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April 26, 2017

Rising Above Lyme | New Collaboration Line at Katya Valera

It's been a while since I've had big news to share about Katya Valera, and now for the first time, I have a collaboration to announce!

My dear fellow Lymie friend Kami Lingren of Living Grace created the phrase "Rising Above Lyme" last year and offered it on tshirts. Being the unpredictable creative that I am, the idea of making Rising Above Lyme jewelry lightning-striked through my brain one day, and I characteristically jumped right in and contacted her with my idea. She, thankfully, loved the idea, and thus began a good couple months of planning and work!

I ended up coming up with four necklace designs, each with their own customization options (expounded on below) and each also coming with an explanation of the RAL phrase, making them equally perfect to purchase for yourself or give as a gift.



Kami created the Rising Above Lyme phrase to inspire others on their own healing journey that their story doesn't have to center around a diagnosis.

"Rising Above" happens from our couches, our homes, and our interactions with others in that we simply say, "I will breathe in this moment. I will face another day. I will cherish this laughter, soak in that sunset, embrace another healing heart." For it's together, with linked arms, that we RISE.


Let's get to know each design!

https://www.etsy.com/listing/525955947/rising-above-lyme-necklace-lyme-disease?ref=shop_home_active_4

The large frame necklace has three pattern options (the middle is my favorite because it's juicy ... like a lime ... and while I do not love Lyme, I do love lime, so...). Kami designed each of them!

https://www.etsy.com/listing/525955947/rising-above-lyme-necklace-lyme-disease?ref=shop_home_active_4

You have your choice of either a silver or bronze frame on chain or a soft green cord. Plus, you can choose the length, so you're covered whether you prefer short or long necklaces.

https://www.etsy.com/listing/525955947/rising-above-lyme-necklace-lyme-disease?ref=shop_home_active_4

There's also a teeny-tiny version!

https://www.etsy.com/listing/526132917/lyme-disease-necklace-rising-above-lyme?ref=shop_home_active_3

The options are the same for this one, and it is offered at either 16" or 18". Of course if you'd prefer a different length, I can happily accommodate that on request.

https://www.etsy.com/listing/526132917/lyme-disease-necklace-rising-above-lyme?ref=shop_home_active_3

https://www.etsy.com/listing/526132917/lyme-disease-necklace-rising-above-lyme?ref=shop_home_active_3

While the first two necklaces are more obvious designs, this necklace is a symbolic take on the phrase, which makes it extra suited for those who wish to show support for a loved one living with Lyme with a more understated style.

https://www.etsy.com/listing/512325752/lyme-disease-support-awareness-necklace?ref=shop_home_active_1

The necklace features a sterling bar atop a frosted lime green glass bead, and they hang from your choice of silver plated or sterling silver chain at the length that you choose.

https://www.etsy.com/listing/512325752/lyme-disease-support-awareness-necklace?ref=shop_home_active_1

And here's what it looks like on a real, live person ... that happens to be Kami herself! :)

http://livinggraceshop.bigcartel.com/product/rising-above-lyme-unisex-jersey-shirt

The fourth style is also very understated and elegant, making it extra versatile.

https://www.etsy.com/listing/512324210/lyme-disease-necklace-minimalist-silver?ref=shop_home_active_2

A vintage, lime wedge-style pendant is set in a silver frame that hangs from your choice of silver plated or sterling silver chain at the length that you choose. So dainty!

https://www.etsy.com/listing/512324210/lyme-disease-necklace-minimalist-silver?ref=shop_home_active_2

You can see all of the necklaces in my shop right here. Any of these necklaces would make a wonderful gift for anyone you know living with Lyme, made by two people who really get it. While Kami and I are both continuing to heal from Lyme, we will always remember the struggles of our hardest days and wish to help those who are similarly suffering.

To top off the excitement of this release, Kami and I are hosting an Instagram giveaway of the bar necklace and the winner's choice of a shirt from her brand new Living Grace shop! Be sure to check out her shop here for some awesome Rising Above Lyme shirts and tanks (plus another new design!), and be sure to enter the giveaway before it ends Friday night! 💚

March 27, 2017

When Christians Fail Us


I have gathered over the past few years that many of us have been disappointed or hurt by Christians. Those of us dealing with chronic illness or any other long-term trial have probably especially encountered some hypocritical actions or words on a Christian’s part when we needed help and love the most. And whether those actions have hurt you, hurt your view of just those people, hurt your view of all proclaiming Christians, or built a wall between you and God altogether, I feel the need to point out that if you too have been hurt by proclaiming Christians, the hurt they have caused you—well-intentioned or not—is a reflection of them and not a reflection of the God that Christians love and serve. Their mistakes are all on them, not on God. 

