health

NEW Fibro Friday Posts Coming!

Now that I’m getting back into the habit of posting blogs, I’m excited to announced that there is NEW Fibro Friday content coming!

I’ve been researching herbs, developing new pain relief oils, trying different therapeutic practices, tinkering with my diet, and giving myself lots of time to figure out what works, and what doesn’t. I can’t wait to tell you all about the discoveries I’ve made over the past year(ish)!

Stay tuned, and thanks for reading!

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Fibro Friday – 5 Red Flags Your Doctor Might Miss

Happy Fibro Friday! I hope you all are doing well and are taking excellent care of yourselves.

I recently started looking back at my health history (thanks to my insurance for the decades-long record). I sometimes will look to see if anything is outdated, or if a diagnosis was slipped in unbeknownst to me. This most recent review didn’t turn up any unknown or outdated information, but I began thinking about my medical experiences and I asked myself, “Is there anything here that could have pointed to me being prone to developing fibromyalgia?” What I found surprised me: I had been diagnosed with multiple conditions over the years, all of which has shown some connection (some weak, some significant) to fibromyalgia. So, for this post, I’m going to tell you what conditions are fibro flags that you or your doctor may have missed on your road to diagnosis and treatment.

Before going further into this discussion, you may want to check out this journal article, titled, “The Prevalence of Fibromyalgia in Other Chronic Pain Conditions“. The researcher, Muhammad Yunus, outlines many of the conditions which have some determined link to fibromyalgia, and Yunus admits that the associations are bidirectional and the interrelationships haven’t been explored fully yet. I highly recommend that you take your time and go through this article as you try to determine if there is any overlap between fibromyalgia and any other conditions you may have.

Flag # 1: History of asthma – A 2020 study of Iraqi fibromyalgia patients confirmed that, “Fibromyalgia (FM) was more common in asthmatic patients compared with controls.” Perhaps it’s the fact that breathing difficulties would (naturally) trigger stress responses in the body, and those repeated stress responses condition the brain to interpret most stimuli to be more urgent than it actually is. Maybe being asthmatic trains the brain to be hyper-sensitive to everything. More study is needed to determine what this means for fibro patients, but it’s certainly something to keep in mind when coming up with a body of “clues” leading to a fibromyalgia diagnosis.

Flag # 2: TMJ syndrome – For several years now, it has been established that TMJ and fibromyalgia are linked, though the nature of the connection is still a bit unclear (a chicken vs. egg argument would fit in this scenario). This article by VeryWell Health references some excellent research on the topic. To put it plainly, it seems that TMJ actually may lay the groundwork for the sensitivity experienced in people that have chronic pain issues. As author Adrienne Dellwo states, “When TMJ occurs before CFS or FMS, it’s possible that TMJ pain contributes to the development of central sensitization. Hypersensitivity of the central nervous system is believed to be a key component of both fibromyalgia and chronic fatigue (also known as myalgic encephalomyelitis).” Again, this area still needs additional research, but there’s no doubting that a connection exists between the two.

Flag # 3: Epstein Barr Virus (Mono) or Lyme disease – Like the two previous red flags, we have to keep in mind that correlation =/= causation. That being said, there is research starting as early as 1987, which indicates that 55% of the test subjects self identified that a viral infection was the cause of their fibromyalgia. Personally, I was infected with mononucleosis in my 20s, and my fibromyalgia symptoms began and sustained after that point, often appearing as a chronic case of influenza or reactivated mono. More recent research confirms that EBV can either cause or contribute to fibromyalgia symptoms, which makes sense, considering that many of EBV’s symptoms overlap significantly with what many fibromyalgia patients experience (fatigue, body aches, even sore throat!) One article states that EBV “highjacks” the immune system, which may explain why fibromyalgia patients that have been infected with EBV tend to experience more sensitivity to viral infections like colds or the flu, as well as sustained symptoms once infected (I personally got a second positive result for the flu nearly a month after initially getting a positive result!) While I haven’t experienced Lyme disease, there is research from as early as 1992 which states that the bacteria responsible for this condition may be a potential cause of fibromyalgia. If you have either of these conditions in your medical history, please know that these may be contributing to your fibromyalgia symptoms.

