. Blogging had been a survival skill when I was in the thick of my autoimmune diagnoses, but now that I’d healed to the point of being able to regularly leave the house for the first time as an adult, I felt like I needed a break. In fact, I was incredibly depressed. I thought it would help to find something to do that didn’t involve thinking about chronic illness all the time. And how lucky I was to be well enough to entertain that thought!

On top of that, my partner, increasingly disabled by his chronic back pain and multitude of herniated discs, had to leave his physically demanding career. It seemed like everything was pointing to me needing to get a job with more stable income. We wound up leaving Austin and buying a cheap house in a very, very small town where we could make ends meet on the bare minimum until we found something suitable for both of us. But two years later, my partner’s health had declined even further, we were both working odd jobs we didn’t really like, and there weren’t a lot of other prospects locally. My mom suggested we move back to our hometown to help out with her pet-sitting business, which was doing really well. And after ten years away, as much as I didn’t like my hometown, being closer to my family sounded nice.

Caretaking Back Home

Grandma with my cat, Starbuck.

So in 2020, we moved again, bought a moldy condo, fixed it up, and became pet sitters. It was the perfect job for our health issues, both physical and mental. Cute puppies and kitties, a little bit of exercise and time outdoors, and short bursts of work multiple times throughout the day instead of one long 8+ hour slog. And even though business took a hit from Covid, it was a great industry to be in, because we only ever interacted with pets and hardly ever had to be around people. I’d also finally started anti-depressants and was feeling a lot more functional. Plus, our location was convenient to my aging grandma, who increasingly needed help with everyday tasks. The pandemic threw a wrench into her plans to move into assisted living, and after a couple of years driving back and forth every day (and dealing with our horrific neighbors), we decided to just sell the condo and move in with her.

By then, my husband’s health issues had progressed to the point where he could no longer pet sit reliably, either. Since 2018, he’d been diagnosed with an anxiety disorder, panic attacks, depression, sleep apnea, narcolepsy, PTSD, and fatty liver disease on top of his back problems, allergies, and severe ADHD. None of the treatments for any of those were helping and none of the doctors we were able to see knew what else to do with him. Of course, it’s a familiar story to me, but it’s so much harder to watch someone you love go through it than it is to do it yourself, and none of my expertise from treating my own conditions was very helpful for any of his. We agreed he’d stay home with grandma while I went to work. This was our norm until grandma’s dementia became too severe for us to manage safely. After a lot of consideration, she moved into assisted living in late 2023, just in time for…

Three New Diagnoses

I’d started having pain in my left ovary in early 2023. I knew it was a cyst (I’ve had PCOS since my teens) and I kept telling myself it would go away on its own, even though I knew I should get it checked out just to make sure it wasn’t cancer. But between work and trying to take care of my family and home, I didn’t find the time and energy until after grandma moved out. Once I got the ball rolling with my doctors, it took two more months to find out it wasn’t cancer (phew!) and another month after that to schedule surgery to remove it, because the pain had become crippling and it was clear it wasn’t going away.

My surgery was at the end of December, 2023. It was a straightforward laparoscopic cystectomy and I went home the same day. But I came home with a new diagnosis of severe endometriosis. This is jumping ahead a bit, but my first two periods after the laparoscopy were so painful (including severe pain in my ovary, as if the cyst hadn’t been removed at all) I knew I needed immediate intervention. After some arguing with my insurance, I was able to try Orlissa, a relatively new endometriosis drug that lowers estrogen and simulates menopause. Fortunately, it’s worked really well so far, buying me some time before needing surgery again. Which is great, because surgery sucked, and didn’t even help.

After surgery, I started having a lot of stomach problems, including severe upper abdominal bloating as well as intense nausea every time I ate or drank anything. I was diagnosed with chronic gastritis and the PPI inhibitor I was prescribed didn’t help much. I did some trial and error and the only things I could reliably stomach were sugary, carbonated drinks like Sprite and gluten-free crackers or pretzels. Not ideal when you have multiple other health problems that require a specific diet that does not include soda or pretzels. I was absolutely miserable for three months, barely eating or drinking, just waiting for the gastritis to subside. But I got lucky again: the Orlissa seems to have helped with that, too. It’s flared up recently due to a high-stress situation in my life, but other than that, I’m eating pretty much normally again. Yay!

But Then, A Colonoscopy

During the laparoscopy, the surgeon noted one more thing. My colon was stuffed! No surprise; I’ve struggled with constipation my entire life and not even the AIP could fix that. Every doctor that’s ever seen inside my abdomen has told me I’m full of shit. But a month later, still hurting from surgery, I was doing colonoscopy prep for the first time since my Celiac test in 2010. It was even more unpleasant than I remembered and I was glad when the whole thing was over.

But my colon, not to be outdone, was full of sessile serrated polyps, a type of precancerous polyp that is very difficult to see and grows quickly. I was diagnosed with SPS, serrated polyposis syndrome, which means I’m going to keep having these polyps develop and nobody really knows why. I have to get annual colonoscopies for the rest of my life. I also have to hope every gastroenterologist I see has really good eyes because sessile serrated polyps are extremely easy to miss. SPS comes with an estimated 1 in 4 risk of developing colon cancer at some point and if you already don’t drink or smoke, there’s not much you can do to decrease that risk. I’ve already had two colonoscopies this year, and I’ll be having at least two more to try to remove all the polyps before they become cancerous.