We tend to expect more of Christians, don't we? I sure do. And we should. 

But humans are still humans even when they are followers of God. 


The difference is the hope that we have and the guidance that we have to do better—and it is up to us to listen to that guidance. But Christians will still fail you and still mess up because that is human nature, something we do not suddenly become totally resistant to when we accept Christ. We know better, and we should do much better, but we will still sadly fail. And while that does not excuse any hurt that has been caused by such failure, it is still the truth. 

So please know: I will fail you; the Christians in your life will fail you, just as anyone in your life will fail you at some point.

But my God will not and cannot fail you. He truly is perfect. His ways are higher than anything that earth’s greatest, deepest minds can begin to process. And He is the reason I have hope.

He is my hope.



He is the reason anyone can have true hope: hope that waits all night while we sleep and meets us when we wake up. Hope that holds our hand through every excruciating moment of chronic illness. Hope that cannot die, no matter the unimaginable pain and sorrow that life can and will bring. Hope that carries us all the way into eternity, to a heaven we cannot imagine where we will finally see our Hope face to face.

I have been hurt, yes, by many Christians. I have wrestled with faith in the face of 6+ years of chronic illness, clinging only to the truths I cannot forget from a lifetime of Christianity. And hope has followed me, waited for me, and burst into glowing brilliance when I finally looked its way. It has not failed me. God has not failed me. 