Flag # 4 – Anxiety or depression – Anxiety and depression are chronic illnesses on their own, and, unsurprisingly, these are almost always present in fibromyalgia patients, too. This article on News Medical is informative and clearly explains the connections between anxiety, depression and fibro. The article, written by Dr. Anaya Mandal, MD, discussed the concurrence of these conditions, and how these overlaps contribute to exacerbated symptoms. According to Dr. Mandal, anxiety, “may increase the severity of pain perception and thus increase the severity of the disease.” Further, when discussing depression, Dr. Mandal writes, “Several studies have speculated that there may be a common pathophysiology between depression and fibromyalgia.” This should be a surprise to no one that has been diagnosed with anxiety or depression: in fact, one favored fibromyalgia treatment – serotonin and norepinephrine reuptake inhibitors, or SNRIs – are classified as antidepressants, and have had fantastic results when used to treat fibro.

Flag # 5 – Childhood traumatic experiences (CTE) – There is still a lot of research needed when it comes to this, but most of the research seems to agree that experiencing trauma in childhood can be a risk factor for fibromyalgia later in life. In fact, there is research that indicates that even the attachment style that we experienced from our primary caregivers may have a lot to do with our neurological health in later years. Interestingly, I have a loving, involved mother and a loving but inconsistent father, who divorced when I was 3 years old. My mother later remarried, and my stepfather was also loving, involved and consistent. So while my home life was stable, the inconsistencies that happened with my father had already made an impact. Further, a serious illness (such as asthma that required multiple hospitalizations in my childhood) is a type of trauma that can also create unhealthy attachment styles, which are a risk factor for fibromyalgia. I’m blessed to have grown up without physical, sexual or emotional abuse, and I’m also fortunate to not have been exposed to drugs or other substance abuse while in utero, but if you’ve had these experiences, your risk of developing fibromyalgia are even higher.

This post was a bit longer and “heavier” than my usual Fibro Friday content, but I wanted to cover something substantial, because I know what it’s like to try to “reverse engineer” your diagnosis and still be left with questions. If any of these red flags apply to you, please take heart. And if you’d like to discuss more about your journey and experiences with fibromyalgia, I’d love to hear about it in the comments.

Take care, and have a great weekend!

health · life curation · relaxation · Uncategorized

Fibro Friday – How I Deal With Chronic Headaches

Happy Fibro Friday! The weather is getting warmer each day, and I find myself feeling happier and more energetic. The summer season is HERE!

June is Migraine and Headache Awareness Month. As someone that has dealt with chronic headaches for almost 20 years, I know a little something about a “mal à la tête” (one of the few phrases I managed to retain decades after taking my last French class). However, I was not aware there was a month dedicated to all of us that have to deal with headaches and migraines on a regular basis. I’m fortunate to have never experienced a migraine (though my mother used to have them when I was younger), but I often have tension headaches and other pain patterns.

The weird thing that I’ve noticed about having that chronic headaches is the fact that I almost always have a low level of pain going on. It’s very similar to how fibromyalgia works: pain is a fairly constant companion, but the level of pain is what makes the difference. My headache may be (on a scale of 0 to 10, with 0 being no pain at all and 10 being severe enough to warrant an emergency room visit) either a 2 or an 8, but never 0. The pain is minimal on some days, but never completely gone. I’ve gotten really adept at functioning without pain medication on any day that’s less than a 5. That may sound awful, but when something has become your normal, you almost don’t recognize it. And, in the case of days where my pain level is a 1 or 2, I often feel ecstatic and like I can conquer the world!