I’ve definitely got some feelings to unpack about this one. I confronted my mortality when I was waiting to find out if my ovarian cyst was cancerous and I was so, so lucky that it wasn’t. Learning I have a chronic colon could-become-cancer problem just a few months later is the worst kind of whiplash. I’m torn between making the most of whatever time I have left by doing everything I ever wanted to accomplish as quickly as possible… and just taking it easy and trying to enjoy each passing moment for what it is, like a Miyazaki character staring at a flower. Everything feels both more meaningful and entirely meaningless and I often wind up sitting, doing nothing, overwhelmed by the choices available to me and the pressure to do something. I have so many unfinished projects, but who will care if I don’t finish them? So many things I’ve put off because I have to work, but if I love my job, is that so bad? And so many fears about what would happen to my partner if I pass before he does. It’s not a fun headspace. With all our issues, it feels like we’re constantly in a holding pattern, waiting for some test results, or a treatment to start, or a follow-up. So much for those brief, shining moments of not thinking about chronic illness.

The Future

Ready for DnD night!

So, where does that leave us? It’s early 2024. I still have hopes and dreams for A Clean Plate. I still have cookbooks I never finished, second editions of my meal plans I never took photos for, and actual hundreds of recipes saved as drafts on the blog, waiting to be formatted for publication. I’d love to get some or all of that out into the world. I’ve toyed with them a few times over the years, but always wind up burned out again, too busy with my job, family, friends, home, and my own health to dedicate the time and energy needed to finish a project. Occasionally, like last week, I’ll throw a recipe onto the site that was pretty much ready to go anyway.

After everything I’ve been through since my surgery, and with my 7-days-a-week sitting business, I don’t see that changing any time soon. I’m just so busy and when I’m not busy, I’m tired. My health has to become my priority again, as does my husband’s, or there’s no point to anything else. After all, I can’t test recipes if my gastritis is too severe to actually eat those recipes. And I can’t finish a cookbook, or a novel, or travel to see far-flung friends and family if I’m in too much pain to work or too poor from being out of work to afford groceries or my medical bills or whatever else I need. Unavoidably, life gets smaller when you’re chronically ill. It doesn’t have to; that’s just the way our culture has decided to do things. If you’re here, you probably already know that. You’ve probably been through similar things, or harder things, or know someone who has.

All that to say, I don’t know what the future holds. I hope I find some semblance of health again and I hope my husband does, too. I hope we have many, many, many happy years in our future, regardless of how we spend them. I hope I get to create something I’m proud of again, whether that’s here or somewhere else. And I hope that even if I don’t, the recipes and meal plans I’ve already put out continue to help people feel better, find hope, and appreciate that they’re not alone in all this. Most of all, I want to thank you for joining me, however long you’ve been here. I hope you all also have many, many, many happy moments until we meet again—whenever and wherever that may be!

8 Comments

  1. So that is where you’ve been…..I’ve followed you for many years and was wondering what had happened in your life. Thank you for sharing. Please check out SarahKleinerWellness.com…her IG account and YouTube videos…..her journey that led her to start incorporating Quantum Biology principles into her life. She has amazing guests and shares amazing healing information. The body was created to heal. Praying you and your husband find your way to being fully well.

  2. My heart goes out to you! I’m sorry you and your husband are suffering so much. May you find many blessings and joy amidst the pain! 🙏

  3. From this Endo warrior to another, please check out Nancy’s Nook for an endo excision specialist. I had stage from (DIE) deep infiltrating endometriosis. Orlissa helps with pain, but it doesn’t stop the growth and has some long term effects that are pretty severe. You mentioned that you did not have relief for your surgery. They may have used eblation (burned) the endo off which causes more pain when it grows back. Look up Nancy’s Nook! Im so sorry you all been having such a hard time!

    1. Thank you, Becky! We are definitely still trying to figure out the long-term plan, but for now, I’m just happy to be symptom-free on Orlissa. I had mildly uncomfortable periods my whole life, but they reached extreme levels of painful after my laparoscopy! I had a feeling it was because it was growing back and if we’d just left it, I might have been better off. Endo sucks, so I’m so sorry you’ve been through it too!

  4. Wow. That’s a lot. Thank you for your honesty and on all the levels: that AIP doesn’t solve everything, that sometimes we just need to step away, that we can’t do it all, and that challenges can help us to see life more clearly. Reading this helps me and I’m sure others to know that we’re not alone and we’re tasked to do what we can, do our best to enjoy what we can, and not stress about what we can’t do. Thank you, Christina. Holding you and your husband in love.

    1. Thank you, Tess! That’s so sweet. I’m glad something resonated. These kinds of things and feelings can feel so isolating and of course it’s always hard to admit when we need help or need to step back from our commitments. Sending you all my best wishes as well!

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