And He never will.


~~~~~

If this kind of hope blows your mind and you have any questions at all, please feel more than welcome to comment or message me.

February 26, 2017

My Alternative Journey to Health

In response to this post of mine being shared on another site recently, many people have wanted to know more specifically what I am doing in my alternative, holistic quest for health. So if that post led you here, welcome! :) I will now endeavor to answer those questions, and if I miss anything, please feel free to comment or contact me. (I do ask that you please read this whole post carefully before commenting.)

HOW IT ALL BEGAN | I had mild health issues and symptoms throughout my childhood and teenage years (they were regarded then only as quirks). In 2010, my body crashed and I began living with debilitating eye pain, headaches, all-over body pain, constant exhaustion, memory problems, IBS, extreme sensitivities to being poked or pushed against, and a plethora of other symptoms, turning my world entirely upside down. (I finally wrote down all the symptoms I could think of a while back, and there were about 75.) In 2011, after testing including an MRI to rule out other possibilities such as arthritis and a brain tumor, I was diagnosed with Fibromyalgia (and a bit later unofficially with Chronic Fatigue Syndrome). 

I then embarked on the traditional route of antidepressants, muscle relaxants, and other prescriptions to attempt to ease the symptoms. Only one helped briefly, and based on what I know about those drugs now, I regret taking them. By 2013, I chose to go off all prescriptions, as they, at best, were not helping. I also eventually chose to quit taking over-the-counter medicines, including pain medication.

HOW I STARTED ALTERNATIVE TREATMENT | In 2013, a friend of a friend suggested an alternative holistic doctor in the area and passed along a DVD that covered this doctor's view and treatment of Fibromyalgia. It was all brand new, mind-blowing, belief-shattering information to me, but I skeptically gave it a chance. During my treatment with this doctor, my most notable improvements were losing about 25 pounds (that I really needed to lose) through addressing my diet needs and a brand new sense of hope I didn't know existed for people like me. After being treated there for about a year, my husband and I happened to move to another state and so started seeing another alternative, holistic doctor that my previous doctor recommended. That is when things really started to get good.

MY ACTUAL DIAGNOSES | This new doctor of mine ran a large number of incredibly in-depth tests to check for everything under the sun: Lupus, Lyme Disease, Epstein-Barr Virus, arthritis, metal poisoning, Celiac Disease, food allergies, gene mutations, hormone imbalances, and a multitude of other imbalances, infections, parasites, viruses, and more. While testing revealed literally a dozen or more problems, among my biggest issues were Lyme Disease (the co-infections Babesia and Bartonella), mercury poisoning, and the unresolved chicken pox virus from when I was five years old, along with gene mutations that inhibit my body from detoxing properly on its own. You can read about a few more of my diagnoses here.

HOW I'M BEING TREATED | My treatment has been made up of three main things: 1) Field Control Therapy, a cutting edge treatment that periodically determines what pernicious agents are affecting your body the most and addresses them by strengthening your body to rid them on its own. 2) Supplements that continually change based on my body's changing needs. 3) Diet changes tailored to my body's needs. I also see a chiropractor for adjustments every so many months. Most alternative doctors either are also chiropractors or have a chiropractor in their office that can do this; I just go to a separate one for these specific needs because it is closer to home. I am currently considering adding another layer of alternative treatment and will definitely write about it if I do and find it to be helpful.

LIFESTYLE CHANGES I'VE MADE | In addition to the treatments listed above, I have made several changes myself that have proven to be hugely beneficial:

1) Removing toxic products from my life and replacing them with non-toxic alternatives. There is a ton of information to be found online about what all ingredients we need to avoid and why. But the bottom line is that all mainstream products (yes, probably the ones you've been using your whole life as I had; think Maybelline makeup, Clorox wipes, Tide detergent, etc.) contain chemicals that we absolutely should not be putting on our bodies--what we put on our bodies is absorbed and just as important as what we eat. You can see some examples of what I do not eat below, as removing toxic foods and ingredients is also vital.

2) Detoxing. In this day and age our bodies are bombarded with harmful, sickness and cancer-causing toxins, from makeup ingredients to food additives to cigarette smoke to EMFs. And while some of us have the MTHFR gene mutation (like I do) that inhibits our body's natural ability to help detox these things, we could all use some help in this department because of the sheer, unprecedented amount of toxins we are being exposed to. A while back I realized that the pain I once would have called "Fibro pain" is frequently actually the build-up of toxins and is eased by detoxing. There are a few suggestions for detoxing practices here and here that I have found very helpful on this journey. I would add to that list oil pulling, which I wrote about here; it alone immensely improved my migraines. (You can browse some of my favorite detox tools here.)

WHAT I DON'T EAT | I do not eat gluten (wheat barley and rye), grains (corn, quinoa, and oats), dairy, soy, nightshades, refined sugar and artificial sweeteners (which means I do not drink pop), table salt, yeast, vegetable oils, and a few fruits and vegetables that I have shown allergies to. While the right diet for each person will vary and is best determined with thorough testing, anyone with autoimmune conditions especially should avoid gluten, grains, dairy, soy, nightshades, refined and artificial sugar, and table salt. I do not eat your typical processed foods and eat organic whenever I can, a change that would behoove anyone, chronic illness or not. The additives and chemicals in today's popular food is absolutely unbelievable. (You can browse some of my favorite foods I've found here.)