A big part of how I manage chronic headaches is that I have an arsenal of things I do BEFORE I choose to use a pain medication. After years of using over-the-counter medication in an attempt to manage neurological and musculoskeletal pain, I became concerned with the long-term effects of these substances. Therefore, I try to avoid them for as long as I can comfortably manage. When I feel a slightly stronger headache, I don’t immediately reach for ibuprofen or acetaminophen anymore. Here’s what I try before I reach for pain

  • Check my hydration levels: I drink some water, because 9 chances out of 10, I’m dehydrated. Starting my day with a large glass of water is a great move that works well when I remember it. I usually keep a large glass of water on my nightstand, so I can sip before I go to bed and finish it in the morning.
  • Use my weighted eye mask: I’ve reviewed my eye mask over here before, and I still love it. There’s something about the counter pressure that really gives me relief. It’s a pretty inexpensive investment (I got mine from Amazon), and I find that laying down for a few minutes with this mask can really help with the pain.
  • Do some jaw and neck stretches: since most of my headaches are tension related, gentle stretching can relieve some of the tightness that contributes to the pain. This may not be particularly helpful if you suffer with migraines, or if your headaches are not tension related. But if you find that you clench your jaw or otherwise hold your face or neck muscles tightly, stretching them gently may help to loosen up those muscles and take off some of the pressure.
  • Pay attention to my triggers and actively avoid them: sometimes seasonal allergies, certain foods, or even particular daily routines can be headache triggers. If I recognize a trigger, I avoid it as much as I can. That can mean avoiding trips outside of the house during the peak pollen or poor air quality days, refraining from bread and other starchy foods, or getting extra sleep so that I don’t have an exhaustion-induced headache.
  • Eat something, and make sure it’s the right food for me: sometimes, the pain comes from eating too late in the day, not eating enough throughout the day, or eating the wrong food. A huge helping of fresh fruits and vegetables tends to give me a little relief. I’m sure it’s because these foods are more easily metabolized by me, but also, fresh fruits and vegetables tend to be very hydrating.

I discuss my practices for dealing with chronic headaches in one of my recent Fibro Friday videos. You can see it below:

Do you have chronic headaches? What have you found that works in helping you to manage them?

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Fibro Friday – National Pain Awareness Month

Happy Fibro Friday! Yesterday kicked off the beginning of National Pain Awareness Month, an observation that I was completely unaware of until a couple of weeks ago. I am using this time to explore the stories shared by other people dealing with chronic pain conditions. I’m also reviewing the resources being shared in various chronic pain spaces.

I’d guessing that most of you are already quite aware of chronic pain: after all, you’re reading a Fibro Friday post! But, if you’re still unsure why a Pain Awareness Month would be needed, I have a few insights that may clarify why this observation is still relevant. For starters, more than 20% of Americans have experienced chronic pain, and it disproportionately affects women, people struggling with poverty and unemployment, and other traditionally disadvantaged groups. Chronic pain is also the #1 reason for doctor’s visits in America, and the pain can severely limit quality of life for those suffering with it. The current chronic pain situation is widespread but poorly understood.

One great resource that I saw is posted on National Today. This post has some great, bite-sized facts about chronic pain, and can be a solid introductory resource for those unfamiliar with chronic pain and its effects (making this an excellent post to share with oblivious friends, family, and even employers). If you’ve had a hard time explaining the effect of your condition to the people in your world – or, if you have struggled with understanding the symptoms that you’re experiencing – this article may be helpful.

I hope that you take some time this month to find out more about the effects of chronic pain, as well as lending support and connecting to those that suffer from chronic pain conditions. I plan on taking some time to learn more as well as lending my voice to the discussions surrounding chronic pain.

That’s it for this week. Take care, and I’ll talk to you all soon!

health · international · life curation · travel

Fibro Friday – Travel-Sized Flare Kits

Happy Fibro Friday, friends! We made it through another week, and I’m excited that I get to share with you some tips that served me well when I traveled several weeks ago.

Because I was traveling for a few weeks out of the country, I had to be mindful that my normal conveniences *may* not be available. The reality of traveling anywhere is that, if you have chronic illness, it’s imperative to have things you need, in case your symptoms flare up.