HOW I AM NOW | Any journey to health is going to be, as my first holistic doctor put it, a marathon and not a sprint. Anyone with as many issues as those of us diagnosed with Fibromyalgia are going to take a lot of time to heal, especially if you have been sick for many years as I have. (I'm pretty sure I was infected with Lyme Disease about 17 years ago.) There is most definitely hope of being "all better" or at least vastly improved, but that is not going to happen overnight or even in just a year--for anyone. As with any chronic illness, there is not a quick fix.

While I am still in this journey to healing, I am the best I have been since I got sick in 2010, and I even have the bloodwork to prove it. This past year, each of my sets of bloodwork came back better and better, a concept I was definitely not familiar with! I know I still have a ways to go, but I accept that because I know this journey of alternative treatment is worth it, not only for improving my health but also for opening my eyes to the truth about health, medications, toxins, diet, and more.

MY TRANSFORMED VIEW OF FIBROMYALGIA AND CFS | Stay with me here and try to understand what I'm saying with an open mind: I firmly believe that diagnoses like Fibromyalgia and Chronic Fatigue Syndrome only describe the symptoms one is experiencing and are not legitimate as end-all diagnoses. I too was once relieved when I was given that diagnosis. And then I learned the truth. The suffering of those of us given these labels is painfully, excruciatingly real--but such a diagnosis is a cop-out. "Fibromyalgia" literally means "muscle pain." Chronic Fatigue is just that: chronic fatigue. Those are symptoms. Do you believe that symptoms, like headaches, extreme pain, exhaustion, memory loss, etc., all just happen on their own, with no cause?

When you see someone with a broken leg, do you assume that their leg just broke on its own? Spontaneously, with no cause but only the diagnosis of "broken leg syndrome" because sometimes that just happens? Or even that the leg is just not working for some inexplicable reason that cannot possibly be determined because sometimes that "just happens"? Of course not! Something had to cause that leg to break--a force of some kind had to come in contact with the body, and the evidence of that occurrence is a broken bone, manifested in pain and the inability to walk.

Similarly, nothing that happens in your body "just happens." There is a cause--or more often a combination of causes, whether infections, viruses, gene mutations, trauma, toxins, parasites, inflammation, and more--manifesting itself  in any and all symptoms you are experiencing. Further, any symptom you experience is your body's way of trying to tell you that something is wrong. It's not your body cruelly deciding to mutiny and ruin your life--every pain, every memory slip, every trembling limb, every moment of panic is your body begging you to help it in the only way it can: by getting your attention.

I grew up being told that anything odd my body did was "just because," even that my symptoms summed up with "Fibromyalgia" happened "just because." I believed that for a long time. And that belief came to a screeching halt when my eyes were opened to the truth through my experience with alternative treatments. I have come to truly believe that "Fibromyalgia" is just a label that mainstream doctors give to people with more problems than they can or want to attempt to help. The average doctor doesn't want to run a ton of time-consuming tests (and often isn't even equipped to), see the same patient frequently for six months or a year or two, work with them, analyze every single part of their body system, determine exactly what dysfunctions are occurring, and treat them all individually, patiently, and thoroughly, no matter how long it takes, without a single prescription. The average doctor wants to prescribe you something to make you "feel better"--just enough to get you through--and send you on your way. I don't want to just "get through." I want to thrive. And mainstream medicine does not offer you that option.

Mine was not a "classic misdiagnosis" because I finally found I had other things resulting in my symptoms; mine was a classic diagnosis. It was determined that I have Fibromyalgia because it hurt in a certain number of places the doctor pushed on and because I tested negative for everything else that they decided to test for. That is a classic Fibromyalgia diagnosis. They didn't make a mistake in giving me that diagnosis; rather, their whole belief system that results in that diagnosis is flawed.

Please keep in mind, I am in no way saying that everyone who has been diagnosed with Fibromyalgia or CFS has the same exact problems I was found to have. But I am saying that I firmly believe everyone who has been diagnosed with Fibromyalgia or CFS has their own unique combination of actual structural and/or neurological and/or metabolic problems that are all teaming up to absolutely ruin their health, and that every one of those root causes is at least treatable or even healable at the source.

Now, if you find all of this insulting to those of us thousands of people diagnosed with Fibromyalgia, I ask that you please go back and reread this and try to see what I am actually saying. I am writing all of this (and all of my other posts on this topic) because I have been where you are. I have reached the end of my rope over and over and sobbed over my body's state more times than I can count. I have earned a college degree only to get sick a few months later and be unable to go get a "real job." I have had my life turned upside down. I have assumed there was nothing that could be done. And then I found out all of the above information and my life completely changed. I went from no hope at all to all the hope in the world simply because I opened my mind and became informed with the truth. None of this is being written to bash anyone who is suffering--it is written to help. I am pouring my heart out, gritting my teeth, and getting through this post not because it's fun or because I think it will be well-received but because I know there are people out there just like me who need it. Surely one or two of you will see the hope in this post and be compelled to become your own advocate and fight for answers and health as I was, and you are why I am writing. I only wish I had learned all of this years ago, and so I am writing for you what I needed to know but did not have access to.

A FEW TIPS | Things to keep in mind:

1) If you're considering going off any medications, please do not do so cold turkey; make sure to check with your doctor first and, if you do, ease off very gradually.

2) If all of the above sounds so promising but you have no idea where to start, the first step is to find a doctor near you. Just search Google for "holistic doctors," "alternative doctors," or "functional medicine doctors" in your area and see what you find. Read their website to see what they say they treat and how they treat it. Ask around and see if someone you know knows one they would recommend, or even if they know someone who would recommend someone (that's how I got started!). Once you find your doctor, he/she will be able to order tests tailored to your needs and walk you through every issue found, one issue at a a time. I highly recommend trying to find one that does Field Control Therapy.

In the meantime, I recommend trying a couple of the lifestyle changes I've made and listed above that can naturally help with many symptoms. But keep in mind, it is all about baby steps--start small, and all your steps will inevitably add up to something great. I know it all can seem overwhelming and even scary, but I want to encourage you that it only seems scary because it's unfamiliar territory, and once you get going on this journey, things will become clearer and more understandable. 

And please know: you are never too old or too many years into sickness to try alternative treatments. There is always hope for improvement!

3) If all of the above sounds absolutely impossible or ridiculous to you, please know that I am just one in thousands being helped by alternative, holistic treatment--and I do not mean just symptoms being soothed but actual causes improving on paper in test results and in day-to-day life.

4) If all of the above sounds like way too much trouble to you, then that is your call and I'm sorry you see it that way. You have to acknowledge the true value of health in order to truly aim for and commit to it. If you want to improve, you have to really want it, more than you want familiarity or even some of your favorite foods. You can be skeptical, as I was, but you must be open-minded and dedicated.

5) No, unfortunately insurance does not generally cover alternative treatments and testing, though it does often cover some. The reason for that is a whole other story.... I know most of us dealing with chronic illness don't exactly have scads of money lying around, and I have said "yes" to things but had to say "no" to others. But each of us needs to weigh the options offered by our alternative doctors and see what we can make happen and what we can't. You do the best you can and will make work what you really want to work.

MY HOPE FOR YOU | As I said before, I know this post will not be well-received by many. A few years ago I would have probably scoffed at it and maybe even laughed. But I'm offering you hope, and if you want to scoff and laugh at hope ... I really can't help you there. You have to reach that point where desperation meets open-mindedness on your own, in your own time.

My hope is that someone reading this has their eyes opened, that the clouds begin to part a bit and you catch a glimpse of the hope that lies in the truth and in the alternative, holistic world. If you are in misery and feel like you are stuck in a life-sentence of Fibromyalgia, CFS, or any chronic diagnosis, you do not have to stay that way. I know this is some mind-blowing stuff, but once you begin to wrap your mind around this temporarily unfamiliar world of alternative treatments, you'll see it's mind-blowing in the best way.

I'm not going to lie and say this is an easy road. Any journey to health is going to hold a multitude of ups and downs. But what worth doing is ever easy? I hope you can see that your health is worth it.

Would you like to hear more about anything in this post? Still have questions? Please feel free to comment below or contact me
You can also check out some of my favorite foods and tools I've found on this journey here.

-----


 Nothing on this blog is to be construed as medical advice,
as I am not a doctor or health professional. I am only 
 a woman with powerful personal experiences to share 
 and am not responsible for any adverse affects from 
 incorporating my suggestions.  No claims about promising
 treatments or approaches are to be taken as guarantees
of improvement or cures. Please do not make any 
drastic changes without consulting a doctor.  

January 5, 2017

Six Years


I look back, and my heart cries over that twenty-three-year-old woman crying on the couch, drowning in the fuzzy, answerless diagnosis of Fibromyalgia and the helpless helplessness of a life doomed to pain, exhaustion, and misery. 

"Fibromyalgia" literally means "muscle pain." That's just a symptom. Chronic Fatigue Syndrome--that's just a symptom. How on earth did I not know that those diagnoses essentially meant nothing, that there had to be infections and viruses and toxins in my body manifesting in my multitudes of symptoms? How did I not know what is no-brainer knowledge to me now? 

Because that kind of thing is a secret. 


That's not how good little people think. We have all grown up in a society that has conditioned us to playing the role of the helpless victim when we need to be taught to play the role of the ruthless advocate, the capable hero in a battle we have every reason and advantage to win. It's just that those we have so dangerously come to trust the most won't tell us how.