I was fortunate that I didn’t have any flares while traveling (yay!) though I did feel ill upon returning to the States. To my credit, I prepared well and that probably created enough energetic “relief” that I was avoid a flare due to stress. Part of my preparation included packing a travel-sized flare kit.

I mentioned my self-care kit a while ago, and I added things to the kit to make it suitable for treating my emotional as well as my physical health. I took an abbreviated version of this kit with me on the road. The contents of my travel kit were as follows:

  • ginger mints and ginger tea
  • journal and pen
  • resistance band and stress ball
  • pain relievers
  • dream water
  • room spray
  • aromatherapeutic oil

I discuss the kit a bit more in this video:

Have you ever prepared a mini flare kit when traveling? What items do you recommend that I add? I’d love to hear your thoughts below!

health

Fibro Friday – Addressing My Wrist Pain

It’s been a while since I’ve done a Fibro Friday post, though I’ve been posting fibro videos over on my YouTube. Last month, I started physical therapy for my wrist pain that I’ve suffered from since 2018(!). I recall when I first had pain in my wrist, which was so intense that I went to the emergency room. The pain made it impossible to write more than a page in my journal at a time. Being unable to write with the same fervor that I used to was a heartbreaking experience and, while I wanted to get relief for the pain, I had far more pressing issues to address (like my other fibro issues). So I shelved the wrist treatment until recently.

So I started physical therapy. I posted this video on June 10th, and I’ve done some therapy sessions after filming this video. In fact, I’ve completed my series of sessions, and now I get to do the work on my own to continue rehabilitating my wrist. So I’ve seen even more progress since I filmed originally. Here’s the video discussing my physical therapy:

Now that I’ve completed physical therapy, I have a much better understanding of what my wrist needs to be its healthiest and strongest. I need exercises that both relieve stress as well as strengthen the muscles. The strengthening is the key point for me: the pain kept me from moving my wrist in a normal way, and due to this, I lost a lot of my original strength. Restoring my wrist strength is crucial to my healing journey. That, along with exercises to help with the flexibility and grip function, will help me to get back to my former glory.

I’m looking forward to giving you all updates in the months to come, as I progress in my healing journey. I’m excited to see how things go!

Anyhoo, that’s it for today. I hope you all have a great weekend. Talk to you all soon!

Uncategorized

Fibro Friday – Make A Fuss For Your Health

Happy Fibro Friday! I hope you all are doing well! I apologize for the premature postings this week: I’ve been concentrating on Vlog-A-Day-In-May and hadn’t gotten a chance to do much writing over here. Rest assured, the prematurely posted blog will be fleshed out and reposted soon.

Today, I’m sharing a vlog that I posted several weeks ago. In this video, I discussed why it’s important to “speak up” when it comes to your health, especially those that are dealing with fibromyalgia. So many times, our voices are silenced because many medical professionals misunderstand or minimize our experiences. Also, when you suffer from chronic pain, it can be difficult to accurately relay your experiences to medical professionals, which makes it challenging to get diagnoses and treatments.

However, we should always continue to “make a fuss”, sharing how we feel with our care providers and the specialists that we work with. We must persist until our concerns are heard, and we get the treatment that we need.

health

Fibro Fridays – My FluRona Experience

Happy Fibro Friday! A few weeks ago, I published two videos over on my YouTube channel, discussing how I had both flu and COVID simultaneously, and all of the shenanigans involved with that experience. I figured I’d share the videos over here, because you all may have missed my story.

So, let me tell you all how it started. I fell ill right after New Year’s Day, and it took several days for me to get tested (there was a huge demand for COVID testing post-holidays), and I couldn’t get examined for nearly a week after I first started showing symptoms. When I was finally able to get tested, it was confirmed that yes, I had COVID, but I also had the flu (yay me). More about that story, as well as my symptoms are in the video below.