That woman who had no idea her diagnoses were just names of symptoms, that she was sick for a reason, that there was healing in her future cried a lot. She lost years to a bogus diagnosis and trying all the ways to help that everyone said to try. And then she found out what was really wrong with her body and learned in the process that thousands and thousands of suffering people are so suffering for many of the same reasons. And that's why that girl who kept crying on the couch back then can't shut up about it all now. Because she learned secrets that flipped her upside-down life rightside-up again and better than it ever was before. And all the other people crying on their couches, drowning in a fog of bogus diagnoses and the helpless helplessness of a life doomed to unending misery need to know:

Healing is yours for the taking if you want it.


I cry over that girl now not so much because she was suffering but more so because she didn't even know she didn't know what was wrong. I thought I had the answer and was simply doing the best I could, the best that anyone could do in such a situation. But I was dead wrong--miraculously, hindsight-is-20/20-gut-wrenchingly wrong.


When I was a teenager, I had this distinct feeling that I would be sick one day. As bizarre as it sounds, you could say I almost saw it coming. But while I had the impression I would be sick in the somewhat distant future, I had no idea at all I would or could later be well one day--and on the way transformed to a completely different person.

Sometimes I have moments of seeing social media posts of mine or hearing my words to others on health and wellness from afar and do a mental double take. Because I distinctly remember Health class back in 2nd/3rd grade and beyond. It was dry, dull, and pointless, made up of food pyramids and admonitions to exercise. (Considering health textbooks are fueled by mainstream views, it's no wonder they didn't exactly light a fire in me to truly care, but I digress.) I had no motivation to care about my health, as most healthy people don't. And well into my twenties, "health" was this abstract, unimportant idea floating in the air, something we all know our whole lives to be important but most of us not really caring to know why. And "eating healthy" held an even less appealing connotation: lots of greens and vegetables with no flavor but filled with deprivation and hunger. If anyone really didn't care about health, it was me.

Funny how you have to lose something to learn what the fuss was about.

If I could change what that girl lying on the couch six years ago is sobbing over, I wouldn't. I wouldn't snap my fingers and make her healthy if I could. Because she would continue to be exactly the same as she was before: floating along in blissful, pill-popping, gluten-filled, sugar-coated ignorance until some other illness caught up with her.

I would not change the what. But I would change the how--I would tell her the truth, the truth that took me years to discover, that I never dreamed existed:

Healing is yours for the taking if you want it. 

 

December 6, 2016

🎉 Katya Valera is FIVE! 🎉


Well, she will be on Friday, December 9th! 🎉


I started Katya Valera on a whim about a year after I got sick, with a name that wasn't even close to Katya Valera, and I can't believe it's been five years.

While I'm still sick (but getting better), Katya Valera is still with me and going stronger than I ever (and, I modestly think, better than ever), and I am so grateful! This little business has been the happiest creative outlet for me while I'm unable to go get a "real job" (though let me tell you, I work, as I put it, "an awful lot for a sick person..."), and I would want to keep it going even if I were healthy.

Of course at this huge milestone, I couldn't go without a massive celebration, so that's what I'm doing! There are FIVE huge events happening all week long in my shop/on Instagram leading up to the big day, and trust me: you don't want to miss any of them!

First up is a giveaway of my most popular piece. I first made this necklace in 2012, and it sold at a jewelry party. I was so bummed it was gone so soon that I decided to make another to list on Etsy, and I've been making and relisting it ever since! 


I more recently added bronze and gold versions to the shop, and you can see them all in the shop right here. And! You can enter to win your choice of the three

https://www.instagram.com/p/BNnfbRqgJdZ/?taken-by=katyavalerajewelry

The giveaway is going on on Instagram and on Facebook, so be sure to enter both places for extra entries! It ends on December 9th--of course--at midnight EST.

The second of the five big events is a special OOAK IG Sale of 11 brand-new, one-of-a-kind pieces not in the shop. They're all posted onInstagram and are priced at at least 15% off! Be sure to take a look, because the sale ends tonight, December 6th, at midnight EST!

https://www.instagram.com/katyavalerajewelry/

And the next event ... I can't tell you about, silly! You'll have to keep an eye out on Instagram and Facebook for it tomorrow! Plus, there's still two more big events after that--so be sure to follow along so you don't miss out on the madness! (Because trust me, what's still coming is definitely some more madness.)
 
And as if this week weren't already special enough, this shop (and my other shop too) is featured in the most special gift guide at MoreThan Lyme

http://www.morethanlyme.org/stories/2016/11/29/the-more-than-lyme-holiday-gift-guide
I was so touched to be included with so many other business-running Lymies, and the intro is the most beautiful, accurate description of what we do that I've ever heard. Be sure to check it out and maybe take advantage of a coupon code you may find in there! 

Thank you so much to everyone who has shopped and followed Katya Valera over the years. I am so thankful she's still going and hope you'll continue to #shopsmall and follow along in the future. Happy celebrating! :)