A couple of weeks later, I went back to the doctor’s office to make sure that I was not contagious. I received a rapid test and a flu test, which confirmed that I was no longer sick with COVID, BUT I was still showing as positive for the flu. I was so confused: I should have been done with both viruses at this point. But, the fact that I was still showing as flu-positive opened the door to considering some additional things that were specific to fibromyalgia. Here’s the video discussing that, and I have a few takeaways that I’m going to mentioned after the break.

Here’s the thing: having any chronic health condition means that all of our internal systems are compromised, even on a minute level. But, as we all know, small leaks sink ships. Little “glitches” in our bodies, such as being in a slightly immunocompromised state, often mean that we get unusual results when we’re sick. Unusual outcomes include extended illness, unexpected side effects/symptoms, and biological/physiological damage that cannot be reasonably explained. Sadly, a lack of compassion when sharing our experiences with others is also something that we have to face when we’re recovering from sickness.

So, that’s the sum of my FluRona experience. I’m glad that I’m *finally* over it and feeling great. And I’m really happy that I get to share my experiences and, hopefully, give a little insight to someone else.

That’s it for today: I hope you all are doing great! Have a great weekend.

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Fibro Fridays – Things I Wish I Knew (After Diagnosis)

I’m taking a little break from protocols (again) to talk about some other things I discovered on my fibromyalgia journey.

Did you all know that getting a diagnosis is just the beginning of the journey? Fibromyalgia is unique in the fact that diagnosis doesn’t automatically result in a clear-cut recovery path. Most of us that have been diagnosed find that there are many things that we still don’t understand about the condition, and most medical professionals are woefully under-exposed/unknowledgeable about fibro. So even after getting a diagnosis, there are a ton of things that we don’t know, and we have to search just to get close to having some answers.

I made a video of the top five things I wish I knew after my fibromyalgia diagnosis. To sum it up briefly, I wish I knew that:

  • Most medicines are largely ineffective.
  • Lifestyle is the key to managing symptoms.
  • This is a problem within the nervous system, not the musculoskeletal system.
  • It may be more beneficial to work with a neurologist than a rheumatologist.
  • Working with a psychologist as soon as you’re diagnosed can be tremendously helpful.

Here’s the video, where I explain these points more in depth:

Is there anything you all wish you knew when you were first diagnosed with fibro? I’d love to hear about it in the comments below!

Have a great weekend, and I’ll talk to you all next week!

health

Fibro Friday – The Lyon Protocol

Happy Friday, friends! We’re back to protocols, after taking a break for the past few Fibro Fridays. As with the other protocol reviews, I’ll be pointing out the philosophy of the healthcare professional/coach/holistic health practitioner, highlights of the protocol, and my thoughts about the protocol.

This week I’m diving into the work of Irene Lyon. Lyon is a nervous system expert that uses somatic neuroplasticity principles to help her clients “rewire” their brains to eliminate the effects of various types of trauma. She has a website with free resources to help people attempting to get to the root of their pain disorders. Also, she has a YouTube channel where she goes into depth with discussing healing principles and techniques. Lyon has degrees in exercise science and biomedical science, as well as 20+ years of practice related to healing the body through somatic experiencing, or how to correct nervous system dysregulation in order to resolve physical and psychological illnesses.

Because Lyon’s work is designed to treat a multitude of illnesses, she doesn’t have a specific protocol for fibromyalgia. However, she has a video where she shares how one of her viewers was able to utilize resources available through Lyon’s website, as well as her video library, to start and progress on her healing journey.

Some of the healing principles promoted by Lyon are as follows:

  • Healthy emotional expression is central to healing physical pain.
  • Understanding the sympathetic and parasympathetic nervous systems and responses are crucial to managing pain.
  • Physical pain is almost invariably rooted in trauma.
  • It’s possible to rewire the brain in order to train it to have a more regulated response to stressors.

I think there are a lot of solid points to Lyon’s protocol, though I feel it would work best when combined with another treatment plan. For anyone that has tried the more traditional healing protocols (with minimal success), this may be a great option to explore.

Are any of you familiar with Irene Lyon’s work? I’d love to hear about it in the comments below! Have a great weekend, and I’ll talk to you all soon.